geneid | 84193 |
---|---|
ensemblid | ENSG00000183576.13 |
hgncid | 20493 |
symbol | SETD3 |
name | SET domain containing 3, actin N3(tau)-histidine methyltransferase |
refseq_nuc | NM_032233.3 |
refseq_prot | NP_115609.2 |
ensembl_nuc | ENST00000331768.10 |
ensembl_prot | ENSP00000327436.5 |
mane_status | MANE Select |
chr | chr14 |
start | 99397748 |
end | 99480859 |
strand | - |
ver | v1.2 |
region | chr14:99397748-99480859 |
region5000 | chr14:99392748-99485859 |
regionname0 | SETD3_chr14_99397748_99480859 |
regionname5000 | SETD3_chr14_99392748_99485859 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 594 | 287 | 74 | 46 | 123 | 12 | 30 | 99 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0002 | 0/0 | 594 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0003 | 0/0 | 594 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0004 | 0/0 | 594 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1785 | 268 | 56 | 46 | 122 | 12 | 30 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
c0002 | 0/0 | 1785 | 10 | 10 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
c0003 | 0/0 | 1785 | 4 | 4 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
c0004 | 0/0 | 1785 | 2 | 2 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
c0005 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
c0006 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
c0007 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
c0008 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
c0009 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
c0010 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1072 | 270 | 61 | 45 | 121 | 12 | 29 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
t0002 | 0/0 | 1073 | 11 | 11 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
t0003 | 0/0 | 1072 | 2 | 2 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
t0004 | 0/0 | 1072 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
t0005 | 0/0 | 1073 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
t0006 | 0/0 | 1072 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
t0007 | 0/0 | 1072 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
t0008 | 0/0 | 1072 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
t0009 | 0/0 | 1072 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
t0010 | 0/0 | 1072 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
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 | 2 | 0 | 0 | 2 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1785 | 268 | 56 | 46 | 122 | 12 | 30 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0002 | 0/0 | 1785 | 10 | 10 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0003 | 0/0 | 1785 | 4 | 4 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0004 | 0/0 | 1785 | 2 | 2 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0007 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0008 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0010 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0002c0006 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0003c0005 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0004c0009 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2856 | 261 | 54 | 45 | 119 | 12 | 29 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0001t0003 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0001t0004 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0001t0006 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0001t0007 | 0/0 | 2856 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0001t0008 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0001t0009 | 0/0 | 2856 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0002t0002 | 0/0 | 2857 | 9 | 9 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0002t0005 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0003t0001 | 0/0 | 2856 | 4 | 4 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0004t0001 | 0/0 | 2856 | 2 | 2 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0007t0002 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0008t0001 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0001c0010t0001 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0002c0006t0002 | 0/0 | 2857 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0003c0005t0010 | 0/0 | 2856 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
a0004c0009t0001 | 0/0 | 2856 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | copy fasta | chr14 | 99392748 | 99485859 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0153 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0003g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0004g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0006g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0007g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0008g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0001t0009g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0002t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0002t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0002t0002g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0002t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0002t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0002t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0002t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0002t0002g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0002t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0003t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0003t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0003t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0004t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0004t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0007t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0008t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0001c0010t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0002c0006t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0003c0005t0010g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
a0004c0009t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0213 | EUR | GBR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0100 | EUR | GBR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0088 | EUR | FIN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0214 | EUR | FIN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00408 | hp1 | a0001 | c0008 | t0001 | g0104 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0042 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | CHS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0197 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0268 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0267 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0191 | EUR | IBS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0028 | EUR | IBS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0114 | EUR | IBS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0190 | EUR | IBS | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0138 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0093 | AMR | PEL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01952 | hp2 | a0001 | c0001 | t0009 | g0112 | AMR | PEL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02055 | hp1 | a0001 | c0007 | t0002 | g0144 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02056 | hp2 | a0001 | c0001 | t0006 | g0083 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0056 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02145 | hp1 | a0001 | c0003 | t0001 | g0141 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CDX | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | CDX | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0282 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02280 | hp2 | a0001 | c0003 | t0001 | g0140 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PEL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0107 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02451 | hp2 | a0001 | c0002 | t0002 | g0130 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0060 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02630 | hp2 | a0002 | c0006 | t0002 | g0143 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0101 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0251 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0066 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02809 | hp1 | a0001 | c0002 | t0002 | g0133 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02965 | hp1 | a0001 | c0004 | t0001 | g0156 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0038 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0152 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02970 | hp2 | a0001 | c0010 | t0001 | g0154 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0216 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0020 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0196 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03130 | hp1 | a0001 | c0002 | t0002 | g0146 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03209 | hp1 | a0003 | c0005 | t0010 | g0284 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0139 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0252 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0132 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0238 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03540 | hp2 | a0001 | c0002 | t0002 | g0129 | AFR | GWD | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03579 | hp1 | a0001 | c0002 | t0002 | g0131 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0249 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | PJL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03831 | hp1 | a0001 | c0001 | t0007 | g0203 | SAS | BEB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | BEB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | BEB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0258 | SAS | STU | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0069 | SAS | BEB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0261 | SAS | BEB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0187 | SAS | STU | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | STU | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0235 | SAS | STU | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | STU | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | YRI | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | YRI | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | CHB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | CHB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18951 | hp1 | a0001 | c0001 | t0008 | g0120 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0231 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19006 | hp2 | a0004 | c0009 | t0001 | g0046 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19043 | hp1 | a0001 | c0002 | t0005 | g0142 | AFR | LWK | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | LWK | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ASW | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0024 | AFR | ASW | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | TSI | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0189 | EUR | TSI | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | TSI | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | TSI | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0047 | SAS | GIH | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | GIH | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | CLM | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02486 | hp2 | a0001 | c0004 | t0001 | g0155 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0271 | AFR | ACB | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03471 | hp1 | a0001 | c0002 | t0002 | g0281 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | USA | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
HG06807 | hp2 | a0001 | c0002 | t0002 | g0280 | AFR | USA | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | LWK | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0031 | REF | REF | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0153 | REF | REF | SETD3_chr14_99392748_99485859 | SETD3 | chr14 | 99392748 | 99485859 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:99398807
|
C | A | 1 | a0003 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.1657G>T | p.Val553Leu | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 1797/2856 | 1657/1785 | 553/594 | chr14 | 99398807 | ||
chr14:99399009
|
G | T | 1 | a0002 | 1 | HG02630.hp2 | missense_variant | MODERATE | c.1455C>A | p.Asn485Lys | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 1595/2856 | 1455/1785 | 485/594 | chr14 | 99399009 | ||
chr14:99463548
|
T | C | 1 | a0004 | 1 | NA19006.hp2 | missense_variant | MODERATE | c.134A>G | p.Lys45Arg | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/13 | 274/2856 | 134/1785 | 45/594 | chr14 | 99463548 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:99404235
|
A | G | 3 | a0001c0002a0001c0007a0002c0006 | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
synonymous_variant | LOW | c.1167T>C | p.Cys389Cys | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/13 | 1307/2856 | 1167/1785 | 389/594 | chr14 | 99404235 | ||
chr14:99405261
|
T | C | 2 | a0001c0007a0002c0006 | 2 | HG02055.hp1 HG02630.hp2 |
synonymous_variant | LOW | c.1035A>G | p.Lys345Lys | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/13 | 1175/2856 | 1035/1785 | 345/594 | chr14 | 99405261 | ||
chr14:99458303
|
G | A | 1 | a0001c0008 | 1 | HG00408.hp1 | synonymous_variant | LOW | c.651C>T | p.Tyr217Tyr | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/13 | 791/2856 | 651/1785 | 217/594 | chr14 | 99458303 | ||
chr14:99458311
|
G | T | 1 | a0001c0004 | 2 | HG02486.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.643C>A | p.Arg215Arg | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/13 | 783/2856 | 643/1785 | 215/594 | chr14 | 99458311 | ||
chr14:99458390
|
G | A | 1 | a0001c0010 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.564C>T | p.Tyr188Tyr | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/13 | 704/2856 | 564/1785 | 188/594 | chr14 | 99458390 | ||
chr14:99461306
|
A | G | 1 | a0001c0003 | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
synonymous_variant | LOW | c.231T>C | p.Asp77Asp | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/13 | 371/2856 | 231/1785 | 77/594 | chr14 | 99461306 | ||
chr14:99465734
|
T | C | 1 | a0001c0010 | 1 | HG02970.hp2 | synonymous_variant | LOW | c.72A>G | p.Glu24Glu | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/13 | 212/2856 | 72/1785 | 24/594 | chr14 | 99465734 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:99397840
|
C | G | 1 | a0001c0001t0006 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*839G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 839 | chr14 | 99397840 | |||||
chr14:99397860
|
C | A | 1 | a0001c0001t0003 | 2 | HG02451.hp1 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*819G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 819 | chr14 | 99397860 | |||||
chr14:99398078
|
T | C | 1 | a0003c0005t0010 | 1 | HG03209.hp1 | 3_prime_UTR_variant | MODIFIER | c.*601A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 601 | chr14 | 99398078 | |||||
chr14:99398087
|
A | G | 1 | a0001c0002t0005 | 1 | NA19043.hp1 | 3_prime_UTR_variant | MODIFIER | c.*592T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 592 | chr14 | 99398087 | |||||
chr14:99398166
|
A | AT | 4 | a0001c0002t0002a0001c0002t0005a0001c0007t0002others(1): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*512dupA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 512 | chr14 | 99398166 | |||||
chr14:99398186
|
C | A | 1 | a0001c0001t0007 | 1 | HG03831.hp1 | 3_prime_UTR_variant | MODIFIER | c.*493G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 493 | chr14 | 99398186 | |||||
chr14:99398363
|
G | A | 1 | a0001c0001t0008 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*316C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 316 | chr14 | 99398363 | |||||
chr14:99398616
|
G | A | 1 | a0001c0001t0009 | 1 | HG01952.hp2 | 3_prime_UTR_variant | MODIFIER | c.*63C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 63 | chr14 | 99398616 | |||||
chr14:99398633
|
C | T | 4 | a0001c0002t0002a0001c0002t0005a0001c0007t0002others(1): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*46G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 13/13 | 46 | chr14 | 99398633 | |||||
chr14:99480782
|
G | A | 1 | a0003c0005t0010 | 1 | HG03209.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-63C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/13 | chr14 | 99480782 | ||||||
chr14:99480793
|
C | G | 1 | a0001c0001t0004 | 1 | NA19085.hp1 | 5_prime_UTR_variant | MODIFIER | c.-74G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/13 | 14988 | chr14 | 99480793 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:99399181
|
G | C | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1339-56C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399181 | ||||||
chr14:99399195
|
C | T | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1339-70G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399195 | ||||||
chr14:99399271
|
T | C | 1 | a0001c0001t0001g0259 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1339-146A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399271 | ||||||
chr14:99399335
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.1339-210G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399335 | ||||||
chr14:99399391
|
C | T | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1339-266G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399391 | ||||||
chr14:99399447
|
ATG | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1339-324_1339-323d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399447 | ||||||
chr14:99399476
|
T | C | 1 | a0001c0001t0001g0163 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1339-351A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399476 | ||||||
chr14:99399489
|
G | A | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1339-364C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399489 | ||||||
chr14:99399586
|
T | G | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1339-461A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399586 | ||||||
chr14:99399741
|
A | AT | 9 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0157others(6): Show | 9 | HG00735.hp2 HG02055.hp2 HG02056.hp1 others(6): Show |
intron_variant | MODIFIER | c.1338+357dupA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399741 | ||||||
chr14:99399741
|
ATT | A | 24 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0069others(21): Show | 24 | HG00738.hp1 HG02027.hp1 HG02056.hp2 others(21): Show |
intron_variant | MODIFIER | c.1338+356_1338+357d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399741 | ||||||
chr14:99399741
|
ATTT | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1338+355_1338+357d others(5): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399741 | ||||||
chr14:99399741
|
ATTTT | A | 11 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0100others(8): Show | 11 | HG00099.hp2 HG01891.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1338+354_1338+357d others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399741 | ||||||
chr14:99399743
|
T | A | 1 | a0001c0001t0001g0255 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1338+356A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399743 | ||||||
chr14:99399744
|
T | A | 22 | a0001c0001t0001g0009a0001c0001t0001g0043a0001c0001t0001g0069others(19): Show | 22 | HG00738.hp1 HG02027.hp1 HG02056.hp2 others(19): Show |
intron_variant | MODIFIER | c.1338+355A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399744 | ||||||
chr14:99399745
|
T | A | 186 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(183): Show | 191 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(188): Show |
intron_variant | MODIFIER | c.1338+354A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399745 | ||||||
chr14:99399746
|
T | A | 11 | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0100others(8): Show | 11 | HG00099.hp2 HG01891.hp2 HG02027.hp2 others(8): Show |
intron_variant | MODIFIER | c.1338+353A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399746 | ||||||
chr14:99399747
|
T | A | 1 | a0001c0001t0001g0279 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1338+352A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399747 | ||||||
chr14:99399835
|
C | T | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1338+264G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399835 | ||||||
chr14:99399846
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1338+253C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399846 | ||||||
chr14:99399982
|
C | T | 17 | a0001c0001t0001g0044a0001c0001t0001g0056a0001c0001t0001g0064others(14): Show | 17 | HG00099.hp2 HG00673.hp1 HG01517.hp1 others(14): Show |
intron_variant | MODIFIER | c.1338+117G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99399982 | ||||||
chr14:99400031
|
G | A | 10 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(7): Show | 10 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.1338+68C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 12/12 | chr14 | 99400031 | ||||||
chr14:99400315
|
G | A | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1178-56C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400315 | ||||||
chr14:99400385
|
C | T | 6 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.1178-126G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400385 | ||||||
chr14:99400392
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1178-133C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400392 | ||||||
chr14:99400439
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.1178-180C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400439 | ||||||
chr14:99400502
|
G | T | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(222): Show |
intron_variant | MODIFIER | c.1178-243C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400502 | ||||||
chr14:99400931
|
G | C | 1 | a0001c0001t0001g0036 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.1178-672C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400931 | ||||||
chr14:99400975
|
A | T | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1178-716T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99400975 | ||||||
chr14:99401138
|
CA | C | 17 | a0001c0001t0001g0028a0001c0001t0001g0149a0001c0001t0001g0150others(14): Show | 17 | HG01515.hp2 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1178-880delT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401138 | ||||||
chr14:99401161
|
C | T | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1178-902G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401161 | ||||||
chr14:99401190
|
C | T | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 131 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1178-931G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401190 | ||||||
chr14:99401402
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1178-1143G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401402 | ||||||
chr14:99401553
|
A | C | 1 | a0001c0001t0001g0114 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1178-1294T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401553 | ||||||
chr14:99401575
|
A | G | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1178-1316T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401575 | ||||||
chr14:99401688
|
A | G | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1178-1429T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401688 | ||||||
chr14:99401971
|
A | AGCACAGG others(4): Show |
12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1178-1713_1178-171 others(15): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401971 | ||||||
chr14:99401973
|
G | A | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1178-1714C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99401973 | ||||||
chr14:99402079
|
G | A | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1178-1820C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402079 | ||||||
chr14:99402150
|
G | C | 2 | a0001c0001t0003g0020a0001c0001t0003g0107 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1178-1891C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402150 | ||||||
chr14:99402198
|
G | A | 24 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(21): Show | 24 | HG00558.hp2 HG00673.hp2 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.1178-1939C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402198 | ||||||
chr14:99402324
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(123): Show | 131 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.1177+1901A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402324 | ||||||
chr14:99402334
|
A | G | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1177+1891T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402334 | ||||||
chr14:99402492
|
G | A | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.1177+1733C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402492 | ||||||
chr14:99402637
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1177+1588C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402637 | ||||||
chr14:99402833
|
A | C | 10 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(7): Show | 10 | HG02055.hp1 HG02451.hp2 HG02630.hp2 others(7): Show |
intron_variant | MODIFIER | c.1177+1392T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402833 | ||||||
chr14:99402835
|
T | C | 1 | a0001c0002t0002g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1177+1390A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402835 | ||||||
chr14:99402918
|
T | C | 1 | a0001c0001t0001g0093 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1177+1307A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402918 | ||||||
chr14:99402939
|
T | C | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1177+1286A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402939 | ||||||
chr14:99402949
|
T | C | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1177+1276A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402949 | ||||||
chr14:99402959
|
T | G | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1177+1266A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99402959 | ||||||
chr14:99403076
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1177+1149G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403076 | ||||||
chr14:99403127
|
G | A | 4 | a0001c0001t0001g0051a0001c0001t0001g0070a0001c0001t0001g0086others(1): Show | 4 | HG02280.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177+1098C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403127 | ||||||
chr14:99403193
|
A | G | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+1032T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403193 | ||||||
chr14:99403252
|
C | T | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02615.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177+973G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403252 | ||||||
chr14:99403298
|
C | T | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+927G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403298 | ||||||
chr14:99403330
|
A | C | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+895T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403330 | ||||||
chr14:99403447
|
A | ACTCTCTC others(7): Show |
1 | a0001c0001t0001g0241 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1177+777_1177+778i others(16): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403447 | ||||||
chr14:99403449
|
A | T | 1 | a0001c0001t0001g0241 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1177+776T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403449 | ||||||
chr14:99403451
|
A | ACTCTCTC others(3): Show |
1 | a0003c0005t0010g0284 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1177+773_1177+774i others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403451 | ||||||
chr14:99403451
|
A | ACTCTCTC others(5): Show |
1 | a0001c0001t0001g0158 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.1177+773_1177+774i others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403451 | ||||||
chr14:99403451
|
A | T | 1 | a0001c0001t0001g0241 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1177+774T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403451 | ||||||
chr14:99403451
|
ACACACTC others(1): Show |
A | 3 | a0001c0002t0002g0146a0001c0007t0002g0144a0002c0006t0002g0143 | 3 | HG02055.hp1 HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1177+766_1177+773d others(10): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403451 | ||||||
chr14:99403451
|
ACACACTC others(3): Show |
A | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.1177+764_1177+773d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403451 | ||||||
chr14:99403451
|
ACACACTC others(11): Show |
A | 4 | a0001c0002t0002g0133a0001c0002t0002g0280a0001c0002t0002g0281others(1): Show | 4 | HG02258.hp2 HG02809.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177+756_1177+773d others(20): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403451 | ||||||
chr14:99403453
|
A | ACTCT | 5 | a0001c0001t0001g0173a0001c0001t0001g0213a0001c0001t0001g0214others(2): Show | 5 | HG00099.hp1 HG00280.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1177+771_1177+772i others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | ||||||
chr14:99403453
|
A | ACTCTCTC others(11): Show |
1 | a0001c0001t0001g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1177+771_1177+772i others(20): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | ||||||
chr14:99403453
|
A | ACTCTCTC others(13): Show |
4 | a0001c0001t0001g0167a0001c0001t0001g0168a0001c0001t0001g0177others(1): Show | 4 | HG00558.hp2 NA18956.hp1 NA18979.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177+771_1177+772i others(22): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | ||||||
chr14:99403453
|
A | ACTCTCTC others(15): Show |
2 | a0001c0001t0001g0174a0001c0001t0001g0185 | 2 | NA18612.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.1177+771_1177+772i others(24): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | ||||||
chr14:99403453
|
A | ACTCTCTC others(17): Show |
2 | a0001c0001t0001g0164a0001c0001t0001g0179 | 2 | HG03041.hp2 NA18941.hp2 |
intron_variant | MODIFIER | c.1177+771_1177+772i others(26): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | ||||||
chr14:99403453
|
A | ACTCTCTC others(25): Show |
1 | a0001c0001t0001g0166 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.1177+771_1177+772i others(34): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | ||||||
chr14:99403453
|
A | T | 6 | a0001c0001t0001g0158a0001c0001t0001g0161a0001c0001t0001g0162others(3): Show | 6 | HG00673.hp2 HG01123.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1177+772T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | ||||||
chr14:99403453
|
ACACTCTC others(3): Show |
A | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.1177+762_1177+771d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | ||||||
chr14:99403453
|
ACACTCTC others(9): Show |
A | 4 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(1): Show | 4 | HG02451.hp2 HG03453.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.1177+756_1177+771d others(18): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403453 | ||||||
chr14:99403455
|
A | ACACT | 9 | a0001c0001t0001g0011a0001c0001t0001g0062a0001c0001t0001g0272others(6): Show | 9 | HG00423.hp2 NA18522.hp2 NA18964.hp1 others(6): Show |
intron_variant | MODIFIER | c.1177+769_1177+770i others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
A | ACTCT | 38 | a0001c0001t0001g0006a0001c0001t0001g0057a0001c0001t0001g0059others(35): Show | 39 | HG00408.hp2 HG00544.hp2 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.1177+766_1177+769d others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
A | ACTCTCTC others(1): Show |
6 | a0001c0001t0001g0196a0001c0001t0001g0207a0001c0001t0001g0209others(3): Show | 6 | HG03098.hp2 NA18941.hp1 NA18957.hp2 others(3): Show |
intron_variant | MODIFIER | c.1177+762_1177+769d others(10): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
A | ACTCTCTC others(3): Show |
2 | a0001c0001t0001g0199a0001c0001t0001g0243 | 2 | NA18948.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.1177+760_1177+769d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
A | ACTCTCTC others(11): Show |
3 | a0001c0001t0001g0172a0001c0001t0001g0175a0001c0001t0001g0181 | 3 | HG03540.hp1 NA18951.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.1177+752_1177+769d others(20): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
A | ACTCTCTC others(13): Show |
2 | a0001c0001t0001g0176a0001c0001t0001g0183 | 2 | HG03579.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.1177+750_1177+769d others(22): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
A | ACTCTCTC others(15): Show |
1 | a0001c0001t0001g0171 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1177+748_1177+769d others(24): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
A | ACTCTCTC others(17): Show |
1 | a0001c0001t0001g0165 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1177+746_1177+769d others(26): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
A | T | 23 | a0001c0001t0001g0158a0001c0001t0001g0161a0001c0001t0001g0162others(20): Show | 23 | HG00099.hp1 HG00280.hp2 HG00558.hp2 others(20): Show |
intron_variant | MODIFIER | c.1177+770T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
ACT | A | 8 | a0001c0001t0001g0061a0001c0001t0001g0109a0001c0001t0001g0110others(5): Show | 8 | HG01496.hp1 HG01891.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.1177+768_1177+769d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
ACTCT | A | 3 | a0001c0001t0001g0005a0001c0004t0001g0155a0001c0004t0001g0156 | 4 | HG01257.hp2 HG01258.hp2 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1177+766_1177+769d others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
ACTCTCT | A | 9 | a0001c0001t0001g0038a0001c0001t0001g0067a0001c0001t0001g0075others(6): Show | 9 | HG02965.hp2 NA18961.hp2 NA18968.hp2 others(6): Show |
intron_variant | MODIFIER | c.1177+764_1177+769d others(8): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
ACTCTCTC others(1): Show |
A | 109 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(106): Show | 113 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.1177+762_1177+769d others(10): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
ACTCTCTC others(3): Show |
A | 2 | a0001c0001t0001g0124a0001c0001t0008g0120 | 2 | NA18951.hp1 NA18964.hp2 |
intron_variant | MODIFIER | c.1177+760_1177+769d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
ACTCTCTC others(5): Show |
A | 2 | a0001c0001t0001g0068a0001c0001t0001g0148 | 2 | HG00738.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.1177+758_1177+769d others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403455
|
ACTCTCTC others(7): Show |
A | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1177+756_1177+769d others(16): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403455 | ||||||
chr14:99403457
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1177+768A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403457 | ||||||
chr14:99403459
|
T | A | 7 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0147others(4): Show | 7 | HG01496.hp1 HG01891.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.1177+766A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403459 | ||||||
chr14:99403461
|
T | A | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1177+764A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403461 | ||||||
chr14:99403463
|
T | A | 11 | a0001c0001t0001g0038a0001c0001t0001g0075a0001c0001t0001g0117others(8): Show | 11 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(8): Show |
intron_variant | MODIFIER | c.1177+762A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403463 | ||||||
chr14:99403465
|
T | A | 1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1177+760A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403465 | ||||||
chr14:99403467
|
T | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0124a0001c0001t0008g0120 | 3 | NA18951.hp1 NA18956.hp2 NA18964.hp2 |
intron_variant | MODIFIER | c.1177+758A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403467 | ||||||
chr14:99403472
|
CTCTCTCT others(11): Show |
C | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1177+735_1177+752d others(20): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403472 | ||||||
chr14:99403488
|
CTTTCTCT others(5): Show |
C | 2 | a0001c0007t0002g0144a0002c0006t0002g0143 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.1177+725_1177+736d others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403488 | ||||||
chr14:99403489
|
T | TCTCTCTC others(8): Show |
1 | a0001c0001t0001g0186 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1177+735_1177+736i others(17): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403489 | ||||||
chr14:99403489
|
T | TCTCTCTC others(12): Show |
1 | a0001c0001t0001g0182 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1177+735_1177+736i others(21): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403489 | ||||||
chr14:99403489
|
T | TCTCTCTC others(14): Show |
1 | a0001c0001t0001g0170 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.1177+735_1177+736i others(23): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403489 | ||||||
chr14:99403490
|
T | C | 9 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(6): Show | 9 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1177+735A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403490 | ||||||
chr14:99403597
|
C | T | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+628G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403597 | ||||||
chr14:99403674
|
G | A | 1 | a0001c0001t0001g0011 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1177+551C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99403674 | ||||||
chr14:99404003
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.1177+222A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99404003 | ||||||
chr14:99404097
|
T | C | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+128A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99404097 | ||||||
chr14:99404199
|
A | T | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1177+26T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 11/12 | chr14 | 99404199 | ||||||
chr14:99404451
|
A | G | 1 | a0001c0001t0001g0108 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1092-141T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404451 | ||||||
chr14:99404570
|
C | T | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1092-260G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404570 | ||||||
chr14:99404574
|
T | A | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1092-264A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404574 | ||||||
chr14:99404626
|
TAAC | T | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.1092-319_1092-317d others(5): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404626 | ||||||
chr14:99404673
|
T | G | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.1092-363A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404673 | ||||||
chr14:99404707
|
C | T | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.1092-397G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404707 | ||||||
chr14:99404844
|
A | G | 8 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.1091+361T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 10/12 | chr14 | 99404844 | ||||||
chr14:99405475
|
T | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(148): Show | 156 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.925-104A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99405475 | ||||||
chr14:99405724
|
A | G | 1 | a0001c0001t0001g0128 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.925-353T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99405724 | ||||||
chr14:99405966
|
T | C | 1 | a0001c0001t0001g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.924+550A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99405966 | ||||||
chr14:99406092
|
G | A | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.924+424C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406092 | ||||||
chr14:99406092
|
G | C | 1 | a0001c0001t0001g0042 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.924+424C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406092 | ||||||
chr14:99406107
|
C | T | 3 | a0001c0002t0002g0280a0001c0002t0002g0281a0001c0002t0002g0282 | 3 | HG02258.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.924+409G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406107 | ||||||
chr14:99406198
|
G | GT | 21 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(18): Show | 21 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(18): Show |
intron_variant | MODIFIER | c.924+317dupA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406198 | ||||||
chr14:99406318
|
C | T | 1 | a0001c0001t0001g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.924+198G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406318 | ||||||
chr14:99406360
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.924+156C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406360 | ||||||
chr14:99406497
|
G | T | 7 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(4): Show | 7 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.924+19C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406497 | ||||||
chr14:99406507
|
G | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0003t0001g0139 | 3 | HG02723.hp1 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.924+9C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 9/12 | chr14 | 99406507 | ||||||
chr14:99406613
|
A | T | 1 | a0001c0001t0001g0253 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.850-23T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99406613 | ||||||
chr14:99406654
|
C | T | 8 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.850-64G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99406654 | ||||||
chr14:99406828
|
T | A | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850-238A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99406828 | ||||||
chr14:99406889
|
C | T | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.850-299G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99406889 | ||||||
chr14:99406896
|
G | T | 1 | a0001c0001t0001g0126 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.850-306C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99406896 | ||||||
chr14:99407134
|
T | C | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.850-544A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407134 | ||||||
chr14:99407261
|
G | A | 4 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 4 | HG01123.hp1 HG01884.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.850-671C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407261 | ||||||
chr14:99407280
|
C | T | 20 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(17): Show | 20 | HG01891.hp2 HG02145.hp1 HG02258.hp2 others(17): Show |
intron_variant | MODIFIER | c.850-690G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407280 | ||||||
chr14:99407330
|
G | A | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.850-740C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407330 | ||||||
chr14:99407341
|
C | T | 14 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(11): Show | 14 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.850-751G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407341 | ||||||
chr14:99407366
|
T | G | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.850-776A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407366 | ||||||
chr14:99407496
|
T | C | 7 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(4): Show | 7 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-906A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407496 | ||||||
chr14:99407538
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0001g0240 | 2 | HG03098.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.850-948T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407538 | ||||||
chr14:99407554
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.850-964C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407554 | ||||||
chr14:99407606
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.850-1016G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407606 | ||||||
chr14:99407782
|
G | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.850-1192C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407782 | ||||||
chr14:99407804
|
C | A | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-1214G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407804 | ||||||
chr14:99407806
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.850-1216A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407806 | ||||||
chr14:99407813
|
C | G | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.850-1223G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407813 | ||||||
chr14:99407819
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.850-1229C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407819 | ||||||
chr14:99407895
|
G | C | 1 | a0001c0001t0001g0272 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850-1305C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407895 | ||||||
chr14:99407897
|
A | C | 1 | a0001c0001t0001g0272 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850-1307T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407897 | ||||||
chr14:99407900
|
T | A | 1 | a0001c0001t0001g0272 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850-1310A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407900 | ||||||
chr14:99407903
|
A | G | 1 | a0001c0001t0001g0272 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850-1313T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407903 | ||||||
chr14:99407908
|
A | T | 1 | a0001c0001t0001g0272 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.850-1318T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407908 | ||||||
chr14:99407920
|
G | C | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.850-1330C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99407920 | ||||||
chr14:99408102
|
T | C | 10 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(7): Show | 10 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-1512A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99408102 | ||||||
chr14:99408451
|
T | A | 10 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(7): Show | 10 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.850-1861A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99408451 | ||||||
chr14:99408748
|
T | G | 1 | a0001c0004t0001g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.850-2158A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99408748 | ||||||
chr14:99409071
|
A | C | 1 | a0001c0001t0001g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.850-2481T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409071 | ||||||
chr14:99409074
|
G | A | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.850-2484C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409074 | ||||||
chr14:99409150
|
C | T | 7 | a0001c0002t0002g0132a0001c0002t0002g0133a0001c0002t0002g0146others(4): Show | 7 | HG02258.hp2 HG02809.hp1 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.850-2560G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409150 | ||||||
chr14:99409326
|
T | C | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-2736A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409326 | ||||||
chr14:99409330
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.850-2740T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409330 | ||||||
chr14:99409367
|
A | C | 4 | a0001c0001t0001g0032a0001c0001t0001g0033a0001c0001t0001g0048others(1): Show | 4 | HG02683.hp1 HG03491.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-2777T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409367 | ||||||
chr14:99409376
|
A | G | 23 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.850-2786T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409376 | ||||||
chr14:99409399
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.850-2809G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409399 | ||||||
chr14:99409492
|
G | A | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.850-2902C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409492 | ||||||
chr14:99409813
|
C | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG02257.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.849+3138G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409813 | ||||||
chr14:99409879
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(133): Show | 141 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.849+3072C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99409879 | ||||||
chr14:99410038
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0077 | 2 | NA18965.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.849+2913A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410038 | ||||||
chr14:99410149
|
G | A | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.849+2802C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410149 | ||||||
chr14:99410168
|
A | G | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(155): Show | 163 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.849+2783T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410168 | ||||||
chr14:99410287
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.849+2664C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410287 | ||||||
chr14:99410333
|
G | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.849+2618C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410333 | ||||||
chr14:99410386
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.849+2565C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410386 | ||||||
chr14:99410512
|
T | C | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.849+2439A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410512 | ||||||
chr14:99410516
|
A | G | 23 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0001t0001g0149others(20): Show | 23 | HG01884.hp2 HG01891.hp2 HG02145.hp1 others(20): Show |
intron_variant | MODIFIER | c.849+2435T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410516 | ||||||
chr14:99410887
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.849+2064G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99410887 | ||||||
chr14:99411128
|
A | AAGAGTGC | 5 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 6 | HG01099.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.849+1816_849+1822d others(9): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411128 | ||||||
chr14:99411275
|
C | T | 11 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(8): Show | 11 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.849+1676G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411275 | ||||||
chr14:99411306
|
A | AAACT | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 154 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(151): Show |
intron_variant | MODIFIER | c.849+1644_849+1645i others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411306 | ||||||
chr14:99411387
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.849+1564C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411387 | ||||||
chr14:99411631
|
A | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+1320T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411631 | ||||||
chr14:99411718
|
ACT | A | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+1231_849+1232d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411718 | ||||||
chr14:99411721
|
C | A | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.849+1230G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411721 | ||||||
chr14:99411799
|
G | A | 8 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 9 | HG02080.hp1 HG02165.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.849+1152C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411799 | ||||||
chr14:99411800
|
T | C | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.849+1151A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411800 | ||||||
chr14:99411891
|
C | T | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.849+1060G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411891 | ||||||
chr14:99411978
|
T | C | 1 | a0001c0001t0001g0015 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.849+973A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99411978 | ||||||
chr14:99412112
|
C | G | 1 | a0001c0001t0001g0259 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.849+839G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412112 | ||||||
chr14:99412167
|
C | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | NA18952.hp1 NA18977.hp2 |
intron_variant | MODIFIER | c.849+784G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412167 | ||||||
chr14:99412244
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(75): Show | 80 | HG00099.hp2 HG00408.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.849+707C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412244 | ||||||
chr14:99412389
|
C | T | 11 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(8): Show | 11 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.849+562G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412389 | ||||||
chr14:99412720
|
A | G | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.849+231T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412720 | ||||||
chr14:99412733
|
C | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.849+218G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412733 | ||||||
chr14:99412810
|
T | A | 1 | a0001c0001t0001g0147 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.849+141A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412810 | ||||||
chr14:99412825
|
T | C | 3 | a0001c0002t0005g0142a0001c0007t0002g0144a0002c0006t0002g0143 | 3 | HG02055.hp1 HG02630.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.849+126A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412825 | ||||||
chr14:99412837
|
T | C | 6 | a0001c0001t0001g0244a0001c0002t0002g0129a0001c0002t0002g0130others(3): Show | 6 | HG02451.hp2 HG02809.hp1 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.849+114A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412837 | ||||||
chr14:99412855
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.849+96C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412855 | ||||||
chr14:99412870
|
A | G | 1 | a0001c0001t0001g0259 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.849+81T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 8/12 | chr14 | 99412870 | ||||||
chr14:99413230
|
C | A | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.735-165G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 7/12 | chr14 | 99413230 | ||||||
chr14:99413276
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.735-211G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 7/12 | chr14 | 99413276 | ||||||
chr14:99413376
|
C | G | 1 | a0001c0001t0001g0076 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.735-311G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 7/12 | chr14 | 99413376 | ||||||
chr14:99413475
|
G | A | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.734+401C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 7/12 | chr14 | 99413475 | ||||||
chr14:99413675
|
T | C | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.734+201A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 7/12 | chr14 | 99413675 | ||||||
chr14:99413856
|
C | T | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.734+20G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 7/12 | chr14 | 99413856 | ||||||
chr14:99413995
|
G | A | 1 | a0001c0001t0001g0181 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.676-61C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99413995 | ||||||
chr14:99414150
|
T | G | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-216A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414150 | ||||||
chr14:99414252
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.676-318T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414252 | ||||||
chr14:99414332
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-398C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414332 | ||||||
chr14:99414398
|
G | A | 1 | a0001c0001t0001g0034 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.676-464C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414398 | ||||||
chr14:99414541
|
C | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.676-607G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414541 | ||||||
chr14:99414670
|
T | C | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-736A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414670 | ||||||
chr14:99414786
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-852A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414786 | ||||||
chr14:99414786
|
T | TAGAC | 250 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(247): Show | 256 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(253): Show |
intron_variant | MODIFIER | c.676-853_676-852ins others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414786 | ||||||
chr14:99414786
|
T | TAGGC | 4 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0049others(1): Show | 4 | NA18963.hp1 NA18978.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-853_676-852ins others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414786 | ||||||
chr14:99414860
|
T | G | 3 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054 | 3 | HG02257.hp1 HG03453.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.676-926A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414860 | ||||||
chr14:99414862
|
C | T | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-928G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414862 | ||||||
chr14:99414903
|
T | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0279 | 2 | HG02293.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.676-969A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99414903 | ||||||
chr14:99415144
|
T | C | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.676-1210A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415144 | ||||||
chr14:99415214
|
G | A | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-1280C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415214 | ||||||
chr14:99415263
|
A | C | 1 | a0001c0001t0001g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.676-1329T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415263 | ||||||
chr14:99415337
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-1403C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415337 | ||||||
chr14:99415351
|
C | T | 1 | a0001c0002t0002g0280 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.676-1417G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415351 | ||||||
chr14:99415824
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.676-1890C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415824 | ||||||
chr14:99415912
|
G | A | 1 | a0001c0001t0006g0083 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.676-1978C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99415912 | ||||||
chr14:99416192
|
T | C | 1 | a0001c0001t0001g0216 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.676-2258A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99416192 | ||||||
chr14:99416519
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.676-2585A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99416519 | ||||||
chr14:99417133
|
T | A | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-3199A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99417133 | ||||||
chr14:99417251
|
C | T | 8 | a0001c0001t0001g0253a0001c0001t0001g0259a0001c0001t0001g0262others(5): Show | 8 | HG00544.hp1 HG01346.hp2 NA18953.hp2 others(5): Show |
intron_variant | MODIFIER | c.676-3317G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99417251 | ||||||
chr14:99417463
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.676-3529T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99417463 | ||||||
chr14:99417734
|
C | A | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | NA18952.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.676-3800G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99417734 | ||||||
chr14:99417988
|
T | TCTCTACC others(22): Show |
1 | a0001c0001t0001g0115 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.676-4083_676-4055d others(31): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99417988 | ||||||
chr14:99418013
|
A | G | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-4079T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99418013 | ||||||
chr14:99418244
|
T | C | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-4310A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99418244 | ||||||
chr14:99418417
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.676-4483G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99418417 | ||||||
chr14:99418727
|
T | A | 1 | a0001c0001t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.676-4793A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99418727 | ||||||
chr14:99418764
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.676-4830A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99418764 | ||||||
chr14:99418953
|
G | A | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-5019C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99418953 | ||||||
chr14:99419085
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.676-5151G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419085 | ||||||
chr14:99419087
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.676-5153G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419087 | ||||||
chr14:99419098
|
C | T | 1 | a0001c0001t0001g0030 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.676-5164G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419098 | ||||||
chr14:99419130
|
T | C | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-5196A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419130 | ||||||
chr14:99419227
|
T | C | 2 | a0001c0002t0002g0281a0001c0002t0002g0282 | 2 | HG02258.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.676-5293A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419227 | ||||||
chr14:99419260
|
C | T | 8 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-5326G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419260 | ||||||
chr14:99419262
|
C | G | 2 | a0001c0001t0001g0006a0001c0001t0001g0198 | 3 | HG02895.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.676-5328G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419262 | ||||||
chr14:99419295
|
C | T | 150 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(147): Show | 155 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.676-5361G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419295 | ||||||
chr14:99419359
|
T | C | 7 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(4): Show | 7 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.676-5425A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419359 | ||||||
chr14:99419475
|
T | C | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-5541A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419475 | ||||||
chr14:99419723
|
C | T | 1 | a0001c0001t0001g0216 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.676-5789G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419723 | ||||||
chr14:99419762
|
G | A | 1 | a0001c0001t0001g0110 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.676-5828C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419762 | ||||||
chr14:99419773
|
TCAAAAAA others(5): Show |
T | 9 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(6): Show | 10 | HG02080.hp1 HG02165.hp2 NA18948.hp1 others(7): Show |
intron_variant | MODIFIER | c.676-5851_676-5840d others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419773 | ||||||
chr14:99419774
|
CA | C | 14 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(11): Show | 14 | HG01891.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.676-5841delT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419774 | ||||||
chr14:99419775
|
AAAAAAAA others(4): Show |
A | 1 | a0001c0001t0001g0067 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.676-5852_676-5842d others(13): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419775 | ||||||
chr14:99419784
|
AAC | A | 8 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-5852_676-5851d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419784 | ||||||
chr14:99419785
|
A | C | 1 | a0001c0001t0001g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.676-5851T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419785 | ||||||
chr14:99419787
|
A | C | 8 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-5853T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99419787 | ||||||
chr14:99420078
|
T | C | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.676-6144A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420078 | ||||||
chr14:99420102
|
C | G | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-6168G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420102 | ||||||
chr14:99420111
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-6177G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420111 | ||||||
chr14:99420446
|
G | A | 1 | a0001c0001t0001g0097 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.676-6512C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420446 | ||||||
chr14:99420532
|
A | T | 6 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0230others(3): Show | 6 | HG00408.hp2 HG01928.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.676-6598T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420532 | ||||||
chr14:99420765
|
C | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(122): Show | 130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.676-6831G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420765 | ||||||
chr14:99420815
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0202 | 2 | NA18952.hp2 NA18968.hp1 |
intron_variant | MODIFIER | c.676-6881G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420815 | ||||||
chr14:99420831
|
C | T | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-6897G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420831 | ||||||
chr14:99420947
|
CG | C | 26 | a0001c0001t0001g0006a0001c0001t0001g0053a0001c0001t0001g0059others(23): Show | 27 | HG00280.hp2 HG00408.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.676-7014delC | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | ||||||
chr14:99420947
|
CGG | C | 23 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0084others(20): Show | 23 | HG00735.hp1 HG01109.hp1 HG01192.hp2 others(20): Show |
intron_variant | MODIFIER | c.676-7015_676-7014d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | ||||||
chr14:99420947
|
CGGG | C | 23 | a0001c0001t0001g0010a0001c0001t0001g0027a0001c0001t0001g0043others(20): Show | 23 | HG00408.hp1 HG01069.hp2 HG01071.hp2 others(20): Show |
intron_variant | MODIFIER | c.676-7016_676-7014d others(5): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | ||||||
chr14:99420947
|
CGGGG | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(93): Show | 101 | HG00280.hp1 HG00558.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.676-7017_676-7014d others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | ||||||
chr14:99420947
|
CGGGGG | C | 28 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0015others(25): Show | 28 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(25): Show |
intron_variant | MODIFIER | c.676-7018_676-7014d others(7): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | ||||||
chr14:99420947
|
CGGGGGGG others(3): Show |
C | 4 | a0001c0001t0001g0226a0001c0002t0002g0133a0001c0002t0002g0280others(1): Show | 4 | HG01891.hp2 HG02809.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-7023_676-7014d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | ||||||
chr14:99420947
|
CGGGGGGG others(4): Show |
C | 10 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(7): Show | 10 | HG01123.hp1 HG01884.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.676-7024_676-7014d others(13): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | ||||||
chr14:99420947
|
CGGGGGGG others(5): Show |
C | 4 | a0001c0002t0002g0132a0001c0002t0002g0282a0002c0006t0002g0143others(1): Show | 4 | HG02258.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-7025_676-7014d others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | ||||||
chr14:99420947
|
CGGGGGGG others(6): Show |
C | 2 | a0001c0001t0001g0229a0001c0007t0002g0144 | 2 | HG02055.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.676-7026_676-7014d others(15): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | ||||||
chr14:99420947
|
CGGGGGGG others(7): Show |
C | 3 | a0001c0002t0002g0146a0001c0002t0005g0142a0001c0010t0001g0154 | 3 | HG02970.hp2 HG03130.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.676-7027_676-7014d others(16): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | ||||||
chr14:99420947
|
CGGGGGGG others(10): Show |
C | 1 | a0001c0001t0001g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.676-7030_676-7014d others(19): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | ||||||
chr14:99420947
|
CGGGGGGG others(17): Show |
C | 2 | a0001c0001t0001g0177a0001c0001t0001g0185 | 2 | NA18986.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.676-7037_676-7014d others(26): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420947 | ||||||
chr14:99420956
|
G | C | 1 | a0001c0001t0001g0098 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.676-7022C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420956 | ||||||
chr14:99420959
|
G | T | 1 | a0001c0001t0001g0034 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.676-7025C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420959 | ||||||
chr14:99420961
|
G | T | 3 | a0001c0001t0001g0113a0001c0001t0001g0196a0001c0001t0001g0233 | 3 | HG01169.hp2 HG02293.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.676-7027C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420961 | ||||||
chr14:99420962
|
G | T | 1 | a0001c0001t0001g0061 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.676-7028C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420962 | ||||||
chr14:99420963
|
G | T | 1 | a0001c0001t0001g0263 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.676-7029C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420963 | ||||||
chr14:99420964
|
G | C | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-7030C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420964 | ||||||
chr14:99420964
|
G | T | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.676-7030C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420964 | ||||||
chr14:99420967
|
G | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(119): Show | 127 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.676-7033C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420967 | ||||||
chr14:99420967
|
GGGGGGGG others(3): Show |
G | 1 | a0001c0001t0001g0150 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.676-7043_676-7034d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420967 | ||||||
chr14:99420968
|
G | T | 6 | a0001c0001t0001g0206a0001c0003t0001g0138a0001c0003t0001g0139others(3): Show | 6 | HG01891.hp2 HG02083.hp1 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.676-7034C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420968 | ||||||
chr14:99420969
|
G | GT | 6 | a0001c0001t0001g0011a0001c0001t0001g0189a0001c0001t0001g0197others(3): Show | 6 | HG01099.hp2 HG03491.hp1 NA18966.hp1 others(3): Show |
intron_variant | MODIFIER | c.676-7036_676-7035i others(3): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420969 | ||||||
chr14:99420969
|
G | T | 78 | a0001c0001t0001g0006a0001c0001t0001g0057a0001c0001t0001g0058others(75): Show | 79 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.676-7035C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420969 | ||||||
chr14:99420972
|
G | T | 4 | a0001c0001t0001g0179a0001c0001t0001g0180a0001c0001t0001g0183others(1): Show | 4 | HG01891.hp1 HG02723.hp2 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-7038C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420972 | ||||||
chr14:99420973
|
G | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(135): Show | 143 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.676-7039C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420973 | ||||||
chr14:99420976
|
G | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-7042C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420976 | ||||||
chr14:99420983
|
G | A | 2 | a0001c0001t0001g0109a0001c0001t0001g0110 | 2 | HG01496.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.676-7049C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99420983 | ||||||
chr14:99421028
|
C | CGTTTCTT others(1): Show |
4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-7102_676-7095d others(10): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421028 | ||||||
chr14:99421044
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.676-7110C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421044 | ||||||
chr14:99421112
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 7 | HG01169.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-7178C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421112 | ||||||
chr14:99421235
|
C | A | 1 | a0001c0001t0001g0105 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.676-7301G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421235 | ||||||
chr14:99421512
|
C | T | 7 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(4): Show | 7 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.676-7578G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421512 | ||||||
chr14:99421606
|
A | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-7672T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421606 | ||||||
chr14:99421777
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-7843C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421777 | ||||||
chr14:99421789
|
A | G | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-7855T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99421789 | ||||||
chr14:99422017
|
G | A | 2 | a0001c0002t0002g0129a0001c0002t0002g0130 | 2 | HG02451.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.676-8083C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422017 | ||||||
chr14:99422078
|
T | C | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-8144A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422078 | ||||||
chr14:99422260
|
G | A | 2 | a0001c0001t0001g0275a0001c0001t0001g0277 | 2 | NA18964.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.676-8326C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422260 | ||||||
chr14:99422368
|
A | G | 1 | a0001c0001t0001g0204 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.676-8434T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422368 | ||||||
chr14:99422550
|
C | T | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.676-8616G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422550 | ||||||
chr14:99422561
|
G | A | 1 | a0001c0001t0001g0250 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.676-8627C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422561 | ||||||
chr14:99422623
|
TAGG | T | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.676-8692_676-8690d others(5): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422623 | ||||||
chr14:99422678
|
C | A | 1 | a0001c0001t0001g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.676-8744G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422678 | ||||||
chr14:99422691
|
A | G | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-8757T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422691 | ||||||
chr14:99422824
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.676-8890G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422824 | ||||||
chr14:99422836
|
C | G | 11 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(8): Show | 11 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.676-8902G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422836 | ||||||
chr14:99422914
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.676-8980C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422914 | ||||||
chr14:99422943
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.676-9009C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99422943 | ||||||
chr14:99423043
|
C | T | 1 | a0001c0001t0001g0098 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.676-9109G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423043 | ||||||
chr14:99423051
|
G | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.676-9117C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423051 | ||||||
chr14:99423167
|
G | T | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.676-9233C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423167 | ||||||
chr14:99423250
|
A | G | 2 | a0001c0007t0002g0144a0002c0006t0002g0143 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.676-9316T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423250 | ||||||
chr14:99423285
|
T | C | 12 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(9): Show | 12 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.676-9351A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423285 | ||||||
chr14:99423350
|
G | A | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-9416C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423350 | ||||||
chr14:99423406
|
A | C | 1 | a0001c0001t0001g0079 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.676-9472T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423406 | ||||||
chr14:99423588
|
C | CA | 84 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0157others(81): Show | 85 | HG00099.hp1 HG00280.hp2 HG00544.hp1 others(82): Show |
intron_variant | MODIFIER | c.676-9655dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAA | 17 | a0001c0001t0001g0033a0001c0001t0001g0193a0001c0001t0001g0198others(14): Show | 17 | HG00423.hp2 HG02293.hp1 HG02293.hp2 others(14): Show |
intron_variant | MODIFIER | c.676-9656_676-9655d others(4): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAA | 9 | a0001c0001t0001g0004a0001c0001t0001g0061a0001c0001t0001g0087others(6): Show | 10 | HG01346.hp1 HG01928.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.676-9658_676-9655d others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0001g0039a0001c0001t0001g0071a0001c0001t0001g0098 | 3 | HG01167.hp2 HG02602.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.676-9666_676-9655d others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0001g0049 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.676-9667_676-9655d others(15): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(7): Show |
1 | a0001c0001t0001g0125 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.676-9668_676-9655d others(16): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(8): Show |
2 | a0001c0001t0001g0134a0001c0001t0001g0145 | 2 | HG00735.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.676-9669_676-9655d others(17): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(10): Show |
1 | a0001c0001t0001g0058 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.676-9671_676-9655d others(19): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0014a0001c0001t0001g0068 | 2 | HG00738.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.676-9672_676-9655d others(20): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(12): Show |
7 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0018others(4): Show | 7 | HG01109.hp2 HG02257.hp2 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-9673_676-9655d others(21): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(13): Show |
7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0031others(4): Show | 7 | HG02074.hp1 HG02074.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.676-9674_676-9655d others(22): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(14): Show |
5 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0052others(2): Show | 5 | HG00673.hp1 HG01952.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.676-9675_676-9655d others(23): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(15): Show |
2 | a0001c0001t0001g0283a0001c0008t0001g0104 | 2 | HG00408.hp1 HG02080.hp1 |
intron_variant | MODIFIER | c.676-9676_676-9655d others(24): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(16): Show |
4 | a0001c0001t0001g0016a0001c0001t0001g0064a0001c0001t0001g0091others(1): Show | 4 | HG02083.hp2 NA18957.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-9677_676-9655d others(25): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(17): Show |
6 | a0001c0001t0001g0040a0001c0001t0001g0053a0001c0001t0001g0055others(3): Show | 6 | HG01952.hp2 HG02630.hp1 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.676-9678_676-9655d others(26): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(18): Show |
7 | a0001c0001t0001g0005a0001c0001t0001g0017a0001c0001t0001g0027others(4): Show | 8 | HG01243.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.676-9679_676-9655d others(27): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(19): Show |
9 | a0001c0001t0001g0029a0001c0001t0001g0041a0001c0001t0001g0050others(6): Show | 9 | HG01081.hp1 HG01192.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.676-9680_676-9655d others(28): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(20): Show |
4 | a0001c0001t0001g0127a0001c0001t0001g0135a0001c0001t0006g0083others(1): Show | 4 | HG01496.hp2 HG02056.hp2 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.676-9655_676-9654i others(29): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(21): Show |
3 | a0001c0001t0001g0057a0001c0001t0001g0072a0001c0001t0003g0020 | 3 | HG02886.hp2 HG03098.hp1 NA18943.hp1 |
intron_variant | MODIFIER | c.676-9655_676-9654i others(30): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(22): Show |
1 | a0001c0001t0003g0107 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.676-9655_676-9654i others(31): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(23): Show |
5 | a0001c0001t0001g0022a0001c0001t0001g0106a0001c0001t0001g0113others(2): Show | 5 | HG01169.hp2 HG03139.hp2 NA18961.hp2 others(2): Show |
intron_variant | MODIFIER | c.676-9655_676-9654i others(32): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(24): Show |
9 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0028others(6): Show | 9 | HG01069.hp2 HG01496.hp1 HG01515.hp2 others(6): Show |
intron_variant | MODIFIER | c.676-9655_676-9654i others(33): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(26): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0124 | 2 | NA18964.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.676-9655_676-9654i others(35): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(27): Show |
7 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(4): Show | 8 | HG01070.hp2 HG01071.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.676-9655_676-9654i others(36): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(28): Show |
3 | a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0099 | 3 | HG02615.hp2 HG02886.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.676-9655_676-9654i others(37): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(29): Show |
2 | a0001c0001t0001g0010a0001c0001t0001g0090 | 2 | HG02809.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.676-9655_676-9654i others(38): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(30): Show |
1 | a0001c0001t0001g0077 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.676-9655_676-9654i others(39): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(31): Show |
3 | a0001c0001t0001g0074a0001c0001t0001g0076a0001c0001t0001g0123 | 3 | NA18977.hp2 NA18985.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.676-9655_676-9654i others(40): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(32): Show |
1 | a0001c0001t0001g0136 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.676-9655_676-9654i others(41): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(33): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0035 | 2 | HG02895.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.676-9655_676-9654i others(42): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(37): Show |
1 | a0001c0001t0001g0019 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.676-9655_676-9654i others(46): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(39): Show |
1 | a0001c0001t0001g0081 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.676-9655_676-9654i others(48): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CAAAAAAA others(45): Show |
1 | a0001c0001t0001g0094 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.676-9655_676-9654i others(54): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
C | CACAAAAA others(28): Show |
1 | a0001c0001t0001g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.676-9655_676-9654i others(37): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
CAAAAAAA others(1): Show |
C | 8 | a0001c0001t0001g0092a0001c0002t0002g0129a0001c0002t0002g0130others(5): Show | 8 | HG02451.hp2 HG02809.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.676-9662_676-9655d others(10): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
CAAAAAAA others(2): Show |
C | 6 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0230others(3): Show | 6 | HG00408.hp2 HG01928.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.676-9663_676-9655d others(11): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423588
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.676-9664_676-9655d others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423588 | ||||||
chr14:99423676
|
A | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0049others(1): Show | 4 | NA18963.hp1 NA18978.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-9742T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423676 | ||||||
chr14:99423821
|
C | T | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.676-9887G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99423821 | ||||||
chr14:99424042
|
A | G | 1 | a0001c0001t0001g0227 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.676-10108T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424042 | ||||||
chr14:99424175
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.676-10241A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424175 | ||||||
chr14:99424240
|
G | A | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-10306C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424240 | ||||||
chr14:99424290
|
G | A | 1 | a0001c0001t0001g0230 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.676-10356C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424290 | ||||||
chr14:99424344
|
G | A | 1 | a0001c0001t0001g0259 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.676-10410C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424344 | ||||||
chr14:99424383
|
A | T | 1 | a0001c0001t0001g0054 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.676-10449T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424383 | ||||||
chr14:99424747
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0168 | 2 | NA18956.hp1 NA18979.hp1 |
intron_variant | MODIFIER | c.676-10813T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424747 | ||||||
chr14:99424870
|
T | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 9 | HG02080.hp1 HG02165.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.676-10936A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99424870 | ||||||
chr14:99425226
|
C | T | 7 | a0001c0001t0001g0199a0001c0001t0001g0207a0001c0001t0001g0208others(4): Show | 7 | HG02056.hp1 NA18941.hp1 NA18948.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-11292G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99425226 | ||||||
chr14:99425481
|
G | C | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.676-11547C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99425481 | ||||||
chr14:99425545
|
G | A | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.676-11611C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99425545 | ||||||
chr14:99425546
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.676-11612G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99425546 | ||||||
chr14:99425616
|
T | A | 1 | a0001c0001t0001g0177 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.676-11682A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99425616 | ||||||
chr14:99425707
|
C | T | 2 | a0001c0001t0001g0179a0001c0001t0001g0184 | 2 | HG01891.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.676-11773G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99425707 | ||||||
chr14:99426028
|
G | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(149): Show | 157 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.676-12094C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426028 | ||||||
chr14:99426051
|
C | T | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-12117G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426051 | ||||||
chr14:99426068
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.676-12134G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426068 | ||||||
chr14:99426069
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.676-12135T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426069 | ||||||
chr14:99426099
|
A | T | 1 | a0001c0001t0001g0177 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.676-12165T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426099 | ||||||
chr14:99426281
|
C | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 132 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.676-12347G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426281 | ||||||
chr14:99426492
|
G | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-12558C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426492 | ||||||
chr14:99426493
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-12559G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426493 | ||||||
chr14:99426505
|
G | C | 1 | a0001c0001t0001g0163 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.676-12571C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426505 | ||||||
chr14:99426707
|
C | T | 7 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(4): Show | 7 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.676-12773G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426707 | ||||||
chr14:99426758
|
CA | C | 4 | a0001c0001t0001g0004a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG01261.hp2 HG01346.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.676-12825delT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426758 | ||||||
chr14:99426761
|
G | C | 1 | a0001c0001t0001g0123 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.676-12827C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426761 | ||||||
chr14:99426889
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.676-12955C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99426889 | ||||||
chr14:99427064
|
C | T | 1 | a0001c0001t0001g0009 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.676-13130G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427064 | ||||||
chr14:99427108
|
C | T | 1 | a0001c0001t0001g0177 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.676-13174G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427108 | ||||||
chr14:99427220
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.676-13286G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427220 | ||||||
chr14:99427231
|
C | T | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-13297G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427231 | ||||||
chr14:99427309
|
A | T | 1 | a0001c0001t0001g0125 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.676-13375T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427309 | ||||||
chr14:99427346
|
A | AAAATATA others(3): Show |
1 | a0001c0001t0001g0202 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.676-13422_676-1341 others(14): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427346 | ||||||
chr14:99427409
|
A | G | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.676-13475T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427409 | ||||||
chr14:99427444
|
C | A | 1 | a0001c0001t0001g0064 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.676-13510G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427444 | ||||||
chr14:99427613
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.676-13679G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427613 | ||||||
chr14:99427732
|
G | A | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-13798C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427732 | ||||||
chr14:99427802
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.676-13868G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99427802 | ||||||
chr14:99428126
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.676-14192G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428126 | ||||||
chr14:99428296
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.676-14362T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428296 | ||||||
chr14:99428297
|
C | T | 13 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(10): Show | 13 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.676-14363G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428297 | ||||||
chr14:99428621
|
G | A | 5 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.676-14687C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428621 | ||||||
chr14:99428853
|
T | C | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.676-14919A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428853 | ||||||
chr14:99428890
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.676-14956A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428890 | ||||||
chr14:99428996
|
C | A | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.676-15062G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99428996 | ||||||
chr14:99429073
|
A | C | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-15139T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99429073 | ||||||
chr14:99429415
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-15481G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99429415 | ||||||
chr14:99429477
|
C | T | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-15543G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99429477 | ||||||
chr14:99429696
|
C | G | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-15762G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99429696 | ||||||
chr14:99430006
|
G | A | 1 | a0001c0001t0001g0225 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.676-16072C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430006 | ||||||
chr14:99430016
|
G | A | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.676-16082C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430016 | ||||||
chr14:99430087
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.676-16153C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430087 | ||||||
chr14:99430107
|
G | C | 1 | a0001c0001t0001g0152 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.676-16173C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430107 | ||||||
chr14:99430227
|
A | G | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.676-16293T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430227 | ||||||
chr14:99430276
|
T | G | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.676-16342A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430276 | ||||||
chr14:99430658
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.676-16724C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430658 | ||||||
chr14:99430835
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.676-16901T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430835 | ||||||
chr14:99430911
|
T | A | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-16977A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430911 | ||||||
chr14:99430926
|
C | A | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.676-16992G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430926 | ||||||
chr14:99430971
|
C | T | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-17037G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99430971 | ||||||
chr14:99431494
|
T | C | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-17560A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99431494 | ||||||
chr14:99431860
|
A | G | 11 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(8): Show | 11 | HG02055.hp1 HG02258.hp2 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.676-17926T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99431860 | ||||||
chr14:99432069
|
C | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.676-18135G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99432069 | ||||||
chr14:99432195
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.676-18261G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99432195 | ||||||
chr14:99432244
|
G | A | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-18310C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99432244 | ||||||
chr14:99432442
|
G | A | 3 | a0001c0002t0002g0280a0001c0002t0002g0281a0001c0002t0002g0282 | 3 | HG02258.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.676-18508C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99432442 | ||||||
chr14:99432533
|
C | T | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.676-18599G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99432533 | ||||||
chr14:99432883
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.676-18949A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99432883 | ||||||
chr14:99433419
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.676-19485C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99433419 | ||||||
chr14:99433506
|
T | C | 9 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(6): Show | 9 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.676-19572A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99433506 | ||||||
chr14:99433732
|
C | T | 8 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-19798G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99433732 | ||||||
chr14:99433988
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.676-20054G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99433988 | ||||||
chr14:99434020
|
C | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.676-20086G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434020 | ||||||
chr14:99434025
|
A | G | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.676-20091T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434025 | ||||||
chr14:99434072
|
T | C | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-20138A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434072 | ||||||
chr14:99434135
|
C | T | 2 | a0001c0007t0002g0144a0002c0006t0002g0143 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.676-20201G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434135 | ||||||
chr14:99434184
|
C | CTG | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 168 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.676-20252_676-2025 others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434184 | ||||||
chr14:99434274
|
C | T | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.676-20340G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434274 | ||||||
chr14:99434447
|
G | A | 8 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-20513C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434447 | ||||||
chr14:99434465
|
C | A | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-20531G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434465 | ||||||
chr14:99434480
|
G | A | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.676-20546C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434480 | ||||||
chr14:99434493
|
G | A | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.676-20559C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434493 | ||||||
chr14:99434715
|
C | A | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.676-20781G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434715 | ||||||
chr14:99434778
|
G | T | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.676-20844C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434778 | ||||||
chr14:99434787
|
T | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.676-20853A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434787 | ||||||
chr14:99434796
|
G | C | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.676-20862C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434796 | ||||||
chr14:99434847
|
C | A | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-20913G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | ||||||
chr14:99434847
|
C | CA | 43 | a0001c0001t0001g0004a0001c0001t0001g0013a0001c0001t0001g0017others(40): Show | 44 | HG00408.hp2 HG00423.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.676-20914dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | ||||||
chr14:99434847
|
C | CAA | 12 | a0001c0001t0001g0149a0001c0001t0001g0152a0001c0001t0001g0164others(9): Show | 12 | HG01891.hp2 HG02280.hp2 HG02970.hp1 others(9): Show |
intron_variant | MODIFIER | c.676-20915_676-2091 others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | ||||||
chr14:99434847
|
C | CAAA | 11 | a0001c0001t0001g0147a0001c0001t0001g0168a0001c0001t0001g0169others(8): Show | 11 | HG00673.hp2 HG01891.hp1 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.676-20916_676-2091 others(7): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | ||||||
chr14:99434847
|
C | CAAAA | 8 | a0001c0001t0001g0165a0001c0001t0001g0166a0001c0001t0001g0173others(5): Show | 8 | HG00558.hp2 HG02027.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-20917_676-2091 others(8): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | ||||||
chr14:99434847
|
CA | C | 89 | a0001c0001t0001g0005a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(87): Show |
intron_variant | MODIFIER | c.676-20914delT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | ||||||
chr14:99434847
|
CAA | C | 7 | a0001c0001t0001g0268a0001c0002t0002g0132a0001c0002t0002g0133others(4): Show | 7 | HG01257.hp1 HG02258.hp2 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.676-20915_676-2091 others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | ||||||
chr14:99434847
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0001g0227a0001c0001t0001g0244 | 2 | HG02080.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.676-20926_676-2091 others(17): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434847 | ||||||
chr14:99434877
|
C | A | 13 | a0001c0001t0001g0075a0001c0001t0001g0149a0001c0001t0001g0150others(10): Show | 13 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.676-20943G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434877 | ||||||
chr14:99434878
|
A | C | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-20944T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434878 | ||||||
chr14:99434943
|
A | C | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.676-21009T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99434943 | ||||||
chr14:99435151
|
C | T | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.676-21217G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435151 | ||||||
chr14:99435170
|
A | G | 1 | a0001c0001t0001g0270 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.676-21236T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435170 | ||||||
chr14:99435228
|
C | CATTA | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.676-21295_676-2129 others(8): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435228 | ||||||
chr14:99435349
|
C | T | 3 | a0001c0002t0002g0280a0001c0002t0002g0281a0001c0002t0002g0282 | 3 | HG02258.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.676-21415G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435349 | ||||||
chr14:99435515
|
T | C | 1 | a0001c0001t0001g0095 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.676-21581A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435515 | ||||||
chr14:99435536
|
T | C | 1 | a0001c0001t0001g0212 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.676-21602A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435536 | ||||||
chr14:99435632
|
G | A | 1 | a0001c0001t0001g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.676-21698C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435632 | ||||||
chr14:99435735
|
C | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0214 | 2 | HG00099.hp1 HG00280.hp2 |
intron_variant | MODIFIER | c.676-21801G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435735 | ||||||
chr14:99435742
|
A | C | 1 | a0001c0001t0001g0077 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.676-21808T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435742 | ||||||
chr14:99435743
|
C | A | 1 | a0001c0001t0001g0077 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.676-21809G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435743 | ||||||
chr14:99435744
|
CT | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(180): Show | 188 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.676-21811delA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435744 | ||||||
chr14:99435745
|
T | C | 1 | a0001c0001t0001g0077 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.676-21811A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435745 | ||||||
chr14:99435777
|
G | A | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.676-21843C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435777 | ||||||
chr14:99435800
|
G | A | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.676-21866C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435800 | ||||||
chr14:99435926
|
G | C | 1 | a0001c0001t0001g0062 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.676-21992C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99435926 | ||||||
chr14:99436060
|
C | G | 1 | a0001c0001t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.676-22126G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436060 | ||||||
chr14:99436121
|
A | G | 2 | a0001c0007t0002g0144a0002c0006t0002g0143 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.675+22158T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436121 | ||||||
chr14:99436136
|
G | A | 1 | a0001c0001t0001g0126 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.675+22143C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436136 | ||||||
chr14:99436393
|
T | G | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+21886A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436393 | ||||||
chr14:99436477
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.675+21802G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436477 | ||||||
chr14:99436533
|
G | A | 1 | a0001c0001t0001g0084 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.675+21746C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436533 | ||||||
chr14:99436583
|
A | G | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+21696T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436583 | ||||||
chr14:99436746
|
C | T | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.675+21533G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436746 | ||||||
chr14:99436878
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.675+21401G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99436878 | ||||||
chr14:99437017
|
T | C | 3 | a0001c0001t0001g0253a0001c0001t0001g0262a0001c0001t0001g0263 | 3 | HG00544.hp1 HG01346.hp2 NA18963.hp2 |
intron_variant | MODIFIER | c.675+21262A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437017 | ||||||
chr14:99437143
|
A | C | 1 | a0001c0002t0002g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.675+21136T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437143 | ||||||
chr14:99437451
|
A | C | 1 | a0001c0001t0001g0187 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.675+20828T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437451 | ||||||
chr14:99437526
|
C | A | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG01123.hp1 HG01884.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+20753G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437526 | ||||||
chr14:99437636
|
C | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.675+20643G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437636 | ||||||
chr14:99437662
|
T | G | 1 | a0001c0001t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.675+20617A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437662 | ||||||
chr14:99437665
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.675+20614C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437665 | ||||||
chr14:99437685
|
G | A | 1 | a0001c0001t0001g0277 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.675+20594C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437685 | ||||||
chr14:99437849
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.675+20430C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437849 | ||||||
chr14:99437890
|
C | T | 7 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(4): Show | 7 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.675+20389G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437890 | ||||||
chr14:99437998
|
C | G | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+20281G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99437998 | ||||||
chr14:99438162
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.675+20117C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438162 | ||||||
chr14:99438234
|
C | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 6 | HG01099.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+20045G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438234 | ||||||
chr14:99438283
|
C | T | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 168 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.675+19996G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438283 | ||||||
chr14:99438515
|
T | G | 2 | a0001c0007t0002g0144a0002c0006t0002g0143 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.675+19764A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438515 | ||||||
chr14:99438697
|
G | A | 1 | a0001c0001t0003g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.675+19582C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438697 | ||||||
chr14:99438706
|
G | A | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+19573C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438706 | ||||||
chr14:99438825
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.675+19454G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438825 | ||||||
chr14:99438826
|
G | A | 2 | a0001c0001t0001g0204a0001c0001t0001g0212 | 2 | HG01099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.675+19453C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438826 | ||||||
chr14:99438838
|
T | C | 1 | a0001c0002t0002g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.675+19441A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99438838 | ||||||
chr14:99439416
|
T | G | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.675+18863A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439416 | ||||||
chr14:99439592
|
G | T | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.675+18687C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439592 | ||||||
chr14:99439616
|
T | C | 8 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(5): Show | 8 | HG02145.hp1 HG02486.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.675+18663A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439616 | ||||||
chr14:99439688
|
A | ATATGTAT others(53): Show |
1 | a0001c0001t0001g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.675+18531_675+1859 others(64): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439688 | ||||||
chr14:99439692
|
GTATT | G | 4 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(1): Show | 4 | HG02970.hp1 HG03471.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.675+18583_675+1858 others(8): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439692 | ||||||
chr14:99439710
|
A | T | 2 | a0001c0007t0002g0144a0002c0006t0002g0143 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.675+18569T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439710 | ||||||
chr14:99439769
|
C | T | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+18510G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99439769 | ||||||
chr14:99440056
|
A | G | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.675+18223T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440056 | ||||||
chr14:99440217
|
T | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0119a0001c0001t0001g0121others(1): Show | 4 | NA18961.hp2 NA18968.hp2 NA18995.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+18062A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440217 | ||||||
chr14:99440302
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.675+17977T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440302 | ||||||
chr14:99440513
|
C | A | 1 | a0001c0001t0001g0211 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.675+17766G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440513 | ||||||
chr14:99440525
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.675+17754G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440525 | ||||||
chr14:99440526
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.675+17753C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440526 | ||||||
chr14:99440676
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.675+17603G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440676 | ||||||
chr14:99440942
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.675+17337A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440942 | ||||||
chr14:99440982
|
G | T | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+17297C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99440982 | ||||||
chr14:99441032
|
C | T | 1 | a0001c0001t0001g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.675+17247G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441032 | ||||||
chr14:99441046
|
C | T | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.675+17233G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441046 | ||||||
chr14:99441156
|
T | C | 1 | a0001c0004t0001g0155 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.675+17123A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441156 | ||||||
chr14:99441195
|
T | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.675+17084A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441195 | ||||||
chr14:99441537
|
C | T | 4 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02809.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+16742G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441537 | ||||||
chr14:99441559
|
T | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.675+16720A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441559 | ||||||
chr14:99441599
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.675+16680C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441599 | ||||||
chr14:99441636
|
A | C | 1 | a0001c0001t0001g0188 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.675+16643T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441636 | ||||||
chr14:99441720
|
G | A | 2 | a0001c0007t0002g0144a0002c0006t0002g0143 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.675+16559C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441720 | ||||||
chr14:99441856
|
T | C | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+16423A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441856 | ||||||
chr14:99441915
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.675+16364C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441915 | ||||||
chr14:99441992
|
G | A | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+16287C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99441992 | ||||||
chr14:99442045
|
G | A | 7 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(4): Show | 7 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.675+16234C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442045 | ||||||
chr14:99442115
|
C | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0039others(23): Show | 27 | HG00423.hp1 HG00558.hp1 HG01261.hp2 others(24): Show |
intron_variant | MODIFIER | c.675+16164G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442115 | ||||||
chr14:99442122
|
G | A | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+16157C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442122 | ||||||
chr14:99442140
|
C | T | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+16139G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442140 | ||||||
chr14:99442292
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.675+15987C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442292 | ||||||
chr14:99442373
|
T | A | 1 | a0001c0001t0001g0216 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.675+15906A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442373 | ||||||
chr14:99442391
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.675+15888G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442391 | ||||||
chr14:99442411
|
G | A | 1 | a0001c0001t0001g0197 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.675+15868C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442411 | ||||||
chr14:99442471
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.675+15808G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442471 | ||||||
chr14:99442723
|
A | G | 1 | a0001c0001t0001g0185 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.675+15556T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442723 | ||||||
chr14:99442959
|
T | C | 156 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(153): Show | 161 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(158): Show |
intron_variant | MODIFIER | c.675+15320A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99442959 | ||||||
chr14:99443065
|
C | T | 1 | a0001c0001t0001g0092 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.675+15214G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443065 | ||||||
chr14:99443255
|
A | AT | 28 | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0052others(25): Show | 28 | HG01081.hp2 HG01123.hp1 HG01258.hp1 others(25): Show |
intron_variant | MODIFIER | c.675+15023dupA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443255 | ||||||
chr14:99443255
|
A | ATT | 6 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0003t0001g0139others(3): Show | 6 | HG02145.hp1 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.675+15022_675+1502 others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443255 | ||||||
chr14:99443255
|
AT | A | 10 | a0001c0001t0001g0014a0001c0001t0001g0034a0001c0001t0001g0035others(7): Show | 10 | HG01167.hp1 HG01517.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.675+15023delA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443255 | ||||||
chr14:99443256
|
T | A | 8 | a0001c0001t0001g0005a0001c0001t0001g0087a0001c0001t0001g0109others(5): Show | 9 | HG01169.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.675+15023A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443256 | ||||||
chr14:99443341
|
T | G | 4 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0049others(1): Show | 4 | NA18963.hp1 NA18978.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.675+14938A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443341 | ||||||
chr14:99443494
|
C | T | 1 | a0001c0004t0001g0155 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.675+14785G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443494 | ||||||
chr14:99443531
|
C | T | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+14748G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443531 | ||||||
chr14:99443644
|
G | A | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+14635C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443644 | ||||||
chr14:99443722
|
T | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.675+14557A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443722 | ||||||
chr14:99443724
|
T | C | 1 | a0001c0001t0001g0039 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.675+14555A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443724 | ||||||
chr14:99443826
|
T | C | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+14453A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443826 | ||||||
chr14:99443829
|
C | T | 1 | a0001c0003t0001g0138 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.675+14450G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443829 | ||||||
chr14:99443851
|
C | T | 6 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(3): Show | 6 | HG02486.hp2 HG02965.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+14428G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443851 | ||||||
chr14:99443885
|
T | A | 2 | a0001c0007t0002g0144a0002c0006t0002g0143 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.675+14394A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99443885 | ||||||
chr14:99444101
|
T | C | 1 | a0001c0007t0002g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.675+14178A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444101 | ||||||
chr14:99444130
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.675+14149G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444130 | ||||||
chr14:99444222
|
A | T | 1 | a0001c0001t0001g0065 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.675+14057T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444222 | ||||||
chr14:99444261
|
T | C | 1 | a0001c0001t0001g0236 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.675+14018A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444261 | ||||||
chr14:99444419
|
T | C | 8 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.675+13860A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444419 | ||||||
chr14:99444438
|
T | C | 14 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0129others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.675+13841A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444438 | ||||||
chr14:99444567
|
ATCAAAAC others(17): Show |
A | 1 | a0001c0001t0001g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.675+13688_675+1371 others(28): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444567 | ||||||
chr14:99444608
|
C | T | 1 | a0001c0001t0001g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.675+13671G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444608 | ||||||
chr14:99444631
|
G | GTAGGATC others(19): Show |
1 | a0001c0001t0001g0106 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.675+13647_675+1364 others(30): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444631 | ||||||
chr14:99444804
|
C | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0088a0001c0001t0001g0089others(2): Show | 6 | HG00280.hp1 HG01070.hp2 HG01071.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+13475G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444804 | ||||||
chr14:99444834
|
C | CA | 23 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(20): Show | 23 | HG01361.hp1 HG01884.hp2 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.675+13444dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444834 | ||||||
chr14:99444885
|
A | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.675+13394T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444885 | ||||||
chr14:99444964
|
T | C | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG01123.hp1 HG01884.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.675+13315A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444964 | ||||||
chr14:99444972
|
A | G | 5 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.675+13307T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99444972 | ||||||
chr14:99445007
|
G | C | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0001g0266 | 3 | NA18953.hp2 NA18974.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.675+13272C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445007 | ||||||
chr14:99445083
|
G | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.675+13196C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445083 | ||||||
chr14:99445117
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02809.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+13162C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445117 | ||||||
chr14:99445182
|
A | T | 1 | a0001c0008t0001g0104 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.675+13097T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445182 | ||||||
chr14:99445235
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.675+13044C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445235 | ||||||
chr14:99445262
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.675+13017G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445262 | ||||||
chr14:99445422
|
T | G | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+12857A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99445422 | ||||||
chr14:99446013
|
G | C | 1 | a0001c0001t0001g0056 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.675+12266C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446013 | ||||||
chr14:99446033
|
G | T | 1 | a0001c0001t0001g0045 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.675+12246C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446033 | ||||||
chr14:99446115
|
G | C | 1 | a0001c0001t0001g0267 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.675+12164C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446115 | ||||||
chr14:99446117
|
C | T | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+12162G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446117 | ||||||
chr14:99446165
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.675+12114C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446165 | ||||||
chr14:99446189
|
G | A | 4 | a0001c0001t0001g0176a0001c0003t0001g0138a0001c0003t0001g0139others(1): Show | 4 | HG01891.hp2 HG02280.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+12090C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446189 | ||||||
chr14:99446417
|
T | C | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+11862A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446417 | ||||||
chr14:99446479
|
C | T | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+11800G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446479 | ||||||
chr14:99446543
|
A | G | 3 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0146 | 3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.675+11736T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446543 | ||||||
chr14:99446926
|
G | A | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+11353C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446926 | ||||||
chr14:99446944
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.675+11335C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446944 | ||||||
chr14:99446975
|
CT | C | 141 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0145others(138): Show | 142 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.675+11303delA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446975 | ||||||
chr14:99446975
|
CTT | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.675+11302_675+1130 others(6): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99446975 | ||||||
chr14:99447117
|
G | A | 2 | a0001c0001t0001g0092a0001c0010t0001g0154 | 2 | HG02970.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.675+11162C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447117 | ||||||
chr14:99447164
|
G | A | 1 | a0001c0001t0001g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.675+11115C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447164 | ||||||
chr14:99447189
|
T | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0093a0001c0001t0001g0094others(1): Show | 5 | HG01261.hp2 HG01346.hp1 HG01928.hp2 others(2): Show |
intron_variant | MODIFIER | c.675+11090A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447189 | ||||||
chr14:99447289
|
T | C | 1 | a0001c0001t0001g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.675+10990A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447289 | ||||||
chr14:99447319
|
A | G | 2 | a0001c0001t0001g0204a0001c0001t0001g0212 | 2 | HG01099.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.675+10960T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447319 | ||||||
chr14:99447334
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.675+10945A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447334 | ||||||
chr14:99447469
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.675+10810T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447469 | ||||||
chr14:99447542
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0001g0137 | 2 | HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.675+10737G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447542 | ||||||
chr14:99447586
|
G | A | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+10693C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447586 | ||||||
chr14:99447589
|
C | T | 1 | a0001c0001t0001g0239 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.675+10690G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447589 | ||||||
chr14:99447734
|
C | T | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+10545G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447734 | ||||||
chr14:99447735
|
G | A | 1 | a0001c0007t0002g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.675+10544C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447735 | ||||||
chr14:99447911
|
C | T | 51 | a0001c0001t0001g0006a0001c0001t0001g0157a0001c0001t0001g0163others(48): Show | 52 | HG00408.hp2 HG00544.hp2 HG00735.hp2 others(49): Show |
intron_variant | MODIFIER | c.675+10368G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99447911 | ||||||
chr14:99448169
|
A | C | 1 | a0001c0001t0001g0063 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.675+10110T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448169 | ||||||
chr14:99448240
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.675+10039C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448240 | ||||||
chr14:99448336
|
G | A | 2 | a0001c0001t0001g0268a0001c0001t0001g0269 | 2 | HG01257.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.675+9943C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448336 | ||||||
chr14:99448488
|
G | A | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(4): Show | 7 | HG01081.hp1 HG01243.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.675+9791C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448488 | ||||||
chr14:99448547
|
C | T | 1 | a0001c0008t0001g0104 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.675+9732G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448547 | ||||||
chr14:99448552
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.675+9727A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448552 | ||||||
chr14:99448554
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.675+9725T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448554 | ||||||
chr14:99448585
|
C | A | 1 | a0001c0001t0001g0187 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.675+9694G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448585 | ||||||
chr14:99448835
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.675+9444C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448835 | ||||||
chr14:99448838
|
G | T | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+9441C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448838 | ||||||
chr14:99448972
|
T | C | 3 | a0001c0001t0001g0134a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG00735.hp1 HG01069.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.675+9307A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99448972 | ||||||
chr14:99449022
|
T | G | 14 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0129others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.675+9257A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449022 | ||||||
chr14:99449270
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.675+9009A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449270 | ||||||
chr14:99449475
|
C | A | 8 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.675+8804G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449475 | ||||||
chr14:99449534
|
A | G | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+8745T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449534 | ||||||
chr14:99449614
|
G | A | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.675+8665C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449614 | ||||||
chr14:99449672
|
A | G | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+8607T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449672 | ||||||
chr14:99449792
|
A | G | 3 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131 | 3 | HG02451.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.675+8487T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449792 | ||||||
chr14:99449829
|
T | C | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+8450A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449829 | ||||||
chr14:99449830
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.675+8449T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449830 | ||||||
chr14:99449960
|
A | C | 1 | a0001c0001t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.675+8319T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99449960 | ||||||
chr14:99450373
|
C | T | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+7906G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99450373 | ||||||
chr14:99450814
|
A | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.675+7465T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99450814 | ||||||
chr14:99450964
|
T | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.675+7315A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99450964 | ||||||
chr14:99450984
|
G | C | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.675+7295C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99450984 | ||||||
chr14:99451237
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.675+7042A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99451237 | ||||||
chr14:99451295
|
G | A | 3 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202 | 3 | NA18952.hp2 NA18968.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.675+6984C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99451295 | ||||||
chr14:99451472
|
T | C | 1 | a0001c0004t0001g0156 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.675+6807A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99451472 | ||||||
chr14:99451527
|
G | A | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+6752C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99451527 | ||||||
chr14:99451600
|
G | T | 1 | a0001c0001t0001g0128 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.675+6679C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99451600 | ||||||
chr14:99451606
|
A | T | 1 | a0001c0001t0001g0128 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.675+6673T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99451606 | ||||||
chr14:99452029
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.675+6250G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452029 | ||||||
chr14:99452080
|
G | C | 2 | a0001c0007t0002g0144a0002c0006t0002g0143 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.675+6199C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452080 | ||||||
chr14:99452170
|
G | A | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+6109C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452170 | ||||||
chr14:99452200
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.675+6079C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452200 | ||||||
chr14:99452357
|
G | A | 1 | a0001c0001t0004g0007 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.675+5922C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452357 | ||||||
chr14:99452418
|
T | G | 4 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0030others(1): Show | 4 | HG01081.hp1 HG01515.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+5861A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452418 | ||||||
chr14:99452470
|
C | T | 6 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0059others(3): Show | 6 | HG02055.hp2 HG02622.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.675+5809G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452470 | ||||||
chr14:99452666
|
A | G | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+5613T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452666 | ||||||
chr14:99452790
|
C | T | 1 | a0002c0006t0002g0143 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.675+5489G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452790 | ||||||
chr14:99452847
|
C | G | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.675+5432G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452847 | ||||||
chr14:99452848
|
G | C | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+5431C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452848 | ||||||
chr14:99452852
|
G | T | 14 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0129others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.675+5427C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452852 | ||||||
chr14:99452898
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0146 | 3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.675+5381C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452898 | ||||||
chr14:99452905
|
A | G | 1 | a0001c0001t0001g0150 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.675+5374T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99452905 | ||||||
chr14:99453239
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.675+5040G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453239 | ||||||
chr14:99453318
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.675+4961C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453318 | ||||||
chr14:99453591
|
G | A | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+4688C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453591 | ||||||
chr14:99453601
|
G | C | 1 | a0001c0001t0001g0236 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.675+4678C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453601 | ||||||
chr14:99453661
|
C | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.675+4618G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453661 | ||||||
chr14:99453673
|
A | T | 1 | a0001c0001t0001g0040 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.675+4606T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453673 | ||||||
chr14:99453739
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.675+4540A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453739 | ||||||
chr14:99453748
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.675+4531G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453748 | ||||||
chr14:99453820
|
C | T | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+4459G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453820 | ||||||
chr14:99453841
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.675+4438G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99453841 | ||||||
chr14:99454014
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.675+4265C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454014 | ||||||
chr14:99454267
|
G | T | 2 | a0001c0001t0001g0254a0001c0001t0001g0255 | 2 | HG00738.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.675+4012C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454267 | ||||||
chr14:99454328
|
G | C | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+3951C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454328 | ||||||
chr14:99454408
|
C | T | 127 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0157others(124): Show | 128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.675+3871G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454408 | ||||||
chr14:99454504
|
A | G | 7 | a0001c0001t0001g0219a0001c0001t0001g0221a0001c0001t0001g0222others(4): Show | 7 | NA18977.hp1 NA18978.hp2 NA18981.hp1 others(4): Show |
intron_variant | MODIFIER | c.675+3775T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454504 | ||||||
chr14:99454518
|
G | A | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.675+3761C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454518 | ||||||
chr14:99454576
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.675+3703A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454576 | ||||||
chr14:99454666
|
C | T | 1 | a0001c0008t0001g0104 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.675+3613G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454666 | ||||||
chr14:99454678
|
A | G | 4 | a0001c0001t0001g0052a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 4 | HG02257.hp1 HG02630.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.675+3601T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454678 | ||||||
chr14:99454703
|
A | C | 1 | a0001c0001t0001g0040 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.675+3576T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454703 | ||||||
chr14:99454704
|
T | A | 1 | a0001c0001t0001g0040 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.675+3575A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454704 | ||||||
chr14:99454768
|
GT | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.675+3510delA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454768 | ||||||
chr14:99454905
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.675+3374C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454905 | ||||||
chr14:99454933
|
G | C | 2 | a0001c0001t0001g0100a0001c0001t0001g0114 | 2 | HG00099.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.675+3346C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454933 | ||||||
chr14:99454949
|
T | C | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.675+3330A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99454949 | ||||||
chr14:99455095
|
G | C | 2 | a0001c0001t0001g0251a0001c0001t0001g0279 | 2 | HG02293.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.675+3184C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99455095 | ||||||
chr14:99455096
|
G | C | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+3183C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99455096 | ||||||
chr14:99455568
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.675+2711T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99455568 | ||||||
chr14:99455584
|
C | T | 1 | a0001c0001t0001g0220 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.675+2695G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99455584 | ||||||
chr14:99455886
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.675+2393C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99455886 | ||||||
chr14:99455930
|
G | A | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+2349C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99455930 | ||||||
chr14:99456069
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.675+2210A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456069 | ||||||
chr14:99456125
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.675+2154T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456125 | ||||||
chr14:99456195
|
A | G | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.675+2084T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456195 | ||||||
chr14:99456201
|
G | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.675+2078C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456201 | ||||||
chr14:99456256
|
A | G | 1 | a0001c0001t0001g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.675+2023T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456256 | ||||||
chr14:99456265
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.675+2014A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456265 | ||||||
chr14:99456439
|
T | C | 2 | a0001c0001t0001g0237a0001c0001t0001g0238 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.675+1840A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456439 | ||||||
chr14:99456445
|
T | A | 1 | a0001c0001t0001g0164 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.675+1834A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456445 | ||||||
chr14:99456723
|
T | G | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.675+1556A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456723 | ||||||
chr14:99456760
|
A | T | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.675+1519T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99456760 | ||||||
chr14:99457070
|
C | A | 2 | a0001c0001t0001g0102a0004c0009t0001g0046 | 2 | NA18979.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.675+1209G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457070 | ||||||
chr14:99457130
|
G | A | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.675+1149C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457130 | ||||||
chr14:99457193
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.675+1086T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457193 | ||||||
chr14:99457225
|
T | A | 1 | a0001c0001t0001g0145 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.675+1054A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457225 | ||||||
chr14:99457229
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.675+1050C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457229 | ||||||
chr14:99457250
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.675+1029A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457250 | ||||||
chr14:99457297
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.675+982G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457297 | ||||||
chr14:99457520
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.675+759G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457520 | ||||||
chr14:99457699
|
G | A | 127 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0157others(124): Show | 128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.675+580C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457699 | ||||||
chr14:99457793
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.675+486A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457793 | ||||||
chr14:99457883
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.675+396C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457883 | ||||||
chr14:99457941
|
T | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0103 | 2 | HG01109.hp2 NA19004.hp2 |
intron_variant | MODIFIER | c.675+338A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99457941 | ||||||
chr14:99458273
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp2 | splice_region_variant&intron_variant | LOW | c.675+6C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 6/12 | chr14 | 99458273 | ||||||
chr14:99458642
|
TAA | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.419-109_419-108del others(2): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458642 | ||||||
chr14:99458663
|
C | T | 3 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | NA18961.hp2 NA18968.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.419-128G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458663 | ||||||
chr14:99458771
|
C | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0146 | 3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.419-236G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458771 | ||||||
chr14:99458774
|
C | CA | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.419-240dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458774 | ||||||
chr14:99458774
|
C | CAA | 12 | a0001c0001t0001g0013a0001c0001t0001g0040a0001c0001t0001g0045others(9): Show | 12 | HG01109.hp2 HG01884.hp2 HG02647.hp1 others(9): Show |
intron_variant | MODIFIER | c.419-241_419-240dup others(2): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458774 | ||||||
chr14:99458774
|
CA | C | 124 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0158others(121): Show | 125 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.419-240delT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458774 | ||||||
chr14:99458856
|
C | T | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.418+257G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 5/12 | chr14 | 99458856 | ||||||
chr14:99459205
|
T | C | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.346-20A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459205 | ||||||
chr14:99459235
|
T | C | 1 | a0001c0001t0001g0027 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.346-50A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459235 | ||||||
chr14:99459254
|
G | A | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.346-69C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459254 | ||||||
chr14:99459265
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.346-80G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459265 | ||||||
chr14:99459297
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.346-112A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459297 | ||||||
chr14:99459305
|
CTTCAAAT others(5): Show |
C | 4 | a0001c0001t0001g0034a0001c0001t0001g0040a0001c0001t0001g0049others(1): Show | 4 | NA18963.hp1 NA18978.hp1 NA18984.hp1 others(1): Show |
intron_variant | MODIFIER | c.346-132_346-121del others(12): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459305 | ||||||
chr14:99459509
|
A | T | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.346-324T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459509 | ||||||
chr14:99459590
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.346-405A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459590 | ||||||
chr14:99459704
|
G | C | 1 | a0001c0001t0001g0186 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.346-519C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459704 | ||||||
chr14:99459706
|
T | C | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.346-521A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459706 | ||||||
chr14:99459823
|
G | C | 3 | a0001c0002t0002g0280a0001c0002t0002g0281a0001c0002t0002g0282 | 3 | HG02258.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.346-638C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459823 | ||||||
chr14:99459899
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.346-714A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99459899 | ||||||
chr14:99460000
|
C | A | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.346-815G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460000 | ||||||
chr14:99460145
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.346-960G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460145 | ||||||
chr14:99460162
|
G | GT | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 135 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(132): Show |
intron_variant | MODIFIER | c.346-978dupA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460162 | ||||||
chr14:99460308
|
A | G | 5 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 6 | HG01099.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.345+884T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460308 | ||||||
chr14:99460419
|
C | T | 1 | a0001c0001t0001g0048 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.345+773G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460419 | ||||||
chr14:99460592
|
G | A | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.345+600C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460592 | ||||||
chr14:99460832
|
A | G | 3 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131 | 3 | HG02451.hp2 HG03540.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.345+360T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99460832 | ||||||
chr14:99461158
|
T | C | 1 | a0001c0001t0001g0137 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.345+34A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 4/12 | chr14 | 99461158 | ||||||
chr14:99461609
|
G | A | 5 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.197-269C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99461609 | ||||||
chr14:99461647
|
A | G | 1 | a0001c0001t0001g0039 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.197-307T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99461647 | ||||||
chr14:99462314
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.197-974A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462314 | ||||||
chr14:99462460
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.196+1026G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462460 | ||||||
chr14:99462481
|
G | A | 1 | a0001c0002t0002g0131 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.196+1005C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462481 | ||||||
chr14:99462587
|
G | A | 96 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0157others(93): Show | 97 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.196+899C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462587 | ||||||
chr14:99462593
|
G | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.196+893C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462593 | ||||||
chr14:99462738
|
C | T | 1 | a0001c0002t0002g0132 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.196+748G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462738 | ||||||
chr14:99462903
|
G | A | 2 | a0001c0001t0003g0020a0001c0001t0003g0107 | 2 | HG02451.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.196+583C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99462903 | ||||||
chr14:99463464
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.196+22C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 3/12 | chr14 | 99463464 | ||||||
chr14:99463705
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.104-127G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99463705 | ||||||
chr14:99463716
|
C | T | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.104-138G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99463716 | ||||||
chr14:99463804
|
G | T | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.104-226C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99463804 | ||||||
chr14:99463809
|
CAA | C | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.104-233_104-232del others(2): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99463809 | ||||||
chr14:99463849
|
T | C | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG02683.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.104-271A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99463849 | ||||||
chr14:99464203
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.104-625C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464203 | ||||||
chr14:99464240
|
C | A | 1 | a0001c0001t0001g0178 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.104-662G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464240 | ||||||
chr14:99464386
|
G | A | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.104-808C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464386 | ||||||
chr14:99464629
|
G | T | 1 | a0001c0001t0001g0253 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.104-1051C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464629 | ||||||
chr14:99464693
|
G | C | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.103+1010C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464693 | ||||||
chr14:99464786
|
T | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.103+917A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464786 | ||||||
chr14:99464821
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.103+882A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464821 | ||||||
chr14:99464903
|
T | C | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.103+800A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464903 | ||||||
chr14:99464916
|
G | C | 1 | a0001c0001t0001g0179 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.103+787C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464916 | ||||||
chr14:99464973
|
C | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.103+730G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99464973 | ||||||
chr14:99465494
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.103+209C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99465494 | ||||||
chr14:99465516
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.103+187G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99465516 | ||||||
chr14:99465625
|
G | A | 1 | a0001c0001t0001g0108 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.103+78C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99465625 | ||||||
chr14:99465627
|
G | A | 1 | a0001c0001t0001g0018 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.103+76C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 2/12 | chr14 | 99465627 | ||||||
chr14:99466004
|
A | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-8-191T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466004 | ||||||
chr14:99466301
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.-8-488T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466301 | ||||||
chr14:99466388
|
G | A | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-8-575C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466388 | ||||||
chr14:99466422
|
G | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-8-609C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466422 | ||||||
chr14:99466485
|
C | T | 1 | a0003c0005t0010g0284 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-8-672G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466485 | ||||||
chr14:99466600
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0146 | 3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-787A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466600 | ||||||
chr14:99466618
|
CGG | C | 21 | a0001c0001t0001g0025a0001c0001t0001g0032a0001c0001t0001g0039others(18): Show | 21 | HG00423.hp1 HG00673.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.-8-807_-8-806delCC | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466618 | ||||||
chr14:99466618
|
CGGG | C | 254 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(251): Show | 260 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(257): Show |
intron_variant | MODIFIER | c.-8-808_-8-806delCC others(1): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466618 | ||||||
chr14:99466621
|
G | A | 1 | a0001c0002t0002g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-8-808C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466621 | ||||||
chr14:99466622
|
G | A | 10 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0132others(7): Show | 10 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-8-809C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466622 | ||||||
chr14:99466626
|
G | C | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-8-813C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466626 | ||||||
chr14:99466631
|
G | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-8-818C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466631 | ||||||
chr14:99466632
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-8-819C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466632 | ||||||
chr14:99466646
|
G | A | 2 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | HG01884.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-8-833C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466646 | ||||||
chr14:99466885
|
G | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(1): Show | 4 | HG02809.hp2 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-8-1072C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99466885 | ||||||
chr14:99467094
|
T | TA | 127 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0157others(124): Show | 128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-8-1282dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467094 | ||||||
chr14:99467210
|
T | C | 3 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140 | 3 | HG01891.hp2 HG02280.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-8-1397A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467210 | ||||||
chr14:99467367
|
T | C | 26 | a0001c0001t0001g0157a0001c0001t0001g0187a0001c0001t0001g0200others(23): Show | 26 | HG00408.hp2 HG00544.hp2 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8-1554A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467367 | ||||||
chr14:99467488
|
C | T | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-8-1675G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467488 | ||||||
chr14:99467489
|
A | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037others(1): Show | 4 | HG02615.hp2 HG02886.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-8-1676T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467489 | ||||||
chr14:99467614
|
G | A | 6 | a0001c0001t0001g0005a0001c0001t0001g0109a0001c0001t0001g0110others(3): Show | 7 | HG01169.hp2 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.-8-1801C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467614 | ||||||
chr14:99467707
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-8-1894G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467707 | ||||||
chr14:99467793
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-8-1980G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467793 | ||||||
chr14:99467796
|
C | T | 1 | a0001c0001t0001g0127 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-8-1983G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467796 | ||||||
chr14:99467824
|
T | C | 127 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0157others(124): Show | 128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-8-2011A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467824 | ||||||
chr14:99467887
|
T | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-8-2074A>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99467887 | ||||||
chr14:99468000
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0146 | 3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-2187C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468000 | ||||||
chr14:99468106
|
G | C | 1 | a0001c0001t0001g0019 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-8-2293C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468106 | ||||||
chr14:99468156
|
T | TA | 119 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0114others(116): Show | 120 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.-8-2344dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468156 | ||||||
chr14:99468582
|
A | G | 26 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(23): Show | 26 | HG00558.hp2 HG00673.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.-8-2769T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468582 | ||||||
chr14:99468642
|
T | TC | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-8-2830dupG | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468642 | ||||||
chr14:99468653
|
C | A | 2 | a0001c0001t0001g0159a0001c0001t0001g0160 | 2 | HG01884.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.-8-2840G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468653 | ||||||
chr14:99468681
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-8-2868A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468681 | ||||||
chr14:99468873
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.-8-3060C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468873 | ||||||
chr14:99468924
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-8-3111T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468924 | ||||||
chr14:99468972
|
A | G | 14 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0129others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-8-3159T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99468972 | ||||||
chr14:99469020
|
C | G | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8-3207G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469020 | ||||||
chr14:99469541
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-8-3728A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469541 | ||||||
chr14:99469565
|
A | G | 277 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(274): Show | 283 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(280): Show |
intron_variant | MODIFIER | c.-8-3752T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469565 | ||||||
chr14:99469668
|
C | T | 2 | a0001c0001t0001g0249a0001c0001t0001g0250 | 2 | HG03654.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.-8-3855G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469668 | ||||||
chr14:99469682
|
G | T | 5 | a0001c0001t0001g0006a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 6 | HG01099.hp2 HG02895.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-8-3869C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469682 | ||||||
chr14:99469889
|
C | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0146 | 3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-8-4076G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469889 | ||||||
chr14:99469898
|
C | G | 1 | a0001c0001t0001g0197 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-8-4085G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469898 | ||||||
chr14:99469921
|
G | A | 121 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0157others(118): Show | 122 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-8-4108C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469921 | ||||||
chr14:99469984
|
G | A | 121 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0157others(118): Show | 122 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(119): Show |
intron_variant | MODIFIER | c.-8-4171C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469984 | ||||||
chr14:99469987
|
C | T | 9 | a0001c0001t0001g0011a0001c0001t0001g0246a0001c0001t0001g0272others(6): Show | 9 | HG00423.hp2 NA18964.hp1 NA18966.hp1 others(6): Show |
intron_variant | MODIFIER | c.-8-4174G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99469987 | ||||||
chr14:99470021
|
A | T | 1 | a0001c0001t0001g0134 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-8-4208T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470021 | ||||||
chr14:99470123
|
G | A | 1 | a0001c0001t0001g0240 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-8-4310C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470123 | ||||||
chr14:99470220
|
G | C | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 284 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(281): Show |
intron_variant | MODIFIER | c.-8-4407C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470220 | ||||||
chr14:99470357
|
C | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.-8-4544G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470357 | ||||||
chr14:99470381
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-8-4568G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470381 | ||||||
chr14:99470610
|
C | G | 28 | a0001c0001t0001g0245a0001c0001t0001g0247a0001c0001t0001g0248others(25): Show | 28 | HG00544.hp1 HG00738.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.-8-4797G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470610 | ||||||
chr14:99470610
|
C | T | 1 | a0001c0001t0001g0246 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-8-4797G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470610 | ||||||
chr14:99470653
|
C | T | 18 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0166others(15): Show | 18 | HG00558.hp2 HG00673.hp2 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.-8-4840G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470653 | ||||||
chr14:99470657
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-8-4844G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99470657 | ||||||
chr14:99471012
|
C | T | 2 | a0001c0007t0002g0144a0002c0006t0002g0143 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-8-5199G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471012 | ||||||
chr14:99471209
|
T | C | 5 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-8-5396A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471209 | ||||||
chr14:99471292
|
C | G | 1 | a0001c0001t0001g0150 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-8-5479G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471292 | ||||||
chr14:99471687
|
T | C | 120 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0157others(117): Show | 121 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.-8-5874A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471687 | ||||||
chr14:99471872
|
C | T | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-8-6059G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471872 | ||||||
chr14:99471875
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-8-6062C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471875 | ||||||
chr14:99471888
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-8-6075A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99471888 | ||||||
chr14:99472003
|
G | A | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-8-6190C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472003 | ||||||
chr14:99472009
|
T | C | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-8-6196A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472009 | ||||||
chr14:99472034
|
T | C | 1 | a0001c0001t0001g0279 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-8-6221A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472034 | ||||||
chr14:99472263
|
G | C | 1 | a0001c0001t0001g0117 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.-8-6450C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472263 | ||||||
chr14:99472280
|
T | C | 1 | a0001c0002t0002g0133 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-8-6467A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472280 | ||||||
chr14:99472466
|
T | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-8-6653A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472466 | ||||||
chr14:99472531
|
T | C | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-8-6718A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472531 | ||||||
chr14:99472674
|
A | G | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-8-6861T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472674 | ||||||
chr14:99472872
|
C | T | 1 | a0001c0001t0001g0164 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.-8-7059G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472872 | ||||||
chr14:99472904
|
T | A | 1 | a0001c0002t0002g0146 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-8-7091A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99472904 | ||||||
chr14:99473050
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.-8-7237G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473050 | ||||||
chr14:99473265
|
A | G | 3 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027 | 3 | HG01243.hp1 HG04115.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-8-7452T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473265 | ||||||
chr14:99473308
|
G | A | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9+7420C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473308 | ||||||
chr14:99473308
|
G | T | 1 | a0001c0001t0001g0246 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.-9+7420C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473308 | ||||||
chr14:99473444
|
A | C | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9+7284T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473444 | ||||||
chr14:99473564
|
T | C | 1 | a0001c0002t0005g0142 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.-9+7164A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473564 | ||||||
chr14:99473579
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0033 | 2 | HG02683.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-9+7149T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473579 | ||||||
chr14:99473684
|
C | G | 4 | a0001c0003t0001g0138a0001c0003t0001g0139a0001c0003t0001g0140others(1): Show | 4 | HG01891.hp2 HG02145.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-9+7044G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473684 | ||||||
chr14:99473991
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-9+6737C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99473991 | ||||||
chr14:99474064
|
C | T | 7 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(4): Show | 7 | HG01081.hp1 HG01243.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.-9+6664G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474064 | ||||||
chr14:99474339
|
A | T | 177 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(174): Show | 182 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.-9+6389T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474339 | ||||||
chr14:99474418
|
G | A | 2 | a0001c0004t0001g0155a0001c0004t0001g0156 | 2 | HG02486.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-9+6310C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474418 | ||||||
chr14:99474549
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.-9+6179A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474549 | ||||||
chr14:99474636
|
G | A | 8 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0122others(5): Show | 8 | NA18951.hp1 NA18961.hp2 NA18964.hp2 others(5): Show |
intron_variant | MODIFIER | c.-9+6092C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474636 | ||||||
chr14:99474825
|
G | C | 1 | a0001c0003t0001g0140 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-9+5903C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474825 | ||||||
chr14:99474851
|
T | A | 275 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(272): Show | 281 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(278): Show |
intron_variant | MODIFIER | c.-9+5877A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474851 | ||||||
chr14:99474875
|
A | AT | 135 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0011others(132): Show | 136 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.-9+5852dupA | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474875 | ||||||
chr14:99474875
|
A | ATT | 7 | a0001c0001t0001g0145a0001c0001t0001g0196a0001c0003t0001g0138others(4): Show | 7 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-9+5851_-9+5852dup others(2): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474875 | ||||||
chr14:99474989
|
G | A | 1 | a0001c0003t0001g0141 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-9+5739C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99474989 | ||||||
chr14:99475417
|
A | C | 9 | a0001c0001t0001g0163a0001c0001t0001g0188a0001c0001t0001g0189others(6): Show | 9 | HG00735.hp2 HG01070.hp1 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+5311T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99475417 | ||||||
chr14:99475659
|
A | G | 1 | a0001c0001t0001g0187 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-9+5069T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99475659 | ||||||
chr14:99475676
|
T | A | 272 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(269): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(275): Show |
intron_variant | MODIFIER | c.-9+5052A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99475676 | ||||||
chr14:99475708
|
G | A | 2 | a0001c0007t0002g0144a0002c0006t0002g0143 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-9+5020C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99475708 | ||||||
chr14:99475818
|
C | G | 1 | a0002c0006t0002g0143 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-9+4910G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99475818 | ||||||
chr14:99475840
|
A | G | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-9+4888T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99475840 | ||||||
chr14:99476109
|
A | G | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-9+4619T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99476109 | ||||||
chr14:99476355
|
G | A | 96 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0157others(93): Show | 97 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(94): Show |
intron_variant | MODIFIER | c.-9+4373C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99476355 | ||||||
chr14:99476393
|
A | T | 1 | a0001c0001t0001g0021 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-9+4335T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99476393 | ||||||
chr14:99476745
|
T | C | 3 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0146 | 3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-9+3983A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99476745 | ||||||
chr14:99476827
|
C | T | 280 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(277): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.-9+3901G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99476827 | ||||||
chr14:99476911
|
C | T | 1 | a0001c0010t0001g0154 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-9+3817G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99476911 | ||||||
chr14:99477051
|
C | T | 1 | a0001c0001t0003g0020 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-9+3677G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477051 | ||||||
chr14:99477123
|
T | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-9+3605A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477123 | ||||||
chr14:99477126
|
T | C | 1 | a0001c0001t0001g0241 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.-9+3602A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477126 | ||||||
chr14:99477358
|
C | CT | 3 | a0001c0002t0002g0280a0001c0002t0002g0281a0001c0002t0002g0282 | 3 | HG02258.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+3369_-9+3370ins others(1): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477358 | ||||||
chr14:99477425
|
T | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.-9+3303A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477425 | ||||||
chr14:99477443
|
A | G | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.-9+3285T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477443 | ||||||
chr14:99477557
|
C | A | 5 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+3171G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477557 | ||||||
chr14:99477723
|
C | T | 2 | a0001c0001t0001g0014a0001c0001t0001g0283 | 2 | HG02080.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.-9+3005G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477723 | ||||||
chr14:99477748
|
C | CA | 267 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(264): Show | 273 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(270): Show |
intron_variant | MODIFIER | c.-9+2979dupT | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477748 | ||||||
chr14:99477748
|
C | CAA | 8 | a0001c0001t0001g0127a0001c0001t0001g0242a0001c0001t0001g0243others(5): Show | 8 | HG02145.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+2978_-9+2979dup others(2): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477748 | ||||||
chr14:99477837
|
TGA | T | 8 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0015others(5): Show | 9 | HG02080.hp1 HG02165.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.-9+2889_-9+2890del others(2): Show |
SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477837 | ||||||
chr14:99477945
|
A | T | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-9+2783T>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99477945 | ||||||
chr14:99478050
|
G | C | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(282): Show |
intron_variant | MODIFIER | c.-9+2678C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99478050 | ||||||
chr14:99478200
|
C | T | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.-9+2528G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99478200 | ||||||
chr14:99478422
|
C | A | 2 | a0001c0007t0002g0144a0002c0006t0002g0143 | 2 | HG02055.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.-9+2306G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99478422 | ||||||
chr14:99478610
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-9+2118C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99478610 | ||||||
chr14:99478904
|
T | C | 1 | a0001c0001t0001g0005 | 2 | HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.-9+1824A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99478904 | ||||||
chr14:99478996
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0001g0162 | 2 | HG02615.hp1 HG02647.hp2 |
intron_variant | MODIFIER | c.-9+1732A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99478996 | ||||||
chr14:99479017
|
G | A | 258 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(255): Show | 264 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(261): Show |
intron_variant | MODIFIER | c.-9+1711C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479017 | ||||||
chr14:99479055
|
T | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-9+1673A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479055 | ||||||
chr14:99479075
|
A | C | 6 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0160others(3): Show | 6 | HG01123.hp1 HG01884.hp1 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.-9+1653T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479075 | ||||||
chr14:99479126
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-9+1602C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479126 | ||||||
chr14:99479355
|
G | A | 3 | a0001c0001t0001g0145a0001c0001t0001g0147a0001c0002t0002g0146 | 3 | HG01884.hp2 HG02647.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-9+1373C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479355 | ||||||
chr14:99479386
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-9+1342C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479386 | ||||||
chr14:99479422
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-9+1306T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479422 | ||||||
chr14:99479507
|
T | A | 8 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.-9+1221A>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479507 | ||||||
chr14:99479569
|
C | A | 1 | a0001c0001t0001g0279 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.-9+1159G>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479569 | ||||||
chr14:99479570
|
T | C | 37 | a0001c0001t0001g0011a0001c0001t0001g0245a0001c0001t0001g0246others(34): Show | 37 | HG00423.hp2 HG00544.hp1 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.-9+1158A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479570 | ||||||
chr14:99479889
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-9+839C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479889 | ||||||
chr14:99479891
|
C | G | 1 | a0001c0001t0001g0128 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-9+837G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479891 | ||||||
chr14:99479892
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-9+836C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99479892 | ||||||
chr14:99480046
|
C | G | 1 | a0001c0001t0001g0157 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.-9+682G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480046 | ||||||
chr14:99480175
|
C | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(128): Show | 136 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.-9+553G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480175 | ||||||
chr14:99480210
|
A | G | 5 | a0001c0002t0002g0129a0001c0002t0002g0130a0001c0002t0002g0131others(2): Show | 5 | HG02451.hp2 HG02809.hp1 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.-9+518T>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480210 | ||||||
chr14:99480240
|
G | T | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(124): Show | 132 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.-9+488C>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480240 | ||||||
chr14:99480300
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-9+428A>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480300 | ||||||
chr14:99480351
|
A | C | 1 | a0001c0001t0001g0012 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-9+377T>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480351 | ||||||
chr14:99480353
|
C | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(273): Show | 282 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.-9+375G>C | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480353 | ||||||
chr14:99480486
|
G | A | 127 | a0001c0001t0001g0006a0001c0001t0001g0011a0001c0001t0001g0157others(124): Show | 128 | HG00099.hp1 HG00280.hp2 HG00408.hp2 others(125): Show |
intron_variant | MODIFIER | c.-9+242C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480486 | ||||||
chr14:99480504
|
G | C | 3 | a0001c0002t0002g0280a0001c0002t0002g0281a0001c0002t0002g0282 | 3 | HG02258.hp2 HG03471.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-9+224C>G | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480504 | ||||||
chr14:99480543
|
G | A | 1 | a0001c0001t0001g0283 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-9+185C>T | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480543 | ||||||
chr14:99480566
|
C | T | 1 | a0001c0001t0001g0011 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-9+162G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480566 | ||||||
chr14:99480632
|
C | T | 1 | a0001c0001t0001g0010 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-9+96G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480632 | ||||||
chr14:99480664
|
C | T | 2 | a0001c0001t0001g0008a0001c0001t0001g0009 | 2 | HG02723.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.-9+64G>A | SETD3 | ENSG00000183576.13 | transcript | ENST00000331768.10 | protein_coding | 1/12 | chr14 | 99480664 |