geneid | 201595 |
---|---|
ensemblid | ENSG00000163527.10 |
hgncid | 30611 |
symbol | STT3B |
name | STT3 oligosaccharyltransferase complex catalytic subunit B |
refseq_nuc | NM_178862.3 |
refseq_prot | NP_849193.1 |
ensembl_nuc | ENST00000295770.4 |
ensembl_prot | ENSP00000295770.2 |
mane_status | MANE Select |
chr | chr3 |
start | 31532925 |
end | 31637616 |
strand | + |
ver | v1.2 |
region | chr3:31532925-31637616 |
region5000 | chr3:31527925-31642616 |
regionname0 | STT3B_chr3_31532925_31637616 |
regionname5000 | STT3B_chr3_31527925_31642616 |
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 | 826 | 339 | 90 | 52 | 163 | 12 | 20 | 136 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0002 | 0/0 | 826 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0003 | 0/0 | 826 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
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 | 2481 | 321 | 76 | 51 | 160 | 12 | 20 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
c0002 | 0/0 | 2481 | 6 | 6 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
c0003 | 0/0 | 2481 | 4 | 4 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
c0004 | 0/0 | 2481 | 3 | 2 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
c0005 | 0/0 | 2481 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
c0006 | 0/0 | 2481 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
c0007 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
c0008 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
c0009 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
c0010 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1627 | 229 | 64 | 42 | 102 | 7 | 13 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
t0002 | 0/0 | 1627 | 52 | 0 | 0 | 49 | 0 | 3 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
t0003 | 1/0 | 1627 | 27 | 15 | 3 | 6 | 0 | 2 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
t0004 | 0/0 | 1627 | 26 | 8 | 6 | 7 | 3 | 2 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
t0005 | 0/0 | 1627 | 4 | 3 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
t0006 | 0/0 | 1627 | 2 | 0 | 0 | 0 | 2 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
t0007 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
t0008 | 0/0 | 1627 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0007 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0168 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0191 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
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 | 2481 | 321 | 76 | 51 | 160 | 12 | 20 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0002 | 0/0 | 2481 | 6 | 6 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0003 | 0/0 | 2481 | 4 | 4 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0004 | 0/0 | 2481 | 3 | 2 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0006 | 0/0 | 2481 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0007 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0009 | 0/0 | 2481 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0010 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0002c0005 | 0/0 | 2481 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0003c0008 | 0/0 | 2481 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4107 | 214 | 52 | 42 | 99 | 7 | 13 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0001t0002 | 0/0 | 4107 | 51 | 0 | 0 | 48 | 0 | 3 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0001t0003 | 1/0 | 4107 | 27 | 15 | 3 | 6 | 0 | 2 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0001t0004 | 0/0 | 4107 | 24 | 8 | 6 | 5 | 3 | 2 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0001t0005 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0001t0006 | 0/0 | 4107 | 2 | 0 | 0 | 0 | 2 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0001t0007 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0001t0008 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0002t0001 | 0/0 | 4107 | 6 | 6 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0003t0001 | 0/0 | 4107 | 4 | 4 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0004t0005 | 0/0 | 4107 | 3 | 2 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0006t0001 | 0/0 | 4107 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0007t0001 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0009t0001 | 0/0 | 4107 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0001c0010t0002 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0002c0005t0004 | 0/0 | 4107 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
a0003c0008t0001 | 0/0 | 4107 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | copy fasta | chr3 | 31527925 | 31642616 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0007 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0168 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0297 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0191 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0003g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0004g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0005g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0006g0115 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0007g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0001t0008g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0002t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0002t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0002t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0002t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0002t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0002t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0003t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0003t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0003t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0004t0005g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0004t0005g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0004t0005g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0006t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0006t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0007t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0009t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0001c0010t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0002c0005t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0002c0005t0004g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
a0003c0008t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0133 | EUR | GBR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0176 | EUR | GBR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | FIN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0183 | EUR | FIN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00423 | hp2 | a0002 | c0005 | t0004 | g0091 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0055 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0041 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00597 | hp2 | a0001 | c0001 | t0007 | g0161 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00621 | hp1 | a0002 | c0005 | t0004 | g0092 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00642 | hp1 | a0001 | c0001 | t0004 | g0180 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0303 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0292 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00735 | hp2 | a0001 | c0001 | t0003 | g0210 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0289 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0256 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01069 | hp1 | a0001 | c0001 | t0004 | g0186 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0308 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01074 | hp1 | a0001 | c0001 | t0004 | g0178 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0266 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0239 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0309 | AMR | PUR | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01261 | hp2 | a0001 | c0001 | t0004 | g0179 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0235 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0236 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0177 | EUR | IBS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0264 | EUR | IBS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01516 | hp2 | a0001 | c0001 | t0006 | g0140 | EUR | IBS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01517 | hp1 | a0001 | c0001 | t0006 | g0115 | EUR | IBS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0011 | EUR | IBS | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0310 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01884 | hp2 | a0001 | c0002 | t0001 | g0216 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0068 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0225 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0234 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01934 | hp1 | a0001 | c0004 | t0005 | g0065 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0174 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0207 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0319 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0185 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02074 | hp2 | a0001 | c0010 | t0002 | g0042 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02080 | hp2 | a0003 | c0008 | t0001 | g0284 | EAS | KHV | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0287 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0093 | EAS | CDX | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | CDX | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0229 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02258 | hp1 | a0001 | c0001 | t0004 | g0194 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0214 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0233 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0145 | AMR | PEL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0015 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02572 | hp1 | a0001 | c0001 | t0004 | g0193 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0007 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0270 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0321 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0318 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02647 | hp1 | a0001 | c0001 | t0003 | g0299 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0297 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0323 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0070 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0290 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0056 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0322 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0196 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0324 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02922 | hp1 | a0001 | c0002 | t0001 | g0217 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02965 | hp1 | a0001 | c0003 | t0001 | g0224 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0311 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0195 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02970 | hp2 | a0001 | c0002 | t0001 | g0221 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03017 | hp1 | a0001 | c0001 | t0003 | g0212 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0119 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03041 | hp2 | a0001 | c0001 | t0004 | g0197 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0192 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0316 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0241 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03139 | hp2 | a0001 | c0004 | t0005 | g0016 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03195 | hp2 | a0001 | c0001 | t0003 | g0188 | AFR | ESN | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03209 | hp1 | a0001 | c0002 | t0001 | g0222 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03209 | hp2 | a0001 | c0009 | t0001 | g0172 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03225 | hp1 | a0001 | c0001 | t0005 | g0219 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0240 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03453 | hp1 | a0001 | c0001 | t0003 | g0189 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0078 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0182 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0314 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0200 | AFR | GWD | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0255 | SAS | STU | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0125 | SAS | STU | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0003 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0206 | SAS | PJL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | BEB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | BEB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG04115 | hp1 | a0001 | c0001 | t0004 | g0184 | SAS | STU | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0162 | SAS | STU | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0173 | SAS | STU | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0143 | SAS | STU | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0312 | AFR | YRI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0226 | AFR | YRI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18612 | hp1 | a0001 | c0001 | t0002 | g0045 | EAS | CHB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | YRI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0030 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18944 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0213 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18964 | hp1 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18978 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18983 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18984 | hp2 | a0001 | c0001 | t0004 | g0094 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0054 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19009 | hp1 | a0001 | c0006 | t0001 | g0089 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19012 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | LWK | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19030 | hp2 | a0001 | c0003 | t0001 | g0326 | AFR | LWK | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0202 | AFR | LWK | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0291 | AFR | LWK | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0050 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0047 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0064 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19068 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19070 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19072 | hp1 | a0001 | c0006 | t0001 | g0116 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19078 | hp2 | a0001 | c0001 | t0008 | g0263 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0052 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19090 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | YRI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0209 | AFR | YRI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0199 | AFR | ASW | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ASW | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | TSI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0088 | EUR | TSI | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0034 | SAS | GIH | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | GIH | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0211 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG01123 | hp2 | a0001 | c0001 | t0004 | g0175 | AMR | CLM | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0317 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02109 | hp2 | a0001 | c0002 | t0001 | g0220 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02486 | hp1 | a0001 | c0002 | t0001 | g0218 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0313 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG02559 | hp2 | a0001 | c0003 | t0001 | g0223 | AFR | ACB | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03471 | hp1 | a0001 | c0007 | t0001 | g0300 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0181 | AFR | MSL | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0203 | AFR | USA | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | USA | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | USA | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | USA | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | LWK | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
NA21309 | hp2 | a0001 | c0004 | t0005 | g0320 | AFR | LWK | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0168 | REF | REF | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0191 | REF | REF | STT3B_chr3_31527925_31642616 | STT3B | chr3 | 31527925 | 31642616 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:31533134
|
G | A | 1 | a0002 | 2 | HG00423.hp2 HG00621.hp1 |
missense_variant | MODERATE | c.136G>A | p.Gly46Ser | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/16 | 210/4107 | 136/2481 | 46/826 | chr3 | 31533134 | ||
chr3:31622111
|
A | G | 1 | a0003 | 1 | HG02080.hp2 | missense_variant | MODERATE | c.1342A>G | p.Ile448Val | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/16 | 1416/4107 | 1342/2481 | 448/826 | chr3 | 31622111 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:31533031
|
C | T | 1 | a0001c0010 | 1 | HG02074.hp2 | synonymous_variant | LOW | c.33C>T | p.His11His | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/16 | 107/4107 | 33/2481 | 11/826 | chr3 | 31533031 | ||
chr3:31533139
|
C | T | 1 | a0001c0009 | 1 | HG03209.hp2 | synonymous_variant | LOW | c.141C>T | p.Gly47Gly | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/16 | 215/4107 | 141/2481 | 47/826 | chr3 | 31533139 | ||
chr3:31533166
|
G | A | 1 | a0001c0006 | 2 | NA19009.hp1 NA19072.hp1 |
synonymous_variant | LOW | c.168G>A | p.Ala56Ala | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/16 | 242/4107 | 168/2481 | 56/826 | chr3 | 31533166 | ||
chr3:31579862
|
A | G | 1 | a0001c0002 | 6 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
synonymous_variant | LOW | c.477A>G | p.Thr159Thr | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/16 | 551/4107 | 477/2481 | 159/826 | chr3 | 31579862 | ||
chr3:31624950
|
C | T | 1 | a0001c0004 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
synonymous_variant | LOW | c.1764C>T | p.Tyr588Tyr | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 12/16 | 1838/4107 | 1764/2481 | 588/826 | chr3 | 31624950 | ||
chr3:31633069
|
A | G | 1 | a0001c0007 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.2322A>G | p.Ala774Ala | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/16 | 2396/4107 | 2322/2481 | 774/826 | chr3 | 31633069 | ||
chr3:31635989
|
C | A | 1 | a0001c0003 | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
synonymous_variant | LOW | c.2406C>A | p.Thr802Thr | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 2480/4107 | 2406/2481 | 802/826 | chr3 | 31635989 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:31636250
|
G | A | 1 | a0001c0001t0006 | 2 | HG01516.hp2 HG01517.hp1 |
3_prime_UTR_variant | MODIFIER | c.*186G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 186 | chr3 | 31636250 | |||||
chr3:31636928
|
A | G | 2 | a0001c0001t0002a0001c0010t0002 | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*864A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 864 | chr3 | 31636928 | |||||
chr3:31636949
|
T | G | 2 | a0001c0001t0005a0001c0004t0005 | 4 | HG01934.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*885T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 885 | chr3 | 31636949 | |||||
chr3:31637020
|
A | G | 2 | a0001c0001t0004a0002c0005t0004 | 26 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*956A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 956 | chr3 | 31637020 | |||||
chr3:31637121
|
G | A | 16 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(13): Show | 315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
3_prime_UTR_variant | MODIFIER | c.*1057G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 1057 | chr3 | 31637121 | |||||
chr3:31637353
|
T | C | 1 | a0001c0001t0007 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1289T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 1289 | chr3 | 31637353 | |||||
chr3:31637563
|
T | G | 1 | a0001c0001t0008 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1499T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 16/16 | 1499 | chr3 | 31637563 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr3:31533337
|
C | T | 1 | a0001c0003t0001g0326 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.314+25C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533337 | ||||||
chr3:31533419
|
C | T | 1 | a0001c0001t0001g0325 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.314+107C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533419 | ||||||
chr3:31533423
|
C | T | 4 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+111C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533423 | ||||||
chr3:31533564
|
A | G | 117 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(114): Show | 122 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(119): Show |
intron_variant | MODIFIER | c.314+252A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533564 | ||||||
chr3:31533652
|
G | C | 1 | a0001c0001t0001g0215 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.314+340G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533652 | ||||||
chr3:31533670
|
A | G | 18 | a0001c0001t0001g0198a0001c0001t0003g0010a0001c0001t0003g0199others(15): Show | 19 | HG00735.hp2 HG01123.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.314+358A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533670 | ||||||
chr3:31533680
|
G | C | 207 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(204): Show | 216 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(213): Show |
intron_variant | MODIFIER | c.314+368G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533680 | ||||||
chr3:31533700
|
G | T | 1 | a0001c0001t0004g0197 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.314+388G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533700 | ||||||
chr3:31533718
|
C | T | 5 | a0001c0001t0004g0192a0001c0001t0004g0193a0001c0001t0004g0194others(2): Show | 5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+406C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533718 | ||||||
chr3:31533779
|
C | T | 1 | a0001c0004t0005g0320 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.314+467C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533779 | ||||||
chr3:31533890
|
T | C | 8 | a0001c0001t0001g0325a0001c0001t0005g0219a0001c0002t0001g0216others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.314+578T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533890 | ||||||
chr3:31533976
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.314+664A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31533976 | ||||||
chr3:31534231
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.314+919G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534231 | ||||||
chr3:31534277
|
T | G | 2 | a0001c0002t0001g0216a0001c0002t0001g0217 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.314+965T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534277 | ||||||
chr3:31534320
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.314+1008C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534320 | ||||||
chr3:31534466
|
C | A | 1 | a0001c0001t0004g0192 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.314+1154C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534466 | ||||||
chr3:31534680
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG00733.hp2 HG02145.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+1368G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534680 | ||||||
chr3:31534885
|
C | G | 3 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319 | 3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.314+1573C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534885 | ||||||
chr3:31534896
|
T | C | 1 | a0001c0006t0001g0089 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.314+1584T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534896 | ||||||
chr3:31534943
|
T | C | 308 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(305): Show | 323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.314+1631T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31534943 | ||||||
chr3:31535001
|
C | A | 1 | a0001c0001t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.314+1689C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535001 | ||||||
chr3:31535105
|
A | C | 1 | a0001c0001t0001g0190 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.314+1793A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535105 | ||||||
chr3:31535125
|
C | CT | 101 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(98): Show | 106 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(103): Show |
intron_variant | MODIFIER | c.314+1814dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31535125 | |||||
chr3:31535335
|
TA | T | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.314+2024delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535335 | ||||||
chr3:31535339
|
T | A | 102 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(99): Show | 107 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(104): Show |
intron_variant | MODIFIER | c.314+2027T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535339 | ||||||
chr3:31535340
|
T | A | 3 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083 | 3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.314+2028T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535340 | ||||||
chr3:31535459
|
C | T | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.314+2147C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535459 | ||||||
chr3:31535463
|
C | A | 1 | a0001c0001t0001g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.314+2151C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535463 | ||||||
chr3:31535551
|
C | T | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.314+2239C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535551 | ||||||
chr3:31535962
|
C | G | 1 | a0001c0002t0001g0222 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.314+2650C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31535962 | ||||||
chr3:31536035
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+2723A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536035 | ||||||
chr3:31536051
|
C | CA | 5 | a0001c0001t0004g0004a0001c0001t0004g0093a0001c0001t0004g0094others(2): Show | 6 | HG00423.hp2 HG00621.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+2747dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31536051 | |||||
chr3:31536052
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.314+2740A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536052 | ||||||
chr3:31536054
|
A | C | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.314+2742A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536054 | ||||||
chr3:31536081
|
T | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 96 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.314+2769T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536081 | ||||||
chr3:31536163
|
A | C | 1 | a0001c0001t0001g0171 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.314+2851A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536163 | ||||||
chr3:31536448
|
A | G | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG01069.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.314+3136A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536448 | ||||||
chr3:31536531
|
A | G | 5 | a0001c0001t0004g0192a0001c0001t0004g0193a0001c0001t0004g0194others(2): Show | 5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+3219A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536531 | ||||||
chr3:31536681
|
A | G | 20 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(17): Show | 20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.314+3369A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31536681 | ||||||
chr3:31537096
|
C | T | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.314+3784C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31537096 | ||||||
chr3:31537100
|
C | T | 192 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.314+3788C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31537100 | ||||||
chr3:31537449
|
G | GTTACTGA | 29 | a0001c0001t0001g0095a0001c0001t0003g0188a0001c0001t0003g0189others(26): Show | 30 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.314+4140_314+4146d others(9): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31537449 | |||||
chr3:31537514
|
G | A | 1 | a0001c0001t0001g0228 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.314+4202G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31537514 | ||||||
chr3:31537586
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.314+4274C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31537586 | ||||||
chr3:31537757
|
C | A | 1 | a0002c0005t0004g0091 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.314+4445C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31537757 | ||||||
chr3:31537770
|
A | G | 1 | a0001c0001t0002g0064 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.314+4458A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31537770 | ||||||
chr3:31538129
|
A | G | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+4817A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538129 | ||||||
chr3:31538129
|
A | T | 3 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319 | 3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.314+4817A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538129 | ||||||
chr3:31538262
|
A | G | 3 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319 | 3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.314+4950A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538262 | ||||||
chr3:31538479
|
A | G | 2 | a0001c0002t0001g0220a0001c0002t0001g0221 | 2 | HG02109.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.314+5167A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538479 | ||||||
chr3:31538488
|
A | AC | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.314+5176_314+5177i others(3): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538488 | ||||||
chr3:31538607
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.314+5295A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538607 | ||||||
chr3:31538639
|
A | G | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+5327A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538639 | ||||||
chr3:31538657
|
C | T | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+5345C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538657 | ||||||
chr3:31538963
|
A | G | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+5651A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31538963 | ||||||
chr3:31539004
|
G | T | 11 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.314+5692G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539004 | ||||||
chr3:31539211
|
T | C | 1 | a0001c0001t0002g0017 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.314+5899T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539211 | ||||||
chr3:31539503
|
C | T | 23 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(20): Show | 23 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(20): Show |
intron_variant | MODIFIER | c.314+6191C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539503 | ||||||
chr3:31539635
|
C | T | 1 | a0001c0001t0001g0168 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.314+6323C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539635 | ||||||
chr3:31539801
|
T | C | 24 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(21): Show | 24 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.314+6489T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539801 | ||||||
chr3:31539881
|
G | A | 90 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 96 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.314+6569G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539881 | ||||||
chr3:31539915
|
A | G | 1 | a0001c0001t0001g0304 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.314+6603A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539915 | ||||||
chr3:31539920
|
C | G | 3 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319 | 3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.314+6608C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31539920 | ||||||
chr3:31540024
|
C | A | 2 | a0001c0001t0001g0308a0001c0001t0001g0309 | 2 | HG01069.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.314+6712C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540024 | ||||||
chr3:31540277
|
A | G | 1 | a0001c0001t0001g0167 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.314+6965A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540277 | ||||||
chr3:31540335
|
C | T | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+7023C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540335 | ||||||
chr3:31540348
|
AG | A | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+7039delG | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31540348 | |||||
chr3:31540392
|
T | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+7080T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540392 | ||||||
chr3:31540457
|
G | A | 18 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(15): Show | 18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.314+7145G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540457 | ||||||
chr3:31540648
|
C | A | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.314+7336C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540648 | ||||||
chr3:31540649
|
G | A | 2 | a0001c0004t0005g0016a0001c0004t0005g0065 | 2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.314+7337G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540649 | ||||||
chr3:31540716
|
A | T | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+7404A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540716 | ||||||
chr3:31540746
|
T | G | 118 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.314+7434T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540746 | ||||||
chr3:31540965
|
C | T | 1 | a0001c0001t0004g0186 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.314+7653C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31540965 | ||||||
chr3:31541034
|
T | A | 1 | a0001c0001t0001g0096 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.314+7722T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541034 | ||||||
chr3:31541063
|
C | G | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.314+7751C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541063 | ||||||
chr3:31541066
|
G | A | 8 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231others(5): Show | 8 | HG01070.hp1 HG01358.hp1 HG01496.hp2 others(5): Show |
intron_variant | MODIFIER | c.314+7754G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541066 | ||||||
chr3:31541213
|
A | C | 24 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(21): Show | 24 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.314+7901A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541213 | ||||||
chr3:31541226
|
T | C | 1 | a0001c0001t0001g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.314+7914T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541226 | ||||||
chr3:31541356
|
T | C | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | NA19007.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.314+8044T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541356 | ||||||
chr3:31541380
|
G | A | 1 | a0001c0001t0003g0199 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.314+8068G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541380 | ||||||
chr3:31541472
|
G | GT | 19 | a0001c0001t0001g0015a0001c0001t0001g0162a0001c0001t0001g0163others(16): Show | 20 | HG00438.hp2 HG00639.hp1 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.314+8175dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31541472 | |||||
chr3:31541478
|
T | G | 1 | a0001c0001t0001g0097 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.314+8166T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541478 | ||||||
chr3:31541528
|
G | A | 3 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072 | 3 | HG01243.hp1 HG02723.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.314+8216G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541528 | ||||||
chr3:31541620
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.314+8308G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541620 | ||||||
chr3:31541871
|
C | G | 1 | a0001c0007t0001g0300 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.314+8559C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541871 | ||||||
chr3:31541911
|
C | T | 1 | a0001c0001t0003g0299 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.314+8599C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541911 | ||||||
chr3:31541932
|
C | G | 3 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319 | 3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.314+8620C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31541932 | ||||||
chr3:31542040
|
C | T | 1 | a0001c0001t0007g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.314+8728C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542040 | ||||||
chr3:31542140
|
G | A | 3 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319 | 3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.314+8828G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542140 | ||||||
chr3:31542168
|
C | T | 1 | a0001c0001t0004g0185 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.314+8856C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542168 | ||||||
chr3:31542344
|
C | G | 1 | a0001c0001t0001g0227 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.314+9032C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542344 | ||||||
chr3:31542402
|
G | A | 6 | a0001c0001t0003g0237a0001c0001t0003g0238a0001c0001t0003g0239others(3): Show | 6 | HG01167.hp2 HG02647.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.314+9090G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542402 | ||||||
chr3:31542598
|
T | G | 1 | a0001c0001t0003g0299 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.314+9286T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542598 | ||||||
chr3:31542761
|
T | C | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.314+9449T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542761 | ||||||
chr3:31542775
|
A | G | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+9463A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542775 | ||||||
chr3:31542791
|
C | G | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.314+9479C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542791 | ||||||
chr3:31542856
|
C | G | 1 | a0001c0001t0003g0214 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.314+9544C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542856 | ||||||
chr3:31542946
|
A | T | 118 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.314+9634A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542946 | ||||||
chr3:31542958
|
C | G | 2 | a0001c0001t0002g0060a0001c0001t0002g0061 | 2 | NA18993.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.314+9646C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542958 | ||||||
chr3:31542959
|
G | C | 1 | a0001c0001t0001g0242 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.314+9647G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542959 | ||||||
chr3:31542964
|
G | A | 2 | a0001c0004t0005g0016a0001c0004t0005g0320 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+9652G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31542964 | ||||||
chr3:31543061
|
A | G | 25 | a0001c0001t0004g0004a0001c0001t0004g0093a0001c0001t0004g0094others(22): Show | 26 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.314+9749A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31543061 | ||||||
chr3:31543067
|
C | CA | 68 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(65): Show | 72 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.314+9772dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31543067 | |||||
chr3:31543067
|
C | CAAAA | 82 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(79): Show | 88 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.314+9769_314+9772d others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31543067 | |||||
chr3:31543067
|
C | CAAAAA | 70 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0066others(67): Show | 73 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(70): Show |
intron_variant | MODIFIER | c.314+9768_314+9772d others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31543067 | |||||
chr3:31543067
|
C | CAAAAAA | 33 | a0001c0001t0001g0067a0001c0001t0001g0070a0001c0001t0001g0072others(30): Show | 34 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.314+9767_314+9772d others(8): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31543067 | |||||
chr3:31543067
|
C | CAAAAAAA | 6 | a0001c0001t0001g0071a0001c0001t0004g0192a0001c0001t0004g0193others(3): Show | 6 | HG01243.hp1 HG02258.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+9766_314+9772d others(9): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31543067 | |||||
chr3:31543328
|
A | G | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.314+10016A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31543328 | ||||||
chr3:31543449
|
A | G | 1 | a0001c0001t0001g0105 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.314+10137A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31543449 | ||||||
chr3:31543468
|
G | C | 1 | a0001c0001t0001g0106 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.314+10156G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31543468 | ||||||
chr3:31543803
|
G | T | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.314+10491G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31543803 | ||||||
chr3:31544038
|
T | C | 1 | a0002c0005t0004g0091 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.314+10726T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31544038 | ||||||
chr3:31544154
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+10842A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31544154 | ||||||
chr3:31544544
|
G | A | 5 | a0001c0001t0001g0285a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+11232G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31544544 | ||||||
chr3:31544711
|
C | G | 5 | a0001c0001t0001g0280a0001c0001t0001g0281a0001c0001t0001g0282others(2): Show | 5 | HG01975.hp2 HG02080.hp2 HG02148.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+11399C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31544711 | ||||||
chr3:31544737
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+11425C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31544737 | ||||||
chr3:31544944
|
G | A | 1 | a0001c0001t0001g0107 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.314+11632G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31544944 | ||||||
chr3:31545076
|
G | A | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.314+11764G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545076 | ||||||
chr3:31545171
|
G | T | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.314+11859G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545171 | ||||||
chr3:31545396
|
G | A | 189 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(186): Show | 199 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(196): Show |
intron_variant | MODIFIER | c.314+12084G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545396 | ||||||
chr3:31545631
|
TTAGTTTC others(17): Show |
T | 118 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.314+12320_314+1234 others(28): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545631 | ||||||
chr3:31545676
|
T | G | 4 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+12364T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545676 | ||||||
chr3:31545759
|
G | A | 1 | a0001c0001t0001g0057 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.314+12447G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545759 | ||||||
chr3:31545814
|
G | GT | 12 | a0001c0001t0001g0069a0001c0001t0001g0155a0001c0001t0001g0156others(9): Show | 12 | HG00438.hp2 HG02027.hp1 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.314+12520dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31545814 | |||||
chr3:31545814
|
G | T | 13 | a0001c0001t0001g0066a0001c0001t0001g0075a0001c0001t0001g0076others(10): Show | 13 | HG01192.hp2 HG01255.hp2 HG02615.hp2 others(10): Show |
intron_variant | MODIFIER | c.314+12502G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545814 | ||||||
chr3:31545814
|
GT | G | 160 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(157): Show | 168 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(165): Show |
intron_variant | MODIFIER | c.314+12520delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31545814 | |||||
chr3:31545814
|
GTT | G | 11 | a0001c0001t0001g0015a0001c0001t0001g0280a0001c0001t0001g0310others(8): Show | 12 | HG00639.hp1 HG01884.hp1 HG01975.hp2 others(9): Show |
intron_variant | MODIFIER | c.314+12519_314+1252 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31545814 | |||||
chr3:31545848
|
C | G | 1 | a0001c0002t0001g0217 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.314+12536C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545848 | ||||||
chr3:31545919
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0315a0001c0001t0001g0316 | 4 | HG00639.hp1 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.314+12607A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31545919 | ||||||
chr3:31546000
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.314+12688C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546000 | ||||||
chr3:31546274
|
G | C | 1 | a0001c0001t0001g0243 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.314+12962G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546274 | ||||||
chr3:31546293
|
TGTA | T | 75 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(72): Show | 79 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.314+12984_314+1298 others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31546293 | |||||
chr3:31546419
|
A | G | 1 | a0001c0001t0004g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.314+13107A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546419 | ||||||
chr3:31546444
|
A | T | 1 | a0001c0001t0001g0090 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.314+13132A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546444 | ||||||
chr3:31546479
|
G | C | 1 | a0001c0001t0002g0026 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.314+13167G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546479 | ||||||
chr3:31546799
|
T | C | 2 | a0001c0004t0005g0016a0001c0004t0005g0320 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+13487T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546799 | ||||||
chr3:31546828
|
T | A | 1 | a0001c0001t0001g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.314+13516T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546828 | ||||||
chr3:31546845
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.314+13533G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546845 | ||||||
chr3:31546916
|
C | G | 1 | a0001c0001t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.314+13604C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546916 | ||||||
chr3:31546925
|
G | A | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.314+13613G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546925 | ||||||
chr3:31546988
|
G | T | 1 | a0001c0001t0001g0154 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.314+13676G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31546988 | ||||||
chr3:31547059
|
T | G | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+13747T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547059 | ||||||
chr3:31547199
|
C | T | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.314+13887C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547199 | ||||||
chr3:31547385
|
C | T | 1 | a0001c0001t0001g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.314+14073C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547385 | ||||||
chr3:31547460
|
T | A | 8 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0298others(5): Show | 8 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.314+14148T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547460 | ||||||
chr3:31547503
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.314+14191G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547503 | ||||||
chr3:31547520
|
C | T | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.314+14208C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547520 | ||||||
chr3:31547790
|
T | A | 10 | a0001c0001t0004g0173a0001c0001t0004g0174a0001c0001t0004g0175others(7): Show | 10 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.314+14478T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547790 | ||||||
chr3:31547853
|
T | C | 1 | a0001c0001t0001g0108 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.314+14541T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31547853 | ||||||
chr3:31548105
|
A | G | 1 | a0001c0001t0001g0074 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.314+14793A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548105 | ||||||
chr3:31548176
|
G | A | 5 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(2): Show | 5 | HG03225.hp1 NA18951.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.314+14864G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548176 | ||||||
chr3:31548209
|
A | G | 1 | a0001c0001t0001g0278 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.314+14897A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548209 | ||||||
chr3:31548335
|
GA | G | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.314+15031delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31548335 | |||||
chr3:31548573
|
T | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.314+15261T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548573 | ||||||
chr3:31548730
|
A | C | 4 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(1): Show | 4 | HG02027.hp2 NA18945.hp1 NA18954.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+15418A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548730 | ||||||
chr3:31548797
|
G | A | 74 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(71): Show | 78 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.314+15485G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548797 | ||||||
chr3:31548878
|
C | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 96 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.314+15566C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548878 | ||||||
chr3:31548934
|
T | C | 1 | a0001c0001t0002g0027 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.314+15622T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31548934 | ||||||
chr3:31549310
|
CT | C | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.314+15999delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549310 | ||||||
chr3:31549412
|
T | G | 1 | a0001c0001t0001g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.314+16100T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549412 | ||||||
chr3:31549530
|
A | G | 1 | a0001c0001t0002g0053 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.314+16218A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549530 | ||||||
chr3:31549586
|
T | C | 1 | a0001c0001t0002g0027 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.314+16274T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549586 | ||||||
chr3:31549741
|
A | G | 13 | a0001c0001t0001g0014a0001c0001t0001g0057a0001c0001t0001g0058others(10): Show | 14 | HG02027.hp2 NA18944.hp1 NA18945.hp1 others(11): Show |
intron_variant | MODIFIER | c.314+16429A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549741 | ||||||
chr3:31549742
|
T | C | 1 | a0001c0001t0001g0098 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.314+16430T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549742 | ||||||
chr3:31549767
|
A | G | 11 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.314+16455A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549767 | ||||||
chr3:31549799
|
G | A | 1 | a0001c0001t0004g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.314+16487G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549799 | ||||||
chr3:31549848
|
A | C | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.314+16536A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549848 | ||||||
chr3:31549894
|
T | C | 2 | a0001c0004t0005g0016a0001c0004t0005g0320 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+16582T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31549894 | ||||||
chr3:31550071
|
ATTAGT | A | 9 | a0001c0001t0002g0021a0001c0001t0002g0028a0001c0001t0002g0029others(6): Show | 9 | NA18942.hp2 NA18944.hp2 NA18993.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+16765_314+1676 others(9): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31550071 | |||||
chr3:31550308
|
A | C | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+16996A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550308 | ||||||
chr3:31550308
|
A | T | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+16996A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550308 | ||||||
chr3:31550513
|
G | A | 1 | a0001c0001t0001g0110 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.314+17201G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550513 | ||||||
chr3:31550656
|
G | A | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+17344G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550656 | ||||||
chr3:31550692
|
T | G | 1 | a0001c0001t0001g0244 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.314+17380T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550692 | ||||||
chr3:31550765
|
T | C | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+17453T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550765 | ||||||
chr3:31550769
|
G | A | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.314+17457G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550769 | ||||||
chr3:31550773
|
G | GT | 4 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.314+17468dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31550773 | |||||
chr3:31550778
|
T | C | 14 | a0001c0001t0001g0014a0001c0001t0001g0228a0001c0001t0001g0242others(11): Show | 15 | HG00558.hp1 HG02027.hp2 NA18945.hp1 others(12): Show |
intron_variant | MODIFIER | c.314+17466T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550778 | ||||||
chr3:31550978
|
G | A | 20 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(17): Show | 20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.314+17666G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31550978 | ||||||
chr3:31551201
|
T | TTTTG | 108 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(105): Show | 114 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(111): Show |
intron_variant | MODIFIER | c.314+17914_314+1791 others(8): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31551201 | |||||
chr3:31551201
|
T | TTTTGTTT others(1): Show |
6 | a0001c0001t0001g0271a0001c0001t0001g0314a0001c0001t0001g0321others(3): Show | 6 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+17910_314+1791 others(12): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31551201 | |||||
chr3:31551226
|
T | G | 1 | a0001c0001t0001g0111 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.314+17914T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551226 | ||||||
chr3:31551255
|
A | G | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.314+17943A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551255 | ||||||
chr3:31551261
|
A | G | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.314+17949A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551261 | ||||||
chr3:31551323
|
C | G | 2 | a0001c0001t0003g0010a0001c0001t0003g0213 | 3 | NA18948.hp2 NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.314+18011C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551323 | ||||||
chr3:31551357
|
A | G | 2 | a0001c0004t0005g0016a0001c0004t0005g0065 | 2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.314+18045A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551357 | ||||||
chr3:31551419
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.314+18107G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551419 | ||||||
chr3:31551692
|
G | C | 1 | a0001c0001t0001g0242 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.314+18380G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551692 | ||||||
chr3:31551781
|
T | C | 1 | a0001c0001t0001g0248 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.314+18469T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551781 | ||||||
chr3:31551840
|
T | C | 1 | a0001c0001t0003g0200 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.314+18528T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551840 | ||||||
chr3:31551882
|
G | GCTTCTAA | 6 | a0001c0002t0001g0216a0001c0002t0001g0217a0001c0002t0001g0218others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+18571_314+1857 others(11): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31551882 | |||||
chr3:31551884
|
A | T | 6 | a0001c0002t0001g0216a0001c0002t0001g0217a0001c0002t0001g0218others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+18572A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551884 | ||||||
chr3:31551886
|
G | C | 6 | a0001c0002t0001g0216a0001c0002t0001g0217a0001c0002t0001g0218others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+18574G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551886 | ||||||
chr3:31551887
|
G | T | 6 | a0001c0002t0001g0216a0001c0002t0001g0217a0001c0002t0001g0218others(3): Show | 6 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.314+18575G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551887 | ||||||
chr3:31551967
|
G | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.314+18655G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31551967 | ||||||
chr3:31551978
|
T | TA | 5 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0032others(2): Show | 7 | NA18950.hp2 NA18962.hp2 NA18973.hp2 others(4): Show |
intron_variant | MODIFIER | c.314+18667dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31551978 | |||||
chr3:31552150
|
G | T | 1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.314+18838G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552150 | ||||||
chr3:31552328
|
G | T | 110 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(107): Show | 116 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.314+19016G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552328 | ||||||
chr3:31552396
|
A | G | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | NA18962.hp1 NA18990.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.314+19084A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552396 | ||||||
chr3:31552494
|
T | C | 9 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(6): Show | 9 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.314+19182T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552494 | ||||||
chr3:31552517
|
CT | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.314+19214delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31552517 | |||||
chr3:31552595
|
A | G | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.314+19283A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552595 | ||||||
chr3:31552617
|
G | A | 1 | a0001c0001t0003g0214 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.314+19305G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552617 | ||||||
chr3:31552712
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.314+19400C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552712 | ||||||
chr3:31552777
|
T | C | 1 | a0001c0001t0001g0288 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.314+19465T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552777 | ||||||
chr3:31552795
|
A | G | 18 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(15): Show | 18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.314+19483A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552795 | ||||||
chr3:31552823
|
G | T | 3 | a0001c0001t0003g0210a0001c0001t0003g0211a0001c0001t0003g0212 | 3 | HG00735.hp2 HG01123.hp1 HG03017.hp1 |
intron_variant | MODIFIER | c.314+19511G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552823 | ||||||
chr3:31552958
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.314+19646C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31552958 | ||||||
chr3:31553097
|
G | A | 2 | a0001c0001t0005g0219a0001c0004t0005g0016 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.314+19785G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553097 | ||||||
chr3:31553101
|
C | CA | 92 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0066others(89): Show | 95 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.314+19807dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31553101 | |||||
chr3:31553101
|
C | CAA | 10 | a0001c0001t0001g0068a0001c0001t0001g0071a0001c0001t0001g0074others(7): Show | 10 | HG01192.hp2 HG01243.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.314+19806_314+1980 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31553101 | |||||
chr3:31553120
|
C | A | 2 | a0001c0001t0001g0198a0001c0001t0001g0322 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.314+19808C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553120 | ||||||
chr3:31553434
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.314+20122T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553434 | ||||||
chr3:31553450
|
G | T | 1 | a0001c0001t0003g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.314+20138G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553450 | ||||||
chr3:31553476
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.314+20164C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553476 | ||||||
chr3:31553570
|
A | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | NA19007.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.314+20258A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553570 | ||||||
chr3:31553608
|
C | T | 5 | a0001c0001t0004g0192a0001c0001t0004g0193a0001c0001t0004g0194others(2): Show | 5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.314+20296C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553608 | ||||||
chr3:31553856
|
T | C | 1 | a0001c0001t0001g0325 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.314+20544T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553856 | ||||||
chr3:31553927
|
ATTTGAGA others(8): Show |
A | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.314+20616_314+2063 others(19): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553927 | ||||||
chr3:31553992
|
A | G | 94 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(91): Show | 99 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(96): Show |
intron_variant | MODIFIER | c.314+20680A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31553992 | ||||||
chr3:31554252
|
T | A | 1 | a0002c0005t0004g0092 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.314+20940T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31554252 | ||||||
chr3:31554529
|
T | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | NA18980.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.314+21217T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31554529 | ||||||
chr3:31554540
|
C | T | 1 | a0001c0001t0001g0160 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.314+21228C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31554540 | ||||||
chr3:31554707
|
T | C | 1 | a0001c0001t0002g0029 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.314+21395T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31554707 | ||||||
chr3:31554714
|
T | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.314+21402T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31554714 | ||||||
chr3:31554884
|
C | A | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-21512C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31554884 | ||||||
chr3:31555119
|
C | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.315-21277C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555119 | ||||||
chr3:31555162
|
T | C | 1 | a0001c0001t0002g0034 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.315-21234T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555162 | ||||||
chr3:31555173
|
T | G | 1 | a0001c0001t0004g0174 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.315-21223T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555173 | ||||||
chr3:31555274
|
T | C | 1 | a0001c0001t0002g0187 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.315-21122T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555274 | ||||||
chr3:31555459
|
A | C | 1 | a0001c0001t0004g0180 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.315-20937A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555459 | ||||||
chr3:31555475
|
G | A | 5 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(2): Show | 6 | HG00733.hp2 HG00741.hp2 HG02145.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-20921G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555475 | ||||||
chr3:31555483
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.315-20913C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555483 | ||||||
chr3:31555680
|
G | T | 1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.315-20716G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555680 | ||||||
chr3:31555716
|
C | T | 184 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(181): Show | 193 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(190): Show |
intron_variant | MODIFIER | c.315-20680C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555716 | ||||||
chr3:31555837
|
T | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0162 | 2 | HG01168.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.315-20559T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555837 | ||||||
chr3:31555848
|
A | G | 1 | a0001c0001t0001g0080 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.315-20548A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555848 | ||||||
chr3:31555942
|
A | G | 25 | a0001c0001t0004g0004a0001c0001t0004g0093a0001c0001t0004g0094others(22): Show | 26 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.315-20454A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555942 | ||||||
chr3:31555982
|
A | T | 1 | a0001c0001t0001g0111 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.315-20414A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31555982 | ||||||
chr3:31556101
|
T | C | 1 | a0001c0001t0002g0035 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.315-20295T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31556101 | ||||||
chr3:31556110
|
C | CT | 6 | a0001c0001t0001g0110a0001c0001t0001g0145a0001c0001t0001g0295others(3): Show | 6 | HG01884.hp2 HG02300.hp2 NA19002.hp1 others(3): Show |
intron_variant | MODIFIER | c.315-20273dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31556110 | |||||
chr3:31556446
|
G | C | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-19950G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31556446 | ||||||
chr3:31556470
|
A | G | 2 | a0001c0002t0001g0216a0001c0002t0001g0217 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.315-19926A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31556470 | ||||||
chr3:31556698
|
T | C | 2 | a0001c0001t0004g0181a0001c0001t0004g0182 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.315-19698T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31556698 | ||||||
chr3:31556705
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.315-19691A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31556705 | ||||||
chr3:31556797
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-19599T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31556797 | ||||||
chr3:31557224
|
G | T | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-19172G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557224 | ||||||
chr3:31557560
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.315-18836G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557560 | ||||||
chr3:31557611
|
G | GTA | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-18777_315-1877 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31557611 | |||||
chr3:31557724
|
C | T | 1 | a0001c0004t0005g0320 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.315-18672C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557724 | ||||||
chr3:31557757
|
C | T | 7 | a0001c0001t0001g0243a0001c0001t0001g0267a0001c0001t0001g0268others(4): Show | 7 | NA18951.hp2 NA18964.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-18639C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557757 | ||||||
chr3:31557781
|
C | T | 1 | a0001c0001t0001g0266 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.315-18615C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557781 | ||||||
chr3:31557784
|
C | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.315-18612C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557784 | ||||||
chr3:31557806
|
A | G | 188 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(185): Show | 197 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(194): Show |
intron_variant | MODIFIER | c.315-18590A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557806 | ||||||
chr3:31557850
|
T | C | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.315-18546T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557850 | ||||||
chr3:31557909
|
C | T | 10 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0075others(7): Show | 10 | HG01192.hp2 HG01255.hp2 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.315-18487C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31557909 | ||||||
chr3:31558029
|
C | T | 1 | a0001c0001t0003g0209 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.315-18367C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31558029 | ||||||
chr3:31558078
|
G | A | 2 | a0001c0004t0005g0016a0001c0004t0005g0065 | 2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.315-18318G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31558078 | ||||||
chr3:31558154
|
A | G | 1 | a0001c0001t0002g0052 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.315-18242A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31558154 | ||||||
chr3:31558287
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.315-18109T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31558287 | ||||||
chr3:31558540
|
C | T | 50 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(47): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.315-17856C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31558540 | ||||||
chr3:31558702
|
T | A | 1 | a0001c0001t0001g0227 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.315-17694T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31558702 | ||||||
chr3:31558863
|
GT | G | 187 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(184): Show | 196 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(193): Show |
intron_variant | MODIFIER | c.315-17519delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31558863 | |||||
chr3:31559021
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.315-17375A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559021 | ||||||
chr3:31559045
|
C | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0265 | 3 | NA18950.hp1 NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.315-17351C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559045 | ||||||
chr3:31559143
|
T | TGG | 10 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0250others(7): Show | 10 | HG01069.hp2 HG01070.hp1 HG01934.hp2 others(7): Show |
intron_variant | MODIFIER | c.315-17250_315-1724 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559143 | |||||
chr3:31559146
|
G | GGT | 7 | a0001c0001t0001g0098a0001c0001t0001g0267a0001c0001t0003g0202others(4): Show | 7 | HG02258.hp2 HG06807.hp1 NA18906.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-17207_315-1720 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | |||||
chr3:31559146
|
GGT | G | 66 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0015others(63): Show | 69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.315-17207_315-1720 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | |||||
chr3:31559146
|
GGTGT | G | 35 | a0001c0001t0001g0009a0001c0001t0001g0088a0001c0001t0001g0104others(32): Show | 36 | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(33): Show |
intron_variant | MODIFIER | c.315-17209_315-1720 others(8): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | |||||
chr3:31559146
|
GGTGTGT | G | 32 | a0001c0001t0001g0007a0001c0001t0001g0076a0001c0001t0001g0078others(29): Show | 33 | HG00735.hp2 HG01069.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.315-17211_315-1720 others(10): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | |||||
chr3:31559146
|
GGTGTGTG others(1): Show |
G | 32 | a0001c0001t0001g0066a0001c0001t0001g0070a0001c0001t0001g0071others(29): Show | 34 | HG00280.hp2 HG00423.hp2 HG00621.hp1 others(31): Show |
intron_variant | MODIFIER | c.315-17213_315-1720 others(12): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | |||||
chr3:31559146
|
GGTGTGTG others(3): Show |
G | 4 | a0001c0001t0001g0067a0001c0001t0001g0073a0001c0001t0001g0084others(1): Show | 4 | HG02257.hp1 HG02615.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-17215_315-1720 others(14): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | |||||
chr3:31559146
|
GGTGTGTG others(5): Show |
G | 5 | a0001c0001t0001g0008a0001c0001t0001g0068a0001c0001t0001g0069others(2): Show | 6 | HG00735.hp1 HG01891.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-17217_315-1720 others(16): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | |||||
chr3:31559146
|
GGTGTGTG others(11): Show |
G | 1 | a0001c0009t0001g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.315-17223_315-1720 others(22): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559146 | |||||
chr3:31559148
|
T | G | 44 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(41): Show | 48 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(45): Show |
intron_variant | MODIFIER | c.315-17248T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559148 | ||||||
chr3:31559150
|
T | G | 4 | a0001c0001t0001g0235a0001c0001t0001g0261a0001c0001t0001g0271others(1): Show | 4 | HG00738.hp1 HG01358.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-17246T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559150 | ||||||
chr3:31559152
|
T | G | 10 | a0001c0001t0001g0009a0001c0001t0001g0107a0001c0001t0001g0151others(7): Show | 11 | HG00639.hp2 HG01070.hp2 HG01928.hp1 others(8): Show |
intron_variant | MODIFIER | c.315-17244T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559152 | ||||||
chr3:31559154
|
T | G | 9 | a0001c0001t0001g0247a0001c0001t0004g0193a0001c0001t0004g0196others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-17242T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559154 | ||||||
chr3:31559179
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0002g0028 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.315-17216_315-1720 others(16): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559179 | ||||||
chr3:31559181
|
GTGTGTGT others(3): Show |
G | 45 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(42): Show | 48 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(45): Show |
intron_variant | MODIFIER | c.315-17214_315-1720 others(14): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559181 | ||||||
chr3:31559183
|
GTGTGTGT others(1): Show |
G | 4 | a0001c0001t0002g0025a0001c0001t0002g0049a0001c0001t0002g0050others(1): Show | 4 | NA19054.hp2 NA19080.hp1 NA19086.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-17212_315-1720 others(12): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559183 | ||||||
chr3:31559191
|
T | G | 1 | a0001c0001t0002g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.315-17205T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559191 | ||||||
chr3:31559349
|
A | ACTTATCT | 218 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(215): Show | 228 | HG00140.hp2 HG00280.hp2 HG00423.hp1 others(225): Show |
intron_variant | MODIFIER | c.315-17043_315-1704 others(11): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31559349 | |||||
chr3:31559443
|
A | G | 2 | a0001c0001t0001g0134a0001c0001t0001g0135 | 2 | HG00673.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.315-16953A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559443 | ||||||
chr3:31559516
|
T | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0190 | 2 | HG02027.hp1 NA18941.hp1 |
intron_variant | MODIFIER | c.315-16880T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559516 | ||||||
chr3:31559609
|
G | T | 111 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(108): Show | 117 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(114): Show |
intron_variant | MODIFIER | c.315-16787G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559609 | ||||||
chr3:31559772
|
G | T | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.315-16624G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31559772 | ||||||
chr3:31560001
|
C | T | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.315-16395C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560001 | ||||||
chr3:31560007
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.315-16389C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560007 | ||||||
chr3:31560086
|
A | G | 1 | a0001c0001t0004g0192 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.315-16310A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560086 | ||||||
chr3:31560121
|
T | C | 11 | a0001c0001t0004g0173a0001c0001t0004g0174a0001c0001t0004g0175others(8): Show | 11 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.315-16275T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560121 | ||||||
chr3:31560331
|
G | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.315-16065G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560331 | ||||||
chr3:31560557
|
A | C | 1 | a0001c0001t0001g0166 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.315-15839A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560557 | ||||||
chr3:31560590
|
G | T | 1 | a0001c0001t0004g0004 | 2 | NA18964.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.315-15806G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560590 | ||||||
chr3:31560618
|
T | A | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(74): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.315-15778T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560618 | ||||||
chr3:31560799
|
C | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-15597C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560799 | ||||||
chr3:31560826
|
T | C | 113 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(110): Show | 119 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(116): Show |
intron_variant | MODIFIER | c.315-15570T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560826 | ||||||
chr3:31560931
|
T | TCATGTTT others(321): Show |
1 | a0001c0001t0003g0213 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.315-15456_315-1545 others(332): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31560931 | |||||
chr3:31560972
|
G | T | 2 | a0001c0001t0002g0047a0001c0001t0002g0048 | 2 | NA18946.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.315-15424G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560972 | ||||||
chr3:31560983
|
A | G | 83 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(80): Show | 88 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.315-15413A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31560983 | ||||||
chr3:31561283
|
A | T | 1 | a0001c0001t0001g0076 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.315-15113A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561283 | ||||||
chr3:31561448
|
T | A | 6 | a0001c0001t0001g0066a0001c0001t0001g0073a0001c0001t0001g0075others(3): Show | 6 | HG01192.hp2 HG01255.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.315-14948T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561448 | ||||||
chr3:31561463
|
G | A | 1 | a0001c0001t0001g0088 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.315-14933G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561463 | ||||||
chr3:31561586
|
T | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-14810T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561586 | ||||||
chr3:31561670
|
G | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-14726G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561670 | ||||||
chr3:31561716
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-14680T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561716 | ||||||
chr3:31561724
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.315-14672G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561724 | ||||||
chr3:31561815
|
T | C | 8 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0136others(5): Show | 8 | HG00544.hp1 NA18965.hp2 NA18982.hp2 others(5): Show |
intron_variant | MODIFIER | c.315-14581T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561815 | ||||||
chr3:31561816
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.315-14580G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561816 | ||||||
chr3:31561855
|
T | C | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-14541T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561855 | ||||||
chr3:31561982
|
G | A | 77 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(74): Show | 81 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.315-14414G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31561982 | ||||||
chr3:31562002
|
C | G | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-14394C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562002 | ||||||
chr3:31562061
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.315-14335C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562061 | ||||||
chr3:31562099
|
A | T | 1 | a0001c0001t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-14297A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562099 | ||||||
chr3:31562224
|
G | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0088 | 2 | HG02145.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.315-14172G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562224 | ||||||
chr3:31562357
|
G | C | 1 | a0001c0001t0004g0093 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.315-14039G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562357 | ||||||
chr3:31562614
|
C | T | 1 | a0001c0001t0001g0142 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.315-13782C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562614 | ||||||
chr3:31562815
|
A | G | 3 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319 | 3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.315-13581A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562815 | ||||||
chr3:31562838
|
G | T | 1 | a0001c0001t0001g0076 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.315-13558G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31562838 | ||||||
chr3:31563156
|
T | C | 1 | a0001c0004t0005g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.315-13240T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31563156 | ||||||
chr3:31563228
|
C | T | 109 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.315-13168C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31563228 | ||||||
chr3:31563368
|
C | G | 1 | a0001c0001t0001g0262 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.315-13028C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31563368 | ||||||
chr3:31563833
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-12563C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31563833 | ||||||
chr3:31563886
|
A | G | 86 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(83): Show | 91 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.315-12510A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31563886 | ||||||
chr3:31564002
|
T | G | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-12394T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564002 | ||||||
chr3:31564053
|
A | G | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG01167.hp1 HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.315-12343A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564053 | ||||||
chr3:31564090
|
A | G | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-12306A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564090 | ||||||
chr3:31564112
|
A | G | 1 | a0001c0001t0003g0201 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.315-12284A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564112 | ||||||
chr3:31564242
|
T | C | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.315-12154T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564242 | ||||||
chr3:31564267
|
G | T | 1 | a0001c0001t0002g0048 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.315-12129G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564267 | ||||||
chr3:31564557
|
G | A | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-11839G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564557 | ||||||
chr3:31564595
|
A | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(191): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.315-11801A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564595 | ||||||
chr3:31564636
|
G | A | 7 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.315-11760G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564636 | ||||||
chr3:31564702
|
G | A | 1 | a0001c0001t0001g0292 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.315-11694G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564702 | ||||||
chr3:31564984
|
T | C | 1 | a0001c0001t0004g0179 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.315-11412T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31564984 | ||||||
chr3:31565073
|
T | C | 1 | a0001c0001t0001g0262 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.315-11323T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565073 | ||||||
chr3:31565269
|
A | C | 1 | a0001c0001t0001g0322 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.315-11127A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565269 | ||||||
chr3:31565288
|
C | G | 284 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(281): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.315-11108C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565288 | ||||||
chr3:31565431
|
T | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.315-10965T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565431 | ||||||
chr3:31565651
|
C | T | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-10745C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565651 | ||||||
chr3:31565846
|
C | A | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-10550C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565846 | ||||||
chr3:31565864
|
T | G | 1 | a0001c0001t0001g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.315-10532T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565864 | ||||||
chr3:31565926
|
A | T | 2 | a0001c0004t0005g0016a0001c0004t0005g0320 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.315-10470A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31565926 | ||||||
chr3:31566295
|
C | T | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.315-10101C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31566295 | ||||||
chr3:31566420
|
G | T | 1 | a0001c0001t0003g0010 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.315-9976G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31566420 | ||||||
chr3:31566451
|
G | A | 1 | a0001c0001t0001g0289 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.315-9945G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31566451 | ||||||
chr3:31566580
|
C | T | 2 | a0001c0001t0006g0115a0001c0001t0006g0140 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.315-9816C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31566580 | ||||||
chr3:31566684
|
A | T | 1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.315-9712A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31566684 | ||||||
chr3:31566761
|
C | T | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-9635C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31566761 | ||||||
chr3:31567491
|
T | C | 4 | a0001c0001t0001g0243a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | NA18964.hp2 NA18965.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-8905T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567491 | ||||||
chr3:31567527
|
C | T | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-8869C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567527 | ||||||
chr3:31567544
|
C | A | 1 | a0001c0001t0003g0237 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.315-8852C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567544 | ||||||
chr3:31567582
|
G | A | 1 | a0001c0001t0002g0048 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.315-8814G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567582 | ||||||
chr3:31567694
|
A | G | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.315-8702A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567694 | ||||||
chr3:31567725
|
A | G | 50 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(47): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.315-8671A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567725 | ||||||
chr3:31567781
|
G | T | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149 | 3 | NA18962.hp1 NA18990.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.315-8615G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567781 | ||||||
chr3:31567825
|
G | A | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-8571G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31567825 | ||||||
chr3:31568029
|
AATCATCA others(20): Show |
A | 1 | a0001c0001t0001g0123 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.315-8365_315-8339d others(29): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31568029 | |||||
chr3:31568112
|
G | T | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-8284G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568112 | ||||||
chr3:31568158
|
G | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | HG01358.hp2 HG01496.hp1 |
intron_variant | MODIFIER | c.315-8238G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568158 | ||||||
chr3:31568792
|
G | T | 1 | a0001c0001t0001g0277 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.315-7604G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568792 | ||||||
chr3:31568837
|
C | G | 1 | a0001c0001t0001g0313 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.315-7559C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568837 | ||||||
chr3:31568868
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.315-7528A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568868 | ||||||
chr3:31568946
|
G | A | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.315-7450G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568946 | ||||||
chr3:31568974
|
A | G | 4 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0001g0145others(1): Show | 4 | HG01358.hp2 HG01496.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.315-7422A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31568974 | ||||||
chr3:31569073
|
G | A | 4 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-7323G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569073 | ||||||
chr3:31569287
|
A | G | 302 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.315-7109A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569287 | ||||||
chr3:31569425
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.315-6971C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569425 | ||||||
chr3:31569432
|
C | A | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-6964C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569432 | ||||||
chr3:31569491
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.315-6905G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569491 | ||||||
chr3:31569550
|
C | A | 1 | a0001c0001t0003g0010 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.315-6846C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569550 | ||||||
chr3:31569609
|
A | G | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.315-6787A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569609 | ||||||
chr3:31569800
|
T | A | 1 | a0001c0001t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-6596T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569800 | ||||||
chr3:31569826
|
G | A | 1 | a0001c0001t0001g0311 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.315-6570G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569826 | ||||||
chr3:31569876
|
A | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | NA19007.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.315-6520A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569876 | ||||||
chr3:31569931
|
T | C | 1 | a0002c0005t0004g0092 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.315-6465T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31569931 | ||||||
chr3:31570126
|
G | A | 20 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(17): Show | 20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.315-6270G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570126 | ||||||
chr3:31570286
|
A | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(191): Show | 204 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(201): Show |
intron_variant | MODIFIER | c.315-6110A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570286 | ||||||
chr3:31570468
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.315-5928C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570468 | ||||||
chr3:31570524
|
G | A | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.315-5872G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570524 | ||||||
chr3:31570687
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.315-5709T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570687 | ||||||
chr3:31570743
|
T | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.315-5653T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570743 | ||||||
chr3:31570846
|
T | C | 9 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(6): Show | 9 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.315-5550T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31570846 | ||||||
chr3:31571029
|
A | G | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-5367A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571029 | ||||||
chr3:31571283
|
A | AT | 190 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(187): Show | 200 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(197): Show |
intron_variant | MODIFIER | c.315-5099dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31571283 | |||||
chr3:31571283
|
A | ATT | 95 | a0001c0001t0001g0015a0001c0001t0001g0057a0001c0001t0001g0058others(92): Show | 100 | HG00140.hp2 HG00423.hp2 HG00438.hp1 others(97): Show |
intron_variant | MODIFIER | c.315-5100_315-5099d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31571283 | |||||
chr3:31571362
|
A | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.315-5034A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571362 | ||||||
chr3:31571384
|
G | A | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.315-5012G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571384 | ||||||
chr3:31571610
|
A | T | 1 | a0001c0001t0004g0193 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.315-4786A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571610 | ||||||
chr3:31571647
|
A | G | 7 | a0001c0001t0001g0286a0001c0001t0001g0298a0001c0001t0001g0321others(4): Show | 7 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.315-4749A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571647 | ||||||
chr3:31571800
|
G | T | 50 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(47): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.315-4596G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571800 | ||||||
chr3:31571934
|
T | TATTA | 118 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.315-4461_315-4458d others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31571934 | |||||
chr3:31571980
|
T | C | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.315-4416T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31571980 | ||||||
chr3:31572015
|
C | CATATTAA others(18): Show |
75 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(72): Show | 79 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.315-4368_315-4344d others(27): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572015 | |||||
chr3:31572015
|
C | CATATTAA others(43): Show |
9 | a0001c0001t0001g0015a0001c0001t0001g0244a0001c0001t0001g0310others(6): Show | 10 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.315-4344_315-4343i others(52): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572015 | |||||
chr3:31572015
|
CATATTAA others(3): Show |
C | 2 | a0001c0001t0003g0207a0001c0001t0003g0208 | 2 | HG02040.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.315-4368_315-4359d others(12): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572015 | |||||
chr3:31572015
|
CATATTAA others(18): Show |
C | 88 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 94 | HG00140.hp1 HG00438.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.315-4368_315-4344d others(27): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572015 | |||||
chr3:31572023
|
TATATATT others(8): Show |
T | 1 | a0001c0004t0005g0320 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.315-4358_315-4344d others(17): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572023 | |||||
chr3:31572026
|
ATATTAAT others(26): Show |
A | 3 | a0001c0001t0001g0102a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | NA18975.hp2 NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.315-4367_315-4335d others(35): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572026 | |||||
chr3:31572035
|
T | TG | 4 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-4361_315-4360i others(3): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572035 | ||||||
chr3:31572037
|
T | TATATTAA others(79): Show |
4 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-4359_315-4358i others(88): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572037 | ||||||
chr3:31572038
|
G | A | 4 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-4358G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572038 | ||||||
chr3:31572038
|
G | GATATATT others(50): Show |
1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.315-4344_315-4343i others(59): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572038 | |||||
chr3:31572038
|
G | GATATATT others(82): Show |
4 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0298others(1): Show | 4 | HG02622.hp2 HG02976.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-4344_315-4343i others(91): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572038 | |||||
chr3:31572056
|
A | ATATTAAT others(24): Show |
8 | a0001c0001t0001g0325a0001c0001t0005g0219a0001c0002t0001g0216others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.315-4333_315-4303d others(33): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr3 | 31572056 | |||||
chr3:31572061
|
A | C | 3 | a0001c0001t0001g0102a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | NA18975.hp2 NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.315-4335A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572061 | ||||||
chr3:31572066
|
A | G | 1 | a0001c0001t0007g0161 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.315-4330A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572066 | ||||||
chr3:31572094
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.315-4302G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572094 | ||||||
chr3:31572094
|
G | T | 8 | a0001c0001t0001g0325a0001c0001t0005g0219a0001c0002t0001g0216others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.315-4302G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572094 | ||||||
chr3:31572231
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.315-4165A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572231 | ||||||
chr3:31572476
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.315-3920C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572476 | ||||||
chr3:31572662
|
G | C | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.315-3734G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572662 | ||||||
chr3:31572779
|
T | G | 1 | a0001c0001t0001g0303 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.315-3617T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572779 | ||||||
chr3:31572820
|
G | A | 8 | a0001c0001t0001g0325a0001c0001t0005g0219a0001c0002t0001g0216others(5): Show | 8 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.315-3576G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572820 | ||||||
chr3:31572843
|
G | A | 4 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0295others(1): Show | 4 | HG02015.hp2 NA18968.hp1 NA18973.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-3553G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31572843 | ||||||
chr3:31573048
|
A | T | 1 | a0001c0001t0002g0059 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.315-3348A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573048 | ||||||
chr3:31573099
|
G | A | 117 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.315-3297G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573099 | ||||||
chr3:31573400
|
A | G | 1 | a0001c0001t0003g0010 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.315-2996A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573400 | ||||||
chr3:31573442
|
G | A | 1 | a0001c0001t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.315-2954G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573442 | ||||||
chr3:31573532
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.315-2864A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573532 | ||||||
chr3:31573572
|
T | C | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.315-2824T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573572 | ||||||
chr3:31573701
|
A | G | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.315-2695A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573701 | ||||||
chr3:31573855
|
A | G | 1 | a0001c0001t0001g0260 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.315-2541A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573855 | ||||||
chr3:31573915
|
G | A | 13 | a0001c0001t0002g0002a0001c0001t0002g0020a0001c0001t0002g0022others(10): Show | 14 | NA18946.hp1 NA18954.hp2 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.315-2481G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31573915 | ||||||
chr3:31574243
|
T | C | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.315-2153T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31574243 | ||||||
chr3:31574290
|
T | C | 99 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(96): Show | 105 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(102): Show |
intron_variant | MODIFIER | c.315-2106T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31574290 | ||||||
chr3:31574504
|
C | T | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG01167.hp1 HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.315-1892C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31574504 | ||||||
chr3:31574576
|
T | C | 1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.315-1820T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31574576 | ||||||
chr3:31574590
|
A | G | 22 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.315-1806A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31574590 | ||||||
chr3:31575181
|
C | T | 20 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(17): Show | 20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.315-1215C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31575181 | ||||||
chr3:31575376
|
G | A | 1 | a0001c0007t0001g0300 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.315-1020G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31575376 | ||||||
chr3:31575466
|
T | G | 2 | a0001c0002t0001g0216a0001c0002t0001g0217 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.315-930T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31575466 | ||||||
chr3:31575467
|
G | T | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-929G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31575467 | ||||||
chr3:31575468
|
G | GT | 4 | a0001c0001t0001g0286a0001c0001t0001g0298a0001c0001t0001g0321others(1): Show | 4 | HG02615.hp1 HG02622.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.315-928_315-927ins others(1): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31575468 | ||||||
chr3:31575497
|
T | C | 5 | a0001c0001t0001g0290a0001c0001t0001g0291a0001c0001t0001g0292others(2): Show | 5 | HG00733.hp1 HG01168.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.315-899T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31575497 | ||||||
chr3:31576167
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.315-229A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31576167 | ||||||
chr3:31576204
|
G | T | 108 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 113 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.315-192G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31576204 | ||||||
chr3:31576220
|
C | T | 1 | a0001c0001t0001g0097 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.315-176C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31576220 | ||||||
chr3:31576233
|
G | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.315-163G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31576233 | ||||||
chr3:31576273
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.315-123G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31576273 | ||||||
chr3:31576353
|
A | G | 1 | a0001c0001t0002g0054 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.315-43A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 1/15 | chr3 | 31576353 | ||||||
chr3:31577056
|
A | G | 5 | a0001c0001t0004g0004a0001c0001t0004g0093a0001c0001t0004g0094others(2): Show | 6 | HG00423.hp2 HG00621.hp1 HG02165.hp1 others(3): Show |
intron_variant | MODIFIER | c.423+552A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577056 | ||||||
chr3:31577178
|
C | T | 186 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(183): Show | 195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.423+674C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577178 | ||||||
chr3:31577243
|
A | G | 1 | a0001c0009t0001g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.423+739A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577243 | ||||||
chr3:31577317
|
T | G | 22 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.423+813T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577317 | ||||||
chr3:31577492
|
T | C | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.423+988T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577492 | ||||||
chr3:31577643
|
C | A | 6 | a0001c0001t0001g0285a0001c0001t0001g0287a0001c0001t0001g0321others(3): Show | 6 | HG02145.hp1 HG02615.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+1139C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577643 | ||||||
chr3:31577745
|
T | C | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.423+1241T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577745 | ||||||
chr3:31577784
|
T | C | 112 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(109): Show | 118 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(115): Show |
intron_variant | MODIFIER | c.423+1280T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31577784 | ||||||
chr3:31578049
|
G | A | 9 | a0001c0001t0003g0010a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 10 | HG00735.hp2 HG01123.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.423+1545G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31578049 | ||||||
chr3:31578567
|
T | TC | 64 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(61): Show | 67 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(64): Show |
intron_variant | MODIFIER | c.424-1235dupC | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31578567 | |||||
chr3:31578569
|
C | T | 1 | a0001c0001t0001g0168 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.424-1240C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31578569 | ||||||
chr3:31578630
|
G | A | 180 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(177): Show | 189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.424-1179G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31578630 | ||||||
chr3:31578806
|
C | T | 1 | a0001c0001t0002g0063 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.424-1003C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31578806 | ||||||
chr3:31578823
|
G | A | 5 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0147others(2): Show | 5 | NA18962.hp1 NA18972.hp1 NA18978.hp1 others(2): Show |
intron_variant | MODIFIER | c.424-986G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31578823 | ||||||
chr3:31578825
|
AAAT | A | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.424-981_424-979del others(3): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31578825 | |||||
chr3:31578864
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.424-945A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31578864 | ||||||
chr3:31579130
|
C | T | 1 | a0001c0001t0003g0240 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.424-679C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579130 | ||||||
chr3:31579185
|
G | A | 1 | a0001c0001t0003g0010 | 2 | NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.424-624G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579185 | ||||||
chr3:31579193
|
A | C | 1 | a0001c0001t0001g0276 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.424-616A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579193 | ||||||
chr3:31579262
|
C | T | 1 | a0001c0001t0005g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.424-547C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579262 | ||||||
chr3:31579352
|
A | C | 1 | a0001c0001t0001g0119 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.424-457A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579352 | ||||||
chr3:31579477
|
T | TA | 38 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(35): Show | 39 | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(36): Show |
intron_variant | MODIFIER | c.424-305dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | |||||
chr3:31579477
|
T | TAA | 8 | a0001c0001t0001g0069a0001c0001t0001g0076a0001c0001t0001g0283others(5): Show | 8 | HG00621.hp1 HG02165.hp1 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.424-306_424-305dup others(2): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | |||||
chr3:31579477
|
T | TAAA | 22 | a0001c0001t0001g0015a0001c0001t0001g0074a0001c0001t0001g0153others(19): Show | 23 | HG01496.hp2 HG01884.hp2 HG01975.hp1 others(20): Show |
intron_variant | MODIFIER | c.424-307_424-305dup others(3): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | |||||
chr3:31579477
|
T | TAAAA | 66 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(63): Show | 71 | HG00544.hp2 HG00639.hp2 HG00673.hp1 others(68): Show |
intron_variant | MODIFIER | c.424-308_424-305dup others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | |||||
chr3:31579477
|
T | TAAAAA | 15 | a0001c0001t0001g0215a0001c0001t0001g0229a0001c0001t0001g0245others(12): Show | 15 | HG00423.hp1 HG00558.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.424-309_424-305dup others(5): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | |||||
chr3:31579477
|
TA | T | 64 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(61): Show | 69 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(66): Show |
intron_variant | MODIFIER | c.424-305delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | |||||
chr3:31579477
|
TAA | T | 10 | a0001c0001t0001g0087a0001c0001t0001g0096a0001c0001t0001g0131others(7): Show | 10 | HG02738.hp2 NA18959.hp1 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.424-306_424-305del others(2): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | |||||
chr3:31579477
|
TAAAA | T | 44 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(41): Show | 47 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(44): Show |
intron_variant | MODIFIER | c.424-308_424-305del others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | |||||
chr3:31579477
|
TAAAAAAA others(6): Show |
T | 1 | a0001c0002t0001g0218 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.424-317_424-305del others(13): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr3 | 31579477 | |||||
chr3:31579478
|
A | T | 3 | a0001c0001t0001g0121a0001c0004t0005g0016a0001c0004t0005g0320 | 3 | HG00544.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.424-331A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579478 | ||||||
chr3:31579522
|
A | G | 325 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(322): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.424-287A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579522 | ||||||
chr3:31579600
|
T | C | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.424-209T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579600 | ||||||
chr3:31579654
|
T | G | 4 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(1): Show | 4 | NA18951.hp1 NA18951.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.424-155T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579654 | ||||||
chr3:31579694
|
A | G | 1 | a0001c0001t0001g0265 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.424-115A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579694 | ||||||
chr3:31579699
|
GC | G | 9 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(6): Show | 9 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.424-109delC | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579699 | ||||||
chr3:31579736
|
T | TAAA | 302 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.424-73_424-72insAA others(1): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579736 | ||||||
chr3:31579778
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.424-31G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 2/15 | chr3 | 31579778 | ||||||
chr3:31580199
|
G | A | 1 | a0001c0001t0001g0303 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.711+103G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31580199 | ||||||
chr3:31580247
|
A | G | 1 | a0001c0001t0001g0117 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.711+151A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31580247 | ||||||
chr3:31580512
|
T | C | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.711+416T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31580512 | ||||||
chr3:31580652
|
T | C | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+556T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31580652 | ||||||
chr3:31580826
|
G | C | 1 | a0001c0001t0001g0314 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.711+730G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31580826 | ||||||
chr3:31580923
|
T | C | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.711+827T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31580923 | ||||||
chr3:31581185
|
A | G | 1 | a0001c0001t0001g0249 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.711+1089A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581185 | ||||||
chr3:31581263
|
A | G | 1 | a0001c0001t0002g0035 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.711+1167A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581263 | ||||||
chr3:31581367
|
C | A | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | HG01167.hp1 HG01192.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.711+1271C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581367 | ||||||
chr3:31581386
|
A | G | 20 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(17): Show | 20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.711+1290A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581386 | ||||||
chr3:31581655
|
T | C | 1 | a0001c0001t0001g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.711+1559T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581655 | ||||||
chr3:31581874
|
C | G | 1 | a0001c0001t0002g0050 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.711+1778C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581874 | ||||||
chr3:31581897
|
A | T | 1 | a0001c0001t0001g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.711+1801A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581897 | ||||||
chr3:31581909
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.711+1813C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581909 | ||||||
chr3:31581972
|
T | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0315a0001c0001t0001g0316 | 4 | HG00639.hp1 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.711+1876T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31581972 | ||||||
chr3:31582030
|
C | T | 1 | a0001c0001t0008g0263 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.711+1934C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582030 | ||||||
chr3:31582151
|
A | AT | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.711+2062dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31582151 | |||||
chr3:31582300
|
C | CT | 119 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.711+2218dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31582300 | |||||
chr3:31582359
|
G | A | 8 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0176others(5): Show | 8 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.711+2263G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582359 | ||||||
chr3:31582394
|
C | G | 20 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(17): Show | 20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.711+2298C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582394 | ||||||
chr3:31582407
|
G | C | 1 | a0001c0001t0004g0193 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.711+2311G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582407 | ||||||
chr3:31582429
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.711+2333G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582429 | ||||||
chr3:31582544
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.711+2448C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582544 | ||||||
chr3:31582722
|
G | A | 1 | a0001c0001t0002g0055 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.711+2626G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582722 | ||||||
chr3:31582815
|
T | C | 1 | a0001c0001t0001g0142 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.711+2719T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31582815 | ||||||
chr3:31583008
|
G | A | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.711+2912G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583008 | ||||||
chr3:31583090
|
C | T | 4 | a0001c0001t0001g0244a0001c0001t0001g0248a0001c0001t0001g0249others(1): Show | 4 | HG00423.hp1 NA18946.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+2994C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583090 | ||||||
chr3:31583097
|
G | T | 1 | a0001c0001t0001g0110 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.711+3001G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583097 | ||||||
chr3:31583194
|
T | C | 1 | a0001c0001t0003g0241 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.711+3098T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583194 | ||||||
chr3:31583312
|
A | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0100a0001c0001t0001g0265 | 4 | NA18950.hp1 NA18980.hp1 NA18999.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+3216A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583312 | ||||||
chr3:31583380
|
A | G | 4 | a0001c0001t0003g0206a0001c0001t0003g0210a0001c0001t0003g0211others(1): Show | 4 | HG00735.hp2 HG01123.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+3284A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583380 | ||||||
chr3:31583505
|
T | C | 9 | a0001c0001t0003g0010a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 10 | HG00735.hp2 HG01123.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.711+3409T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583505 | ||||||
chr3:31583515
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.711+3419G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583515 | ||||||
chr3:31583779
|
T | G | 11 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.711+3683T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31583779 | ||||||
chr3:31584082
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.711+3986G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584082 | ||||||
chr3:31584135
|
A | G | 1 | a0001c0001t0002g0034 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.711+4039A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584135 | ||||||
chr3:31584307
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.711+4211G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584307 | ||||||
chr3:31584380
|
C | G | 1 | a0001c0001t0002g0050 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.711+4284C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584380 | ||||||
chr3:31584433
|
A | G | 1 | a0001c0001t0003g0206 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.711+4337A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584433 | ||||||
chr3:31584516
|
A | G | 1 | a0001c0001t0001g0324 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.711+4420A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584516 | ||||||
chr3:31584604
|
T | C | 7 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(4): Show | 7 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.711+4508T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584604 | ||||||
chr3:31584650
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.711+4554C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584650 | ||||||
chr3:31584784
|
C | T | 1 | a0001c0001t0002g0019 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.711+4688C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31584784 | ||||||
chr3:31585107
|
A | ATAAGTAC others(10): Show |
1 | a0001c0001t0002g0025 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.711+5012_711+5028d others(19): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31585107 | |||||
chr3:31585108
|
T | G | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.711+5012T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585108 | ||||||
chr3:31585118
|
G | C | 1 | a0001c0001t0001g0013 | 2 | NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.711+5022G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585118 | ||||||
chr3:31585273
|
G | A | 26 | a0001c0001t0004g0004a0001c0001t0004g0093a0001c0001t0004g0094others(23): Show | 27 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.711+5177G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585273 | ||||||
chr3:31585332
|
A | C | 1 | a0001c0001t0001g0114 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.711+5236A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585332 | ||||||
chr3:31585333
|
C | A | 1 | a0001c0001t0001g0114 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.711+5237C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585333 | ||||||
chr3:31585347
|
C | A | 1 | a0001c0001t0001g0166 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.711+5251C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585347 | ||||||
chr3:31585375
|
G | T | 2 | a0001c0001t0001g0113a0001c0001t0001g0130 | 2 | NA18963.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.711+5279G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585375 | ||||||
chr3:31585555
|
GGTTTT | G | 10 | a0001c0001t0001g0312a0001c0001t0001g0313a0001c0001t0001g0325others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.711+5475_711+5479d others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31585555 | |||||
chr3:31585839
|
T | G | 18 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(15): Show | 18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.711+5743T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31585839 | ||||||
chr3:31586097
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.711+6001C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586097 | ||||||
chr3:31586287
|
T | G | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.711+6191T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586287 | ||||||
chr3:31586327
|
G | GAAAT | 302 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.711+6233_711+6236d others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31586327 | |||||
chr3:31586527
|
T | C | 2 | a0001c0004t0005g0016a0001c0004t0005g0320 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.711+6431T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586527 | ||||||
chr3:31586571
|
G | T | 13 | a0001c0001t0002g0002a0001c0001t0002g0020a0001c0001t0002g0022others(10): Show | 14 | NA18946.hp1 NA18954.hp2 NA18959.hp2 others(11): Show |
intron_variant | MODIFIER | c.711+6475G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586571 | ||||||
chr3:31586847
|
T | C | 302 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.711+6751T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586847 | ||||||
chr3:31586870
|
T | G | 3 | a0001c0001t0001g0101a0001c0001t0001g0123a0001c0001t0001g0133 | 3 | HG00140.hp1 HG00280.hp1 HG00642.hp2 |
intron_variant | MODIFIER | c.711+6774T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586870 | ||||||
chr3:31586923
|
T | C | 5 | a0001c0001t0004g0192a0001c0001t0004g0193a0001c0001t0004g0194others(2): Show | 5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.711+6827T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31586923 | ||||||
chr3:31587079
|
A | C | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.711+6983A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587079 | ||||||
chr3:31587230
|
T | G | 1 | a0001c0001t0001g0303 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.711+7134T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587230 | ||||||
chr3:31587235
|
A | G | 1 | a0001c0001t0001g0143 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.711+7139A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587235 | ||||||
chr3:31587255
|
T | A | 1 | a0001c0001t0001g0104 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.711+7159T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587255 | ||||||
chr3:31587267
|
A | AAAAG | 121 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(118): Show | 128 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(125): Show |
intron_variant | MODIFIER | c.711+7172_711+7175d others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31587267 | |||||
chr3:31587303
|
A | T | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.711+7207A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587303 | ||||||
chr3:31587309
|
C | T | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.711+7213C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587309 | ||||||
chr3:31587414
|
T | A | 1 | a0001c0004t0005g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.711+7318T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587414 | ||||||
chr3:31587812
|
T | A | 1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.711+7716T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31587812 | ||||||
chr3:31588042
|
G | A | 1 | a0001c0001t0003g0207 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.711+7946G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588042 | ||||||
chr3:31588046
|
A | T | 5 | a0001c0001t0001g0285a0001c0001t0001g0321a0001c0001t0001g0322others(2): Show | 5 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.711+7950A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588046 | ||||||
chr3:31588096
|
C | T | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.711+8000C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588096 | ||||||
chr3:31588215
|
G | T | 3 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319 | 3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.711+8119G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588215 | ||||||
chr3:31588240
|
G | T | 4 | a0001c0001t0001g0321a0001c0001t0001g0322a0001c0001t0001g0323others(1): Show | 4 | HG02615.hp1 HG02717.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.711+8144G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588240 | ||||||
chr3:31588244
|
G | A | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.711+8148G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588244 | ||||||
chr3:31588244
|
G | T | 1 | a0001c0001t0001g0122 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.711+8148G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588244 | ||||||
chr3:31588265
|
T | G | 1 | a0001c0001t0001g0315 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.711+8169T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588265 | ||||||
chr3:31588457
|
T | G | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.712-8341T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588457 | ||||||
chr3:31588487
|
ATGCAC | A | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-8309_712-8305d others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31588487 | |||||
chr3:31588822
|
G | T | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.712-7976G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588822 | ||||||
chr3:31588923
|
G | GT | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-7874dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31588923 | |||||
chr3:31588978
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0082 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.712-7820A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31588978 | ||||||
chr3:31589094
|
A | G | 1 | a0001c0001t0001g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.712-7704A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589094 | ||||||
chr3:31589112
|
G | C | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.712-7686G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589112 | ||||||
chr3:31589386
|
C | T | 2 | a0001c0004t0005g0016a0001c0004t0005g0065 | 2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.712-7412C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589386 | ||||||
chr3:31589555
|
G | T | 193 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.712-7243G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589555 | ||||||
chr3:31589650
|
A | C | 1 | a0001c0001t0001g0166 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.712-7148A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589650 | ||||||
chr3:31589684
|
T | A | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.712-7114T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589684 | ||||||
chr3:31589861
|
A | G | 7 | a0001c0001t0002g0024a0001c0001t0002g0038a0001c0001t0002g0045others(4): Show | 7 | HG03942.hp1 NA18612.hp1 NA18941.hp2 others(4): Show |
intron_variant | MODIFIER | c.712-6937A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589861 | ||||||
chr3:31589890
|
T | A | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.712-6908T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589890 | ||||||
chr3:31589902
|
A | G | 1 | a0001c0001t0004g0184 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.712-6896A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31589902 | ||||||
chr3:31590134
|
C | A | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.712-6664C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590134 | ||||||
chr3:31590144
|
C | G | 1 | a0001c0001t0001g0267 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.712-6654C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590144 | ||||||
chr3:31590239
|
G | C | 50 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(47): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.712-6559G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590239 | ||||||
chr3:31590253
|
T | C | 1 | a0001c0001t0001g0267 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.712-6545T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590253 | ||||||
chr3:31590299
|
A | G | 1 | a0001c0001t0002g0024 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.712-6499A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590299 | ||||||
chr3:31590315
|
C | T | 8 | a0001c0001t0004g0174a0001c0001t0004g0175a0001c0001t0004g0176others(5): Show | 8 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(5): Show |
intron_variant | MODIFIER | c.712-6483C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590315 | ||||||
chr3:31590643
|
A | G | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-6155A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590643 | ||||||
chr3:31590701
|
G | A | 1 | a0001c0001t0003g0299 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.712-6097G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590701 | ||||||
chr3:31590925
|
T | G | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.712-5873T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31590925 | ||||||
chr3:31591057
|
T | G | 5 | a0001c0001t0004g0192a0001c0001t0004g0193a0001c0001t0004g0194others(2): Show | 5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.712-5741T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591057 | ||||||
chr3:31591170
|
C | T | 1 | a0001c0001t0003g0241 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.712-5628C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591170 | ||||||
chr3:31591444
|
C | T | 1 | a0001c0009t0001g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.712-5354C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591444 | ||||||
chr3:31591509
|
T | A | 1 | a0001c0009t0001g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.712-5289T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591509 | ||||||
chr3:31591520
|
C | A | 2 | a0001c0001t0001g0076a0001c0001t0001g0078 | 2 | HG03453.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.712-5278C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591520 | ||||||
chr3:31591540
|
A | G | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.712-5258A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591540 | ||||||
chr3:31591655
|
C | G | 1 | a0001c0001t0001g0243 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.712-5143C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591655 | ||||||
chr3:31591679
|
G | A | 1 | a0001c0001t0001g0290 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.712-5119G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591679 | ||||||
chr3:31591913
|
G | A | 1 | a0001c0001t0001g0304 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.712-4885G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591913 | ||||||
chr3:31591929
|
G | A | 73 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(70): Show | 77 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.712-4869G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31591929 | ||||||
chr3:31592091
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.712-4707A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592091 | ||||||
chr3:31592137
|
G | A | 25 | a0001c0001t0004g0004a0001c0001t0004g0093a0001c0001t0004g0094others(22): Show | 26 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.712-4661G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592137 | ||||||
chr3:31592173
|
A | G | 1 | a0001c0004t0005g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.712-4625A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592173 | ||||||
chr3:31592320
|
G | A | 1 | a0001c0004t0005g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.712-4478G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592320 | ||||||
chr3:31592416
|
CA | C | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.712-4380delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31592416 | |||||
chr3:31592428
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.712-4370T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592428 | ||||||
chr3:31592524
|
A | G | 2 | a0001c0001t0001g0169a0001c0001t0001g0170 | 2 | NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.712-4274A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592524 | ||||||
chr3:31592629
|
T | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.712-4169T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592629 | ||||||
chr3:31592630
|
A | G | 9 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0287others(6): Show | 9 | HG02145.hp1 HG02615.hp1 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.712-4168A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592630 | ||||||
chr3:31592771
|
C | G | 1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.712-4027C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592771 | ||||||
chr3:31592772
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.712-4026G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592772 | ||||||
chr3:31592967
|
C | T | 9 | a0001c0001t0001g0015a0001c0001t0001g0287a0001c0001t0001g0310others(6): Show | 10 | HG00639.hp1 HG01884.hp1 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.712-3831C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592967 | ||||||
chr3:31592987
|
G | A | 9 | a0001c0001t0003g0010a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 10 | HG00735.hp2 HG01123.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.712-3811G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592987 | ||||||
chr3:31592996
|
G | A | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.712-3802G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592996 | ||||||
chr3:31592998
|
G | T | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.712-3800G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31592998 | ||||||
chr3:31593045
|
G | A | 90 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 96 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.712-3753G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593045 | ||||||
chr3:31593266
|
TGTGA | T | 8 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0201others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.712-3529_712-3526d others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31593266 | |||||
chr3:31593384
|
C | T | 1 | a0001c0001t0001g0068 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.712-3414C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593384 | ||||||
chr3:31593730
|
A | G | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.712-3068A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593730 | ||||||
chr3:31593751
|
T | TA | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-3047_712-3046i others(3): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593751 | ||||||
chr3:31593752
|
C | T | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-3046C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593752 | ||||||
chr3:31593905
|
T | C | 2 | a0001c0002t0001g0216a0001c0002t0001g0217 | 2 | HG01884.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.712-2893T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593905 | ||||||
chr3:31593953
|
A | G | 1 | a0001c0007t0001g0300 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.712-2845A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593953 | ||||||
chr3:31593976
|
T | C | 8 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0298others(5): Show | 8 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.712-2822T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31593976 | ||||||
chr3:31594018
|
T | C | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-2780T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594018 | ||||||
chr3:31594040
|
T | G | 2 | a0001c0001t0001g0013a0001c0001t0001g0265 | 3 | NA18950.hp1 NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.712-2758T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594040 | ||||||
chr3:31594059
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.712-2739C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594059 | ||||||
chr3:31594084
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.712-2714A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594084 | ||||||
chr3:31594135
|
A | C | 22 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.712-2663A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594135 | ||||||
chr3:31594206
|
T | C | 1 | a0001c0004t0005g0320 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.712-2592T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594206 | ||||||
chr3:31594436
|
G | GT | 7 | a0001c0001t0001g0085a0001c0001t0001g0152a0001c0001t0001g0294others(4): Show | 7 | HG01993.hp2 HG02071.hp1 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.712-2349dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31594436 | |||||
chr3:31594436
|
G | GTTT | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.712-2351_712-2349d others(5): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | INFO_REALIGN_3_PRIME | chr3 | 31594436 | |||||
chr3:31594534
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.712-2264A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594534 | ||||||
chr3:31594618
|
C | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.712-2180C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594618 | ||||||
chr3:31594656
|
G | A | 1 | a0001c0001t0003g0202 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.712-2142G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594656 | ||||||
chr3:31594722
|
C | A | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.712-2076C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594722 | ||||||
chr3:31594811
|
C | G | 1 | a0001c0001t0001g0095 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.712-1987C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594811 | ||||||
chr3:31594854
|
C | T | 1 | a0001c0001t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.712-1944C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31594854 | ||||||
chr3:31595019
|
T | G | 2 | a0001c0004t0005g0016a0001c0004t0005g0065 | 2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.712-1779T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595019 | ||||||
chr3:31595155
|
G | T | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.712-1643G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595155 | ||||||
chr3:31595315
|
A | G | 1 | a0001c0001t0005g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.712-1483A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595315 | ||||||
chr3:31595354
|
A | G | 76 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(73): Show | 80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.712-1444A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595354 | ||||||
chr3:31595401
|
G | A | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.712-1397G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595401 | ||||||
chr3:31595408
|
G | T | 310 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(307): Show | 326 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(323): Show |
intron_variant | MODIFIER | c.712-1390G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595408 | ||||||
chr3:31595433
|
G | T | 1 | a0001c0001t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.712-1365G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595433 | ||||||
chr3:31595501
|
T | G | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.712-1297T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595501 | ||||||
chr3:31595557
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.712-1241A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595557 | ||||||
chr3:31595745
|
A | T | 22 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.712-1053A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595745 | ||||||
chr3:31595769
|
C | T | 15 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319others(12): Show | 15 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.712-1029C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595769 | ||||||
chr3:31595972
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.712-826C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31595972 | ||||||
chr3:31596152
|
G | A | 3 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324 | 3 | HG02717.hp2 HG02809.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.712-646G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31596152 | ||||||
chr3:31596295
|
C | T | 1 | a0001c0001t0002g0027 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.712-503C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31596295 | ||||||
chr3:31596456
|
G | T | 1 | a0001c0001t0001g0138 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.712-342G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31596456 | ||||||
chr3:31596486
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.712-312A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31596486 | ||||||
chr3:31596490
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.712-308T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31596490 | ||||||
chr3:31596771
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.712-27A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 3/15 | chr3 | 31596771 | ||||||
chr3:31596870
|
T | G | 1 | a0001c0001t0001g0264 | 1 | HG01516.hp1 | splice_region_variant&intron_variant | LOW | c.777+7T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31596870 | ||||||
chr3:31596872
|
T | A | 1 | a0001c0001t0001g0311 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.777+9T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31596872 | ||||||
chr3:31596902
|
G | C | 26 | a0001c0001t0004g0004a0001c0001t0004g0093a0001c0001t0004g0094others(23): Show | 27 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.777+39G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31596902 | ||||||
chr3:31597182
|
C | T | 7 | a0001c0001t0001g0325a0001c0002t0001g0216a0001c0002t0001g0217others(4): Show | 7 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.777+319C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597182 | ||||||
chr3:31597305
|
G | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.777+442G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597305 | ||||||
chr3:31597410
|
G | C | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.777+547G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597410 | ||||||
chr3:31597527
|
G | A | 1 | a0001c0001t0004g0174 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.777+664G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597527 | ||||||
chr3:31597635
|
A | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.777+772A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597635 | ||||||
chr3:31597749
|
G | A | 1 | a0001c0001t0001g0162 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.777+886G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597749 | ||||||
chr3:31597840
|
A | AT | 58 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0007others(55): Show | 62 | HG00140.hp1 HG00280.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.777+979dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 31597840 | |||||
chr3:31597840
|
A | ATT | 29 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0085others(26): Show | 31 | HG00438.hp2 HG00544.hp1 HG00597.hp2 others(28): Show |
intron_variant | MODIFIER | c.777+978_777+979dup others(2): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 31597840 | |||||
chr3:31597840
|
A | T | 3 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0004t0005g0065 | 3 | HG01934.hp1 HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.777+977A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597840 | ||||||
chr3:31597843
|
A | T | 146 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(143): Show | 153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.777+980A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597843 | ||||||
chr3:31597846
|
T | A | 2 | a0001c0001t0001g0318a0001c0001t0002g0045 | 2 | HG02630.hp1 NA18612.hp1 |
intron_variant | MODIFIER | c.777+983T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597846 | ||||||
chr3:31597884
|
G | A | 6 | a0001c0001t0002g0002a0001c0001t0002g0020a0001c0001t0002g0022others(3): Show | 7 | NA18954.hp2 NA18959.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.777+1021G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597884 | ||||||
chr3:31597940
|
A | G | 8 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0298others(5): Show | 8 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.777+1077A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31597940 | ||||||
chr3:31598079
|
G | C | 17 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(14): Show | 17 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.777+1216G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31598079 | ||||||
chr3:31598409
|
T | TA | 22 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.777+1548dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 31598409 | |||||
chr3:31598627
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.778-1733A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31598627 | ||||||
chr3:31598713
|
T | C | 22 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.778-1647T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31598713 | ||||||
chr3:31598735
|
A | G | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-1625A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31598735 | ||||||
chr3:31598755
|
T | C | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.778-1605T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31598755 | ||||||
chr3:31598812
|
C | CT | 9 | a0001c0001t0001g0285a0001c0001t0001g0286a0001c0001t0001g0298others(6): Show | 9 | HG02615.hp1 HG02622.hp2 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.778-1534dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr3 | 31598812 | |||||
chr3:31598865
|
A | T | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-1495A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31598865 | ||||||
chr3:31599105
|
A | G | 203 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.778-1255A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31599105 | ||||||
chr3:31599415
|
C | A | 1 | a0001c0001t0001g0258 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.778-945C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31599415 | ||||||
chr3:31599415
|
C | G | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.778-945C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31599415 | ||||||
chr3:31599437
|
T | C | 4 | a0001c0001t0005g0219a0001c0004t0005g0016a0001c0004t0005g0065others(1): Show | 4 | HG01934.hp1 HG03139.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.778-923T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31599437 | ||||||
chr3:31599605
|
G | A | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.778-755G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31599605 | ||||||
chr3:31599719
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.778-641G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31599719 | ||||||
chr3:31600069
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.778-291T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31600069 | ||||||
chr3:31600105
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.778-255A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31600105 | ||||||
chr3:31600140
|
C | T | 1 | a0001c0001t0004g0175 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.778-220C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31600140 | ||||||
chr3:31600201
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.778-159G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31600201 | ||||||
chr3:31600343
|
C | A | 10 | a0001c0001t0004g0173a0001c0001t0004g0174a0001c0001t0004g0175others(7): Show | 10 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.778-17C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 4/15 | chr3 | 31600343 | ||||||
chr3:31600545
|
A | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 124 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(121): Show |
intron_variant | MODIFIER | c.877+86A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31600545 | ||||||
chr3:31600785
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.877+326T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31600785 | ||||||
chr3:31600925
|
C | G | 1 | a0001c0001t0001g0101 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.877+466C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31600925 | ||||||
chr3:31600949
|
A | G | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.877+490A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31600949 | ||||||
chr3:31600978
|
A | T | 1 | a0001c0001t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.877+519A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31600978 | ||||||
chr3:31601216
|
C | T | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(45): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.877+757C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601216 | ||||||
chr3:31601217
|
G | A | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.877+758G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601217 | ||||||
chr3:31601335
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.877+876T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601335 | ||||||
chr3:31601553
|
C | A | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.877+1094C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601553 | ||||||
chr3:31601574
|
T | C | 6 | a0001c0001t0003g0199a0001c0001t0003g0201a0001c0001t0003g0202others(3): Show | 6 | HG02258.hp2 HG02451.hp2 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+1115T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601574 | ||||||
chr3:31601623
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.877+1164G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601623 | ||||||
chr3:31601642
|
G | C | 5 | a0001c0001t0004g0192a0001c0001t0004g0193a0001c0001t0004g0194others(2): Show | 5 | HG02258.hp1 HG02572.hp1 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.877+1183G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601642 | ||||||
chr3:31601784
|
C | G | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.877+1325C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31601784 | ||||||
chr3:31602081
|
G | C | 1 | a0001c0001t0001g0128 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.877+1622G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602081 | ||||||
chr3:31602229
|
G | A | 50 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(47): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.877+1770G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602229 | ||||||
chr3:31602239
|
A | G | 1 | a0001c0001t0003g0299 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.877+1780A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602239 | ||||||
chr3:31602303
|
C | CT | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.877+1855dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31602303 | |||||
chr3:31602320
|
A | T | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.877+1861A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602320 | ||||||
chr3:31602660
|
A | AT | 13 | a0001c0001t0001g0086a0001c0001t0001g0112a0001c0001t0001g0124others(10): Show | 13 | HG01993.hp2 HG02145.hp2 HG02622.hp2 others(10): Show |
intron_variant | MODIFIER | c.877+2223dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31602660 | |||||
chr3:31602660
|
A | T | 7 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0137others(4): Show | 7 | HG00544.hp1 NA18965.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.877+2201A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602660 | ||||||
chr3:31602660
|
AT | A | 97 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(94): Show | 102 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(99): Show |
intron_variant | MODIFIER | c.877+2223delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31602660 | |||||
chr3:31602660
|
ATT | A | 59 | a0001c0001t0001g0015a0001c0001t0001g0255a0001c0001t0001g0281others(56): Show | 60 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(57): Show |
intron_variant | MODIFIER | c.877+2222_877+2223d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31602660 | |||||
chr3:31602660
|
ATTT | A | 68 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(65): Show | 72 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.877+2221_877+2223d others(5): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31602660 | |||||
chr3:31602793
|
T | C | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.877+2334T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602793 | ||||||
chr3:31602824
|
C | G | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.877+2365C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602824 | ||||||
chr3:31602833
|
T | C | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.877+2374T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602833 | ||||||
chr3:31602874
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.877+2415A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602874 | ||||||
chr3:31602885
|
T | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.877+2426T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602885 | ||||||
chr3:31602905
|
G | T | 118 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 125 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(122): Show |
intron_variant | MODIFIER | c.877+2446G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31602905 | ||||||
chr3:31603098
|
T | A | 5 | a0001c0001t0001g0012a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 6 | HG00673.hp1 HG02165.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.877+2639T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603098 | ||||||
chr3:31603122
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.877+2663G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603122 | ||||||
chr3:31603145
|
T | C | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.877+2686T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603145 | ||||||
chr3:31603155
|
AAGTTT | A | 3 | a0001c0001t0001g0139a0001c0001t0001g0145a0001c0001t0001g0154 | 3 | HG01358.hp2 HG02148.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.877+2701_877+2705d others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31603155 | |||||
chr3:31603251
|
A | T | 317 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(314): Show | 333 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(330): Show |
intron_variant | MODIFIER | c.877+2792A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603251 | ||||||
chr3:31603330
|
T | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.877+2871T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603330 | ||||||
chr3:31603427
|
T | G | 2 | a0001c0001t0004g0181a0001c0001t0004g0182 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.877+2968T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603427 | ||||||
chr3:31603568
|
T | TTG | 3 | a0001c0001t0003g0238a0001c0001t0003g0239a0001c0001t0003g0240 | 3 | HG01167.hp2 HG02723.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.877+3111_877+3112d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31603568 | |||||
chr3:31603681
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.877+3222A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603681 | ||||||
chr3:31603723
|
G | GTA | 50 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(47): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.877+3267_877+3268d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31603723 | |||||
chr3:31603769
|
TA | T | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.877+3311delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31603769 | ||||||
chr3:31604056
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.877+3597T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604056 | ||||||
chr3:31604069
|
T | C | 51 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0002g0001others(48): Show | 54 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(51): Show |
intron_variant | MODIFIER | c.877+3610T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604069 | ||||||
chr3:31604108
|
T | A | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.877+3649T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604108 | ||||||
chr3:31604137
|
G | T | 2 | a0001c0001t0001g0251a0001c0001t0001g0258 | 2 | NA18975.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.877+3678G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604137 | ||||||
chr3:31604192
|
A | G | 203 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(200): Show | 213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.877+3733A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604192 | ||||||
chr3:31604227
|
T | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.877+3768T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604227 | ||||||
chr3:31604251
|
C | G | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.877+3792C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604251 | ||||||
chr3:31604283
|
G | A | 28 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0004g0004others(25): Show | 29 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.877+3824G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604283 | ||||||
chr3:31604637
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.877+4178T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31604637 | ||||||
chr3:31605018
|
A | G | 3 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319 | 3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.877+4559A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31605018 | ||||||
chr3:31605031
|
T | G | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.877+4572T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31605031 | ||||||
chr3:31605501
|
GGTGA | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 94 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.877+5045_877+5048d others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31605501 | |||||
chr3:31605772
|
G | A | 25 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(22): Show | 25 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(22): Show |
intron_variant | MODIFIER | c.877+5313G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31605772 | ||||||
chr3:31605925
|
C | T | 1 | a0001c0001t0001g0322 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.877+5466C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31605925 | ||||||
chr3:31606215
|
A | G | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.877+5756A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31606215 | ||||||
chr3:31606224
|
G | A | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.877+5765G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31606224 | ||||||
chr3:31606501
|
CA | C | 87 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(84): Show | 93 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(90): Show |
intron_variant | MODIFIER | c.877+6044delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31606501 | |||||
chr3:31606736
|
C | T | 88 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(85): Show | 94 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.877+6277C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31606736 | ||||||
chr3:31606815
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.877+6356A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31606815 | ||||||
chr3:31606816
|
G | C | 1 | a0001c0001t0001g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.877+6357G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31606816 | ||||||
chr3:31607214
|
T | G | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.877+6755T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607214 | ||||||
chr3:31607314
|
C | A | 1 | a0001c0001t0001g0310 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.877+6855C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607314 | ||||||
chr3:31607397
|
C | G | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0277 | 3 | NA18945.hp1 NA18954.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.877+6938C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607397 | ||||||
chr3:31607454
|
A | G | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.877+6995A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607454 | ||||||
chr3:31607489
|
G | A | 2 | a0001c0004t0005g0016a0001c0004t0005g0065 | 2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.877+7030G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607489 | ||||||
chr3:31607622
|
A | G | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.877+7163A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607622 | ||||||
chr3:31607692
|
A | G | 22 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.877+7233A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607692 | ||||||
chr3:31607752
|
G | GGTT | 200 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(197): Show | 211 | HG00140.hp1 HG00280.hp1 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.877+7299_877+7301d others(5): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31607752 | |||||
chr3:31607758
|
TGTG | T | 22 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.877+7302_877+7304d others(5): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31607758 | |||||
chr3:31607761
|
G | T | 279 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(276): Show | 294 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(291): Show |
intron_variant | MODIFIER | c.877+7302G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607761 | ||||||
chr3:31607846
|
C | T | 114 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 121 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(118): Show |
intron_variant | MODIFIER | c.878-7259C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31607846 | ||||||
chr3:31608037
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.878-7068G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608037 | ||||||
chr3:31608213
|
G | A | 107 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(104): Show | 112 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(109): Show |
intron_variant | MODIFIER | c.878-6892G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608213 | ||||||
chr3:31608257
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.878-6848A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608257 | ||||||
chr3:31608289
|
G | T | 5 | a0001c0001t0001g0251a0001c0001t0001g0254a0001c0001t0001g0257others(2): Show | 5 | NA18942.hp1 NA18948.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-6816G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608289 | ||||||
chr3:31608350
|
C | T | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.878-6755C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608350 | ||||||
chr3:31608365
|
A | C | 25 | a0001c0001t0004g0004a0001c0001t0004g0093a0001c0001t0004g0094others(22): Show | 26 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.878-6740A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608365 | ||||||
chr3:31608421
|
GA | G | 90 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(87): Show | 95 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.878-6681delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31608421 | |||||
chr3:31608520
|
T | C | 2 | a0001c0004t0005g0016a0001c0004t0005g0320 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.878-6585T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608520 | ||||||
chr3:31608652
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.878-6453C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608652 | ||||||
chr3:31608692
|
A | G | 1 | a0001c0001t0002g0063 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.878-6413A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608692 | ||||||
chr3:31608796
|
C | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.878-6309C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608796 | ||||||
chr3:31608830
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0169a0001c0001t0001g0170 | 3 | NA18975.hp2 NA18991.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.878-6275G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608830 | ||||||
chr3:31608901
|
G | C | 1 | a0001c0001t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.878-6204G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608901 | ||||||
chr3:31608995
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.878-6110G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31608995 | ||||||
chr3:31609008
|
A | T | 119 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.878-6097A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609008 | ||||||
chr3:31609016
|
G | A | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.878-6089G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609016 | ||||||
chr3:31609404
|
A | G | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.878-5701A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609404 | ||||||
chr3:31609767
|
G | A | 1 | a0001c0001t0004g0173 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.878-5338G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609767 | ||||||
chr3:31609795
|
G | A | 73 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(70): Show | 77 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(74): Show |
intron_variant | MODIFIER | c.878-5310G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609795 | ||||||
chr3:31609843
|
G | A | 119 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(116): Show | 126 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(123): Show |
intron_variant | MODIFIER | c.878-5262G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609843 | ||||||
chr3:31609866
|
C | T | 2 | a0001c0001t0004g0181a0001c0001t0004g0182 | 2 | HG03471.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.878-5239C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609866 | ||||||
chr3:31609877
|
A | G | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.878-5228A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31609877 | ||||||
chr3:31610036
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878-5069T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31610036 | ||||||
chr3:31610394
|
G | A | 1 | a0001c0001t0001g0190 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.878-4711G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31610394 | ||||||
chr3:31610416
|
C | T | 1 | a0001c0001t0001g0323 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.878-4689C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31610416 | ||||||
chr3:31610480
|
C | CTGCAA | 120 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.878-4621_878-4617d others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31610480 | |||||
chr3:31610523
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.878-4582G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31610523 | ||||||
chr3:31610543
|
A | G | 2 | a0001c0001t0003g0299a0001c0004t0005g0320 | 2 | HG02647.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.878-4562A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31610543 | ||||||
chr3:31610806
|
C | T | 1 | a0001c0001t0003g0237 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.878-4299C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31610806 | ||||||
chr3:31611062
|
G | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.878-4043G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611062 | ||||||
chr3:31611435
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.878-3670A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611435 | ||||||
chr3:31611470
|
C | T | 1 | a0001c0004t0005g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.878-3635C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611470 | ||||||
chr3:31611486
|
G | A | 91 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(88): Show | 97 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(94): Show |
intron_variant | MODIFIER | c.878-3619G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611486 | ||||||
chr3:31611530
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.878-3575G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611530 | ||||||
chr3:31611744
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878-3361G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611744 | ||||||
chr3:31611745
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0265 | 3 | NA18950.hp1 NA18999.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.878-3360C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31611745 | ||||||
chr3:31612546
|
A | G | 120 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.878-2559A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31612546 | ||||||
chr3:31612567
|
A | G | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.878-2538A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31612567 | ||||||
chr3:31612734
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.878-2371G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31612734 | ||||||
chr3:31612914
|
T | C | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878-2191T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31612914 | ||||||
chr3:31612964
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0109 | 3 | HG02896.hp1 HG02897.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.878-2141T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31612964 | ||||||
chr3:31612974
|
A | G | 10 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.878-2131A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31612974 | ||||||
chr3:31613062
|
T | G | 2 | a0001c0001t0005g0219a0001c0004t0005g0016 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.878-2043T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613062 | ||||||
chr3:31613103
|
G | A | 2 | a0001c0001t0005g0219a0001c0004t0005g0016 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.878-2002G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613103 | ||||||
chr3:31613106
|
G | A | 10 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.878-1999G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613106 | ||||||
chr3:31613134
|
G | T | 10 | a0001c0001t0004g0173a0001c0001t0004g0174a0001c0001t0004g0175others(7): Show | 10 | HG00140.hp2 HG00642.hp1 HG01069.hp1 others(7): Show |
intron_variant | MODIFIER | c.878-1971G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613134 | ||||||
chr3:31613158
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.878-1947C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613158 | ||||||
chr3:31613159
|
G | A | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.878-1946G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613159 | ||||||
chr3:31613194
|
A | G | 20 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(17): Show | 20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.878-1911A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613194 | ||||||
chr3:31613200
|
A | G | 22 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(19): Show | 22 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(19): Show |
intron_variant | MODIFIER | c.878-1905A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613200 | ||||||
chr3:31613274
|
C | A | 1 | a0001c0004t0005g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.878-1831C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613274 | ||||||
chr3:31613283
|
G | C | 1 | a0001c0001t0001g0155 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.878-1822G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613283 | ||||||
chr3:31613459
|
C | G | 1 | a0001c0001t0001g0230 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.878-1646C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613459 | ||||||
chr3:31613624
|
C | G | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.878-1481C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613624 | ||||||
chr3:31613667
|
CT | C | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.878-1428delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr3 | 31613667 | |||||
chr3:31613676
|
T | C | 1 | a0001c0001t0001g0264 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.878-1429T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613676 | ||||||
chr3:31613761
|
C | T | 14 | a0001c0001t0001g0015a0001c0001t0001g0285a0001c0001t0001g0287others(11): Show | 15 | HG00639.hp1 HG01884.hp1 HG02145.hp1 others(12): Show |
intron_variant | MODIFIER | c.878-1344C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613761 | ||||||
chr3:31613927
|
G | A | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.878-1178G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31613927 | ||||||
chr3:31614018
|
T | A | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878-1087T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614018 | ||||||
chr3:31614027
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878-1078A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614027 | ||||||
chr3:31614150
|
C | T | 90 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(87): Show | 95 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(92): Show |
intron_variant | MODIFIER | c.878-955C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614150 | ||||||
chr3:31614172
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.878-933C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614172 | ||||||
chr3:31614173
|
G | C | 4 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0122others(1): Show | 4 | NA18612.hp2 NA18944.hp1 NA18997.hp2 others(1): Show |
intron_variant | MODIFIER | c.878-932G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614173 | ||||||
chr3:31614296
|
G | A | 1 | a0001c0001t0001g0168 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.878-809G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614296 | ||||||
chr3:31614362
|
C | T | 2 | a0001c0004t0005g0016a0001c0004t0005g0065 | 2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.878-743C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614362 | ||||||
chr3:31614467
|
C | T | 4 | a0001c0001t0001g0008a0001c0001t0001g0113a0001c0001t0001g0130others(1): Show | 5 | NA18963.hp2 NA18968.hp2 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.878-638C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614467 | ||||||
chr3:31614721
|
C | CAT | 193 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.878-384_878-383ins others(2): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614721 | ||||||
chr3:31614726
|
A | G | 1 | a0001c0001t0001g0257 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.878-379A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614726 | ||||||
chr3:31614770
|
GT | G | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.878-334delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31614770 | ||||||
chr3:31615050
|
T | G | 1 | a0001c0009t0001g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.878-55T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 5/15 | chr3 | 31615050 | ||||||
chr3:31615283
|
T | G | 1 | a0001c0001t0001g0257 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.976+80T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615283 | ||||||
chr3:31615347
|
G | C | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.976+144G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615347 | ||||||
chr3:31615480
|
T | A | 1 | a0001c0001t0001g0257 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.976+277T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615480 | ||||||
chr3:31615509
|
G | A | 20 | a0001c0001t0004g0004a0001c0001t0004g0093a0001c0001t0004g0094others(17): Show | 21 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(18): Show |
intron_variant | MODIFIER | c.976+306G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615509 | ||||||
chr3:31615593
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.976+390C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615593 | ||||||
chr3:31615710
|
G | A | 25 | a0001c0001t0004g0004a0001c0001t0004g0093a0001c0001t0004g0094others(22): Show | 26 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(23): Show |
intron_variant | MODIFIER | c.976+507G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615710 | ||||||
chr3:31615929
|
A | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0315a0001c0001t0001g0316 | 4 | HG00639.hp1 HG02451.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.976+726A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31615929 | ||||||
chr3:31615945
|
ACTC | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.976+745_976+747del others(3): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 31615945 | |||||
chr3:31616211
|
G | T | 1 | a0001c0001t0002g0035 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.977-718G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31616211 | ||||||
chr3:31616290
|
A | T | 1 | a0001c0001t0001g0257 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.977-639A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31616290 | ||||||
chr3:31616376
|
C | CT | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.977-551dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr3 | 31616376 | |||||
chr3:31616447
|
A | G | 11 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(8): Show | 11 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.977-482A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31616447 | ||||||
chr3:31616498
|
T | C | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.977-431T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31616498 | ||||||
chr3:31616772
|
G | A | 1 | a0001c0001t0001g0105 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.977-157G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31616772 | ||||||
chr3:31616861
|
C | T | 2 | a0001c0001t0002g0018a0001c0001t0002g0019 | 2 | NA19007.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.977-68C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 6/15 | chr3 | 31616861 | ||||||
chr3:31617186
|
C | CT | 27 | a0001c0001t0001g0113a0001c0001t0001g0136a0001c0001t0004g0004others(24): Show | 28 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.1123+126dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 31617186 | |||||
chr3:31617186
|
C | CTT | 89 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(86): Show | 95 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1123+125_1123+126d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 31617186 | |||||
chr3:31617186
|
CT | C | 47 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(44): Show | 50 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(47): Show |
intron_variant | MODIFIER | c.1123+126delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr3 | 31617186 | |||||
chr3:31617222
|
G | T | 2 | a0001c0001t0003g0010a0001c0001t0003g0213 | 3 | NA18948.hp2 NA18983.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.1123+147G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | chr3 | 31617222 | ||||||
chr3:31617429
|
C | T | 2 | a0001c0001t0001g0286a0001c0001t0001g0298 | 2 | HG02622.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1123+354C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | chr3 | 31617429 | ||||||
chr3:31617517
|
G | T | 2 | a0001c0004t0005g0016a0001c0004t0005g0065 | 2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1124-423G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | chr3 | 31617517 | ||||||
chr3:31617846
|
G | A | 1 | a0001c0001t0003g0210 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1124-94G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 7/15 | chr3 | 31617846 | ||||||
chr3:31618003
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1172+15A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618003 | ||||||
chr3:31618011
|
G | A | 1 | a0001c0004t0005g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1172+23G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618011 | ||||||
chr3:31618262
|
T | C | 120 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(117): Show | 127 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(124): Show |
intron_variant | MODIFIER | c.1172+274T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618262 | ||||||
chr3:31618287
|
T | TTACCTAA others(2): Show |
301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1172+301_1172+302i others(11): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 31618287 | |||||
chr3:31618456
|
T | G | 1 | a0001c0001t0001g0273 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1172+468T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618456 | ||||||
chr3:31618469
|
A | C | 1 | a0001c0001t0001g0298 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1172+481A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618469 | ||||||
chr3:31618628
|
G | C | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1172+640G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618628 | ||||||
chr3:31618865
|
T | C | 2 | a0001c0001t0001g0306a0001c0001t0001g0307 | 2 | NA18951.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1173-811T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31618865 | ||||||
chr3:31618937
|
TTATAA | T | 18 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(15): Show | 18 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1173-733_1173-729d others(7): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr3 | 31618937 | |||||
chr3:31619040
|
C | T | 1 | a0001c0004t0005g0016 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1173-636C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31619040 | ||||||
chr3:31619261
|
T | C | 1 | a0001c0001t0002g0040 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1173-415T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 8/15 | chr3 | 31619261 | ||||||
chr3:31619851
|
A | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1327+21A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31619851 | ||||||
chr3:31620132
|
G | T | 1 | a0001c0001t0001g0069 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1327+302G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620132 | ||||||
chr3:31620148
|
G | A | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1327+318G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620148 | ||||||
chr3:31620262
|
G | A | 32 | a0001c0001t0001g0106a0001c0001t0001g0117a0001c0001t0001g0138others(29): Show | 33 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(30): Show |
intron_variant | MODIFIER | c.1327+432G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620262 | ||||||
chr3:31620274
|
C | CAA | 74 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(71): Show | 78 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(75): Show |
intron_variant | MODIFIER | c.1327+460_1327+461d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 31620274 | |||||
chr3:31620274
|
CA | C | 7 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318others(4): Show | 7 | HG01515.hp2 HG02055.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.1327+461delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 31620274 | |||||
chr3:31620277
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1327+447A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620277 | ||||||
chr3:31620285
|
A | G | 1 | a0001c0001t0005g0219 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1327+455A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620285 | ||||||
chr3:31620349
|
A | G | 2 | a0001c0004t0005g0016a0001c0004t0005g0320 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1327+519A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620349 | ||||||
chr3:31620356
|
G | A | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1327+526G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620356 | ||||||
chr3:31620365
|
G | A | 76 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(73): Show | 80 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.1327+535G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620365 | ||||||
chr3:31620417
|
C | T | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.1327+587C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620417 | ||||||
chr3:31620560
|
C | T | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 316 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(313): Show |
intron_variant | MODIFIER | c.1327+730C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620560 | ||||||
chr3:31620681
|
G | T | 46 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(43): Show | 49 | HG00438.hp1 HG00558.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1327+851G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620681 | ||||||
chr3:31620865
|
T | C | 8 | a0001c0001t0001g0015a0001c0001t0001g0310a0001c0001t0001g0311others(5): Show | 9 | HG00639.hp1 HG01884.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1327+1035T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620865 | ||||||
chr3:31620892
|
C | T | 2 | a0001c0004t0005g0016a0001c0004t0005g0065 | 2 | HG01934.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1327+1062C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31620892 | ||||||
chr3:31620901
|
TTCTCTAG others(1): Show |
T | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(45): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.1327+1073_1327+108 others(12): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 31620901 | |||||
chr3:31621148
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1328-949A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31621148 | ||||||
chr3:31621583
|
A | G | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1328-514A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31621583 | ||||||
chr3:31621655
|
A | C | 2 | a0001c0001t0001g0267a0001c0001t0001g0268 | 2 | NA18964.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.1328-442A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31621655 | ||||||
chr3:31621676
|
G | A | 1 | a0001c0001t0001g0118 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1328-421G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31621676 | ||||||
chr3:31621711
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1328-386G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31621711 | ||||||
chr3:31621984
|
C | T | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1328-113C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31621984 | ||||||
chr3:31622013
|
T | C | 1 | a0001c0001t0002g0062 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1328-84T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | chr3 | 31622013 | ||||||
chr3:31622023
|
A | AGTGTG | 325 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(322): Show | 341 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(338): Show |
intron_variant | MODIFIER | c.1328-72_1328-71ins others(5): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr3 | 31622023 | |||||
chr3:31622377
|
C | G | 1 | a0001c0001t0001g0100 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.1539+69C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31622377 | ||||||
chr3:31622679
|
C | T | 108 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 113 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.1539+371C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31622679 | ||||||
chr3:31622807
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1539+499G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31622807 | ||||||
chr3:31622896
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1539+588G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31622896 | ||||||
chr3:31622933
|
G | A | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1539+625G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31622933 | ||||||
chr3:31623023
|
T | A | 1 | a0001c0001t0001g0156 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.1540-651T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31623023 | ||||||
chr3:31623156
|
TG | T | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1540-517delG | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31623156 | ||||||
chr3:31623226
|
G | A | 84 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(81): Show | 90 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1540-448G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31623226 | ||||||
chr3:31623281
|
A | G | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.1540-393A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31623281 | ||||||
chr3:31623354
|
A | C | 3 | a0001c0001t0001g0317a0001c0001t0001g0318a0001c0001t0001g0319 | 3 | HG02055.hp1 HG02109.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.1540-320A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 10/15 | chr3 | 31623354 | ||||||
chr3:31623913
|
G | A | 4 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(1): Show | 4 | NA18951.hp1 NA18951.hp2 NA18969.hp2 others(1): Show |
intron_variant | MODIFIER | c.1727+52G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31623913 | ||||||
chr3:31624077
|
G | A | 10 | a0001c0001t0001g0305a0001c0001t0001g0306a0001c0001t0001g0307others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1727+216G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624077 | ||||||
chr3:31624088
|
G | T | 1 | a0001c0001t0001g0118 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1727+227G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624088 | ||||||
chr3:31624221
|
C | T | 1 | a0001c0002t0001g0221 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1727+360C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624221 | ||||||
chr3:31624231
|
C | A | 2 | a0001c0001t0002g0021a0001c0001t0002g0030 | 2 | NA18942.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.1727+370C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624231 | ||||||
chr3:31624236
|
G | T | 3 | a0001c0004t0005g0016a0001c0004t0005g0065a0001c0004t0005g0320 | 3 | HG01934.hp1 HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1727+375G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624236 | ||||||
chr3:31624295
|
T | C | 2 | a0001c0004t0005g0016a0001c0004t0005g0320 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1727+434T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624295 | ||||||
chr3:31624667
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1728-247C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624667 | ||||||
chr3:31624670
|
CT | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0011a0001c0001t0001g0012others(125): Show | 136 | HG00423.hp1 HG00438.hp1 HG00544.hp2 others(133): Show |
intron_variant | MODIFIER | c.1728-227delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 31624670 | |||||
chr3:31624749
|
C | T | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.1728-165C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624749 | ||||||
chr3:31624764
|
CT | C | 75 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(72): Show | 79 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(76): Show |
intron_variant | MODIFIER | c.1728-140delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr3 | 31624764 | |||||
chr3:31624865
|
C | A | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1728-49C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 11/15 | chr3 | 31624865 | ||||||
chr3:31625118
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1899+33C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 12/15 | chr3 | 31625118 | ||||||
chr3:31625186
|
C | T | 1 | a0001c0009t0001g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1899+101C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 12/15 | chr3 | 31625186 | ||||||
chr3:31625799
|
A | G | 302 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.1900-155A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 12/15 | chr3 | 31625799 | ||||||
chr3:31626141
|
T | C | 7 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0137others(4): Show | 7 | HG00544.hp1 NA18965.hp2 NA18982.hp2 others(4): Show |
intron_variant | MODIFIER | c.2073+14T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31626141 | ||||||
chr3:31626625
|
G | T | 1 | a0001c0001t0001g0169 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2073+498G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31626625 | ||||||
chr3:31626668
|
G | T | 1 | a0001c0001t0004g0195 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2073+541G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31626668 | ||||||
chr3:31626763
|
A | G | 1 | a0001c0001t0001g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2073+636A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31626763 | ||||||
chr3:31626808
|
A | G | 79 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(76): Show | 83 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.2073+681A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31626808 | ||||||
chr3:31627235
|
C | G | 1 | a0001c0004t0005g0065 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2073+1108C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627235 | ||||||
chr3:31627268
|
T | C | 302 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.2073+1141T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627268 | ||||||
chr3:31627597
|
G | A | 3 | a0001c0001t0001g0245a0001c0001t0001g0246a0001c0001t0001g0247 | 3 | HG00558.hp1 NA19065.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.2073+1470G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627597 | ||||||
chr3:31627694
|
G | A | 20 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(17): Show | 20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.2073+1567G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627694 | ||||||
chr3:31627722
|
C | T | 1 | a0001c0001t0001g0006 | 2 | NA18977.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.2074-1576C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627722 | ||||||
chr3:31627802
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2074-1496A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627802 | ||||||
chr3:31627830
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2074-1468C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31627830 | ||||||
chr3:31628011
|
T | TA | 114 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 120 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(117): Show |
intron_variant | MODIFIER | c.2074-1275dupA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 31628011 | |||||
chr3:31628011
|
T | TAA | 6 | a0001c0001t0001g0009a0001c0001t0001g0107a0001c0001t0001g0151others(3): Show | 7 | HG00639.hp2 HG01070.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.2074-1276_2074-127 others(6): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 31628011 | |||||
chr3:31628219
|
T | TG | 58 | a0001c0001t0001g0067a0001c0001t0001g0071a0001c0001t0001g0072others(55): Show | 58 | HG00423.hp1 HG00423.hp2 HG00438.hp1 others(55): Show |
intron_variant | MODIFIER | c.2074-1072dupG | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr3 | 31628219 | |||||
chr3:31628306
|
C | T | 1 | a0001c0001t0002g0044 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2074-992C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31628306 | ||||||
chr3:31628455
|
C | T | 1 | a0001c0001t0002g0050 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2074-843C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31628455 | ||||||
chr3:31628495
|
G | A | 1 | a0001c0001t0002g0056 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2074-803G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31628495 | ||||||
chr3:31628526
|
T | C | 13 | a0001c0001t0001g0285a0001c0001t0001g0287a0001c0001t0001g0317others(10): Show | 13 | HG01891.hp2 HG02055.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.2074-772T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31628526 | ||||||
chr3:31628819
|
T | C | 8 | a0001c0001t0003g0199a0001c0001t0003g0200a0001c0001t0003g0201others(5): Show | 8 | HG02258.hp2 HG02451.hp2 HG02486.hp2 others(5): Show |
intron_variant | MODIFIER | c.2074-479T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31628819 | ||||||
chr3:31628997
|
T | C | 1 | a0001c0001t0001g0285 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2074-301T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31628997 | ||||||
chr3:31629066
|
A | G | 1 | a0001c0001t0001g0150 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2074-232A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31629066 | ||||||
chr3:31629186
|
C | T | 1 | a0001c0001t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2074-112C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 13/15 | chr3 | 31629186 | ||||||
chr3:31629514
|
A | G | 1 | a0001c0001t0001g0132 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2187+103A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629514 | ||||||
chr3:31629594
|
A | G | 9 | a0001c0001t0003g0010a0001c0001t0003g0205a0001c0001t0003g0206others(6): Show | 10 | HG00735.hp2 HG01123.hp1 HG02040.hp2 others(7): Show |
intron_variant | MODIFIER | c.2187+183A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629594 | ||||||
chr3:31629645
|
A | T | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2187+234A>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629645 | ||||||
chr3:31629719
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.2187+308C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629719 | ||||||
chr3:31629779
|
A | C | 1 | a0001c0001t0002g0035 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.2187+368A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629779 | ||||||
chr3:31629807
|
T | A | 1 | a0001c0001t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2187+396T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629807 | ||||||
chr3:31629831
|
T | C | 3 | a0001c0001t0005g0219a0001c0004t0005g0016a0001c0004t0005g0320 | 3 | HG03139.hp2 HG03225.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2187+420T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629831 | ||||||
chr3:31629861
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2187+450T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31629861 | ||||||
chr3:31630209
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.2187+798A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630209 | ||||||
chr3:31630250
|
C | T | 1 | a0001c0001t0004g0177 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2187+839C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630250 | ||||||
chr3:31630665
|
G | A | 193 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(190): Show | 203 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(200): Show |
intron_variant | MODIFIER | c.2187+1254G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630665 | ||||||
chr3:31630725
|
A | G | 7 | a0001c0001t0001g0325a0001c0002t0001g0216a0001c0002t0001g0217others(4): Show | 7 | HG01884.hp2 HG02109.hp2 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.2187+1314A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630725 | ||||||
chr3:31630795
|
GT | G | 192 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(189): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.2187+1392delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 31630795 | |||||
chr3:31630796
|
T | G | 80 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(77): Show | 84 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.2187+1385T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630796 | ||||||
chr3:31630803
|
T | G | 1 | a0001c0010t0002g0042 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2187+1392T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630803 | ||||||
chr3:31630804
|
G | GT | 6 | a0001c0001t0001g0254a0001c0001t0001g0285a0001c0001t0001g0289others(3): Show | 6 | HG00738.hp1 HG03195.hp1 NA18951.hp2 others(3): Show |
intron_variant | MODIFIER | c.2187+1403dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 31630804 | |||||
chr3:31630804
|
G | T | 1 | a0001c0010t0002g0042 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.2187+1393G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630804 | ||||||
chr3:31630828
|
G | T | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2187+1417G>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630828 | ||||||
chr3:31630835
|
C | T | 1 | a0001c0001t0002g0025 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.2187+1424C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31630835 | ||||||
chr3:31631017
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.2187+1606C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31631017 | ||||||
chr3:31631039
|
T | C | 1 | a0001c0001t0004g0196 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2187+1628T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31631039 | ||||||
chr3:31631078
|
C | T | 2 | a0001c0001t0005g0219a0001c0004t0005g0016 | 2 | HG03139.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.2187+1667C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31631078 | ||||||
chr3:31631583
|
T | A | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2188-1352T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31631583 | ||||||
chr3:31631781
|
G | A | 1 | a0001c0001t0001g0287 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2188-1154G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31631781 | ||||||
chr3:31631978
|
C | T | 80 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(77): Show | 84 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(81): Show |
intron_variant | MODIFIER | c.2188-957C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31631978 | ||||||
chr3:31632082
|
C | CT | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(46): Show | 52 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(49): Show |
intron_variant | MODIFIER | c.2188-852dupT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 31632082 | |||||
chr3:31632098
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2188-837C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632098 | ||||||
chr3:31632226
|
C | T | 14 | a0001c0001t0002g0001a0001c0001t0002g0017a0001c0001t0002g0023others(11): Show | 16 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(13): Show |
intron_variant | MODIFIER | c.2188-709C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632226 | ||||||
chr3:31632549
|
C | T | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2188-386C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632549 | ||||||
chr3:31632669
|
GT | G | 103 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(100): Show | 107 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.2188-250delT | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 31632669 | |||||
chr3:31632669
|
GTT | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(87): Show | 95 | HG00140.hp1 HG00280.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.2188-251_2188-250d others(4): Show |
STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr3 | 31632669 | |||||
chr3:31632670
|
T | G | 78 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(75): Show | 82 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.2188-265T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632670 | ||||||
chr3:31632671
|
T | G | 1 | a0001c0001t0001g0290 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.2188-264T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632671 | ||||||
chr3:31632673
|
T | G | 26 | a0001c0001t0004g0004a0001c0001t0004g0093a0001c0001t0004g0094others(23): Show | 27 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.2188-262T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632673 | ||||||
chr3:31632763
|
A | G | 4 | a0001c0001t0001g0243a0001c0001t0001g0267a0001c0001t0001g0268others(1): Show | 4 | NA18964.hp2 NA18965.hp1 NA18986.hp1 others(1): Show |
intron_variant | MODIFIER | c.2188-172A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 14/15 | chr3 | 31632763 | ||||||
chr3:31633276
|
G | A | 4 | a0001c0001t0001g0003a0001c0001t0001g0086a0001c0001t0001g0087others(1): Show | 5 | HG00733.hp2 HG02145.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.2400+129G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633276 | ||||||
chr3:31633316
|
A | C | 2 | a0001c0001t0003g0188a0001c0001t0003g0189 | 2 | HG03195.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.2400+169A>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633316 | ||||||
chr3:31633422
|
T | C | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.2400+275T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633422 | ||||||
chr3:31633481
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0068a0001c0001t0001g0069 | 3 | HG01891.hp1 HG02257.hp1 HG02572.hp2 |
intron_variant | MODIFIER | c.2400+334G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633481 | ||||||
chr3:31633615
|
TA | T | 108 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(105): Show | 113 | HG00423.hp1 HG00544.hp2 HG00558.hp1 others(110): Show |
intron_variant | MODIFIER | c.2400+469delA | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633615 | ||||||
chr3:31633671
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2400+524A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633671 | ||||||
chr3:31633686
|
T | G | 1 | a0001c0001t0001g0106 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2400+539T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633686 | ||||||
chr3:31633769
|
C | A | 1 | a0001c0001t0001g0112 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2400+622C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31633769 | ||||||
chr3:31634043
|
G | A | 1 | a0001c0001t0001g0106 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2400+896G>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634043 | ||||||
chr3:31634174
|
G | C | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.2400+1027G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634174 | ||||||
chr3:31634655
|
C | T | 50 | a0001c0001t0001g0311a0001c0001t0002g0001a0001c0001t0002g0002others(47): Show | 53 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(50): Show |
intron_variant | MODIFIER | c.2401-1329C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634655 | ||||||
chr3:31634676
|
A | G | 1 | a0001c0001t0001g0198 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2401-1308A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634676 | ||||||
chr3:31634805
|
T | A | 1 | a0001c0009t0001g0172 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.2401-1179T>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634805 | ||||||
chr3:31634848
|
A | G | 28 | a0001c0001t0003g0188a0001c0001t0003g0189a0001c0001t0004g0004others(25): Show | 29 | HG00140.hp2 HG00280.hp2 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.2401-1136A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634848 | ||||||
chr3:31634876
|
C | A | 21 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(18): Show | 21 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(18): Show |
intron_variant | MODIFIER | c.2401-1108C>A | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31634876 | ||||||
chr3:31635048
|
A | G | 3 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0277 | 3 | NA18945.hp1 NA18954.hp1 NA18997.hp1 |
intron_variant | MODIFIER | c.2401-936A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635048 | ||||||
chr3:31635134
|
C | T | 1 | a0001c0007t0001g0300 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2401-850C>T | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635134 | ||||||
chr3:31635221
|
A | G | 2 | a0001c0004t0005g0016a0001c0004t0005g0320 | 2 | HG03139.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2401-763A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635221 | ||||||
chr3:31635252
|
A | G | 20 | a0001c0001t0001g0066a0001c0001t0001g0067a0001c0001t0001g0068others(17): Show | 20 | HG01192.hp2 HG01243.hp1 HG01255.hp2 others(17): Show |
intron_variant | MODIFIER | c.2401-732A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635252 | ||||||
chr3:31635435
|
T | C | 1 | a0001c0001t0002g0045 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2401-549T>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635435 | ||||||
chr3:31635458
|
T | G | 1 | a0001c0001t0001g0303 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2401-526T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635458 | ||||||
chr3:31635536
|
A | G | 1 | a0001c0001t0001g0321 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.2401-448A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635536 | ||||||
chr3:31635567
|
C | G | 4 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(1): Show | 4 | HG01891.hp2 HG02559.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2401-417C>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635567 | ||||||
chr3:31635569
|
A | G | 1 | a0001c0001t0003g0241 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2401-415A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635569 | ||||||
chr3:31635632
|
G | C | 1 | a0001c0001t0001g0100 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.2401-352G>C | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635632 | ||||||
chr3:31635898
|
A | G | 1 | a0001c0001t0001g0102 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.2401-86A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635898 | ||||||
chr3:31635903
|
T | G | 302 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(299): Show | 317 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(314): Show |
intron_variant | MODIFIER | c.2401-81T>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635903 | ||||||
chr3:31635940
|
A | G | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0017others(45): Show | 51 | HG00438.hp1 HG00558.hp2 HG00597.hp1 others(48): Show |
intron_variant | MODIFIER | c.2401-44A>G | STT3B | ENSG00000163527.10 | transcript | ENST00000295770.4 | protein_coding | 15/15 | chr3 | 31635940 |