geneid | 7371 |
---|---|
ensemblid | ENSG00000143179.16 |
hgncid | 12562 |
symbol | UCK2 |
name | uridine-cytidine kinase 2 |
refseq_nuc | NM_012474.5 |
refseq_prot | NP_036606.2 |
ensembl_nuc | ENST00000367879.9 |
ensembl_prot | ENSP00000356853.4 |
mane_status | MANE Select |
chr | chr1 |
start | 165827614 |
end | 165911618 |
strand | + |
ver | v1.2 |
region | chr1:165827614-165911618 |
region5000 | chr1:165822614-165916618 |
regionname0 | UCK2_chr1_165827614_165911618 |
regionname5000 | UCK2_chr1_165822614_165916618 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 261 | 319 | 89 | 62 | 120 | 14 | 34 | 94 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0002 | 0/0 | 261 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 786 | 295 | 88 | 57 | 105 | 13 | 32 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
c0002 | 0/0 | 786 | 24 | 1 | 5 | 15 | 1 | 2 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
c0003 | 0/0 | 786 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4016 | 89 | 6 | 26 | 45 | 4 | 8 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0002 | 0/0 | 4015 | 43 | 11 | 10 | 8 | 4 | 10 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0003 | 0/0 | 4015 | 33 | 0 | 8 | 19 | 1 | 5 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0004 | 0/0 | 4015 | 29 | 16 | 2 | 10 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0005 | 0/0 | 4015 | 22 | 1 | 6 | 12 | 1 | 2 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0006 | 0/0 | 4015 | 22 | 22 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0007 | 0/0 | 4015 | 15 | 2 | 6 | 0 | 2 | 5 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0008 | 0/0 | 4016 | 10 | 0 | 3 | 4 | 0 | 3 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0009 | 0/0 | 4015 | 9 | 9 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0010 | 0/0 | 4015 | 6 | 0 | 0 | 6 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0011 | 0/0 | 4015 | 6 | 0 | 0 | 6 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0012 | 0/0 | 4016 | 4 | 4 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0013 | 0/0 | 4015 | 3 | 3 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0014 | 0/0 | 4015 | 3 | 0 | 0 | 3 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0015 | 0/0 | 4015 | 2 | 0 | 0 | 2 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0016 | 0/0 | 4015 | 2 | 2 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0017 | 0/0 | 4015 | 2 | 2 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0018 | 0/0 | 4016 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0019 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0020 | 0/0 | 4015 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0021 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0022 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0023 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0024 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0025 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0026 | 0/0 | 4016 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0027 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0028 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0029 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0030 | 0/0 | 4015 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0031 | 0/0 | 4015 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0032 | 0/0 | 4015 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0033 | 0/0 | 4016 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0034 | 0/0 | 4015 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0035 | 0/0 | 4016 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0036 | 0/0 | 4015 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
t0037 | 0/0 | 4016 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
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 | 3 | 0 | 3 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 786 | 295 | 88 | 57 | 105 | 13 | 32 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0002 | 0/0 | 786 | 24 | 1 | 5 | 15 | 1 | 2 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0002c0003 | 0/0 | 786 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4801 | 89 | 6 | 26 | 45 | 4 | 8 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0002 | 0/0 | 4800 | 43 | 11 | 10 | 8 | 4 | 10 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0003 | 0/0 | 4800 | 33 | 0 | 8 | 19 | 1 | 5 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0004 | 0/0 | 4800 | 29 | 16 | 2 | 10 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0005 | 0/0 | 4800 | 2 | 0 | 2 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0006 | 0/0 | 4800 | 22 | 22 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0007 | 0/0 | 4800 | 15 | 2 | 6 | 0 | 2 | 5 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0008 | 0/0 | 4801 | 10 | 0 | 3 | 4 | 0 | 3 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0009 | 0/0 | 4800 | 8 | 8 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0010 | 0/0 | 4800 | 6 | 0 | 0 | 6 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0011 | 0/0 | 4800 | 6 | 0 | 0 | 6 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0012 | 0/0 | 4801 | 4 | 4 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0013 | 0/0 | 4800 | 3 | 3 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0014 | 0/0 | 4800 | 3 | 0 | 0 | 3 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0016 | 0/0 | 4800 | 2 | 2 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0017 | 0/0 | 4800 | 2 | 2 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0018 | 0/0 | 4801 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0019 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0021 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0022 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0023 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0024 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0025 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0026 | 0/0 | 4801 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0027 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0028 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0029 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0030 | 0/0 | 4800 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0031 | 0/0 | 4800 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0032 | 0/0 | 4800 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0033 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0035 | 0/0 | 4801 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0036 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0001t0037 | 0/0 | 4801 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0002t0005 | 0/0 | 4800 | 20 | 1 | 4 | 12 | 1 | 2 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0002t0015 | 0/0 | 4800 | 2 | 0 | 0 | 2 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0002t0020 | 0/0 | 4800 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0001c0002t0034 | 0/0 | 4800 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
a0002c0003t0009 | 0/0 | 4800 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | copy fasta | chr1 | 165822614 | 165916618 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0301 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0294 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0023 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0128 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0003g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0266 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0004g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0005g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0005g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0295 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0006g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0020 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0007g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0008g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0008g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0008g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0008g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0008g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0008g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0008g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0008g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0008g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0008g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0009g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0009g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0009g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0009g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0009g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0009g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0009g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0009g0296 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0010g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0010g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0010g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0010g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0010g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0010g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0011g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0011g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0011g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0011g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0011g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0011g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0012g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0012g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0012g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0013g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0013g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0013g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0014g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0014g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0014g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0016g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0016g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0017g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0017g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0018g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0019g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0021g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0022g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0023g0302 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0024g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0025g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0026g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0027g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0028g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0029g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0030g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0031g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0032g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0033g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0035g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0036g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0001t0037g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0005g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0015g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0015g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0020g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0001c0002t0034g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
a0002c0003t0009g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0179 | EUR | GBR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00099 | hp2 | a0001 | c0001 | t0004 | g0266 | EUR | GBR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0180 | EUR | GBR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00140 | hp2 | a0001 | c0001 | t0007 | g0020 | EUR | GBR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00323 | hp1 | a0001 | c0001 | t0007 | g0171 | EUR | FIN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0263 | EUR | FIN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0230 | EAS | CHS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0268 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | CHS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | CHS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0023 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0254 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00738 | hp2 | a0001 | c0001 | t0007 | g0271 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0004 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0003 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01099 | hp1 | a0001 | c0001 | t0007 | g0265 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01106 | hp1 | a0001 | c0002 | t0005 | g0125 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0157 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01175 | hp2 | a0001 | c0002 | t0005 | g0101 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01192 | hp1 | a0001 | c0002 | t0005 | g0269 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01192 | hp2 | a0001 | c0001 | t0008 | g0255 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01243 | hp1 | a0001 | c0001 | t0004 | g0065 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0156 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0246 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01256 | hp1 | a0001 | c0002 | t0005 | g0082 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0273 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0250 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0274 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0038 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01261 | hp2 | a0001 | c0001 | t0007 | g0264 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0173 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01433 | hp2 | a0001 | c0001 | t0007 | g0129 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01496 | hp1 | a0001 | c0001 | t0007 | g0140 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01515 | hp1 | a0001 | c0001 | t0032 | g0259 | EUR | IBS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0272 | EUR | IBS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0161 | EUR | IBS | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0120 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01884 | hp2 | a0001 | c0001 | t0007 | g0064 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01891 | hp1 | a0001 | c0001 | t0006 | g0117 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01891 | hp2 | a0001 | c0001 | t0006 | g0119 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01943 | hp1 | a0001 | c0001 | t0008 | g0153 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0316 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0015 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02040 | hp2 | a0001 | c0002 | t0005 | g0186 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02055 | hp1 | a0001 | c0001 | t0006 | g0295 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0111 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02080 | hp1 | a0001 | c0002 | t0005 | g0099 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0041 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02129 | hp1 | a0001 | c0002 | t0005 | g0228 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02132 | hp1 | a0001 | c0001 | t0002 | g0209 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02132 | hp2 | a0001 | c0001 | t0010 | g0258 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02135 | hp1 | a0001 | c0001 | t0010 | g0247 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02135 | hp2 | a0001 | c0002 | t0005 | g0219 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02145 | hp1 | a0001 | c0001 | t0004 | g0009 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02145 | hp2 | a0001 | c0002 | t0005 | g0303 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02148 | hp2 | a0001 | c0001 | t0002 | g0037 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CDX | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02155 | hp2 | a0001 | c0002 | t0005 | g0307 | EAS | CDX | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02257 | hp1 | a0001 | c0001 | t0023 | g0302 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02257 | hp2 | a0001 | c0001 | t0006 | g0049 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02258 | hp1 | a0001 | c0001 | t0013 | g0317 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02273 | hp1 | a0001 | c0001 | t0008 | g0036 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0034 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0279 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0304 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0314 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02300 | hp1 | a0001 | c0002 | t0034 | g0126 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0224 | AMR | PEL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02451 | hp1 | a0001 | c0001 | t0036 | g0136 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02451 | hp2 | a0001 | c0001 | t0019 | g0079 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02523 | hp1 | a0001 | c0001 | t0008 | g0014 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0061 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02572 | hp2 | a0001 | c0001 | t0022 | g0297 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02602 | hp1 | a0001 | c0002 | t0005 | g0081 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0107 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02615 | hp2 | a0001 | c0001 | t0009 | g0105 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0298 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0163 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0278 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0108 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02723 | hp1 | a0001 | c0001 | t0002 | g0294 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0280 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02735 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02809 | hp1 | a0001 | c0001 | t0029 | g0132 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02809 | hp2 | a0001 | c0001 | t0009 | g0063 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0301 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02886 | hp2 | a0001 | c0001 | t0009 | g0290 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0114 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02896 | hp1 | a0001 | c0001 | t0004 | g0300 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02896 | hp2 | a0001 | c0001 | t0006 | g0283 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0299 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0013 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0062 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02965 | hp1 | a0001 | c0001 | t0009 | g0012 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02965 | hp2 | a0001 | c0001 | t0004 | g0293 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02976 | hp1 | a0001 | c0001 | t0004 | g0112 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02976 | hp2 | a0001 | c0001 | t0017 | g0289 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0115 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03098 | hp1 | a0001 | c0001 | t0002 | g0113 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03098 | hp2 | a0001 | c0001 | t0006 | g0121 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03130 | hp1 | a0001 | c0001 | t0009 | g0276 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03130 | hp2 | a0001 | c0001 | t0012 | g0010 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03139 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03139 | hp2 | a0001 | c0001 | t0009 | g0296 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0094 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03195 | hp2 | a0001 | c0001 | t0016 | g0066 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03209 | hp1 | a0001 | c0001 | t0021 | g0135 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03225 | hp1 | a0001 | c0001 | t0004 | g0118 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03225 | hp2 | a0001 | c0001 | t0004 | g0282 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0042 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03239 | hp2 | a0001 | c0001 | t0007 | g0127 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03453 | hp1 | a0001 | c0001 | t0027 | g0084 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0305 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03486 | hp1 | a0001 | c0001 | t0006 | g0285 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0167 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0240 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03491 | hp1 | a0001 | c0001 | t0008 | g0073 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0085 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0002 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03492 | hp2 | a0001 | c0001 | t0008 | g0072 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03516 | hp1 | a0001 | c0001 | t0017 | g0288 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03516 | hp2 | a0001 | c0001 | t0013 | g0083 | AFR | ESN | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03540 | hp1 | a0001 | c0001 | t0006 | g0110 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03540 | hp2 | a0002 | c0003 | t0009 | g0080 | AFR | GWD | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03579 | hp1 | a0001 | c0001 | t0006 | g0116 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03579 | hp2 | a0001 | c0001 | t0016 | g0286 | AFR | MSL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03654 | hp1 | a0001 | c0001 | t0003 | g0164 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0308 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03704 | hp2 | a0001 | c0001 | t0007 | g0022 | SAS | PJL | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0060 | SAS | BEB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0089 | SAS | BEB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03927 | hp1 | a0001 | c0001 | t0030 | g0051 | SAS | BEB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0019 | SAS | BEB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0096 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0122 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG04199 | hp1 | a0001 | c0002 | t0005 | g0088 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0174 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0074 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0090 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0102 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0044 | SAS | STU | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18522 | hp1 | a0001 | c0001 | t0012 | g0103 | AFR | YRI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18522 | hp2 | a0001 | c0001 | t0006 | g0104 | AFR | YRI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0212 | EAS | CHB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | CHB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18747 | hp1 | a0001 | c0002 | t0020 | g0193 | EAS | CHB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | CHB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0032 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18941 | hp2 | a0001 | c0002 | t0015 | g0226 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18944 | hp2 | a0001 | c0001 | t0011 | g0253 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18945 | hp1 | a0001 | c0001 | t0008 | g0166 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0033 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18946 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18946 | hp2 | a0001 | c0001 | t0008 | g0234 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0059 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18951 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18956 | hp1 | a0001 | c0001 | t0018 | g0197 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18956 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18957 | hp1 | a0001 | c0001 | t0011 | g0225 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18960 | hp1 | a0001 | c0002 | t0005 | g0141 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18964 | hp1 | a0001 | c0001 | t0026 | g0210 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18964 | hp2 | a0001 | c0001 | t0035 | g0199 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18969 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18973 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18979 | hp2 | a0001 | c0001 | t0010 | g0093 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18980 | hp1 | a0001 | c0002 | t0005 | g0029 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18983 | hp1 | a0001 | c0001 | t0004 | g0310 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18983 | hp2 | a0001 | c0002 | t0005 | g0147 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18984 | hp2 | a0001 | c0001 | t0010 | g0261 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18985 | hp2 | a0001 | c0001 | t0003 | g0313 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18992 | hp2 | a0001 | c0001 | t0004 | g0256 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18993 | hp2 | a0001 | c0002 | t0005 | g0146 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA18995 | hp2 | a0001 | c0001 | t0003 | g0223 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19000 | hp1 | a0001 | c0001 | t0011 | g0201 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19000 | hp2 | a0001 | c0002 | t0005 | g0237 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0206 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19005 | hp1 | a0001 | c0001 | t0011 | g0043 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0211 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19009 | hp1 | a0001 | c0001 | t0011 | g0145 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19009 | hp2 | a0001 | c0001 | t0010 | g0252 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19030 | hp1 | a0001 | c0001 | t0025 | g0275 | AFR | LWK | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19030 | hp2 | a0001 | c0001 | t0004 | g0284 | AFR | LWK | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19043 | hp1 | a0001 | c0001 | t0013 | g0134 | AFR | LWK | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0095 | AFR | LWK | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19055 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19056 | hp2 | a0001 | c0002 | t0005 | g0183 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19057 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19062 | hp1 | a0001 | c0001 | t0014 | g0016 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19062 | hp2 | a0001 | c0001 | t0004 | g0262 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19064 | hp2 | a0001 | c0001 | t0031 | g0233 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19065 | hp1 | a0001 | c0001 | t0008 | g0046 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19065 | hp2 | a0001 | c0002 | t0005 | g0077 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19068 | hp2 | a0001 | c0001 | t0011 | g0244 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19070 | hp2 | a0001 | c0002 | t0015 | g0248 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19074 | hp1 | a0001 | c0001 | t0003 | g0151 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19075 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19078 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19086 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19086 | hp2 | a0001 | c0001 | t0014 | g0017 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19088 | hp1 | a0001 | c0001 | t0004 | g0175 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19089 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0312 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19091 | hp1 | a0001 | c0001 | t0014 | g0018 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19091 | hp2 | a0001 | c0001 | t0010 | g0170 | EAS | JPT | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19240 | hp1 | a0001 | c0001 | t0009 | g0292 | AFR | YRI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0067 | AFR | YRI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0138 | AFR | ASW | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA20129 | hp2 | a0001 | c0001 | t0007 | g0055 | AFR | ASW | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0160 | EUR | TSI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0260 | EUR | TSI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0128 | EUR | TSI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA20805 | hp2 | a0001 | c0002 | t0005 | g0057 | EUR | TSI | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA20905 | hp1 | a0001 | c0001 | t0007 | g0091 | SAS | GIH | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA20905 | hp2 | a0001 | c0001 | t0008 | g0028 | SAS | GIH | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0281 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02486 | hp1 | a0001 | c0001 | t0028 | g0106 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02486 | hp2 | a0001 | c0001 | t0006 | g0168 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02559 | hp1 | a0001 | c0001 | t0033 | g0008 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG02559 | hp2 | a0001 | c0001 | t0037 | g0287 | AFR | ACB | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0277 | AFR | USA | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0109 | AFR | USA | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0315 | AFR | USA | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0133 | AFR | USA | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA21309 | hp1 | a0001 | c0001 | t0024 | g0078 | AFR | LWK | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
NA21309 | hp2 | a0001 | c0001 | t0004 | g0137 | AFR | LWK | UCK2_chr1_165822614_165916618 | UCK2 | chr1 | 165822614 | 165916618 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:165891238
|
A | G | 1 | a0002 | 1 | HG03540.hp2 | missense_variant | MODERATE | c.272A>G | p.Asn91Ser | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/7 | 492/4801 | 272/786 | 91/261 | chr1 | 165891238 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:165896241
|
G | A | 1 | a0001c0002 | 24 | HG01106.hp1 HG01175.hp2 HG01192.hp1 others(21): Show |
synonymous_variant | LOW | c.408G>A | p.Gly136Gly | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/7 | 628/4801 | 408/786 | 136/261 | chr1 | 165896241 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:165827669
|
C | T | 2 | a0001c0001t0017a0001c0001t0037 | 3 | HG02559.hp2 HG02976.hp2 HG03516.hp1 |
5_prime_UTR_variant | MODIFIER | c.-165C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/7 | 165 | chr1 | 165827669 | |||||
chr1:165827819
|
G | C | 1 | a0001c0001t0018 | 1 | NA18956.hp1 | 5_prime_UTR_variant | MODIFIER | c.-15G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/7 | 15 | chr1 | 165827819 | |||||
chr1:165907909
|
A | G | 1 | a0001c0001t0036 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*86A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 86 | chr1 | 165907909 | |||||
chr1:165908040
|
A | G | 1 | a0001c0001t0035 | 1 | NA18964.hp2 | 3_prime_UTR_variant | MODIFIER | c.*217A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 217 | chr1 | 165908040 | |||||
chr1:165908102
|
A | T | 2 | a0001c0001t0011a0001c0002t0034 | 7 | HG02300.hp1 NA18944.hp2 NA18957.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*279A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 279 | chr1 | 165908102 | |||||
chr1:165908338
|
A | C | 12 | a0001c0001t0003a0001c0001t0004a0001c0001t0007others(9): Show | 96 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(93): Show |
3_prime_UTR_variant | MODIFIER | c.*515A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 515 | chr1 | 165908338 | |||||
chr1:165908423
|
T | C | 1 | a0001c0001t0019 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*600T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 600 | chr1 | 165908423 | |||||
chr1:165908433
|
CT | C | 31 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(28): Show | 212 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*622delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 622 | INFO_REALIGN_3_PRIME | chr1 | 165908433 | ||||
chr1:165908514
|
G | A | 5 | a0001c0001t0005a0001c0002t0005a0001c0002t0015others(2): Show | 26 | HG01070.hp2 HG01071.hp1 HG01106.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*691G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 691 | chr1 | 165908514 | |||||
chr1:165908552
|
C | T | 2 | a0001c0001t0007a0001c0001t0032 | 16 | HG00140.hp2 HG00323.hp1 HG00738.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*729C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 729 | chr1 | 165908552 | |||||
chr1:165908751
|
G | A | 1 | a0001c0001t0032 | 1 | HG01515.hp1 | 3_prime_UTR_variant | MODIFIER | c.*928G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 928 | chr1 | 165908751 | |||||
chr1:165908753
|
C | T | 1 | a0001c0001t0025 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*930C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 930 | chr1 | 165908753 | |||||
chr1:165908909
|
C | T | 1 | a0001c0001t0031 | 1 | NA19064.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1086C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1086 | chr1 | 165908909 | |||||
chr1:165909038
|
A | C | 1 | a0001c0001t0010 | 6 | HG02132.hp2 HG02135.hp1 NA18979.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1215A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1215 | chr1 | 165909038 | |||||
chr1:165909183
|
C | T | 3 | a0001c0001t0019a0001c0001t0024a0001c0001t0036 | 3 | HG02451.hp1 HG02451.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1360C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1360 | chr1 | 165909183 | |||||
chr1:165909261
|
C | T | 4 | a0001c0001t0003a0001c0001t0010a0001c0001t0011others(1): Show | 46 | HG00438.hp2 HG00639.hp1 HG00673.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*1438C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1438 | chr1 | 165909261 | |||||
chr1:165909389
|
C | G | 1 | a0001c0002t0015 | 2 | NA18941.hp2 NA19070.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1566C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1566 | chr1 | 165909389 | |||||
chr1:165909477
|
G | T | 1 | a0001c0002t0020 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1654G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1654 | chr1 | 165909477 | |||||
chr1:165909541
|
T | C | 1 | a0001c0001t0027 | 1 | HG03453.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1718T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1718 | chr1 | 165909541 | |||||
chr1:165909566
|
C | T | 1 | a0001c0001t0026 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1743C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1743 | chr1 | 165909566 | |||||
chr1:165909674
|
C | T | 4 | a0001c0001t0006a0001c0001t0016a0001c0001t0022others(1): Show | 26 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1851C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1851 | chr1 | 165909674 | |||||
chr1:165909766
|
A | G | 1 | a0001c0001t0008 | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1943A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1943 | chr1 | 165909766 | |||||
chr1:165909783
|
T | C | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*1960T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 1960 | chr1 | 165909783 | |||||
chr1:165909825
|
T | C | 39 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
3_prime_UTR_variant | MODIFIER | c.*2002T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2002 | chr1 | 165909825 | |||||
chr1:165910021
|
C | G | 1 | a0001c0001t0014 | 3 | NA19062.hp1 NA19086.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2198C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2198 | chr1 | 165910021 | |||||
chr1:165910042
|
T | G | 1 | a0001c0001t0008 | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2219T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2219 | chr1 | 165910042 | |||||
chr1:165910385
|
A | C | 11 | a0001c0001t0002a0001c0001t0005a0001c0001t0013others(8): Show | 78 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(75): Show |
3_prime_UTR_variant | MODIFIER | c.*2562A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2562 | chr1 | 165910385 | |||||
chr1:165910495
|
C | T | 1 | a0001c0001t0023 | 1 | HG02257.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2672C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2672 | chr1 | 165910495 | |||||
chr1:165910500
|
G | A | 1 | a0001c0001t0021 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2677G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2677 | chr1 | 165910500 | |||||
chr1:165910584
|
A | G | 1 | a0001c0001t0033 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2761A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2761 | chr1 | 165910584 | |||||
chr1:165910608
|
G | A | 1 | a0001c0001t0028 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2785G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2785 | chr1 | 165910608 | |||||
chr1:165910654
|
A | G | 1 | a0001c0001t0008 | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2831A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2831 | chr1 | 165910654 | |||||
chr1:165910794
|
A | G | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
3_prime_UTR_variant | MODIFIER | c.*2971A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 2971 | chr1 | 165910794 | |||||
chr1:165910874
|
T | A | 1 | a0001c0001t0016 | 2 | HG03195.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3051T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3051 | chr1 | 165910874 | |||||
chr1:165910874
|
T | C | 37 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
3_prime_UTR_variant | MODIFIER | c.*3051T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3051 | chr1 | 165910874 | |||||
chr1:165910957
|
G | A | 1 | a0001c0001t0013 | 3 | HG02258.hp1 HG03516.hp2 NA19043.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3134G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3134 | chr1 | 165910957 | |||||
chr1:165911084
|
C | G | 3 | a0001c0001t0019a0001c0001t0024a0001c0001t0036 | 3 | HG02451.hp1 HG02451.hp2 NA21309.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3261C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3261 | chr1 | 165911084 | |||||
chr1:165911193
|
A | G | 3 | a0001c0001t0009a0001c0001t0017a0002c0003t0009 | 11 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*3370A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3370 | chr1 | 165911193 | |||||
chr1:165911377
|
C | G | 1 | a0001c0001t0022 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3554C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3554 | chr1 | 165911377 | |||||
chr1:165911465
|
T | C | 1 | a0001c0001t0029 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3642T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 7/7 | 3642 | chr1 | 165911465 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:165828075
|
G | C | 2 | a0001c0001t0005g0003a0001c0001t0005g0004 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.99+143G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828075 | ||||||
chr1:165828076
|
T | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0004g0007 | 3 | HG01978.hp1 NA18944.hp1 NA19078.hp2 |
intron_variant | MODIFIER | c.99+144T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828076 | ||||||
chr1:165828081
|
C | G | 1 | a0001c0001t0013g0317 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.99+149C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828081 | ||||||
chr1:165828103
|
C | CG | 11 | a0001c0001t0001g0306a0001c0001t0001g0311a0001c0001t0001g0314others(8): Show | 11 | HG01978.hp2 HG02129.hp2 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+173dupG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165828103 | |||||
chr1:165828112
|
C | T | 41 | a0001c0001t0001g0291a0001c0001t0001g0301a0001c0001t0001g0306others(38): Show | 41 | HG01978.hp2 HG02055.hp1 HG02109.hp2 others(38): Show |
intron_variant | MODIFIER | c.99+180C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828112 | ||||||
chr1:165828312
|
C | T | 1 | a0001c0001t0025g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+380C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828312 | ||||||
chr1:165828619
|
T | C | 19 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0009others(16): Show | 19 | HG02109.hp2 HG02145.hp1 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+687T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828619 | ||||||
chr1:165828729
|
C | A | 301 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(298): Show | 304 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(301): Show |
intron_variant | MODIFIER | c.99+797C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828729 | ||||||
chr1:165828774
|
G | T | 101 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0165others(98): Show | 101 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.99+842G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165828774 | ||||||
chr1:165829089
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.99+1157T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829089 | ||||||
chr1:165829160
|
T | C | 1 | a0001c0001t0001g0011 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.99+1228T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829160 | ||||||
chr1:165829163
|
T | C | 4 | a0001c0001t0004g0009a0001c0001t0012g0010a0001c0001t0025g0275others(1): Show | 4 | HG02145.hp1 HG02559.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+1231T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829163 | ||||||
chr1:165829406
|
G | A | 1 | a0001c0001t0009g0292 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.99+1474G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829406 | ||||||
chr1:165829480
|
G | T | 1 | a0001c0001t0010g0258 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.99+1548G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829480 | ||||||
chr1:165829596
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.99+1664C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829596 | ||||||
chr1:165829643
|
G | C | 1 | a0001c0001t0009g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.99+1711G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829643 | ||||||
chr1:165829785
|
G | A | 95 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0021others(92): Show | 98 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.99+1853G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829785 | ||||||
chr1:165829903
|
A | G | 25 | a0001c0001t0001g0142a0001c0001t0001g0143a0001c0001t0001g0144others(22): Show | 25 | HG00673.hp1 HG00741.hp1 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.99+1971A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165829903 | ||||||
chr1:165830046
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.99+2114C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830046 | ||||||
chr1:165830207
|
G | C | 13 | a0001c0001t0001g0301a0001c0001t0002g0294a0001c0001t0004g0293others(10): Show | 13 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+2275G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830207 | ||||||
chr1:165830216
|
C | T | 16 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(13): Show | 16 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+2284C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830216 | ||||||
chr1:165830239
|
A | G | 1 | a0001c0001t0025g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+2307A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830239 | ||||||
chr1:165830318
|
A | T | 5 | a0001c0001t0004g0009a0001c0001t0012g0010a0001c0001t0025g0275others(2): Show | 5 | HG02145.hp1 HG02451.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+2386A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830318 | ||||||
chr1:165830330
|
AT | A | 255 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(252): Show | 258 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(255): Show |
intron_variant | MODIFIER | c.99+2410delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165830330 | |||||
chr1:165830333
|
T | A | 4 | a0001c0001t0004g0009a0001c0001t0032g0259a0001c0001t0033g0008others(1): Show | 4 | HG01515.hp1 HG02145.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+2401T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830333 | ||||||
chr1:165830417
|
C | T | 1 | a0001c0001t0003g0257 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.99+2485C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830417 | ||||||
chr1:165830482
|
G | T | 95 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0021others(92): Show | 98 | HG00140.hp2 HG00639.hp2 HG00733.hp1 others(95): Show |
intron_variant | MODIFIER | c.99+2550G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830482 | ||||||
chr1:165830566
|
C | T | 1 | a0001c0001t0004g0305 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.99+2634C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830566 | ||||||
chr1:165830571
|
C | T | 2 | a0001c0001t0001g0291a0001c0001t0009g0290 | 2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.99+2639C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830571 | ||||||
chr1:165830615
|
A | G | 242 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(239): Show | 245 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.99+2683A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830615 | ||||||
chr1:165830617
|
G | GC | 122 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0165others(119): Show | 122 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(119): Show |
intron_variant | MODIFIER | c.99+2687dupC | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165830617 | |||||
chr1:165830619
|
C | T | 1 | a0001c0001t0009g0292 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.99+2687C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830619 | ||||||
chr1:165830701
|
A | G | 13 | a0001c0001t0001g0301a0001c0001t0002g0294a0001c0001t0004g0293others(10): Show | 13 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+2769A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830701 | ||||||
chr1:165830756
|
G | A | 1 | a0001c0001t0025g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+2824G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830756 | ||||||
chr1:165830772
|
A | G | 147 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0165others(144): Show | 147 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.99+2840A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830772 | ||||||
chr1:165830819
|
A | C | 2 | a0001c0001t0001g0100a0001c0002t0005g0101 | 2 | HG01175.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.99+2887A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830819 | ||||||
chr1:165830823
|
C | T | 1 | a0001c0001t0004g0256 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.99+2891C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165830823 | ||||||
chr1:165831038
|
G | A | 16 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(13): Show | 16 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+3106G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831038 | ||||||
chr1:165831040
|
C | T | 3 | a0001c0001t0006g0119a0001c0001t0006g0120a0001c0001t0006g0121 | 3 | HG01884.hp1 HG01891.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.99+3108C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831040 | ||||||
chr1:165831217
|
A | G | 2 | a0001c0001t0001g0098a0001c0002t0005g0099 | 2 | HG02080.hp1 NA19057.hp1 |
intron_variant | MODIFIER | c.99+3285A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831217 | ||||||
chr1:165831228
|
G | A | 1 | a0001c0001t0004g0293 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.99+3296G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831228 | ||||||
chr1:165831453
|
A | G | 16 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(13): Show | 16 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.99+3521A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831453 | ||||||
chr1:165831534
|
G | T | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+3602G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831534 | ||||||
chr1:165831541
|
G | A | 1 | a0001c0001t0009g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+3609G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831541 | ||||||
chr1:165831545
|
T | C | 1 | a0001c0001t0004g0013 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.99+3613T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831545 | ||||||
chr1:165831584
|
C | T | 1 | a0001c0002t0005g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+3652C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831584 | ||||||
chr1:165831677
|
A | G | 131 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0165others(128): Show | 131 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(128): Show |
intron_variant | MODIFIER | c.99+3745A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831677 | ||||||
chr1:165831873
|
C | A | 1 | a0001c0001t0008g0014 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.99+3941C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831873 | ||||||
chr1:165831989
|
G | A | 1 | a0001c0001t0012g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.99+4057G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165831989 | ||||||
chr1:165832013
|
C | A | 10 | a0001c0001t0002g0279a0001c0001t0004g0282a0001c0001t0004g0284others(7): Show | 10 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+4081C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832013 | ||||||
chr1:165832084
|
G | T | 10 | a0001c0001t0002g0279a0001c0001t0004g0282a0001c0001t0004g0284others(7): Show | 10 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+4152G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832084 | ||||||
chr1:165832397
|
A | G | 18 | a0001c0001t0001g0301a0001c0001t0002g0294a0001c0001t0004g0009others(15): Show | 18 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(15): Show |
intron_variant | MODIFIER | c.99+4465A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832397 | ||||||
chr1:165832488
|
T | C | 38 | a0001c0001t0001g0011a0001c0001t0001g0019a0001c0001t0001g0021others(35): Show | 39 | HG00140.hp2 HG00733.hp1 HG01175.hp1 others(36): Show |
intron_variant | MODIFIER | c.99+4556T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832488 | ||||||
chr1:165832516
|
G | A | 3 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0006g0049 | 3 | HG02257.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.99+4584G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832516 | ||||||
chr1:165832570
|
T | C | 15 | a0001c0001t0001g0301a0001c0001t0002g0294a0001c0001t0003g0122others(12): Show | 15 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+4638T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832570 | ||||||
chr1:165832889
|
T | G | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.99+4957T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832889 | ||||||
chr1:165832946
|
C | T | 3 | a0001c0001t0004g0009a0001c0001t0012g0010a0001c0001t0033g0008 | 3 | HG02145.hp1 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.99+5014C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832946 | ||||||
chr1:165832947
|
G | A | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG00639.hp2 HG01358.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+5015G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165832947 | ||||||
chr1:165833089
|
T | C | 34 | a0001c0001t0001g0291a0001c0001t0002g0108a0001c0001t0002g0109others(31): Show | 34 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(31): Show |
intron_variant | MODIFIER | c.99+5157T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833089 | ||||||
chr1:165833145
|
C | G | 19 | a0001c0001t0002g0108a0001c0001t0002g0109a0001c0001t0002g0113others(16): Show | 19 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+5213C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833145 | ||||||
chr1:165833191
|
C | G | 13 | a0001c0001t0001g0306a0001c0001t0001g0311a0001c0001t0001g0314others(10): Show | 13 | HG01192.hp2 HG01978.hp2 HG02129.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+5259C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833191 | ||||||
chr1:165833233
|
G | A | 15 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(12): Show | 15 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+5301G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833233 | ||||||
chr1:165833361
|
C | G | 3 | a0001c0001t0001g0314a0001c0001t0001g0315a0001c0001t0001g0316 | 3 | HG01978.hp2 HG02293.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.99+5429C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833361 | ||||||
chr1:165833438
|
T | C | 15 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(12): Show | 15 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+5506T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833438 | ||||||
chr1:165833480
|
C | T | 1 | a0001c0001t0004g0118 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.99+5548C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833480 | ||||||
chr1:165833531
|
C | T | 1 | a0001c0001t0008g0255 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.99+5599C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833531 | ||||||
chr1:165833613
|
T | G | 1 | a0001c0001t0003g0164 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.99+5681T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833613 | ||||||
chr1:165833709
|
A | G | 15 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(12): Show | 15 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+5777A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833709 | ||||||
chr1:165833794
|
G | A | 15 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(12): Show | 15 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+5862G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833794 | ||||||
chr1:165833926
|
A | G | 5 | a0001c0001t0002g0133a0001c0001t0013g0134a0001c0001t0013g0317others(2): Show | 5 | HG02258.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+5994A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833926 | ||||||
chr1:165833931
|
T | C | 15 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(12): Show | 15 | HG02109.hp2 HG02280.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+5999T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165833931 | ||||||
chr1:165834023
|
T | A | 15 | a0001c0001t0001g0301a0001c0001t0002g0294a0001c0001t0003g0122others(12): Show | 15 | HG02055.hp1 HG02145.hp2 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.99+6091T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834023 | ||||||
chr1:165834175
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.99+6243G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834175 | ||||||
chr1:165834414
|
T | G | 32 | a0001c0001t0001g0301a0001c0001t0001g0306a0001c0001t0001g0311others(29): Show | 32 | HG01192.hp2 HG01978.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.99+6482T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834414 | ||||||
chr1:165834580
|
G | T | 20 | a0001c0001t0001g0301a0001c0001t0002g0294a0001c0001t0003g0122others(17): Show | 20 | HG02055.hp1 HG02145.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.99+6648G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834580 | ||||||
chr1:165834681
|
T | A | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+6749T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834681 | ||||||
chr1:165834713
|
C | T | 12 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(9): Show | 12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+6781C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834713 | ||||||
chr1:165834757
|
G | A | 1 | a0001c0001t0029g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99+6825G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834757 | ||||||
chr1:165834818
|
C | T | 1 | a0001c0001t0004g0254 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.99+6886C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834818 | ||||||
chr1:165834896
|
G | A | 12 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(9): Show | 12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+6964G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834896 | ||||||
chr1:165834993
|
C | T | 1 | a0001c0001t0002g0161 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.99+7061C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165834993 | ||||||
chr1:165835006
|
CT | C | 12 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(9): Show | 12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+7082delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165835006 | |||||
chr1:165835060
|
A | G | 3 | a0001c0001t0004g0009a0001c0001t0012g0010a0001c0001t0033g0008 | 3 | HG02145.hp1 HG02559.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.99+7128A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165835060 | ||||||
chr1:165835314
|
T | TATATATA others(43): Show |
12 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(9): Show | 12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+7401_99+7402ins others(50): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165835314 | |||||
chr1:165835359
|
G | GTTA | 3 | a0001c0001t0006g0104a0001c0001t0008g0166a0001c0001t0036g0136 | 3 | HG02451.hp1 NA18522.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.99+7448_99+7450dup others(3): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165835359 | |||||
chr1:165835359
|
GTTA | G | 12 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(9): Show | 12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+7448_99+7450del others(3): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165835359 | |||||
chr1:165835505
|
C | A | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+7573C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165835505 | ||||||
chr1:165835659
|
A | G | 1 | a0001c0001t0004g0254 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.99+7727A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165835659 | ||||||
chr1:165835667
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.99+7735A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165835667 | ||||||
chr1:165835792
|
A | G | 1 | a0001c0001t0011g0253 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.99+7860A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165835792 | ||||||
chr1:165836119
|
T | G | 2 | a0001c0001t0001g0291a0001c0001t0009g0290 | 2 | HG02886.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.99+8187T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836119 | ||||||
chr1:165836214
|
G | T | 1 | a0001c0001t0012g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.99+8282G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836214 | ||||||
chr1:165836222
|
C | T | 215 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(212): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.99+8290C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836222 | ||||||
chr1:165836223
|
C | T | 215 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(212): Show | 218 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(215): Show |
intron_variant | MODIFIER | c.99+8291C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836223 | ||||||
chr1:165836233
|
C | A | 12 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(9): Show | 12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+8301C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836233 | ||||||
chr1:165836240
|
C | A | 12 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(9): Show | 12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+8308C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836240 | ||||||
chr1:165836245
|
C | A | 12 | a0001c0001t0001g0291a0001c0001t0002g0279a0001c0001t0004g0282others(9): Show | 12 | HG02109.hp2 HG02280.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+8313C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836245 | ||||||
chr1:165836347
|
T | G | 1 | a0001c0002t0005g0307 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.99+8415T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836347 | ||||||
chr1:165836396
|
T | A | 12 | a0001c0001t0001g0306a0001c0001t0001g0311a0001c0001t0001g0314others(9): Show | 12 | HG01192.hp2 HG01978.hp2 HG02129.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+8464T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836396 | ||||||
chr1:165836405
|
C | A | 4 | a0001c0001t0002g0015a0001c0001t0014g0016a0001c0001t0014g0017others(1): Show | 4 | HG02027.hp2 NA19062.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+8473C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836405 | ||||||
chr1:165836559
|
C | T | 1 | a0001c0001t0010g0252 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.99+8627C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836559 | ||||||
chr1:165836595
|
T | C | 3 | a0001c0001t0002g0001a0001c0001t0002g0056a0001c0002t0005g0057 | 5 | HG01081.hp1 HG01099.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+8663T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836595 | ||||||
chr1:165836600
|
A | G | 1 | a0001c0001t0001g0047 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.99+8668A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836600 | ||||||
chr1:165836688
|
G | A | 1 | a0001c0001t0002g0260 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.99+8756G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836688 | ||||||
chr1:165836757
|
G | A | 1 | a0001c0001t0010g0170 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.99+8825G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836757 | ||||||
chr1:165836800
|
T | A | 1 | a0001c0001t0002g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+8868T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836800 | ||||||
chr1:165836873
|
T | C | 3 | a0001c0001t0006g0167a0001c0001t0006g0168a0001c0001t0006g0277 | 3 | HG02486.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.99+8941T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836873 | ||||||
chr1:165836941
|
C | T | 1 | a0001c0001t0009g0292 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.99+9009C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165836941 | ||||||
chr1:165837004
|
G | T | 1 | a0001c0001t0001g0251 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.99+9072G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165837004 | ||||||
chr1:165837053
|
A | C | 15 | a0001c0001t0001g0306a0001c0001t0001g0311a0001c0001t0001g0314others(12): Show | 15 | HG01192.hp2 HG01978.hp2 HG02129.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+9121A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165837053 | ||||||
chr1:165837152
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.99+9220T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165837152 | ||||||
chr1:165837240
|
T | C | 1 | a0001c0001t0004g0059 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.99+9308T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165837240 | ||||||
chr1:165837315
|
T | G | 1 | a0001c0001t0002g0015 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.99+9383T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165837315 | ||||||
chr1:165837847
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.99+9915C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165837847 | ||||||
chr1:165838575
|
T | G | 24 | a0001c0001t0001g0052a0001c0001t0001g0123a0001c0001t0001g0124others(21): Show | 24 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(21): Show |
intron_variant | MODIFIER | c.99+10643T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165838575 | ||||||
chr1:165838610
|
G | A | 2 | a0001c0001t0004g0118a0001c0001t0033g0008 | 2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.99+10678G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165838610 | ||||||
chr1:165838681
|
A | G | 1 | a0001c0001t0002g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.99+10749A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165838681 | ||||||
chr1:165838892
|
A | G | 1 | a0001c0001t0002g0160 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.99+10960A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165838892 | ||||||
chr1:165838966
|
T | C | 1 | a0001c0001t0004g0175 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.99+11034T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165838966 | ||||||
chr1:165838979
|
C | T | 140 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(137): Show | 142 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(139): Show |
intron_variant | MODIFIER | c.99+11047C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165838979 | ||||||
chr1:165839667
|
G | A | 2 | a0001c0002t0005g0081a0001c0002t0005g0082 | 2 | HG01256.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.99+11735G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839667 | ||||||
chr1:165839738
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.99+11806G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839738 | ||||||
chr1:165839750
|
A | G | 156 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(153): Show | 158 | HG00438.hp2 HG00673.hp1 HG00673.hp2 others(155): Show |
intron_variant | MODIFIER | c.99+11818A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839750 | ||||||
chr1:165839773
|
T | C | 12 | a0001c0001t0002g0113a0001c0001t0004g0112a0001c0001t0004g0114others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+11841T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839773 | ||||||
chr1:165839840
|
C | T | 4 | a0001c0001t0004g0282a0001c0001t0004g0284a0001c0001t0006g0283others(1): Show | 4 | HG02451.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+11908C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839840 | ||||||
chr1:165839851
|
C | G | 133 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(130): Show | 135 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(132): Show |
intron_variant | MODIFIER | c.99+11919C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839851 | ||||||
chr1:165839932
|
C | T | 111 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(108): Show | 112 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.99+12000C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839932 | ||||||
chr1:165839933
|
G | A | 1 | a0001c0001t0002g0174 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.99+12001G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839933 | ||||||
chr1:165839952
|
G | A | 1 | a0001c0002t0005g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.99+12020G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165839952 | ||||||
chr1:165840023
|
A | G | 1 | a0001c0001t0009g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+12091A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840023 | ||||||
chr1:165840127
|
C | G | 1 | a0001c0001t0002g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+12195C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840127 | ||||||
chr1:165840164
|
C | G | 2 | a0001c0001t0004g0284a0001c0001t0006g0283 | 2 | HG02896.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.99+12232C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840164 | ||||||
chr1:165840330
|
A | G | 1 | a0001c0001t0009g0276 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.99+12398A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840330 | ||||||
chr1:165840353
|
A | G | 193 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(190): Show | 195 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.99+12421A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840353 | ||||||
chr1:165840416
|
A | G | 1 | a0001c0002t0015g0248 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.99+12484A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840416 | ||||||
chr1:165840676
|
G | A | 2 | a0001c0001t0003g0208a0001c0001t0004g0256 | 2 | NA18992.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.99+12744G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840676 | ||||||
chr1:165840693
|
C | T | 12 | a0001c0001t0002g0113a0001c0001t0004g0112a0001c0001t0004g0114others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+12761C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840693 | ||||||
chr1:165840926
|
A | G | 75 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(72): Show | 75 | HG00673.hp2 HG01261.hp1 HG01943.hp2 others(72): Show |
intron_variant | MODIFIER | c.99+12994A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165840926 | ||||||
chr1:165841094
|
C | T | 9 | a0001c0001t0002g0095a0001c0001t0002g0273a0001c0001t0002g0274others(6): Show | 9 | HG01256.hp2 HG01258.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+13162C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841094 | ||||||
chr1:165841095
|
G | T | 12 | a0001c0001t0002g0113a0001c0001t0004g0112a0001c0001t0004g0114others(9): Show | 12 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.99+13163G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841095 | ||||||
chr1:165841097
|
A | ATG | 8 | a0001c0001t0002g0162a0001c0001t0009g0062a0001c0001t0009g0063others(5): Show | 8 | HG02559.hp1 HG02809.hp2 HG02922.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+13179_99+13180d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841097 | |||||
chr1:165841097
|
A | G | 1 | a0001c0001t0003g0044 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.99+13165A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841097 | ||||||
chr1:165841109
|
G | GTATATA | 8 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0002g0263others(5): Show | 8 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+13178_99+13179i others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841109 | |||||
chr1:165841109
|
G | GTATATAT others(3): Show |
3 | a0001c0001t0009g0105a0001c0001t0009g0276a0001c0001t0028g0106 | 3 | HG02486.hp1 HG02615.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.99+13178_99+13179i others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841109 | |||||
chr1:165841109
|
GTGTA | G | 11 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0002g0139others(8): Show | 11 | HG00673.hp1 HG01516.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+13179_99+13182d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841109 | |||||
chr1:165841111
|
G | A | 13 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0002g0263others(10): Show | 13 | HG00323.hp1 HG00323.hp2 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.99+13179G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841111 | ||||||
chr1:165841111
|
G | GTA | 3 | a0001c0001t0002g0058a0001c0001t0004g0061a0001c0001t0007g0140 | 3 | HG01496.hp1 HG02109.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.99+13200_99+13201d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841111 | |||||
chr1:165841111
|
G | GTATA | 8 | a0001c0001t0001g0052a0001c0001t0001g0172a0001c0001t0001g0267others(5): Show | 8 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+13198_99+13201d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841111 | |||||
chr1:165841111
|
G | GTGTA | 11 | a0001c0001t0002g0108a0001c0001t0002g0133a0001c0001t0002g0279others(8): Show | 11 | HG02055.hp1 HG02280.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+13180_99+13181i others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841111 | |||||
chr1:165841111
|
GTA | G | 116 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+13200_99+13201d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841111 | |||||
chr1:165841111
|
GTATA | G | 134 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(131): Show | 136 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(133): Show |
intron_variant | MODIFIER | c.99+13198_99+13201d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841111 | |||||
chr1:165841111
|
GTATATA | G | 3 | a0001c0001t0002g0209a0001c0001t0010g0252a0001c0001t0026g0210 | 3 | HG02132.hp1 NA18964.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.99+13196_99+13201d others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165841111 | |||||
chr1:165841113
|
A | G | 5 | a0001c0001t0002g0160a0001c0001t0004g0282a0001c0001t0004g0284others(2): Show | 5 | HG02451.hp2 HG02896.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+13181A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841113 | ||||||
chr1:165841115
|
A | G | 114 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(111): Show | 115 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(112): Show |
intron_variant | MODIFIER | c.99+13183A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841115 | ||||||
chr1:165841117
|
A | G | 1 | a0001c0001t0004g0007 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.99+13185A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841117 | ||||||
chr1:165841407
|
C | T | 3 | a0001c0001t0009g0105a0001c0001t0025g0275a0001c0001t0028g0106 | 3 | HG02486.hp1 HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.99+13475C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841407 | ||||||
chr1:165841433
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.99+13501A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841433 | ||||||
chr1:165841454
|
G | C | 1 | a0001c0001t0008g0255 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.99+13522G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841454 | ||||||
chr1:165841497
|
T | C | 1 | a0001c0001t0002g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.99+13565T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841497 | ||||||
chr1:165841572
|
C | T | 1 | a0001c0001t0006g0121 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.99+13640C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841572 | ||||||
chr1:165841673
|
C | G | 2 | a0001c0001t0004g0009a0001c0001t0004g0305 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+13741C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841673 | ||||||
chr1:165841815
|
T | G | 172 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(169): Show | 174 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(171): Show |
intron_variant | MODIFIER | c.99+13883T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841815 | ||||||
chr1:165841824
|
G | A | 2 | a0001c0001t0004g0118a0001c0001t0033g0008 | 2 | HG02559.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.99+13892G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841824 | ||||||
chr1:165841856
|
C | T | 2 | a0001c0001t0010g0093a0001c0001t0010g0247 | 2 | HG02135.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.99+13924C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165841856 | ||||||
chr1:165842176
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.99+14244C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842176 | ||||||
chr1:165842249
|
C | A | 154 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(151): Show | 156 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(153): Show |
intron_variant | MODIFIER | c.99+14317C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842249 | ||||||
chr1:165842447
|
A | G | 15 | a0001c0001t0001g0052a0001c0001t0001g0123a0001c0001t0001g0124others(12): Show | 15 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+14515A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842447 | ||||||
chr1:165842464
|
T | C | 1 | a0001c0001t0003g0211 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.99+14532T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842464 | ||||||
chr1:165842492
|
C | T | 116 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+14560C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842492 | ||||||
chr1:165842505
|
G | A | 4 | a0001c0001t0002g0162a0001c0001t0012g0010a0001c0001t0017g0288others(1): Show | 4 | HG02976.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+14573G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842505 | ||||||
chr1:165842705
|
C | G | 1 | a0001c0001t0004g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.99+14773C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842705 | ||||||
chr1:165842848
|
C | T | 116 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+14916C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842848 | ||||||
chr1:165842870
|
A | G | 2 | a0001c0001t0003g0158a0001c0001t0003g0159 | 2 | HG01257.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.99+14938A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842870 | ||||||
chr1:165842883
|
A | C | 155 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(152): Show | 157 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(154): Show |
intron_variant | MODIFIER | c.99+14951A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842883 | ||||||
chr1:165842932
|
C | G | 6 | a0001c0001t0002g0139a0001c0001t0002g0161a0001c0001t0002g0174others(3): Show | 6 | HG00673.hp1 HG01516.hp2 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+15000C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165842932 | ||||||
chr1:165843047
|
G | T | 3 | a0001c0001t0004g0013a0001c0001t0004g0094a0001c0001t0004g0304 | 3 | HG02280.hp2 HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.99+15115G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843047 | ||||||
chr1:165843090
|
TTC | T | 116 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(113): Show | 117 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.99+15160_99+15161d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165843090 | |||||
chr1:165843457
|
A | C | 1 | a0001c0001t0009g0290 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.99+15525A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843457 | ||||||
chr1:165843562
|
G | A | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+15630G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843562 | ||||||
chr1:165843769
|
C | T | 172 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(169): Show | 174 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(171): Show |
intron_variant | MODIFIER | c.99+15837C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843769 | ||||||
chr1:165843802
|
A | G | 1 | a0001c0002t0005g0082 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.99+15870A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843802 | ||||||
chr1:165843884
|
A | T | 2 | a0001c0001t0001g0124a0001c0001t0007g0264 | 2 | HG01261.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.99+15952A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843884 | ||||||
chr1:165843941
|
A | G | 5 | a0001c0001t0001g0035a0001c0001t0002g0034a0001c0001t0002g0037others(2): Show | 5 | HG01261.hp1 HG02004.hp1 HG02148.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+16009A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165843941 | ||||||
chr1:165844008
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.99+16076G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844008 | ||||||
chr1:165844171
|
G | A | 2 | a0001c0001t0004g0009a0001c0001t0004g0305 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+16239G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844171 | ||||||
chr1:165844173
|
C | A | 2 | a0001c0001t0009g0105a0001c0001t0028g0106 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.99+16241C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844173 | ||||||
chr1:165844271
|
G | A | 309 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(306): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.99+16339G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844271 | ||||||
chr1:165844279
|
C | T | 1 | a0001c0002t0015g0248 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.99+16347C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844279 | ||||||
chr1:165844280
|
A | C | 5 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0006g0049others(2): Show | 5 | HG02257.hp2 HG02647.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+16348A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844280 | ||||||
chr1:165844483
|
C | G | 143 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(140): Show | 145 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(142): Show |
intron_variant | MODIFIER | c.99+16551C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844483 | ||||||
chr1:165844523
|
T | G | 1 | a0001c0001t0002g0308 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.99+16591T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844523 | ||||||
chr1:165844625
|
G | A | 134 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(131): Show | 135 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(132): Show |
intron_variant | MODIFIER | c.99+16693G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844625 | ||||||
chr1:165844783
|
TTGAA | T | 4 | a0001c0001t0004g0282a0001c0001t0004g0284a0001c0001t0006g0283others(1): Show | 4 | HG02451.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+16855_99+16858d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165844783 | |||||
chr1:165844807
|
A | G | 1 | a0001c0001t0003g0203 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.99+16875A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844807 | ||||||
chr1:165844844
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.99+16912G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844844 | ||||||
chr1:165844864
|
T | G | 20 | a0001c0001t0002g0108a0001c0001t0002g0133a0001c0001t0002g0162others(17): Show | 20 | HG02055.hp1 HG02280.hp1 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.99+16932T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844864 | ||||||
chr1:165844965
|
C | T | 6 | a0001c0001t0001g0301a0001c0001t0004g0065a0001c0001t0004g0148others(3): Show | 6 | HG01243.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+17033C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165844965 | ||||||
chr1:165845041
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.99+17109C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165845041 | ||||||
chr1:165845332
|
C | T | 2 | a0001c0001t0004g0009a0001c0001t0004g0305 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+17400C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165845332 | ||||||
chr1:165845468
|
T | G | 2 | a0001c0001t0001g0182a0001c0002t0005g0183 | 2 | HG02523.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.99+17536T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165845468 | ||||||
chr1:165845510
|
C | T | 1 | a0002c0003t0009g0080 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.99+17578C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165845510 | ||||||
chr1:165845926
|
G | A | 1 | a0001c0001t0008g0046 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.99+17994G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165845926 | ||||||
chr1:165846075
|
T | G | 2 | a0001c0001t0004g0262a0001c0001t0010g0261 | 2 | NA18984.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.99+18143T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165846075 | ||||||
chr1:165846446
|
T | TAAACA | 8 | a0001c0001t0004g0282a0001c0001t0004g0284a0001c0001t0006g0283others(5): Show | 8 | HG02451.hp2 HG02486.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+18535_99+18539d others(7): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165846446 | |||||
chr1:165846446
|
TAAACA | T | 13 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0002g0092others(10): Show | 13 | HG00673.hp1 HG00735.hp2 HG01516.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+18535_99+18539d others(7): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165846446 | |||||
chr1:165846446
|
TAAACAAA others(3): Show |
T | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+18530_99+18539d others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165846446 | |||||
chr1:165846597
|
A | G | 1 | a0001c0001t0029g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.99+18665A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165846597 | ||||||
chr1:165846702
|
T | C | 166 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(163): Show | 168 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(165): Show |
intron_variant | MODIFIER | c.99+18770T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165846702 | ||||||
chr1:165846710
|
G | C | 1 | a0001c0001t0002g0213 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.99+18778G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165846710 | ||||||
chr1:165846946
|
T | C | 1 | a0001c0001t0001g0152 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.99+19014T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165846946 | ||||||
chr1:165847000
|
G | A | 1 | a0001c0001t0033g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+19068G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847000 | ||||||
chr1:165847003
|
T | C | 1 | a0001c0001t0016g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99+19071T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847003 | ||||||
chr1:165847091
|
C | T | 309 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(306): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.99+19159C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847091 | ||||||
chr1:165847123
|
A | T | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.99+19191A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847123 | ||||||
chr1:165847136
|
A | G | 1 | a0001c0001t0016g0286 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.99+19204A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847136 | ||||||
chr1:165847238
|
A | G | 1 | a0001c0001t0007g0157 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.99+19306A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847238 | ||||||
chr1:165847373
|
G | GT | 3 | a0001c0001t0007g0064a0001c0001t0007g0171a0001c0002t0005g0269 | 3 | HG00323.hp1 HG01192.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.99+19442dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165847373 | |||||
chr1:165847452
|
C | T | 5 | a0001c0001t0002g0273a0001c0001t0002g0274a0001c0001t0006g0167others(2): Show | 5 | HG01256.hp2 HG01258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+19520C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847452 | ||||||
chr1:165847724
|
C | T | 31 | a0001c0001t0002g0108a0001c0001t0002g0133a0001c0001t0002g0139others(28): Show | 31 | HG00673.hp1 HG01516.hp2 HG02055.hp1 others(28): Show |
intron_variant | MODIFIER | c.99+19792C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847724 | ||||||
chr1:165847858
|
C | T | 2 | a0001c0001t0006g0278a0001c0001t0007g0140 | 2 | HG01496.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.99+19926C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165847858 | ||||||
chr1:165848340
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.99+20408G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165848340 | ||||||
chr1:165848374
|
G | A | 1 | a0001c0001t0001g0184 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.99+20442G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165848374 | ||||||
chr1:165848559
|
C | CG | 11 | a0001c0001t0002g0113a0001c0001t0004g0112a0001c0001t0004g0114others(8): Show | 11 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+20628dupG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165848559 | |||||
chr1:165848660
|
C | A | 180 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(177): Show | 182 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(179): Show |
intron_variant | MODIFIER | c.99+20728C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165848660 | ||||||
chr1:165848662
|
A | C | 180 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(177): Show | 182 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(179): Show |
intron_variant | MODIFIER | c.99+20730A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165848662 | ||||||
chr1:165848678
|
C | A | 1 | a0001c0001t0007g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.99+20746C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165848678 | ||||||
chr1:165849020
|
G | T | 3 | a0001c0001t0014g0016a0001c0001t0014g0017a0001c0001t0014g0018 | 3 | NA19062.hp1 NA19086.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.99+21088G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165849020 | ||||||
chr1:165849042
|
T | C | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.99+21110T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165849042 | ||||||
chr1:165849384
|
G | A | 138 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(135): Show | 140 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(137): Show |
intron_variant | MODIFIER | c.99+21452G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165849384 | ||||||
chr1:165849653
|
G | T | 2 | a0001c0001t0009g0105a0001c0001t0028g0106 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.99+21721G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165849653 | ||||||
chr1:165849763
|
C | T | 6 | a0001c0001t0001g0301a0001c0001t0004g0065a0001c0001t0004g0148others(3): Show | 6 | HG01243.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+21831C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165849763 | ||||||
chr1:165849911
|
C | T | 2 | a0001c0001t0009g0105a0001c0001t0028g0106 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.99+21979C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165849911 | ||||||
chr1:165850010
|
A | G | 43 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0089others(40): Show | 45 | HG01081.hp1 HG01099.hp2 HG01106.hp1 others(42): Show |
intron_variant | MODIFIER | c.99+22078A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850010 | ||||||
chr1:165850221
|
C | T | 5 | a0001c0001t0007g0090a0001c0001t0007g0091a0001c0001t0007g0157others(2): Show | 5 | HG01109.hp2 HG01256.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.99+22289C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850221 | ||||||
chr1:165850233
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.99+22301C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850233 | ||||||
chr1:165850292
|
G | A | 1 | a0001c0001t0002g0214 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.99+22360G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850292 | ||||||
chr1:165850420
|
G | A | 180 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(177): Show | 182 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(179): Show |
intron_variant | MODIFIER | c.99+22488G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850420 | ||||||
chr1:165850602
|
C | T | 11 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0002g0092others(8): Show | 11 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.99+22670C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850602 | ||||||
chr1:165850616
|
AT | A | 186 | a0001c0001t0001g0040a0001c0001t0001g0045a0001c0001t0001g0050others(183): Show | 188 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(185): Show |
intron_variant | MODIFIER | c.99+22704delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850616 | |||||
chr1:165850616
|
ATT | A | 102 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(99): Show | 103 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(100): Show |
intron_variant | MODIFIER | c.99+22703_99+22704d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850616 | |||||
chr1:165850616
|
ATTT | A | 21 | a0001c0001t0001g0025a0001c0001t0001g0142a0001c0001t0001g0143others(18): Show | 21 | HG00438.hp1 HG00639.hp1 HG00741.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+22702_99+22704d others(5): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850616 | |||||
chr1:165850711
|
C | T | 2 | a0001c0001t0007g0090a0001c0001t0007g0091 | 2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.99+22779C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850711 | ||||||
chr1:165850743
|
C | T | 117 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(114): Show | 118 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(115): Show |
intron_variant | MODIFIER | c.99+22811C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850743 | ||||||
chr1:165850813
|
G | A | 5 | a0001c0001t0002g0273a0001c0001t0002g0274a0001c0001t0006g0167others(2): Show | 5 | HG01256.hp2 HG01258.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+22881G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850813 | ||||||
chr1:165850927
|
AT | A | 8 | a0001c0001t0004g0061a0001c0001t0004g0112a0001c0001t0006g0278others(5): Show | 8 | HG01496.hp1 HG02572.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+23022delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850927 | |||||
chr1:165850927
|
ATTT | A | 21 | a0001c0001t0002g0108a0001c0001t0002g0133a0001c0001t0002g0162others(18): Show | 21 | HG02055.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+23020_99+23022d others(5): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850927 | |||||
chr1:165850927
|
ATTTTT | A | 115 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(112): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.99+23018_99+23022d others(7): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850927 | |||||
chr1:165850927
|
ATTTTTT | A | 6 | a0001c0001t0001g0185a0001c0001t0002g0176a0001c0001t0002g0263others(3): Show | 6 | HG00323.hp1 HG00323.hp2 HG01099.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+23017_99+23022d others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850927 | |||||
chr1:165850927
|
ATTTTTTT others(1): Show |
A | 8 | a0001c0001t0002g0213a0001c0001t0006g0111a0001c0001t0006g0119others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+23015_99+23022d others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850927 | |||||
chr1:165850927
|
ATTTTTTT others(5): Show |
A | 13 | a0001c0001t0002g0139a0001c0001t0002g0161a0001c0001t0002g0174others(10): Show | 13 | HG00673.hp1 HG01516.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+23011_99+23022d others(14): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850927 | |||||
chr1:165850940
|
T | A | 1 | a0001c0001t0009g0105 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.99+23008T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850940 | ||||||
chr1:165850954
|
T | A | 15 | a0001c0001t0002g0113a0001c0001t0002g0213a0001c0001t0003g0039others(12): Show | 15 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+23022T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850954 | ||||||
chr1:165850954
|
T | TA | 9 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0003g0087others(6): Show | 9 | HG01257.hp2 HG03041.hp1 HG03139.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+23024dupA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850954 | |||||
chr1:165850954
|
T | TTA | 97 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(94): Show | 99 | HG00438.hp2 HG00673.hp2 HG00735.hp2 others(96): Show |
intron_variant | MODIFIER | c.99+23022_99+23023i others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850954 | ||||||
chr1:165850954
|
T | TTTA | 19 | a0001c0001t0001g0086a0001c0001t0001g0235a0001c0001t0001g0236others(16): Show | 19 | HG00733.hp2 HG01070.hp2 HG01071.hp1 others(16): Show |
intron_variant | MODIFIER | c.99+23022_99+23023i others(5): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165850954 | ||||||
chr1:165850977
|
GTTGCTTG others(3): Show |
G | 1 | a0001c0001t0025g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.99+23047_99+23056d others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165850977 | |||||
chr1:165851137
|
C | T | 6 | a0001c0001t0001g0301a0001c0001t0004g0065a0001c0001t0004g0148others(3): Show | 6 | HG01243.hp1 HG02717.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.99+23205C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851137 | ||||||
chr1:165851146
|
T | C | 21 | a0001c0001t0002g0108a0001c0001t0002g0133a0001c0001t0002g0162others(18): Show | 21 | HG02055.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+23214T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851146 | ||||||
chr1:165851176
|
A | C | 21 | a0001c0001t0002g0108a0001c0001t0002g0133a0001c0001t0002g0162others(18): Show | 21 | HG02055.hp1 HG02145.hp1 HG02559.hp1 others(18): Show |
intron_variant | MODIFIER | c.99+23244A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851176 | ||||||
chr1:165851251
|
A | G | 1 | a0001c0002t0005g0307 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.99+23319A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851251 | ||||||
chr1:165851418
|
C | T | 1 | a0001c0001t0010g0170 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.99+23486C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851418 | ||||||
chr1:165851552
|
A | G | 4 | a0001c0001t0004g0282a0001c0001t0004g0284a0001c0001t0006g0283others(1): Show | 4 | HG02451.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+23620A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851552 | ||||||
chr1:165851588
|
G | A | 1 | a0001c0001t0007g0271 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.99+23656G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851588 | ||||||
chr1:165851692
|
G | C | 138 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(135): Show | 140 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(137): Show |
intron_variant | MODIFIER | c.99+23760G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851692 | ||||||
chr1:165851695
|
T | C | 3 | a0001c0001t0009g0105a0001c0001t0025g0275a0001c0001t0028g0106 | 3 | HG02486.hp1 HG02615.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.99+23763T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851695 | ||||||
chr1:165851794
|
C | G | 10 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0002g0092others(7): Show | 10 | HG02145.hp1 HG02257.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+23862C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851794 | ||||||
chr1:165851813
|
A | G | 2 | a0001c0001t0004g0262a0001c0001t0010g0261 | 2 | NA18984.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.99+23881A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165851813 | ||||||
chr1:165852040
|
A | G | 1 | a0001c0001t0033g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+24108A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852040 | ||||||
chr1:165852091
|
G | A | 180 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(177): Show | 182 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(179): Show |
intron_variant | MODIFIER | c.99+24159G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852091 | ||||||
chr1:165852193
|
A | G | 1 | a0001c0001t0009g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.99+24261A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852193 | ||||||
chr1:165852453
|
A | C | 1 | a0001c0001t0008g0234 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.99+24521A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852453 | ||||||
chr1:165852604
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.99+24672T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852604 | ||||||
chr1:165852670
|
A | G | 2 | a0001c0001t0002g0176a0001c0001t0002g0178 | 2 | NA18954.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.99+24738A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852670 | ||||||
chr1:165852726
|
C | T | 2 | a0001c0001t0003g0232a0001c0001t0031g0233 | 2 | NA18973.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.99+24794C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852726 | ||||||
chr1:165852775
|
G | T | 1 | a0001c0001t0001g0239 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.99+24843G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852775 | ||||||
chr1:165852939
|
C | T | 137 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(134): Show | 139 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(136): Show |
intron_variant | MODIFIER | c.99+25007C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165852939 | ||||||
chr1:165853036
|
A | G | 1 | a0001c0001t0009g0063 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.99+25104A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853036 | ||||||
chr1:165853042
|
GCCT | G | 13 | a0001c0001t0002g0139a0001c0001t0002g0161a0001c0001t0002g0174others(10): Show | 13 | HG00673.hp1 HG01516.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.99+25111_99+25113d others(5): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853042 | ||||||
chr1:165853356
|
AT | A | 22 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(19): Show | 22 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(19): Show |
intron_variant | MODIFIER | c.99+25435delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165853356 | |||||
chr1:165853358
|
T | A | 135 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(132): Show | 137 | HG00438.hp2 HG00733.hp2 HG00735.hp2 others(134): Show |
intron_variant | MODIFIER | c.99+25426T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853358 | ||||||
chr1:165853491
|
C | G | 1 | a0001c0002t0005g0077 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.99+25559C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853491 | ||||||
chr1:165853503
|
G | A | 7 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0002g0092others(4): Show | 7 | HG02257.hp2 HG02258.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+25571G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853503 | ||||||
chr1:165853535
|
C | T | 1 | a0001c0002t0005g0303 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.99+25603C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853535 | ||||||
chr1:165853654
|
T | C | 133 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(130): Show | 134 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(131): Show |
intron_variant | MODIFIER | c.99+25722T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853654 | ||||||
chr1:165853803
|
T | C | 168 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(165): Show | 170 | HG00438.hp2 HG00673.hp1 HG00733.hp2 others(167): Show |
intron_variant | MODIFIER | c.99+25871T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165853803 | ||||||
chr1:165854496
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.99+26564C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165854496 | ||||||
chr1:165854556
|
C | T | 1 | a0001c0001t0001g0024 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.99+26624C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165854556 | ||||||
chr1:165854598
|
A | AAAAT | 46 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0030others(43): Show | 46 | HG01261.hp1 HG01515.hp1 HG01943.hp2 others(43): Show |
intron_variant | MODIFIER | c.99+26710_99+26713d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165854598 | |||||
chr1:165854598
|
A | AAAATAAA others(1): Show |
6 | a0001c0001t0001g0097a0001c0001t0001g0200a0001c0001t0001g0202others(3): Show | 6 | HG02027.hp1 HG02735.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+26706_99+26713d others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165854598 | |||||
chr1:165854598
|
AAAAT | A | 154 | a0001c0001t0001g0019a0001c0001t0001g0040a0001c0001t0001g0045others(151): Show | 156 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(153): Show |
intron_variant | MODIFIER | c.99+26710_99+26713d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165854598 | |||||
chr1:165854598
|
AAAATAAA others(1): Show |
A | 10 | a0001c0001t0001g0149a0001c0001t0002g0095a0001c0001t0002g0139others(7): Show | 10 | HG00673.hp1 HG00735.hp2 HG01516.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+26706_99+26713d others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165854598 | |||||
chr1:165854598
|
AAAATAAA others(5): Show |
A | 1 | a0001c0001t0001g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.99+26702_99+26713d others(14): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165854598 | |||||
chr1:165854598
|
AAAATAAA others(13): Show |
A | 1 | a0001c0001t0006g0167 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.99+26694_99+26713d others(22): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165854598 | |||||
chr1:165854803
|
G | A | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.99+26871G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165854803 | ||||||
chr1:165854824
|
A | G | 1 | a0001c0001t0004g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.99+26892A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165854824 | ||||||
chr1:165854881
|
C | G | 3 | a0001c0001t0004g0154a0001c0001t0004g0155a0001c0001t0011g0043 | 3 | NA19005.hp1 NA19057.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.99+26949C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165854881 | ||||||
chr1:165855107
|
A | G | 4 | a0001c0001t0006g0104a0001c0001t0006g0115a0001c0001t0006g0116others(1): Show | 4 | HG01891.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+27175A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855107 | ||||||
chr1:165855169
|
A | G | 1 | a0001c0001t0001g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.99+27237A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855169 | ||||||
chr1:165855254
|
T | C | 1 | a0001c0002t0005g0186 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.99+27322T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855254 | ||||||
chr1:165855510
|
C | CT | 9 | a0001c0001t0001g0052a0001c0001t0001g0124a0001c0001t0001g0172others(6): Show | 9 | HG00099.hp2 HG00639.hp2 HG00738.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+27596dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165855510 | |||||
chr1:165855510
|
CT | C | 7 | a0001c0001t0001g0239a0001c0001t0004g0059a0001c0001t0004g0112others(4): Show | 7 | HG02647.hp2 HG02976.hp1 NA18942.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+27596delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165855510 | |||||
chr1:165855666
|
G | A | 10 | a0001c0001t0002g0113a0001c0001t0004g0112a0001c0001t0004g0114others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+27734G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855666 | ||||||
chr1:165855682
|
C | T | 2 | a0001c0001t0009g0105a0001c0001t0028g0106 | 2 | HG02486.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.99+27750C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855682 | ||||||
chr1:165855741
|
C | T | 1 | a0001c0002t0005g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.99+27809C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855741 | ||||||
chr1:165855896
|
A | G | 97 | a0001c0001t0001g0045a0001c0001t0001g0086a0001c0001t0001g0130others(94): Show | 97 | HG00438.hp2 HG00673.hp2 HG00733.hp2 others(94): Show |
intron_variant | MODIFIER | c.99+27964A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855896 | ||||||
chr1:165855907
|
G | A | 1 | a0001c0001t0033g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+27975G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855907 | ||||||
chr1:165855929
|
G | A | 204 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0024others(201): Show | 207 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(204): Show |
intron_variant | MODIFIER | c.99+27997G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165855929 | ||||||
chr1:165856050
|
A | G | 1 | a0001c0001t0002g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.99+28118A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856050 | ||||||
chr1:165856062
|
C | T | 1 | a0001c0001t0023g0302 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.99+28130C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856062 | ||||||
chr1:165856157
|
A | G | 1 | a0001c0002t0005g0183 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.99+28225A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856157 | ||||||
chr1:165856230
|
G | A | 23 | a0001c0001t0001g0052a0001c0001t0001g0123a0001c0001t0001g0124others(20): Show | 23 | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(20): Show |
intron_variant | MODIFIER | c.99+28298G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856230 | ||||||
chr1:165856285
|
G | T | 6 | a0001c0001t0001g0035a0001c0001t0002g0034a0001c0001t0002g0037others(3): Show | 6 | HG01261.hp1 HG02004.hp1 HG02148.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+28353G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856285 | ||||||
chr1:165856329
|
GTCTGATA others(974): Show |
G | 1 | a0001c0001t0033g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.99+28428_99+29408d others(2): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165856329 | |||||
chr1:165856350
|
A | T | 2 | a0001c0001t0003g0232a0001c0001t0031g0233 | 2 | NA18973.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.99+28418A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856350 | ||||||
chr1:165856354
|
A | G | 1 | a0001c0001t0001g0076 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.99+28422A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856354 | ||||||
chr1:165856361
|
C | T | 1 | a0001c0001t0004g0061 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.99+28429C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856361 | ||||||
chr1:165856406
|
A | AT | 88 | a0001c0001t0001g0019a0001c0001t0001g0076a0001c0001t0001g0143others(85): Show | 90 | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(87): Show |
intron_variant | MODIFIER | c.99+28488dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165856406 | |||||
chr1:165856406
|
AT | A | 8 | a0001c0001t0004g0112a0001c0001t0006g0111a0001c0001t0006g0119others(5): Show | 8 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+28488delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165856406 | |||||
chr1:165856420
|
T | G | 1 | a0001c0001t0001g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.99+28488T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856420 | ||||||
chr1:165856447
|
C | T | 1 | a0001c0001t0004g0282 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.99+28515C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856447 | ||||||
chr1:165856497
|
C | A | 8 | a0001c0001t0004g0009a0001c0001t0004g0118a0001c0001t0004g0305others(5): Show | 8 | HG02145.hp1 HG02723.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+28565C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856497 | ||||||
chr1:165856752
|
G | A | 22 | a0001c0001t0001g0045a0001c0001t0001g0249a0001c0001t0001g0250others(19): Show | 22 | HG00735.hp2 HG01243.hp1 HG01257.hp1 others(19): Show |
intron_variant | MODIFIER | c.99+28820G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856752 | ||||||
chr1:165856901
|
G | GTT | 10 | a0001c0001t0002g0034a0001c0001t0002g0037a0001c0001t0002g0038others(7): Show | 10 | HG00673.hp2 HG01261.hp1 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.99+28987_99+28988d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165856901 | |||||
chr1:165856901
|
GT | G | 187 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(184): Show | 188 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(185): Show |
intron_variant | MODIFIER | c.99+28988delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165856901 | |||||
chr1:165856907
|
T | G | 64 | a0001c0001t0001g0040a0001c0001t0001g0097a0001c0001t0001g0177others(61): Show | 66 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(63): Show |
intron_variant | MODIFIER | c.99+28975T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856907 | ||||||
chr1:165856955
|
G | A | 1 | a0001c0001t0008g0234 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.99+29023G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165856955 | ||||||
chr1:165856957
|
AG | A | 84 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(81): Show |
intron_variant | MODIFIER | c.99+29027delG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165856957 | |||||
chr1:165857012
|
G | A | 1 | a0001c0001t0006g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.99+29080G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857012 | ||||||
chr1:165857069
|
C | G | 30 | a0001c0001t0001g0301a0001c0001t0002g0095a0001c0001t0002g0109others(27): Show | 30 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(27): Show |
intron_variant | MODIFIER | c.99+29137C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857069 | ||||||
chr1:165857131
|
C | T | 4 | a0001c0001t0010g0093a0001c0001t0010g0170a0001c0001t0010g0247others(1): Show | 4 | HG02135.hp1 NA18979.hp2 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+29199C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857131 | ||||||
chr1:165857292
|
C | T | 1 | a0001c0001t0012g0163 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.99+29360C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857292 | ||||||
chr1:165857498
|
G | T | 1 | a0001c0001t0001g0097 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.99+29566G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857498 | ||||||
chr1:165857508
|
G | A | 263 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(260): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.99+29576G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857508 | ||||||
chr1:165857653
|
C | A | 3 | a0001c0001t0008g0028a0001c0001t0008g0072a0001c0001t0008g0073 | 3 | HG03491.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.99+29721C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857653 | ||||||
chr1:165857665
|
A | G | 1 | a0001c0001t0001g0054 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.99+29733A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857665 | ||||||
chr1:165857784
|
C | A | 2 | a0001c0001t0016g0066a0001c0001t0016g0286 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.99+29852C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857784 | ||||||
chr1:165857889
|
T | C | 1 | a0001c0001t0023g0302 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.99+29957T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165857889 | ||||||
chr1:165858145
|
T | C | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.99+30213T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858145 | ||||||
chr1:165858186
|
A | T | 7 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0009g0012others(4): Show | 7 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.99+30254A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858186 | ||||||
chr1:165858251
|
G | T | 49 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0042others(46): Show | 51 | HG00099.hp2 HG00323.hp2 HG01081.hp1 others(48): Show |
intron_variant | MODIFIER | c.99+30319G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858251 | ||||||
chr1:165858257
|
G | T | 11 | a0001c0001t0004g0009a0001c0001t0004g0118a0001c0001t0004g0305others(8): Show | 11 | HG02145.hp1 HG02451.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.99+30325G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858257 | ||||||
chr1:165858452
|
C | T | 1 | a0001c0002t0005g0077 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.99+30520C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858452 | ||||||
chr1:165858453
|
G | A | 2 | a0001c0001t0006g0049a0001c0001t0033g0008 | 2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.99+30521G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858453 | ||||||
chr1:165858504
|
G | A | 1 | a0001c0001t0007g0127 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.99+30572G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858504 | ||||||
chr1:165858671
|
AG | A | 17 | a0001c0001t0001g0301a0001c0001t0004g0059a0001c0001t0004g0065others(14): Show | 17 | HG00735.hp2 HG01243.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+30741delG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165858671 | |||||
chr1:165858745
|
A | G | 1 | a0001c0001t0003g0033 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.99+30813A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858745 | ||||||
chr1:165858894
|
T | C | 8 | a0001c0001t0002g0095a0001c0001t0002g0109a0001c0001t0002g0113others(5): Show | 8 | HG02258.hp1 HG02451.hp2 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+30962T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165858894 | ||||||
chr1:165859078
|
G | A | 1 | a0001c0001t0021g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-31126G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859078 | ||||||
chr1:165859085
|
C | T | 1 | a0001c0001t0009g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-31119C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859085 | ||||||
chr1:165859178
|
AGTGG | A | 36 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0301others(33): Show | 36 | HG00673.hp1 HG00735.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.100-31018_100-3101 others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165859178 | |||||
chr1:165859257
|
T | TA | 11 | a0001c0001t0004g0009a0001c0001t0004g0118a0001c0001t0004g0305others(8): Show | 11 | HG02145.hp1 HG02451.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-30946dupA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165859257 | |||||
chr1:165859299
|
T | C | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.100-30905T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859299 | ||||||
chr1:165859301
|
C | T | 4 | a0001c0001t0009g0105a0001c0001t0017g0288a0001c0001t0017g0289others(1): Show | 4 | HG02615.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-30903C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859301 | ||||||
chr1:165859307
|
G | A | 15 | a0001c0001t0002g0034a0001c0001t0002g0037a0001c0001t0002g0038others(12): Show | 15 | HG00673.hp2 HG01261.hp1 HG02148.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-30897G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859307 | ||||||
chr1:165859434
|
G | A | 1 | a0001c0001t0010g0252 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.100-30770G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859434 | ||||||
chr1:165859566
|
A | G | 1 | a0001c0001t0029g0132 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.100-30638A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859566 | ||||||
chr1:165859611
|
C | T | 1 | a0001c0001t0012g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-30593C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859611 | ||||||
chr1:165859652
|
G | A | 17 | a0001c0001t0001g0301a0001c0001t0004g0059a0001c0001t0004g0065others(14): Show | 17 | HG00735.hp2 HG01243.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-30552G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859652 | ||||||
chr1:165859919
|
T | G | 101 | a0001c0001t0001g0030a0001c0001t0001g0052a0001c0001t0001g0100others(98): Show | 102 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.100-30285T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859919 | ||||||
chr1:165859964
|
A | G | 2 | a0001c0001t0006g0049a0001c0001t0033g0008 | 2 | HG02257.hp2 HG02559.hp1 |
intron_variant | MODIFIER | c.100-30240A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165859964 | ||||||
chr1:165860041
|
G | A | 1 | a0001c0002t0034g0126 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.100-30163G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860041 | ||||||
chr1:165860057
|
A | G | 2 | a0001c0001t0003g0205a0001c0001t0003g0206 | 2 | HG00673.hp2 NA19002.hp2 |
intron_variant | MODIFIER | c.100-30147A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860057 | ||||||
chr1:165860060
|
T | C | 1 | a0001c0001t0001g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.100-30144T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860060 | ||||||
chr1:165860070
|
G | A | 1 | a0001c0001t0008g0014 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.100-30134G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860070 | ||||||
chr1:165860108
|
C | T | 1 | a0002c0003t0009g0080 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.100-30096C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860108 | ||||||
chr1:165860495
|
C | T | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.100-29709C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860495 | ||||||
chr1:165860561
|
A | C | 98 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(95): Show | 99 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.100-29643A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860561 | ||||||
chr1:165860720
|
G | T | 20 | a0001c0001t0001g0301a0001c0001t0003g0208a0001c0001t0004g0059others(17): Show | 20 | HG00735.hp2 HG01243.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.100-29484G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860720 | ||||||
chr1:165860726
|
A | G | 1 | a0001c0001t0012g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-29478A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860726 | ||||||
chr1:165860772
|
T | C | 14 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0053others(11): Show | 14 | HG00099.hp1 HG00140.hp1 HG00738.hp1 others(11): Show |
intron_variant | MODIFIER | c.100-29432T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860772 | ||||||
chr1:165860810
|
A | G | 1 | a0001c0001t0003g0041 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.100-29394A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860810 | ||||||
chr1:165860937
|
A | G | 3 | a0001c0001t0008g0028a0001c0001t0008g0072a0001c0001t0008g0073 | 3 | HG03491.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.100-29267A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860937 | ||||||
chr1:165860947
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.100-29257G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165860947 | ||||||
chr1:165861079
|
G | C | 97 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(94): Show | 98 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.100-29125G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861079 | ||||||
chr1:165861080
|
G | A | 3 | a0001c0001t0006g0278a0001c0001t0006g0295a0001c0001t0007g0140 | 3 | HG01496.hp1 HG02055.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.100-29124G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861080 | ||||||
chr1:165861247
|
C | T | 8 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(5): Show | 8 | HG00673.hp2 HG02523.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-28957C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861247 | ||||||
chr1:165861394
|
C | T | 4 | a0001c0001t0002g0109a0001c0001t0002g0113a0001c0001t0004g0137others(1): Show | 4 | HG02451.hp2 HG03098.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-28810C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861394 | ||||||
chr1:165861403
|
C | T | 98 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(95): Show | 99 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.100-28801C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861403 | ||||||
chr1:165861525
|
A | G | 129 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(126): Show | 130 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.100-28679A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861525 | ||||||
chr1:165861553
|
A | G | 4 | a0001c0001t0002g0109a0001c0001t0002g0113a0001c0001t0004g0137others(1): Show | 4 | HG02451.hp2 HG03098.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-28651A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861553 | ||||||
chr1:165861576
|
C | T | 1 | a0001c0002t0005g0088 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.100-28628C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861576 | ||||||
chr1:165861590
|
C | T | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.100-28614C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861590 | ||||||
chr1:165861614
|
C | A | 7 | a0001c0001t0001g0030a0001c0001t0001g0152a0001c0001t0001g0188others(4): Show | 7 | HG00741.hp2 HG01255.hp2 HG01975.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-28590C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861614 | ||||||
chr1:165861615
|
G | A | 98 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(95): Show | 99 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.100-28589G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861615 | ||||||
chr1:165861627
|
C | CA | 34 | a0001c0001t0001g0005a0001c0001t0001g0019a0001c0001t0001g0024others(31): Show | 34 | HG00099.hp1 HG00738.hp1 HG01070.hp1 others(31): Show |
intron_variant | MODIFIER | c.100-28555dupA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861627 | |||||
chr1:165861627
|
C | CAA | 8 | a0001c0001t0001g0071a0001c0001t0001g0086a0001c0001t0001g0130others(5): Show | 8 | HG01106.hp1 HG01109.hp1 HG01943.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-28556_100-2855 others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861627 | |||||
chr1:165861634
|
AAAAAAAA others(9): Show |
A | 6 | a0001c0001t0001g0047a0001c0001t0001g0184a0001c0001t0001g0185others(3): Show | 6 | NA18985.hp1 NA18992.hp1 NA19000.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-28560_100-2854 others(20): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861634 | |||||
chr1:165861635
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0001g0191 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.100-28559_100-2854 others(19): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861635 | |||||
chr1:165861640
|
AAAAAAAA others(3): Show |
A | 1 | a0001c0002t0005g0307 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.100-28551_100-2854 others(14): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861640 | |||||
chr1:165861641
|
AAAAAAAA others(2): Show |
A | 27 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0002g0074others(24): Show | 27 | HG00099.hp2 HG01192.hp1 HG02040.hp2 others(24): Show |
intron_variant | MODIFIER | c.100-28554_100-2854 others(13): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861641 | |||||
chr1:165861642
|
AAAAAAAA others(1): Show |
A | 29 | a0001c0001t0002g0001a0001c0001t0002g0034a0001c0001t0002g0038others(26): Show | 31 | HG01081.hp1 HG01081.hp2 HG01099.hp2 others(28): Show |
intron_variant | MODIFIER | c.100-28554_100-2854 others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861642 | |||||
chr1:165861643
|
AAAAAAAC | A | 37 | a0001c0001t0001g0301a0001c0001t0002g0015a0001c0001t0002g0037others(34): Show | 37 | HG00323.hp2 HG00735.hp2 HG01243.hp1 others(34): Show |
intron_variant | MODIFIER | c.100-28554_100-2854 others(11): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861643 | |||||
chr1:165861644
|
AAAAAAC | A | 17 | a0001c0001t0002g0095a0001c0001t0002g0139a0001c0001t0003g0044others(14): Show | 17 | HG00673.hp1 HG00738.hp2 HG01261.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-28554_100-2854 others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861644 | |||||
chr1:165861645
|
AAAAAC | A | 63 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0142others(60): Show | 64 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(61): Show |
intron_variant | MODIFIER | c.100-28554_100-2855 others(9): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861645 | |||||
chr1:165861646
|
AAAAC | A | 35 | a0001c0001t0001g0123a0001c0001t0001g0238a0001c0001t0001g0243others(32): Show | 35 | HG00438.hp2 HG00735.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.100-28554_100-2855 others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165861646 | |||||
chr1:165861649
|
AC | A | 8 | a0001c0001t0002g0108a0001c0001t0006g0104a0001c0001t0006g0115others(5): Show | 8 | HG01496.hp1 HG01891.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-28554delC | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861649 | ||||||
chr1:165861650
|
C | A | 91 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(88): Show | 91 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(88): Show |
intron_variant | MODIFIER | c.100-28554C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861650 | ||||||
chr1:165861660
|
C | A | 211 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(208): Show | 214 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.100-28544C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861660 | ||||||
chr1:165861737
|
A | G | 57 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(54): Show | 59 | HG00099.hp2 HG00323.hp2 HG01081.hp1 others(56): Show |
intron_variant | MODIFIER | c.100-28467A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861737 | ||||||
chr1:165861856
|
C | T | 84 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0301others(81): Show | 86 | HG00099.hp2 HG00323.hp2 HG00735.hp2 others(83): Show |
intron_variant | MODIFIER | c.100-28348C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861856 | ||||||
chr1:165861882
|
G | C | 4 | a0001c0001t0009g0105a0001c0001t0017g0288a0001c0001t0017g0289others(1): Show | 4 | HG02615.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-28322G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861882 | ||||||
chr1:165861891
|
A | C | 97 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(94): Show | 98 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(95): Show |
intron_variant | MODIFIER | c.100-28313A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165861891 | ||||||
chr1:165862066
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.100-28138G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862066 | ||||||
chr1:165862103
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.100-28101A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862103 | ||||||
chr1:165862113
|
C | T | 1 | a0001c0001t0006g0049 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.100-28091C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862113 | ||||||
chr1:165862161
|
T | C | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.100-28043T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862161 | ||||||
chr1:165862163
|
T | C | 1 | a0001c0002t0020g0193 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.100-28041T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862163 | ||||||
chr1:165862168
|
A | C | 1 | a0001c0001t0023g0302 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100-28036A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862168 | ||||||
chr1:165862412
|
A | G | 212 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(209): Show | 215 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.100-27792A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862412 | ||||||
chr1:165862585
|
G | A | 1 | a0001c0001t0003g0257 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.100-27619G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862585 | ||||||
chr1:165862681
|
G | A | 1 | a0001c0001t0008g0046 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.100-27523G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862681 | ||||||
chr1:165862791
|
C | A | 1 | a0001c0001t0012g0280 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100-27413C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862791 | ||||||
chr1:165862801
|
G | A | 4 | a0001c0001t0009g0105a0001c0001t0017g0288a0001c0001t0017g0289others(1): Show | 4 | HG02615.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-27403G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862801 | ||||||
chr1:165862848
|
G | T | 102 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0301others(99): Show | 104 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(101): Show |
intron_variant | MODIFIER | c.100-27356G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862848 | ||||||
chr1:165862984
|
C | G | 94 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0301others(91): Show | 96 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.100-27220C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165862984 | ||||||
chr1:165863039
|
C | G | 118 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(115): Show | 119 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.100-27165C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863039 | ||||||
chr1:165863219
|
C | G | 1 | a0001c0001t0009g0296 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100-26985C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863219 | ||||||
chr1:165863746
|
G | T | 94 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0301others(91): Show | 96 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.100-26458G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863746 | ||||||
chr1:165863750
|
T | G | 9 | a0001c0001t0002g0095a0001c0001t0002g0139a0001c0001t0002g0273others(6): Show | 9 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-26454T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863750 | ||||||
chr1:165863767
|
A | G | 54 | a0001c0001t0001g0100a0001c0001t0001g0181a0001c0001t0001g0218others(51): Show | 55 | HG00438.hp1 HG00438.hp2 HG00639.hp1 others(52): Show |
intron_variant | MODIFIER | c.100-26437A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863767 | ||||||
chr1:165863897
|
A | G | 94 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0301others(91): Show | 96 | HG00099.hp2 HG00323.hp2 HG00673.hp1 others(93): Show |
intron_variant | MODIFIER | c.100-26307A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863897 | ||||||
chr1:165863931
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0202 | 2 | HG02027.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.100-26273A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863931 | ||||||
chr1:165863978
|
CTTCTT | C | 3 | a0001c0001t0002g0108a0001c0001t0002g0133a0001c0001t0002g0294 | 3 | HG02717.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.100-26218_100-2621 others(9): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165863978 | |||||
chr1:165863982
|
T | C | 1 | a0001c0001t0002g0058 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.100-26222T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863982 | ||||||
chr1:165863996
|
G | A | 8 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(5): Show | 8 | HG00673.hp2 HG02523.hp1 HG03491.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-26208G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165863996 | ||||||
chr1:165864011
|
C | A | 212 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(209): Show | 215 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(212): Show |
intron_variant | MODIFIER | c.100-26193C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864011 | ||||||
chr1:165864074
|
AG | A | 98 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(95): Show | 99 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.100-26129delG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864074 | ||||||
chr1:165864108
|
T | C | 214 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(211): Show | 217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.100-26096T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864108 | ||||||
chr1:165864133
|
A | G | 4 | a0001c0001t0002g0109a0001c0001t0002g0113a0001c0001t0004g0137others(1): Show | 4 | HG02451.hp2 HG03098.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-26071A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864133 | ||||||
chr1:165864168
|
G | A | 1 | a0001c0002t0005g0186 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.100-26036G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864168 | ||||||
chr1:165864195
|
G | T | 1 | a0001c0001t0003g0033 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.100-26009G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864195 | ||||||
chr1:165864239
|
C | T | 1 | a0001c0001t0012g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-25965C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864239 | ||||||
chr1:165864367
|
G | T | 1 | a0001c0001t0006g0278 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.100-25837G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864367 | ||||||
chr1:165864625
|
G | T | 1 | a0001c0001t0002g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100-25579G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864625 | ||||||
chr1:165864745
|
T | C | 2 | a0001c0001t0001g0048a0001c0001t0001g0050 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.100-25459T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864745 | ||||||
chr1:165864821
|
AG | A | 54 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(51): Show | 56 | HG00099.hp2 HG00323.hp2 HG01081.hp1 others(53): Show |
intron_variant | MODIFIER | c.100-25379delG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165864821 | |||||
chr1:165864845
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.100-25359A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864845 | ||||||
chr1:165864880
|
T | G | 214 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(211): Show | 217 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(214): Show |
intron_variant | MODIFIER | c.100-25324T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864880 | ||||||
chr1:165864886
|
A | C | 213 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(210): Show | 216 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.100-25318A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165864886 | ||||||
chr1:165865015
|
G | A | 213 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0052others(210): Show | 216 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(213): Show |
intron_variant | MODIFIER | c.100-25189G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865015 | ||||||
chr1:165865150
|
T | C | 1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.100-25054T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865150 | ||||||
chr1:165865217
|
G | A | 1 | a0001c0001t0021g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-24987G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865217 | ||||||
chr1:165865252
|
A | G | 24 | a0001c0001t0001g0301a0001c0001t0002g0217a0001c0001t0003g0208others(21): Show | 24 | HG00735.hp2 HG01243.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.100-24952A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865252 | ||||||
chr1:165865368
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.100-24836G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865368 | ||||||
chr1:165865573
|
T | C | 13 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(10): Show | 13 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-24631T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865573 | ||||||
chr1:165865646
|
A | G | 2 | a0001c0001t0002g0162a0001c0001t0002g0270 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.100-24558A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865646 | ||||||
chr1:165865957
|
A | G | 127 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(124): Show | 128 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(125): Show |
intron_variant | MODIFIER | c.100-24247A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865957 | ||||||
chr1:165865998
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.100-24206G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165865998 | ||||||
chr1:165866070
|
G | A | 13 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(10): Show | 13 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-24134G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165866070 | ||||||
chr1:165866127
|
C | T | 217 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(214): Show | 220 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(217): Show |
intron_variant | MODIFIER | c.100-24077C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165866127 | ||||||
chr1:165866154
|
A | G | 165 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(162): Show | 168 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(165): Show |
intron_variant | MODIFIER | c.100-24050A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165866154 | ||||||
chr1:165866218
|
A | G | 66 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(63): Show | 68 | HG00323.hp2 HG00673.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.100-23986A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165866218 | ||||||
chr1:165866366
|
C | T | 1 | a0001c0001t0030g0051 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.100-23838C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165866366 | ||||||
chr1:165866489
|
A | G | 24 | a0001c0001t0001g0301a0001c0001t0002g0217a0001c0001t0003g0208others(21): Show | 24 | HG00735.hp2 HG01243.hp1 HG02486.hp1 others(21): Show |
intron_variant | MODIFIER | c.100-23715A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165866489 | ||||||
chr1:165867118
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.100-23086T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867118 | ||||||
chr1:165867155
|
C | T | 10 | a0001c0001t0004g0009a0001c0001t0004g0305a0001c0001t0009g0062others(7): Show | 10 | HG02145.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-23049C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867155 | ||||||
chr1:165867199
|
A | T | 2 | a0001c0001t0004g0013a0001c0001t0004g0094 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.100-23005A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867199 | ||||||
chr1:165867230
|
T | C | 4 | a0001c0001t0002g0109a0001c0001t0002g0113a0001c0001t0004g0137others(1): Show | 4 | HG03098.hp1 HG06807.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-22974T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867230 | ||||||
chr1:165867468
|
T | A | 4 | a0001c0001t0006g0115a0001c0001t0006g0116a0001c0001t0006g0117others(1): Show | 4 | HG01891.hp1 HG03041.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-22736T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867468 | ||||||
chr1:165867512
|
A | G | 13 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(10): Show | 13 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-22692A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867512 | ||||||
chr1:165867845
|
A | G | 1 | a0001c0001t0004g0254 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.100-22359A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867845 | ||||||
chr1:165867957
|
C | T | 4 | a0001c0001t0006g0107a0001c0001t0006g0110a0001c0001t0006g0298others(1): Show | 4 | HG02572.hp2 HG02615.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-22247C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165867957 | ||||||
chr1:165868498
|
G | A | 13 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(10): Show | 13 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-21706G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165868498 | ||||||
chr1:165868578
|
A | G | 1 | a0001c0001t0009g0296 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.100-21626A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165868578 | ||||||
chr1:165868625
|
T | G | 6 | a0001c0001t0010g0093a0001c0001t0010g0170a0001c0001t0010g0247others(3): Show | 6 | HG02132.hp2 HG02135.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-21579T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165868625 | ||||||
chr1:165868740
|
T | A | 2 | a0001c0001t0024g0078a0001c0001t0027g0084 | 2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.100-21464T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165868740 | ||||||
chr1:165868741
|
C | T | 89 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(86): Show | 90 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(87): Show |
intron_variant | MODIFIER | c.100-21463C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165868741 | ||||||
chr1:165868745
|
G | A | 1 | a0001c0001t0009g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-21459G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165868745 | ||||||
chr1:165869033
|
A | G | 1 | a0001c0001t0027g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.100-21171A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869033 | ||||||
chr1:165869047
|
C | A | 2 | a0001c0001t0004g0009a0001c0001t0004g0305 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.100-21157C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869047 | ||||||
chr1:165869091
|
A | G | 1 | a0001c0001t0004g0310 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.100-21113A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869091 | ||||||
chr1:165869138
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0124 | 2 | HG01109.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.100-21066C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869138 | ||||||
chr1:165869151
|
A | T | 1 | a0001c0001t0012g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-21053A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869151 | ||||||
chr1:165869358
|
AC | A | 10 | a0001c0001t0004g0009a0001c0001t0004g0305a0001c0001t0009g0062others(7): Show | 10 | HG02145.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-20845delC | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869358 | ||||||
chr1:165869365
|
A | G | 10 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(7): Show | 10 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-20839A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869365 | ||||||
chr1:165869417
|
T | G | 3 | a0001c0001t0006g0167a0001c0001t0006g0168a0001c0001t0006g0277 | 3 | HG02486.hp2 HG03486.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.100-20787T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869417 | ||||||
chr1:165869484
|
T | G | 1 | a0001c0001t0007g0090 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.100-20720T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869484 | ||||||
chr1:165869622
|
C | T | 1 | a0001c0002t0005g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.100-20582C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869622 | ||||||
chr1:165869644
|
A | T | 1 | a0001c0001t0001g0242 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.100-20560A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869644 | ||||||
chr1:165869659
|
C | CT | 16 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0001g0152others(13): Show | 16 | HG01496.hp1 HG01515.hp2 HG01975.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-20522dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165869659 | |||||
chr1:165869659
|
C | CTT | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(107): Show |
intron_variant | MODIFIER | c.100-20523_100-2052 others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165869659 | |||||
chr1:165869659
|
C | CTTT | 17 | a0001c0001t0001g0098a0001c0001t0001g0251a0001c0001t0001g0291others(14): Show | 17 | HG00673.hp2 HG01106.hp1 HG01192.hp2 others(14): Show |
intron_variant | MODIFIER | c.100-20524_100-2052 others(7): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165869659 | |||||
chr1:165869659
|
C | T | 1 | a0001c0001t0012g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-20545C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869659 | ||||||
chr1:165869659
|
CT | C | 134 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0142others(131): Show | 137 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.100-20522delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165869659 | |||||
chr1:165869659
|
CTT | C | 10 | a0001c0001t0001g0123a0001c0001t0002g0015a0001c0001t0002g0138others(7): Show | 10 | HG00735.hp1 HG01070.hp2 HG01071.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-20523_100-2052 others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165869659 | |||||
chr1:165869690
|
TG | T | 257 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(254): Show | 258 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(255): Show |
intron_variant | MODIFIER | c.100-20509delG | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165869690 | |||||
chr1:165869713
|
C | T | 2 | a0001c0001t0002g0162a0001c0001t0002g0270 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.100-20491C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869713 | ||||||
chr1:165869784
|
G | A | 1 | a0001c0002t0005g0303 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-20420G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869784 | ||||||
chr1:165869794
|
T | C | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-20410T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165869794 | ||||||
chr1:165870196
|
A | G | 5 | a0001c0001t0001g0031a0001c0001t0001g0149a0001c0001t0001g0198others(2): Show | 5 | NA18942.hp2 NA18964.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-20008A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870196 | ||||||
chr1:165870201
|
AT | A | 286 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(283): Show | 289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.100-19984delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165870201 | |||||
chr1:165870201
|
ATT | A | 18 | a0001c0001t0003g0208a0001c0001t0004g0059a0001c0001t0004g0065others(15): Show | 18 | HG00735.hp2 HG01243.hp1 HG02486.hp1 others(15): Show |
intron_variant | MODIFIER | c.100-19985_100-1998 others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165870201 | |||||
chr1:165870260
|
C | T | 6 | a0001c0001t0002g0109a0001c0001t0002g0113a0001c0001t0004g0137others(3): Show | 6 | HG03098.hp1 HG03453.hp1 HG06807.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-19944C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870260 | ||||||
chr1:165870263
|
TAATTTTA others(108): Show |
T | 13 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(10): Show | 13 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-19913_100-1979 others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165870263 | |||||
chr1:165870291
|
TTGCTCAC others(108): Show |
T | 1 | a0001c0001t0001g0031 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.100-19752_100-1963 others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165870291 | |||||
chr1:165870313
|
C | T | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-19891C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870313 | ||||||
chr1:165870495
|
A | G | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(107): Show |
intron_variant | MODIFIER | c.100-19709A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870495 | ||||||
chr1:165870510
|
T | C | 2 | a0001c0001t0019g0079a0001c0001t0036g0136 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.100-19694T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870510 | ||||||
chr1:165870777
|
GT | G | 104 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(101): Show |
intron_variant | MODIFIER | c.100-19426delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870777 | ||||||
chr1:165870843
|
A | T | 6 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0009g0105others(3): Show | 6 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-19361A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870843 | ||||||
chr1:165870880
|
C | T | 13 | a0001c0001t0003g0204a0001c0001t0003g0205a0001c0001t0003g0206others(10): Show | 13 | HG00673.hp2 HG01192.hp2 HG01943.hp1 others(10): Show |
intron_variant | MODIFIER | c.100-19324C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870880 | ||||||
chr1:165870903
|
C | T | 5 | a0001c0001t0011g0043a0001c0001t0011g0201a0001c0001t0011g0225others(2): Show | 5 | NA18944.hp2 NA18957.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-19301C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870903 | ||||||
chr1:165870907
|
G | A | 110 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(107): Show | 110 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(107): Show |
intron_variant | MODIFIER | c.100-19297G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165870907 | ||||||
chr1:165871064
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.100-19140G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871064 | ||||||
chr1:165871167
|
G | T | 2 | a0001c0001t0001g0027a0001c0001t0001g0187 | 2 | HG02738.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.100-19037G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871167 | ||||||
chr1:165871174
|
C | T | 104 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(101): Show |
intron_variant | MODIFIER | c.100-19030C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871174 | ||||||
chr1:165871344
|
A | G | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.100-18860A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871344 | ||||||
chr1:165871387
|
T | C | 8 | a0001c0001t0001g0045a0001c0001t0001g0098a0001c0001t0001g0249others(5): Show | 8 | HG01257.hp1 HG01258.hp1 HG01975.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-18817T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871387 | ||||||
chr1:165871591
|
A | G | 1 | a0001c0001t0008g0046 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.100-18613A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871591 | ||||||
chr1:165871763
|
C | T | 1 | a0001c0001t0037g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.100-18441C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165871763 | ||||||
chr1:165872025
|
C | CT | 125 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(122): Show | 125 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(122): Show |
intron_variant | MODIFIER | c.100-18167dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165872025 | |||||
chr1:165872036
|
T | C | 1 | a0001c0001t0007g0020 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.100-18168T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165872036 | ||||||
chr1:165872381
|
T | G | 1 | a0001c0001t0012g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-17823T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165872381 | ||||||
chr1:165872517
|
A | T | 3 | a0001c0001t0008g0028a0001c0001t0008g0072a0001c0001t0008g0073 | 3 | HG03491.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.100-17687A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165872517 | ||||||
chr1:165872531
|
T | A | 4 | a0001c0001t0001g0131a0001c0001t0001g0144a0001c0001t0001g0235others(1): Show | 4 | HG00733.hp2 HG01070.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-17673T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165872531 | ||||||
chr1:165872531
|
T | TA | 8 | a0001c0001t0002g0095a0001c0001t0002g0139a0001c0001t0002g0174others(5): Show | 8 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.100-17667dupA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165872531 | |||||
chr1:165872776
|
C | T | 6 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0009g0105others(3): Show | 6 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-17428C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165872776 | ||||||
chr1:165872777
|
G | A | 12 | a0001c0001t0004g0009a0001c0001t0004g0305a0001c0001t0009g0062others(9): Show | 12 | HG02145.hp1 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-17427G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165872777 | ||||||
chr1:165873042
|
C | T | 1 | a0001c0001t0033g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100-17162C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873042 | ||||||
chr1:165873111
|
C | T | 4 | a0001c0001t0002g0109a0001c0001t0002g0113a0001c0001t0004g0137others(1): Show | 4 | HG03098.hp1 HG06807.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-17093C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873111 | ||||||
chr1:165873158
|
T | G | 1 | a0001c0001t0012g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-17046T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873158 | ||||||
chr1:165873222
|
C | T | 5 | a0001c0002t0005g0029a0001c0002t0005g0077a0001c0002t0005g0237others(2): Show | 5 | HG02155.hp2 NA18747.hp1 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-16982C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873222 | ||||||
chr1:165873488
|
C | T | 98 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(95): Show | 98 | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(95): Show |
intron_variant | MODIFIER | c.100-16716C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873488 | ||||||
chr1:165873599
|
C | T | 2 | a0001c0001t0019g0079a0001c0001t0036g0136 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.100-16605C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873599 | ||||||
chr1:165873759
|
G | A | 6 | a0001c0001t0001g0048a0001c0001t0001g0050a0001c0001t0009g0105others(3): Show | 6 | HG02615.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.100-16445G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873759 | ||||||
chr1:165873832
|
C | T | 90 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(87): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.100-16372C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873832 | ||||||
chr1:165873838
|
C | G | 1 | a0001c0001t0001g0189 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.100-16366C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165873838 | ||||||
chr1:165874149
|
CAG | C | 5 | a0001c0001t0009g0105a0001c0001t0012g0010a0001c0001t0017g0288others(2): Show | 5 | HG02615.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-16054_100-1605 others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874149 | ||||||
chr1:165874209
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.100-15995C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874209 | ||||||
chr1:165874438
|
C | T | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-15766C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874438 | ||||||
chr1:165874538
|
A | G | 2 | a0001c0001t0002g0133a0001c0001t0002g0294 | 2 | HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.100-15666A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874538 | ||||||
chr1:165874609
|
A | G | 1 | a0001c0002t0005g0303 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.100-15595A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874609 | ||||||
chr1:165874786
|
A | G | 4 | a0001c0001t0009g0105a0001c0001t0017g0288a0001c0001t0017g0289others(1): Show | 4 | HG02615.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-15418A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874786 | ||||||
chr1:165874827
|
T | A | 1 | a0001c0001t0033g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.100-15377T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874827 | ||||||
chr1:165874859
|
C | G | 9 | a0001c0001t0004g0137a0001c0001t0009g0062a0001c0001t0009g0063others(6): Show | 9 | HG02647.hp1 HG02723.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-15345C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874859 | ||||||
chr1:165874895
|
G | A | 1 | a0001c0001t0008g0014 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.100-15309G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165874895 | ||||||
chr1:165875038
|
C | CAA | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-15150_100-1514 others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165875038 | |||||
chr1:165875038
|
CA | C | 118 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(115): Show | 119 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.100-15149delA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165875038 | |||||
chr1:165875368
|
T | A | 3 | a0001c0001t0008g0028a0001c0001t0008g0072a0001c0001t0008g0073 | 3 | HG03491.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.100-14836T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165875368 | ||||||
chr1:165875493
|
G | C | 1 | a0001c0001t0003g0229 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.100-14711G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165875493 | ||||||
chr1:165875695
|
T | C | 9 | a0001c0001t0006g0067a0001c0001t0006g0111a0001c0001t0006g0119others(6): Show | 9 | HG01884.hp1 HG01891.hp2 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-14509T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165875695 | ||||||
chr1:165875748
|
G | A | 1 | a0001c0001t0009g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-14456G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165875748 | ||||||
chr1:165875805
|
C | T | 105 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(102): Show | 106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.100-14399C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165875805 | ||||||
chr1:165875867
|
G | T | 1 | a0001c0001t0001g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.100-14337G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165875867 | ||||||
chr1:165876213
|
C | A | 1 | a0001c0002t0005g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.100-13991C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876213 | ||||||
chr1:165876237
|
C | G | 2 | a0001c0001t0002g0042a0001c0001t0002g0240 | 2 | HG03239.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.100-13967C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876237 | ||||||
chr1:165876245
|
G | A | 4 | a0001c0001t0002g0217a0001c0001t0014g0016a0001c0001t0014g0017others(1): Show | 4 | NA19010.hp1 NA19062.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-13959G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876245 | ||||||
chr1:165876317
|
A | G | 1 | a0001c0001t0019g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-13887A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876317 | ||||||
chr1:165876407
|
T | C | 60 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(57): Show | 62 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.100-13797T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876407 | ||||||
chr1:165876504
|
A | G | 1 | a0001c0001t0002g0309 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.100-13700A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876504 | ||||||
chr1:165876662
|
A | G | 1 | a0001c0001t0007g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.100-13542A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876662 | ||||||
chr1:165876781
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.100-13423A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876781 | ||||||
chr1:165876890
|
G | A | 3 | a0001c0001t0013g0083a0001c0001t0013g0134a0001c0001t0013g0317 | 3 | HG02258.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.100-13314G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165876890 | ||||||
chr1:165877189
|
A | G | 1 | a0001c0001t0021g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-13015A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877189 | ||||||
chr1:165877199
|
G | T | 1 | a0001c0001t0009g0012 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.100-13005G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877199 | ||||||
chr1:165877278
|
CATTTT | C | 105 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(102): Show | 106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.100-12925_100-1292 others(9): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877278 | ||||||
chr1:165877432
|
C | T | 1 | a0001c0001t0006g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.100-12772C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877432 | ||||||
chr1:165877441
|
C | T | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-12763C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877441 | ||||||
chr1:165877468
|
C | T | 5 | a0001c0001t0011g0043a0001c0001t0011g0201a0001c0001t0011g0225others(2): Show | 5 | NA18944.hp2 NA18957.hp1 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-12736C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877468 | ||||||
chr1:165877470
|
G | A | 7 | a0001c0001t0008g0014a0001c0001t0008g0036a0001c0001t0008g0046others(4): Show | 7 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-12734G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877470 | ||||||
chr1:165877519
|
G | T | 1 | a0001c0001t0019g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-12685G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877519 | ||||||
chr1:165877575
|
T | C | 1 | a0001c0001t0002g0001 | 3 | HG01081.hp1 HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.100-12629T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877575 | ||||||
chr1:165877616
|
G | A | 1 | a0001c0001t0027g0084 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.100-12588G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877616 | ||||||
chr1:165877642
|
G | A | 1 | a0001c0001t0009g0292 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.100-12562G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877642 | ||||||
chr1:165877643
|
T | C | 1 | a0001c0001t0023g0302 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100-12561T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165877643 | ||||||
chr1:165878252
|
T | C | 105 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(102): Show | 106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.100-11952T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878252 | ||||||
chr1:165878329
|
T | C | 60 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(57): Show | 62 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(59): Show |
intron_variant | MODIFIER | c.100-11875T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878329 | ||||||
chr1:165878335
|
CT | C | 105 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(102): Show | 106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.100-11856delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165878335 | |||||
chr1:165878374
|
G | A | 16 | a0001c0001t0002g0095a0001c0001t0002g0109a0001c0001t0002g0113others(13): Show | 16 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(13): Show |
intron_variant | MODIFIER | c.100-11830G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878374 | ||||||
chr1:165878413
|
C | T | 3 | a0001c0001t0004g0137a0001c0001t0009g0012a0001c0001t0009g0296 | 3 | HG02965.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100-11791C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878413 | ||||||
chr1:165878519
|
C | T | 1 | a0001c0001t0002g0095 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.100-11685C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878519 | ||||||
chr1:165878619
|
C | T | 1 | a0001c0001t0001g0212 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.100-11585C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878619 | ||||||
chr1:165878649
|
C | T | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-11555C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878649 | ||||||
chr1:165878712
|
C | T | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-11492C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165878712 | ||||||
chr1:165879172
|
G | A | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-11032G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879172 | ||||||
chr1:165879447
|
G | A | 2 | a0001c0001t0009g0062a0001c0001t0009g0276 | 2 | HG02922.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.100-10757G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879447 | ||||||
chr1:165879473
|
A | G | 1 | a0001c0002t0005g0088 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.100-10731A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879473 | ||||||
chr1:165879545
|
T | TTTA | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-10635_100-1063 others(7): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | |||||
chr1:165879545
|
T | TTTATTA | 8 | a0001c0001t0002g0095a0001c0001t0002g0109a0001c0001t0002g0113others(5): Show | 8 | HG00673.hp1 HG02258.hp1 HG03098.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-10638_100-1063 others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | |||||
chr1:165879545
|
T | TTTATTAT others(2): Show |
9 | a0001c0001t0002g0070a0001c0001t0002g0162a0001c0001t0002g0270others(6): Show | 9 | HG01081.hp2 HG01256.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-10641_100-1063 others(13): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | |||||
chr1:165879545
|
T | TTTATTAT others(5): Show |
94 | a0001c0001t0001g0100a0001c0001t0002g0001a0001c0001t0002g0015others(91): Show | 97 | HG00099.hp2 HG00323.hp2 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.100-10644_100-1063 others(16): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | |||||
chr1:165879545
|
T | TTTATTAT others(8): Show |
23 | a0001c0001t0002g0042a0001c0001t0002g0056a0001c0001t0002g0096others(20): Show | 23 | HG00639.hp1 HG01243.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.100-10647_100-1063 others(19): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | |||||
chr1:165879545
|
T | TTTATTAT others(11): Show |
33 | a0001c0001t0001g0052a0001c0001t0001g0123a0001c0001t0001g0142others(30): Show | 33 | HG00323.hp1 HG00639.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.100-10650_100-1063 others(22): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | |||||
chr1:165879545
|
T | TTTATTAT others(14): Show |
11 | a0001c0001t0001g0172a0001c0001t0003g0208a0001c0001t0004g0175others(8): Show | 11 | HG00140.hp2 HG01071.hp2 HG01099.hp1 others(8): Show |
intron_variant | MODIFIER | c.100-10653_100-1063 others(25): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | |||||
chr1:165879545
|
T | TTTATTAT others(17): Show |
1 | a0001c0001t0007g0157 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.100-10656_100-1063 others(28): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | |||||
chr1:165879545
|
T | TTTATTAT others(20): Show |
2 | a0001c0001t0004g0282a0001c0001t0007g0055 | 2 | HG03225.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.100-10633_100-1063 others(31): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165879545 | |||||
chr1:165879572
|
T | A | 1 | a0001c0001t0004g0312 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.100-10632T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879572 | ||||||
chr1:165879688
|
T | G | 11 | a0001c0001t0002g0095a0001c0001t0002g0109a0001c0001t0002g0113others(8): Show | 11 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-10516T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879688 | ||||||
chr1:165879819
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.100-10385A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879819 | ||||||
chr1:165879976
|
G | T | 202 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(199): Show | 205 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(202): Show |
intron_variant | MODIFIER | c.100-10228G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165879976 | ||||||
chr1:165880062
|
A | T | 1 | a0001c0001t0003g0204 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100-10142A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880062 | ||||||
chr1:165880200
|
C | T | 1 | a0001c0001t0003g0164 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.100-10004C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880200 | ||||||
chr1:165880260
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.100-9944C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880260 | ||||||
chr1:165880483
|
G | A | 1 | a0001c0001t0002g0108 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.100-9721G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880483 | ||||||
chr1:165880559
|
TTTTGGGG others(3): Show |
T | 2 | a0001c0001t0008g0072a0001c0001t0008g0073 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.100-9643_100-9634d others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880559 | |||||
chr1:165880560
|
TTTGG | T | 4 | a0001c0001t0008g0014a0001c0001t0008g0036a0001c0001t0008g0046others(1): Show | 4 | HG01192.hp2 HG02273.hp1 HG02523.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-9643_100-9640d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880560 | ||||||
chr1:165880562
|
TGG | T | 37 | a0001c0001t0001g0031a0001c0001t0001g0047a0001c0001t0001g0048others(34): Show | 37 | HG00438.hp1 HG00741.hp1 HG00741.hp2 others(34): Show |
intron_variant | MODIFIER | c.100-9638_100-9637d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880562 | |||||
chr1:165880562
|
TGGGGGTG others(6): Show |
T | 1 | a0001c0001t0003g0032 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.100-9641_100-9629d others(15): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880562 | ||||||
chr1:165880562
|
TGGGGGTG others(10): Show |
T | 17 | a0001c0001t0001g0123a0001c0001t0003g0211a0001c0001t0003g0229others(14): Show | 17 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-9641_100-9625d others(19): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880562 | ||||||
chr1:165880562
|
TGGGGGTG others(12): Show |
T | 89 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0142others(86): Show | 90 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.100-9641_100-9623d others(21): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880562 | ||||||
chr1:165880562
|
TGGGGGTG others(14): Show |
T | 1 | a0001c0001t0003g0204 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100-9641_100-9621d others(23): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880562 | ||||||
chr1:165880563
|
G | T | 1 | a0001c0001t0007g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.100-9641G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880563 | ||||||
chr1:165880564
|
GGGGT | G | 40 | a0001c0001t0001g0011a0001c0001t0001g0025a0001c0001t0001g0030others(37): Show | 40 | HG00673.hp1 HG00733.hp2 HG01070.hp1 others(37): Show |
intron_variant | MODIFIER | c.100-9638_100-9635d others(6): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | |||||
chr1:165880564
|
GGGGTGT | G | 16 | a0001c0001t0001g0054a0001c0001t0001g0179a0001c0001t0001g0187others(13): Show | 16 | HG00099.hp1 HG01516.hp1 HG02027.hp1 others(13): Show |
intron_variant | MODIFIER | c.100-9638_100-9633d others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | |||||
chr1:165880564
|
GGGGTGTG others(7): Show |
G | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-9638_100-9625d others(16): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | |||||
chr1:165880564
|
GGGGTGTG others(9): Show |
G | 1 | a0001c0001t0004g0137 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.100-9638_100-9623d others(18): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | |||||
chr1:165880564
|
GGGGTGTG others(11): Show |
G | 10 | a0001c0001t0001g0040a0001c0001t0009g0012a0001c0001t0009g0062others(7): Show | 10 | HG02040.hp1 HG02647.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-9638_100-9621d others(20): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | |||||
chr1:165880564
|
GGGGTGTG others(15): Show |
G | 2 | a0001c0001t0002g0162a0001c0001t0002g0270 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.100-9638_100-9617d others(24): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | |||||
chr1:165880564
|
GGGGTGTG others(19): Show |
G | 1 | a0001c0001t0002g0001 | 3 | HG01081.hp1 HG01099.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.100-9638_100-9613d others(28): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | |||||
chr1:165880564
|
GGGGTGTG others(21): Show |
G | 52 | a0001c0001t0002g0015a0001c0001t0002g0034a0001c0001t0002g0037others(49): Show | 52 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(49): Show |
intron_variant | MODIFIER | c.100-9638_100-9611d others(30): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880564 | |||||
chr1:165880566
|
G | T | 36 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0019others(33): Show | 36 | HG00140.hp1 HG00738.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.100-9638G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880566 | ||||||
chr1:165880566
|
GGTGTGTG others(21): Show |
G | 1 | a0001c0001t0002g0038 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.100-9616_100-9589d others(30): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165880566 | |||||
chr1:165880567
|
GTGTGTGT others(12): Show |
G | 1 | a0001c0001t0007g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.100-9636_100-9618d others(21): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880567 | ||||||
chr1:165880578
|
T | G | 1 | a0001c0001t0003g0032 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.100-9626T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880578 | ||||||
chr1:165880582
|
T | G | 17 | a0001c0001t0001g0123a0001c0001t0003g0211a0001c0001t0003g0229others(14): Show | 17 | HG00099.hp2 HG00639.hp1 HG00735.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-9622T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880582 | ||||||
chr1:165880584
|
T | G | 89 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0142others(86): Show | 90 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.100-9620T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880584 | ||||||
chr1:165880586
|
T | G | 1 | a0001c0001t0003g0204 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100-9618T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880586 | ||||||
chr1:165880614
|
T | A | 2 | a0001c0001t0019g0079a0001c0001t0036g0136 | 2 | HG02451.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.100-9590T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880614 | ||||||
chr1:165880719
|
A | G | 1 | a0001c0001t0010g0261 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.100-9485A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880719 | ||||||
chr1:165880872
|
G | A | 1 | a0001c0001t0002g0309 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.100-9332G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165880872 | ||||||
chr1:165881083
|
G | A | 1 | a0001c0001t0001g0026 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.100-9121G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881083 | ||||||
chr1:165881133
|
A | G | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-9071A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881133 | ||||||
chr1:165881182
|
T | TA | 119 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(116): Show | 119 | HG00099.hp1 HG00438.hp1 HG00733.hp2 others(116): Show |
intron_variant | MODIFIER | c.100-8998dupA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165881182 | |||||
chr1:165881182
|
T | TAA | 9 | a0001c0001t0001g0089a0001c0001t0001g0124a0001c0001t0001g0187others(6): Show | 9 | HG02738.hp1 HG02738.hp2 HG02809.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-8999_100-8998d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165881182 | |||||
chr1:165881182
|
TA | T | 66 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(63): Show | 68 | HG00140.hp2 HG00323.hp2 HG01070.hp2 others(65): Show |
intron_variant | MODIFIER | c.100-8998delA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165881182 | |||||
chr1:165881359
|
T | G | 112 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(109): Show | 113 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(110): Show |
intron_variant | MODIFIER | c.100-8845T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881359 | ||||||
chr1:165881363
|
G | T | 2 | a0001c0001t0001g0124a0001c0001t0001g0187 | 2 | HG02738.hp1 HG02738.hp2 |
intron_variant | MODIFIER | c.100-8841G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881363 | ||||||
chr1:165881461
|
T | A | 4 | a0001c0001t0009g0105a0001c0001t0017g0288a0001c0001t0017g0289others(1): Show | 4 | HG02615.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-8743T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881461 | ||||||
chr1:165881551
|
G | T | 1 | a0001c0002t0005g0099 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.100-8653G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881551 | ||||||
chr1:165881784
|
G | A | 1 | a0001c0001t0003g0041 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.100-8420G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165881784 | ||||||
chr1:165882053
|
G | T | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.100-8151G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882053 | ||||||
chr1:165882447
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.100-7757T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882447 | ||||||
chr1:165882559
|
C | T | 3 | a0001c0001t0003g0002a0001c0001t0003g0224a0001c0001t0003g0268 | 4 | HG00639.hp1 HG02300.hp2 HG03490.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-7645C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882559 | ||||||
chr1:165882564
|
A | G | 4 | a0001c0001t0009g0105a0001c0001t0017g0288a0001c0001t0017g0289others(1): Show | 4 | HG02615.hp2 HG02976.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.100-7640A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882564 | ||||||
chr1:165882577
|
G | T | 1 | a0001c0001t0012g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-7627G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882577 | ||||||
chr1:165882588
|
G | C | 11 | a0001c0001t0002g0095a0001c0001t0002g0109a0001c0001t0002g0113others(8): Show | 11 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-7616G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882588 | ||||||
chr1:165882596
|
C | A | 1 | a0001c0001t0021g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-7608C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882596 | ||||||
chr1:165882807
|
C | A | 1 | a0001c0001t0003g0204 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100-7397C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882807 | ||||||
chr1:165882942
|
G | A | 1 | a0001c0001t0023g0302 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.100-7262G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882942 | ||||||
chr1:165882975
|
C | T | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.100-7229C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165882975 | ||||||
chr1:165883015
|
C | G | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.100-7189C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883015 | ||||||
chr1:165883038
|
A | T | 1 | a0001c0001t0003g0204 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.100-7166A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883038 | ||||||
chr1:165883080
|
T | C | 10 | a0001c0001t0004g0137a0001c0001t0009g0012a0001c0001t0009g0062others(7): Show | 10 | HG02647.hp1 HG02723.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-7124T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883080 | ||||||
chr1:165883137
|
A | G | 1 | a0001c0001t0002g0161 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.100-7067A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883137 | ||||||
chr1:165883783
|
C | T | 54 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(51): Show | 56 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(53): Show |
intron_variant | MODIFIER | c.100-6421C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883783 | ||||||
chr1:165883914
|
C | T | 2 | a0001c0001t0017g0288a0001c0001t0017g0289 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.100-6290C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883914 | ||||||
chr1:165883992
|
T | C | 107 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(104): Show | 107 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.100-6212T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165883992 | ||||||
chr1:165884065
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.100-6139G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165884065 | ||||||
chr1:165884116
|
A | G | 10 | a0001c0001t0004g0137a0001c0001t0009g0012a0001c0001t0009g0062others(7): Show | 10 | HG02647.hp1 HG02723.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-6088A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165884116 | ||||||
chr1:165884246
|
C | T | 10 | a0001c0001t0004g0137a0001c0001t0009g0012a0001c0001t0009g0062others(7): Show | 10 | HG02647.hp1 HG02723.hp2 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-5958C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165884246 | ||||||
chr1:165884330
|
C | G | 15 | a0001c0001t0002g0015a0001c0001t0002g0096a0001c0001t0002g0138others(12): Show | 15 | HG01070.hp2 HG01071.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.100-5874C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165884330 | ||||||
chr1:165884368
|
G | A | 1 | a0001c0001t0007g0020 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.100-5836G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165884368 | ||||||
chr1:165884432
|
C | G | 1 | a0001c0001t0010g0258 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.100-5772C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165884432 | ||||||
chr1:165885040
|
G | T | 1 | a0001c0001t0012g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.100-5164G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165885040 | ||||||
chr1:165885661
|
G | A | 1 | a0001c0001t0001g0143 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.100-4543G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165885661 | ||||||
chr1:165885705
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.100-4499C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165885705 | ||||||
chr1:165885907
|
A | G | 2 | a0001c0001t0017g0288a0001c0001t0017g0289 | 2 | HG02976.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.100-4297A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165885907 | ||||||
chr1:165886063
|
G | A | 7 | a0001c0001t0008g0014a0001c0001t0008g0036a0001c0001t0008g0046others(4): Show | 7 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-4141G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886063 | ||||||
chr1:165886085
|
G | A | 1 | a0001c0001t0004g0118 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100-4119G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886085 | ||||||
chr1:165886161
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0089a0001c0001t0001g0179 | 3 | HG00099.hp1 HG01358.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.100-4043T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886161 | ||||||
chr1:165886270
|
G | C | 1 | a0001c0001t0004g0282 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.100-3934G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886270 | ||||||
chr1:165886304
|
AT | A | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-3893delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165886304 | |||||
chr1:165886352
|
T | C | 1 | a0001c0001t0003g0223 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.100-3852T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886352 | ||||||
chr1:165886522
|
T | G | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-3682T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886522 | ||||||
chr1:165886578
|
C | T | 5 | a0001c0001t0009g0105a0001c0001t0012g0010a0001c0001t0017g0288others(2): Show | 5 | HG02615.hp2 HG02976.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-3626C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886578 | ||||||
chr1:165886580
|
C | T | 11 | a0001c0001t0002g0095a0001c0001t0002g0109a0001c0001t0002g0113others(8): Show | 11 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-3624C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886580 | ||||||
chr1:165886883
|
T | C | 68 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(65): Show | 70 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(67): Show |
intron_variant | MODIFIER | c.100-3321T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165886883 | ||||||
chr1:165887078
|
C | T | 58 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(55): Show | 60 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.100-3126C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165887078 | ||||||
chr1:165887138
|
G | C | 1 | a0001c0001t0007g0020 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.100-3066G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165887138 | ||||||
chr1:165887483
|
G | A | 1 | a0001c0001t0007g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.100-2721G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165887483 | ||||||
chr1:165887543
|
A | G | 3 | a0001c0001t0014g0016a0001c0001t0014g0017a0001c0001t0014g0018 | 3 | NA19062.hp1 NA19086.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.100-2661A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165887543 | ||||||
chr1:165887637
|
G | A | 3 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0192 | 3 | NA18995.hp1 NA19007.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.100-2567G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165887637 | ||||||
chr1:165887771
|
T | TC | 109 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(106): Show | 110 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(107): Show |
intron_variant | MODIFIER | c.100-2425dupC | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165887771 | |||||
chr1:165888135
|
A | G | 3 | a0001c0001t0004g0137a0001c0001t0009g0012a0001c0001t0009g0296 | 3 | HG02965.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.100-2069A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888135 | ||||||
chr1:165888247
|
A | G | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.100-1957A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888247 | ||||||
chr1:165888432
|
C | T | 1 | a0001c0001t0002g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.100-1772C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888432 | ||||||
chr1:165888434
|
G | C | 11 | a0001c0001t0002g0095a0001c0001t0002g0109a0001c0001t0002g0113others(8): Show | 11 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.100-1770G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888434 | ||||||
chr1:165888482
|
G | A | 1 | a0001c0001t0007g0171 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.100-1722G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888482 | ||||||
chr1:165888642
|
C | CT | 56 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(53): Show | 58 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.100-1538dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165888642 | |||||
chr1:165888642
|
CT | C | 51 | a0001c0001t0001g0025a0001c0001t0001g0030a0001c0001t0001g0045others(48): Show | 51 | HG00673.hp1 HG00733.hp2 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.100-1538delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165888642 | |||||
chr1:165888642
|
CTT | C | 88 | a0001c0001t0001g0052a0001c0001t0001g0100a0001c0001t0001g0123others(85): Show | 89 | HG00099.hp2 HG00140.hp2 HG00438.hp2 others(86): Show |
intron_variant | MODIFIER | c.100-1539_100-1538d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165888642 | |||||
chr1:165888642
|
CTTT | C | 8 | a0001c0001t0003g0032a0001c0001t0003g0039a0001c0001t0003g0087others(5): Show | 8 | HG00323.hp1 HG02896.hp2 HG03195.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-1540_100-1538d others(5): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165888642 | |||||
chr1:165888750
|
T | C | 1 | a0001c0001t0008g0036 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.100-1454T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888750 | ||||||
chr1:165888973
|
G | C | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.100-1231G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888973 | ||||||
chr1:165888999
|
A | T | 2 | a0001c0001t0004g0013a0001c0001t0004g0094 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.100-1205A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165888999 | ||||||
chr1:165889117
|
C | T | 90 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(87): Show | 90 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(87): Show |
intron_variant | MODIFIER | c.100-1087C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889117 | ||||||
chr1:165889151
|
G | A | 56 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(53): Show | 58 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(55): Show |
intron_variant | MODIFIER | c.100-1053G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889151 | ||||||
chr1:165889216
|
T | C | 1 | a0001c0001t0021g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.100-988T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889216 | ||||||
chr1:165889232
|
G | A | 10 | a0001c0001t0002g0095a0001c0001t0002g0109a0001c0001t0002g0113others(7): Show | 10 | HG00673.hp1 HG01256.hp2 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-972G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889232 | ||||||
chr1:165889504
|
C | G | 1 | a0001c0001t0037g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.100-700C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889504 | ||||||
chr1:165889631
|
T | C | 2 | a0001c0001t0004g0304a0001c0001t0029g0132 | 2 | HG02280.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.100-573T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889631 | ||||||
chr1:165889645
|
C | T | 2 | a0001c0001t0016g0066a0001c0001t0016g0286 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.100-559C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889645 | ||||||
chr1:165889669
|
C | T | 2 | a0001c0001t0012g0010a0001c0001t0012g0103 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.100-535C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889669 | ||||||
chr1:165889688
|
C | CT | 132 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.100-497dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165889688 | |||||
chr1:165889688
|
CT | C | 18 | a0001c0001t0002g0178a0001c0001t0003g0032a0001c0001t0003g0041others(15): Show | 18 | HG00323.hp1 HG01192.hp2 HG01943.hp1 others(15): Show |
intron_variant | MODIFIER | c.100-497delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr1 | 165889688 | |||||
chr1:165889713
|
A | T | 1 | a0001c0001t0004g0118 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.100-491A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889713 | ||||||
chr1:165889789
|
C | T | 12 | a0001c0001t0004g0137a0001c0001t0009g0012a0001c0001t0009g0062others(9): Show | 12 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.100-415C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165889789 | ||||||
chr1:165890146
|
C | T | 1 | a0001c0001t0004g0305 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.100-58C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 1/6 | chr1 | 165890146 | ||||||
chr1:165890381
|
G | A | 1 | a0001c0001t0007g0264 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.259+18G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890381 | ||||||
chr1:165890382
|
G | T | 1 | a0001c0001t0007g0264 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.259+19G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890382 | ||||||
chr1:165890393
|
C | G | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.259+30C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890393 | ||||||
chr1:165890403
|
G | GTGT | 10 | a0001c0001t0002g0056a0001c0001t0007g0020a0001c0001t0007g0055others(7): Show | 10 | HG00140.hp2 HG01099.hp1 HG01109.hp2 others(7): Show |
intron_variant | MODIFIER | c.259+43_259+45dupTT others(1): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr1 | 165890403 | |||||
chr1:165890503
|
G | A | 3 | a0001c0001t0003g0156a0001c0001t0003g0158a0001c0001t0003g0159 | 3 | HG01255.hp1 HG01257.hp2 HG01358.hp2 |
intron_variant | MODIFIER | c.259+140G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890503 | ||||||
chr1:165890601
|
G | A | 1 | a0001c0001t0007g0140 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.259+238G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890601 | ||||||
chr1:165890619
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.259+256G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890619 | ||||||
chr1:165890717
|
A | G | 1 | a0001c0001t0025g0275 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.259+354A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890717 | ||||||
chr1:165890809
|
A | C | 1 | a0001c0002t0015g0226 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.260-417A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890809 | ||||||
chr1:165890863
|
A | G | 1 | a0001c0001t0023g0302 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.260-363A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890863 | ||||||
chr1:165890934
|
A | C | 1 | a0001c0001t0002g0070 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.260-292A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 2/6 | chr1 | 165890934 | ||||||
chr1:165891494
|
G | A | 1 | a0001c0001t0009g0290 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.356+172G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891494 | ||||||
chr1:165891549
|
C | T | 1 | a0001c0001t0002g0085 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.356+227C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891549 | ||||||
chr1:165891569
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.356+247A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891569 | ||||||
chr1:165891576
|
A | C | 207 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(204): Show | 209 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.356+254A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891576 | ||||||
chr1:165891623
|
A | G | 1 | a0001c0002t0005g0141 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.356+301A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891623 | ||||||
chr1:165891630
|
C | T | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(203): Show | 208 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.356+308C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891630 | ||||||
chr1:165891866
|
T | G | 1 | a0001c0001t0010g0252 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.356+544T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891866 | ||||||
chr1:165891998
|
C | T | 12 | a0001c0001t0004g0137a0001c0001t0009g0012a0001c0001t0009g0062others(9): Show | 12 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(9): Show |
intron_variant | MODIFIER | c.356+676C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165891998 | ||||||
chr1:165892002
|
T | C | 1 | a0001c0001t0001g0019 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.356+680T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892002 | ||||||
chr1:165892146
|
T | TCTGAAAC others(2353): Show |
2 | a0001c0001t0016g0066a0001c0001t0016g0286 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.356+841_356+842ins others(2360): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2287): Show |
5 | a0001c0001t0006g0049a0001c0001t0006g0107a0001c0001t0006g0110others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.356+832_356+833ins others(2294): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2344): Show |
1 | a0001c0001t0001g0212 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2351): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2349): Show |
1 | a0001c0001t0001g0200 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2356): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2349): Show |
1 | a0001c0001t0001g0192 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2356): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2352): Show |
1 | a0001c0001t0001g0030 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2350): Show |
1 | a0001c0001t0001g0150 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0001g0184 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2350): Show |
1 | a0001c0001t0001g0207 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2350): Show |
2 | a0001c0001t0001g0054a0001c0001t0001g0089 | 2 | HG01516.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2344): Show |
1 | a0001c0001t0001g0097 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2351): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2350): Show |
14 | a0001c0001t0001g0025a0001c0001t0001g0031a0001c0001t0001g0045others(11): Show | 14 | HG01257.hp1 HG01975.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0001g0048 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2350): Show |
1 | a0001c0001t0001g0144 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2350): Show |
1 | a0001c0001t0006g0283 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2350): Show |
1 | a0001c0001t0001g0086 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2357): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0001g0130 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2300): Show |
1 | a0001c0001t0001g0102 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2307): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2352): Show |
1 | a0001c0001t0001g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0001g0245 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2352): Show |
1 | a0001c0001t0001g0185 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2124): Show |
1 | a0001c0001t0001g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2131): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2345): Show |
1 | a0001c0001t0036g0136 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2352): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0019g0079 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
6 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0100others(3): Show | 6 | HG00099.hp1 HG00639.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
43 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0026others(40): Show | 43 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
2 | a0001c0001t0001g0198a0001c0001t0026g0210 | 2 | NA18964.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2311): Show |
3 | a0001c0001t0001g0238a0001c0001t0001g0241a0001c0001t0001g0243 | 3 | NA18951.hp2 NA19002.hp1 NA19058.hp1 |
intron_variant | MODIFIER | c.356+832_356+833ins others(2318): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0001g0131 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
3 | a0001c0001t0001g0076a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | NA18973.hp2 NA19007.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0037g0287 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2352): Show |
1 | a0001c0001t0001g0181 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
4 | a0001c0001t0001g0021a0001c0001t0001g0024a0001c0001t0001g0143others(1): Show | 4 | HG00140.hp1 HG00741.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2353): Show |
1 | a0001c0001t0001g0165 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2360): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2352): Show |
1 | a0001c0001t0001g0047 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2352): Show |
1 | a0001c0001t0001g0235 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2356): Show |
1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2363): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2355): Show |
1 | a0001c0001t0001g0191 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2362): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2313): Show |
1 | a0001c0001t0001g0251 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2320): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2353): Show |
1 | a0001c0001t0001g0019 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2360): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2351): Show |
1 | a0001c0001t0001g0301 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2358): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2369): Show |
1 | a0001c0001t0023g0302 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2376): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2126): Show |
1 | a0001c0001t0001g0242 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.356+832_356+833ins others(2133): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2352): Show |
2 | a0001c0001t0001g0011a0001c0001t0001g0195 | 2 | NA19064.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.356+832_356+833ins others(2359): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892146
|
T | TCTGAAAC others(2353): Show |
1 | a0001c0001t0006g0116 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.356+832_356+833ins others(2360): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr1 | 165892146 | |||||
chr1:165892186
|
G | A | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.356+864G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892186 | ||||||
chr1:165892223
|
C | T | 1 | a0001c0001t0001g0316 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.356+901C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892223 | ||||||
chr1:165892224
|
G | A | 1 | a0001c0002t0005g0237 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.356+902G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892224 | ||||||
chr1:165892328
|
G | A | 7 | a0001c0001t0008g0014a0001c0001t0008g0036a0001c0001t0008g0046others(4): Show | 7 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.356+1006G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892328 | ||||||
chr1:165892356
|
T | C | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(203): Show | 208 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.356+1034T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892356 | ||||||
chr1:165892408
|
C | A | 6 | a0001c0001t0002g0108a0001c0001t0002g0133a0001c0001t0002g0294others(3): Show | 6 | HG02280.hp2 HG02717.hp1 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.356+1086C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892408 | ||||||
chr1:165892552
|
C | A | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.356+1230C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892552 | ||||||
chr1:165892608
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.356+1286G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892608 | ||||||
chr1:165892677
|
C | G | 1 | a0001c0001t0012g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.356+1355C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892677 | ||||||
chr1:165892849
|
G | A | 1 | a0001c0001t0023g0302 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.356+1527G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165892849 | ||||||
chr1:165893027
|
C | T | 62 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(59): Show | 64 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(61): Show |
intron_variant | MODIFIER | c.356+1705C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165893027 | ||||||
chr1:165893034
|
A | G | 2 | a0001c0001t0012g0010a0001c0001t0012g0103 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.356+1712A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165893034 | ||||||
chr1:165893086
|
T | A | 132 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.356+1764T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165893086 | ||||||
chr1:165894026
|
T | A | 3 | a0001c0001t0004g0137a0001c0001t0009g0012a0001c0001t0009g0296 | 3 | HG02965.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.357-2164T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894026 | ||||||
chr1:165894392
|
T | G | 3 | a0001c0001t0002g0108a0001c0001t0002g0133a0001c0001t0002g0294 | 3 | HG02717.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.357-1798T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894392 | ||||||
chr1:165894417
|
A | G | 1 | a0001c0001t0006g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.357-1773A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894417 | ||||||
chr1:165894449
|
A | G | 3 | a0001c0001t0008g0028a0001c0001t0008g0072a0001c0001t0008g0073 | 3 | HG03491.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.357-1741A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894449 | ||||||
chr1:165894485
|
C | T | 2 | a0001c0001t0001g0241a0001c0001t0001g0251 | 2 | NA19002.hp1 NA19078.hp1 |
intron_variant | MODIFIER | c.357-1705C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894485 | ||||||
chr1:165894671
|
T | C | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.357-1519T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894671 | ||||||
chr1:165894676
|
G | A | 2 | a0001c0001t0002g0174a0001c0001t0003g0313 | 2 | HG04199.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.357-1514G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894676 | ||||||
chr1:165894689
|
C | T | 1 | a0001c0001t0003g0173 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.357-1501C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894689 | ||||||
chr1:165894716
|
C | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG02895.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.357-1474C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165894716 | ||||||
chr1:165895071
|
C | A | 200 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(197): Show | 202 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(199): Show |
intron_variant | MODIFIER | c.357-1119C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165895071 | ||||||
chr1:165895137
|
A | G | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.357-1053A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165895137 | ||||||
chr1:165895243
|
G | A | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.357-947G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165895243 | ||||||
chr1:165895450
|
T | A | 132 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(129): Show | 132 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(129): Show |
intron_variant | MODIFIER | c.357-740T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165895450 | ||||||
chr1:165895607
|
G | A | 1 | a0001c0001t0004g0118 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.357-583G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165895607 | ||||||
chr1:165895742
|
G | A | 3 | a0001c0001t0002g0108a0001c0001t0002g0133a0001c0001t0002g0294 | 3 | HG02717.hp1 HG02723.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.357-448G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165895742 | ||||||
chr1:165896023
|
G | A | 1 | a0001c0002t0005g0228 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.357-167G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165896023 | ||||||
chr1:165896063
|
G | A | 57 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(54): Show | 59 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(56): Show |
intron_variant | MODIFIER | c.357-127G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 3/6 | chr1 | 165896063 | ||||||
chr1:165896457
|
G | A | 120 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(117): Show | 120 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.499+125G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165896457 | ||||||
chr1:165896536
|
G | C | 1 | a0001c0001t0010g0247 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.499+204G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165896536 | ||||||
chr1:165896864
|
A | G | 1 | a0001c0001t0006g0283 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.499+532A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165896864 | ||||||
chr1:165896870
|
T | C | 11 | a0001c0001t0009g0012a0001c0001t0009g0062a0001c0001t0009g0063others(8): Show | 11 | HG02615.hp2 HG02809.hp2 HG02886.hp2 others(8): Show |
intron_variant | MODIFIER | c.499+538T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165896870 | ||||||
chr1:165896976
|
A | C | 3 | a0001c0001t0004g0118a0001c0001t0004g0304a0001c0001t0029g0132 | 3 | HG02280.hp2 HG02809.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.499+644A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165896976 | ||||||
chr1:165896990
|
C | T | 1 | a0001c0001t0033g0008 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.499+658C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165896990 | ||||||
chr1:165897059
|
C | T | 1 | a0001c0001t0008g0166 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.499+727C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897059 | ||||||
chr1:165897212
|
G | T | 1 | a0001c0001t0007g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.499+880G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897212 | ||||||
chr1:165897364
|
C | T | 1 | a0001c0001t0003g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.499+1032C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897364 | ||||||
chr1:165897478
|
G | A | 3 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0096 | 3 | HG02735.hp2 HG04115.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.499+1146G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897478 | ||||||
chr1:165897652
|
C | T | 58 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(55): Show | 60 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(57): Show |
intron_variant | MODIFIER | c.499+1320C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897652 | ||||||
chr1:165897711
|
C | T | 2 | a0001c0001t0012g0010a0001c0001t0012g0103 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.499+1379C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897711 | ||||||
chr1:165897889
|
A | C | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.499+1557A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897889 | ||||||
chr1:165897931
|
A | G | 39 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(36): Show | 39 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.499+1599A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165897931 | ||||||
chr1:165898205
|
C | T | 218 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(215): Show | 220 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(217): Show |
intron_variant | MODIFIER | c.499+1873C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898205 | ||||||
chr1:165898248
|
GGC | G | 39 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(36): Show | 39 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.499+1917_499+1918d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898248 | ||||||
chr1:165898252
|
A | C | 39 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(36): Show | 39 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.499+1920A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898252 | ||||||
chr1:165898253
|
A | C | 39 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(36): Show | 39 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.499+1921A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898253 | ||||||
chr1:165898256
|
GTGCAAAT others(1): Show |
G | 39 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(36): Show | 39 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.499+1925_499+1932d others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898256 | ||||||
chr1:165898263
|
T | C | 1 | a0001c0001t0008g0234 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.499+1931T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898263 | ||||||
chr1:165898266
|
G | A | 59 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(56): Show | 61 | HG00323.hp2 HG01070.hp2 HG01071.hp1 others(58): Show |
intron_variant | MODIFIER | c.499+1934G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898266 | ||||||
chr1:165898375
|
C | T | 2 | a0001c0001t0012g0010a0001c0001t0012g0103 | 2 | HG03130.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.499+2043C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898375 | ||||||
chr1:165898400
|
T | C | 18 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0107others(15): Show | 18 | HG01884.hp1 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.499+2068T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898400 | ||||||
chr1:165898482
|
A | G | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.499+2150A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898482 | ||||||
chr1:165898503
|
C | T | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2171C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898503 | ||||||
chr1:165898509
|
T | C | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2177T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898509 | ||||||
chr1:165898590
|
C | T | 2 | a0001c0001t0012g0163a0001c0001t0012g0280 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.499+2258C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898590 | ||||||
chr1:165898618
|
G | A | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2286G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898618 | ||||||
chr1:165898746
|
C | A | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2414C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898746 | ||||||
chr1:165898780
|
T | A | 39 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(36): Show | 39 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(36): Show |
intron_variant | MODIFIER | c.499+2448T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898780 | ||||||
chr1:165898833
|
C | T | 1 | a0001c0002t0015g0226 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.499+2501C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898833 | ||||||
chr1:165898932
|
T | C | 206 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(203): Show | 208 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(205): Show |
intron_variant | MODIFIER | c.499+2600T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898932 | ||||||
chr1:165898970
|
T | C | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2638T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165898970 | ||||||
chr1:165899094
|
T | G | 1 | a0001c0001t0012g0280 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.499+2762T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899094 | ||||||
chr1:165899259
|
T | C | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2927T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899259 | ||||||
chr1:165899308
|
C | A | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2976C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899308 | ||||||
chr1:165899309
|
T | C | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+2977T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899309 | ||||||
chr1:165899332
|
G | A | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+3000G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899332 | ||||||
chr1:165899380
|
A | G | 1 | a0001c0001t0023g0302 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.499+3048A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899380 | ||||||
chr1:165899468
|
A | C | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+3136A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899468 | ||||||
chr1:165899509
|
T | C | 1 | a0001c0001t0002g0308 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.499+3177T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899509 | ||||||
chr1:165899529
|
A | G | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.499+3197A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899529 | ||||||
chr1:165899650
|
T | C | 49 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(46): Show | 49 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.499+3318T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899650 | ||||||
chr1:165899658
|
C | T | 7 | a0001c0001t0008g0014a0001c0001t0008g0036a0001c0001t0008g0046others(4): Show | 7 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(4): Show |
intron_variant | MODIFIER | c.499+3326C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899658 | ||||||
chr1:165899733
|
G | C | 5 | a0001c0001t0008g0036a0001c0001t0008g0046a0001c0001t0008g0153others(2): Show | 5 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(2): Show |
intron_variant | MODIFIER | c.499+3401G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899733 | ||||||
chr1:165899801
|
A | C | 49 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(46): Show | 49 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(46): Show |
intron_variant | MODIFIER | c.500-3381A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899801 | ||||||
chr1:165899850
|
C | G | 5 | a0001c0001t0001g0130a0001c0001t0001g0131a0001c0001t0001g0144others(2): Show | 5 | HG00733.hp2 HG01070.hp1 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-3332C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899850 | ||||||
chr1:165899896
|
T | C | 1 | a0001c0001t0001g0306 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.500-3286T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899896 | ||||||
chr1:165899932
|
A | G | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.500-3250A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165899932 | ||||||
chr1:165900013
|
A | G | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.500-3169A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900013 | ||||||
chr1:165900040
|
C | T | 1 | a0001c0001t0001g0026 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.500-3142C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900040 | ||||||
chr1:165900063
|
G | A | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.500-3119G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900063 | ||||||
chr1:165900081
|
G | A | 3 | a0001c0001t0008g0028a0001c0001t0008g0072a0001c0001t0008g0073 | 3 | HG03491.hp1 HG03492.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.500-3101G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900081 | ||||||
chr1:165900110
|
G | A | 2 | a0001c0001t0002g0138a0001c0001t0002g0160 | 2 | NA20129.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.500-3072G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900110 | ||||||
chr1:165900130
|
T | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-3052T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900130 | ||||||
chr1:165900183
|
C | T | 1 | a0001c0001t0003g0044 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.500-2999C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900183 | ||||||
chr1:165900194
|
T | C | 74 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(71): Show | 76 | HG00673.hp1 HG01070.hp2 HG01071.hp1 others(73): Show |
intron_variant | MODIFIER | c.500-2988T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900194 | ||||||
chr1:165900235
|
G | A | 1 | a0001c0001t0001g0291 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.500-2947G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900235 | ||||||
chr1:165900356
|
G | T | 47 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(44): Show | 47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-2826G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900356 | ||||||
chr1:165900374
|
T | C | 5 | a0001c0001t0006g0104a0001c0001t0006g0115a0001c0001t0006g0116others(2): Show | 5 | HG01891.hp1 HG03041.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-2808T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900374 | ||||||
chr1:165900376
|
T | C | 47 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(44): Show | 47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-2806T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900376 | ||||||
chr1:165900453
|
T | A | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-2729T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900453 | ||||||
chr1:165900463
|
T | C | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.500-2719T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900463 | ||||||
chr1:165900605
|
A | G | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.500-2577A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900605 | ||||||
chr1:165900665
|
GT | G | 47 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(44): Show | 47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-2515delT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165900665 | |||||
chr1:165900714
|
G | A | 23 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(20): Show | 23 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(20): Show |
intron_variant | MODIFIER | c.500-2468G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900714 | ||||||
chr1:165900834
|
A | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(89): Show | 92 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(89): Show |
intron_variant | MODIFIER | c.500-2348A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900834 | ||||||
chr1:165900854
|
G | C | 1 | a0001c0001t0002g0279 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.500-2328G>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165900854 | ||||||
chr1:165901026
|
T | C | 47 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(44): Show | 47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-2156T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901026 | ||||||
chr1:165901066
|
G | A | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.500-2116G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901066 | ||||||
chr1:165901070
|
C | T | 37 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(34): Show | 37 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.500-2112C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901070 | ||||||
chr1:165901076
|
C | T | 6 | a0001c0001t0001g0152a0001c0001t0001g0249a0001c0001t0001g0250others(3): Show | 6 | HG01257.hp1 HG01258.hp1 HG01975.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-2106C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901076 | ||||||
chr1:165901152
|
G | A | 1 | a0001c0001t0002g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.500-2030G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901152 | ||||||
chr1:165901257
|
T | G | 2 | a0001c0001t0004g0013a0001c0001t0004g0094 | 2 | HG02922.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.500-1925T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901257 | ||||||
chr1:165901260
|
C | T | 2 | a0001c0001t0016g0066a0001c0001t0016g0286 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.500-1922C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901260 | ||||||
chr1:165901286
|
G | A | 77 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(74): Show | 79 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(76): Show |
intron_variant | MODIFIER | c.500-1896G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901286 | ||||||
chr1:165901292
|
C | T | 3 | a0001c0001t0012g0163a0001c0001t0012g0280a0001c0001t0033g0008 | 3 | HG02559.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.500-1890C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901292 | ||||||
chr1:165901325
|
G | A | 1 | a0001c0001t0012g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.500-1857G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901325 | ||||||
chr1:165901329
|
A | G | 124 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(121): Show | 126 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(123): Show |
intron_variant | MODIFIER | c.500-1853A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901329 | ||||||
chr1:165901422
|
C | T | 74 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(71): Show | 76 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(73): Show |
intron_variant | MODIFIER | c.500-1760C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901422 | ||||||
chr1:165901431
|
G | T | 315 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(312): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.500-1751G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901431 | ||||||
chr1:165901546
|
C | A | 2 | a0001c0001t0003g0222a0001c0001t0003g0313 | 2 | HG01433.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.500-1636C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901546 | ||||||
chr1:165901563
|
T | C | 47 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(44): Show | 47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-1619T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901563 | ||||||
chr1:165901593
|
A | G | 37 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(34): Show | 37 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.500-1589A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901593 | ||||||
chr1:165901611
|
T | C | 5 | a0001c0001t0006g0049a0001c0001t0006g0107a0001c0001t0006g0110others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-1571T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901611 | ||||||
chr1:165901636
|
G | A | 3 | a0001c0001t0012g0163a0001c0001t0012g0280a0001c0001t0033g0008 | 3 | HG02559.hp1 HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.500-1546G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901636 | ||||||
chr1:165901693
|
A | G | 2 | a0001c0001t0007g0090a0001c0001t0007g0091 | 2 | HG04204.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.500-1489A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901693 | ||||||
chr1:165901782
|
T | C | 47 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(44): Show | 47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.500-1400T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901782 | ||||||
chr1:165901818
|
A | C | 3 | a0001c0001t0013g0083a0001c0001t0013g0134a0001c0001t0013g0317 | 3 | HG02258.hp1 HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.500-1364A>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901818 | ||||||
chr1:165901852
|
A | G | 1 | a0001c0001t0021g0135 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.500-1330A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165901852 | ||||||
chr1:165901947
|
C | CA | 157 | a0001c0001t0001g0030a0001c0001t0002g0001a0001c0001t0002g0015others(154): Show | 160 | HG00099.hp2 HG00140.hp2 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.500-1217dupA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165901947 | |||||
chr1:165901947
|
C | CAA | 34 | a0001c0001t0002g0075a0001c0001t0002g0096a0001c0001t0002g0213others(31): Show | 34 | HG00323.hp1 HG01433.hp1 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.500-1218_500-1217d others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165901947 | |||||
chr1:165901947
|
C | CAAA | 22 | a0001c0001t0006g0104a0001c0001t0006g0115a0001c0001t0006g0116others(19): Show | 22 | HG01891.hp1 HG02451.hp1 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.500-1219_500-1217d others(5): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165901947 | |||||
chr1:165902031
|
C | G | 169 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(166): Show | 172 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.500-1151C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902031 | ||||||
chr1:165902052
|
G | A | 1 | a0001c0001t0002g0214 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.500-1130G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902052 | ||||||
chr1:165902129
|
G | A | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.500-1053G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902129 | ||||||
chr1:165902148
|
A | G | 1 | a0001c0002t0005g0101 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.500-1034A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902148 | ||||||
chr1:165902193
|
G | A | 2 | a0001c0001t0002g0162a0001c0001t0002g0270 | 2 | HG01081.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.500-989G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902193 | ||||||
chr1:165902371
|
T | C | 37 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(34): Show | 37 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.500-811T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902371 | ||||||
chr1:165902428
|
T | A | 2 | a0001c0001t0004g0009a0001c0001t0004g0305 | 2 | HG02145.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.500-754T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902428 | ||||||
chr1:165902437
|
GA | G | 14 | a0001c0001t0004g0114a0001c0001t0004g0304a0001c0001t0009g0012others(11): Show | 14 | HG02280.hp2 HG02615.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.500-733delA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902437 | |||||
chr1:165902442
|
A | G | 1 | a0001c0001t0035g0199 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.500-740A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902442 | ||||||
chr1:165902468
|
G | A | 75 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(72): Show | 77 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(74): Show |
intron_variant | MODIFIER | c.500-714G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902468 | ||||||
chr1:165902481
|
G | A | 2 | a0001c0001t0012g0163a0001c0001t0012g0280 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.500-701G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902481 | ||||||
chr1:165902592
|
A | AT | 53 | a0001c0001t0003g0002a0001c0001t0003g0023a0001c0001t0003g0041others(50): Show | 54 | HG00099.hp2 HG00639.hp1 HG00733.hp1 others(51): Show |
intron_variant | MODIFIER | c.500-563dupT | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATT | 37 | a0001c0001t0003g0087a0001c0001t0003g0122a0001c0001t0003g0205others(34): Show | 37 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(34): Show |
intron_variant | MODIFIER | c.500-564_500-563dup others(2): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTT | 6 | a0001c0001t0007g0090a0001c0001t0007g0157a0001c0001t0019g0079others(3): Show | 6 | HG01109.hp2 HG01515.hp1 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.500-565_500-563dup others(3): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(1): Show |
18 | a0001c0001t0002g0095a0001c0001t0002g0109a0001c0001t0002g0113others(15): Show | 18 | HG00673.hp1 HG01070.hp2 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.500-570_500-563dup others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(2): Show |
15 | a0001c0001t0002g0174a0001c0001t0002g0273a0001c0001t0005g0003others(12): Show | 15 | HG01071.hp1 HG01106.hp1 HG01175.hp2 others(12): Show |
intron_variant | MODIFIER | c.500-571_500-563dup others(9): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(3): Show |
7 | a0001c0001t0002g0274a0001c0001t0002g0294a0001c0001t0025g0275others(4): Show | 7 | HG01258.hp2 HG02080.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.500-572_500-563dup others(10): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(4): Show |
26 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0031others(23): Show | 26 | HG00099.hp1 HG00438.hp1 HG00639.hp2 others(23): Show |
intron_variant | MODIFIER | c.500-573_500-563dup others(11): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(5): Show |
24 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0025others(21): Show | 24 | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.500-574_500-563dup others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(6): Show |
15 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0054others(12): Show | 15 | HG00735.hp1 HG01496.hp2 HG01516.hp1 others(12): Show |
intron_variant | MODIFIER | c.500-575_500-563dup others(13): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(7): Show |
8 | a0001c0001t0001g0071a0001c0001t0001g0165a0001c0001t0001g0185others(5): Show | 8 | HG01515.hp2 HG01943.hp2 NA18964.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-576_500-563dup others(14): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(8): Show |
3 | a0001c0001t0001g0027a0001c0001t0001g0150a0001c0001t0001g0184 | 3 | NA18954.hp1 NA18979.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.500-577_500-563dup others(15): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(9): Show |
2 | a0001c0001t0001g0024a0001c0001t0001g0180 | 2 | HG00140.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.500-578_500-563dup others(16): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(11): Show |
1 | a0001c0001t0001g0236 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.500-580_500-563dup others(18): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(13): Show |
1 | a0001c0001t0001g0047 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.500-582_500-563dup others(20): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(14): Show |
1 | a0001c0001t0001g0086 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.500-583_500-563dup others(21): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
A | ATTTTTTT others(20): Show |
1 | a0001c0001t0001g0124 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.500-589_500-563dup others(27): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
ATTTT | A | 31 | a0001c0001t0001g0050a0001c0001t0001g0301a0001c0001t0002g0001others(28): Show | 33 | HG00323.hp2 HG01081.hp1 HG01081.hp2 others(30): Show |
intron_variant | MODIFIER | c.500-566_500-563del others(4): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
ATTTTTTT others(1): Show |
A | 8 | a0001c0001t0001g0098a0001c0001t0001g0152a0001c0001t0001g0249others(5): Show | 8 | HG01257.hp1 HG01258.hp1 HG01975.hp1 others(5): Show |
intron_variant | MODIFIER | c.500-570_500-563del others(8): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
ATTTTTTT others(5): Show |
A | 4 | a0001c0001t0004g0175a0001c0001t0004g0216a0001c0001t0004g0256others(1): Show | 4 | NA18969.hp1 NA18992.hp2 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-574_500-563del others(12): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902592
|
ATTTTTTT others(6): Show |
A | 5 | a0001c0001t0003g0032a0001c0001t0003g0033a0001c0001t0003g0039others(2): Show | 5 | NA18941.hp1 NA18945.hp2 NA19002.hp2 others(2): Show |
intron_variant | MODIFIER | c.500-575_500-563del others(13): Show |
UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr1 | 165902592 | |||||
chr1:165902593
|
T | A | 3 | a0001c0001t0006g0119a0001c0001t0006g0121a0001c0001t0006g0278 | 3 | HG01891.hp2 HG02647.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.500-589T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902593 | ||||||
chr1:165902634
|
C | T | 1 | a0001c0001t0006g0285 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.500-548C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902634 | ||||||
chr1:165902744
|
C | T | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.500-438C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902744 | ||||||
chr1:165902768
|
G | A | 2 | a0001c0001t0001g0185a0001c0001t0001g0191 | 2 | NA18985.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.500-414G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902768 | ||||||
chr1:165902794
|
C | T | 5 | a0001c0001t0006g0049a0001c0001t0006g0107a0001c0001t0006g0110others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-388C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902794 | ||||||
chr1:165902830
|
T | A | 1 | a0001c0001t0006g0117 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.500-352T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902830 | ||||||
chr1:165902880
|
A | G | 1 | a0001c0001t0007g0129 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.500-302A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902880 | ||||||
chr1:165902900
|
A | G | 4 | a0001c0001t0011g0043a0001c0001t0011g0201a0001c0001t0011g0225others(1): Show | 4 | NA18944.hp2 NA18957.hp1 NA19000.hp1 others(1): Show |
intron_variant | MODIFIER | c.500-282A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902900 | ||||||
chr1:165902922
|
G | A | 5 | a0001c0001t0006g0049a0001c0001t0006g0107a0001c0001t0006g0110others(2): Show | 5 | HG02257.hp2 HG02572.hp2 HG02615.hp1 others(2): Show |
intron_variant | MODIFIER | c.500-260G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902922 | ||||||
chr1:165902931
|
C | T | 2 | a0001c0001t0016g0066a0001c0001t0016g0286 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.500-251C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165902931 | ||||||
chr1:165903018
|
C | T | 1 | a0001c0001t0003g0230 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.500-164C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165903018 | ||||||
chr1:165903025
|
G | A | 1 | a0001c0001t0001g0316 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.500-157G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165903025 | ||||||
chr1:165903083
|
T | C | 1 | a0001c0001t0004g0262 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.500-99T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 4/6 | chr1 | 165903083 | ||||||
chr1:165903340
|
C | T | 1 | a0001c0002t0005g0269 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.597+61C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165903340 | ||||||
chr1:165903542
|
A | G | 5 | a0001c0001t0001g0149a0001c0001t0001g0198a0001c0001t0001g0239others(2): Show | 5 | NA18942.hp1 NA18964.hp1 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.597+263A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165903542 | ||||||
chr1:165903648
|
A | G | 4 | a0001c0001t0001g0076a0001c0001t0001g0189a0001c0001t0001g0190others(1): Show | 4 | NA18973.hp2 NA18995.hp1 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.597+369A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165903648 | ||||||
chr1:165903668
|
C | A | 32 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(29): Show | 34 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(31): Show |
intron_variant | MODIFIER | c.597+389C>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165903668 | ||||||
chr1:165903718
|
C | T | 1 | a0001c0001t0009g0290 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.597+439C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165903718 | ||||||
chr1:165904085
|
G | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.597+806G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904085 | ||||||
chr1:165904155
|
T | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.597+876T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904155 | ||||||
chr1:165904272
|
C | G | 47 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(44): Show | 47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.597+993C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904272 | ||||||
chr1:165904373
|
A | G | 1 | a0001c0001t0012g0010 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.597+1094A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904373 | ||||||
chr1:165904382
|
A | G | 126 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(123): Show | 128 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(125): Show |
intron_variant | MODIFIER | c.597+1103A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904382 | ||||||
chr1:165904530
|
T | G | 37 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(34): Show | 37 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(34): Show |
intron_variant | MODIFIER | c.597+1251T>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904530 | ||||||
chr1:165904537
|
G | A | 26 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(23): Show | 26 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.597+1258G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904537 | ||||||
chr1:165904549
|
C | T | 2 | a0001c0001t0012g0163a0001c0001t0012g0280 | 2 | HG02647.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.597+1270C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904549 | ||||||
chr1:165904703
|
A | G | 1 | a0001c0001t0006g0115 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.598-1218A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904703 | ||||||
chr1:165904775
|
A | G | 1 | a0001c0001t0002g0096 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.598-1146A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904775 | ||||||
chr1:165904778
|
T | C | 47 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(44): Show | 47 | HG01192.hp2 HG01884.hp1 HG01891.hp1 others(44): Show |
intron_variant | MODIFIER | c.598-1143T>C | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904778 | ||||||
chr1:165904791
|
G | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.598-1130G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165904791 | ||||||
chr1:165905184
|
G | A | 76 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(73): Show | 78 | HG00323.hp2 HG00673.hp1 HG01070.hp2 others(75): Show |
intron_variant | MODIFIER | c.598-737G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165905184 | ||||||
chr1:165905221
|
G | A | 3 | a0001c0001t0002g0058a0001c0001t0002g0092a0001c0001t0002g0279 | 3 | HG02109.hp1 HG02258.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.598-700G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165905221 | ||||||
chr1:165905638
|
G | A | 317 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(314): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.598-283G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165905638 | ||||||
chr1:165905675
|
A | T | 1 | a0001c0001t0001g0187 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.598-246A>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 5/6 | chr1 | 165905675 | ||||||
chr1:165906057
|
C | G | 4 | a0001c0001t0004g0175a0001c0001t0004g0216a0001c0001t0004g0256others(1): Show | 4 | NA18969.hp1 NA18992.hp2 NA19088.hp1 others(1): Show |
intron_variant | MODIFIER | c.646+88C>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906057 | ||||||
chr1:165906272
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.646+303C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906272 | ||||||
chr1:165906363
|
A | G | 26 | a0001c0001t0006g0049a0001c0001t0006g0067a0001c0001t0006g0104others(23): Show | 26 | HG01884.hp1 HG01891.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.646+394A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906363 | ||||||
chr1:165906439
|
C | T | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.646+470C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906439 | ||||||
chr1:165906473
|
A | G | 10 | a0001c0001t0008g0014a0001c0001t0008g0028a0001c0001t0008g0036others(7): Show | 10 | HG01192.hp2 HG01943.hp1 HG02273.hp1 others(7): Show |
intron_variant | MODIFIER | c.646+504A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906473 | ||||||
chr1:165906577
|
T | A | 1 | a0001c0001t0006g0285 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.646+608T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906577 | ||||||
chr1:165906706
|
A | G | 141 | a0001c0001t0003g0002a0001c0001t0003g0023a0001c0001t0003g0032others(138): Show | 142 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.646+737A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906706 | ||||||
chr1:165906726
|
C | T | 2 | a0001c0001t0016g0066a0001c0001t0016g0286 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.646+757C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906726 | ||||||
chr1:165906735
|
G | A | 93 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0011others(90): Show | 93 | HG00099.hp1 HG00140.hp1 HG00438.hp1 others(90): Show |
intron_variant | MODIFIER | c.646+766G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906735 | ||||||
chr1:165906890
|
T | A | 1 | a0001c0001t0003g0122 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.647-794T>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906890 | ||||||
chr1:165906940
|
A | G | 2 | a0001c0001t0011g0145a0001c0001t0011g0244 | 2 | NA19009.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.647-744A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906940 | ||||||
chr1:165906947
|
C | T | 1 | a0001c0001t0007g0022 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.647-737C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165906947 | ||||||
chr1:165907033
|
A | G | 1 | a0001c0001t0024g0078 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.647-651A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907033 | ||||||
chr1:165907091
|
G | A | 1 | a0001c0001t0032g0259 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.647-593G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907091 | ||||||
chr1:165907316
|
G | A | 1 | a0001c0001t0012g0103 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.647-368G>A | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907316 | ||||||
chr1:165907341
|
C | T | 220 | a0001c0001t0002g0001a0001c0001t0002g0015a0001c0001t0002g0034others(217): Show | 223 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.647-343C>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907341 | ||||||
chr1:165907373
|
CA | C | 3 | a0001c0001t0019g0079a0001c0001t0024g0078a0001c0001t0036g0136 | 3 | HG02451.hp1 HG02451.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.647-310delA | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907373 | ||||||
chr1:165907428
|
G | T | 2 | a0001c0001t0016g0066a0001c0001t0016g0286 | 2 | HG03195.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.647-256G>T | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907428 | ||||||
chr1:165907468
|
A | G | 131 | a0001c0001t0003g0002a0001c0001t0003g0023a0001c0001t0003g0032others(128): Show | 132 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(129): Show |
intron_variant | MODIFIER | c.647-216A>G | UCK2 | ENSG00000143179.16 | transcript | ENST00000367879.9 | protein_coding | 6/6 | chr1 | 165907468 |