geneid | 9044 |
---|---|
ensemblid | ENSG00000095564.15 |
hgncid | 17307 |
symbol | BTAF1 |
name | B-TFIID TATA-box binding protein associated factor 1 |
refseq_nuc | NM_003972.3 |
refseq_prot | NP_003963.1 |
ensembl_nuc | ENST00000265990.12 |
ensembl_prot | ENSP00000265990.6 |
mane_status | MANE Select |
chr | chr10 |
start | 91923770 |
end | 92031437 |
strand | + |
ver | v1.2 |
region | chr10:91923770-92031437 |
region5000 | chr10:91918770-92036437 |
regionname0 | BTAF1_chr10_91923770_92031437 |
regionname5000 | BTAF1_chr10_91918770_92036437 |
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 | 1849 | 322 | 87 | 62 | 123 | 11 | 37 | 95 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0002 | 0/0 | 1849 | 2 | 0 | 0 | 2 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0003 | 0/0 | 1849 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0004 | 0/0 | 1411 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0005 | 0/0 | 1849 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0006 | 0/0 | 1857 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0007 | 0/0 | 1849 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0008 | 0/0 | 1849 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
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 | 5550 | 307 | 77 | 61 | 121 | 11 | 35 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0002 | 0/0 | 5550 | 4 | 4 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0003 | 0/0 | 5550 | 3 | 3 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0004 | 0/0 | 5550 | 3 | 3 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0005 | 0/0 | 5550 | 2 | 0 | 0 | 2 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0006 | 0/0 | 5550 | 2 | 0 | 0 | 0 | 0 | 2 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0007 | 0/0 | 5550 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0008 | 0/0 | 5550 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0009 | 0/0 | 5550 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0010 | 0/0 | 5550 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0011 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0012 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0013 | 0/0 | 5550 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0014 | 0/0 | 5550 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
c0015 | 0/0 | 5550 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2812 | 155 | 64 | 28 | 39 | 3 | 20 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
t0002 | 0/0 | 2812 | 90 | 6 | 19 | 50 | 4 | 11 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
t0003 | 0/0 | 2816 | 60 | 3 | 13 | 33 | 5 | 6 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
t0004 | 0/0 | 2814 | 8 | 7 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
t0005 | 0/0 | 2812 | 4 | 4 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
t0006 | 0/0 | 2815 | 3 | 0 | 0 | 3 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
t0007 | 0/0 | 2814 | 3 | 3 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
t0008 | 0/0 | 2812 | 2 | 0 | 0 | 2 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
t0009 | 0/0 | 2812 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
t0010 | 0/0 | 2816 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
t0011 | 0/0 | 2812 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
t0012 | 0/1 | 2812 | 1 | 0 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
t0013 | 0/0 | 2812 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
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 | 5550 | 307 | 77 | 61 | 121 | 11 | 35 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0002 | 0/0 | 5550 | 4 | 4 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0003 | 0/0 | 5550 | 3 | 3 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0004 | 0/0 | 5550 | 3 | 3 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0006 | 0/0 | 5550 | 2 | 0 | 0 | 0 | 0 | 2 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0010 | 0/0 | 5550 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0012 | 0/0 | 5550 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0013 | 0/0 | 5550 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0002c0005 | 0/0 | 5550 | 2 | 0 | 0 | 2 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0003c0014 | 0/0 | 5550 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0004c0008 | 0/0 | 5550 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0005c0009 | 0/0 | 5550 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0006c0011 | 0/0 | 5574 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0007c0015 | 0/0 | 5550 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0008c0007 | 0/0 | 5550 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 8361 | 140 | 53 | 27 | 38 | 3 | 18 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0001t0002 | 0/0 | 8361 | 86 | 6 | 19 | 46 | 4 | 11 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0001t0003 | 0/0 | 8365 | 56 | 3 | 13 | 31 | 4 | 5 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0001t0004 | 0/0 | 8363 | 8 | 7 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0001t0005 | 0/0 | 8361 | 4 | 4 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0001t0006 | 0/0 | 8364 | 3 | 0 | 0 | 3 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0001t0007 | 0/0 | 8363 | 3 | 3 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0001t0008 | 0/0 | 8361 | 2 | 0 | 0 | 2 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0001t0009 | 0/0 | 8361 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0001t0010 | 0/0 | 8365 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0001t0011 | 0/0 | 8361 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0001t0012 | 0/1 | 8361 | 1 | 0 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0001t0013 | 0/0 | 8361 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0002t0001 | 0/0 | 8361 | 4 | 4 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0003t0001 | 0/0 | 8361 | 3 | 3 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0004t0001 | 0/0 | 8361 | 3 | 3 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0006t0001 | 0/0 | 8361 | 2 | 0 | 0 | 0 | 0 | 2 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0010t0001 | 0/0 | 8361 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0012t0001 | 0/0 | 8361 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0001c0013t0002 | 0/0 | 8361 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0002c0005t0003 | 0/0 | 8365 | 2 | 0 | 0 | 2 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0003c0014t0002 | 0/0 | 8361 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0004c0008t0001 | 0/0 | 8361 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0005c0009t0003 | 0/0 | 8365 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0006c0011t0002 | 0/0 | 8385 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0007c0015t0003 | 0/0 | 8365 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
a0008c0007t0002 | 0/0 | 8361 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | copy fasta | chr10 | 91918770 | 92036437 |
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 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0150 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0001g0329 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0200 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0003g0312 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0004g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0004g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0004g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0004g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0004g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0004g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0005g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0005g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0005g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0005g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0006g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0007g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0007g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0007g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0008g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0008g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0009g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0010g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0011g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0012g0113 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0001t0013g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0002t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0002t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0003t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0003t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0003t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0004t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0004t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0004t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0006t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0010t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0012t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0001c0013t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0002c0005t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0002c0005t0003g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0003c0014t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0004c0008t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0005c0009t0003g0210 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0006c0011t0002g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0007c0015t0003g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
a0008c0007t0002g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0002 | g0164 | EUR | GBR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0221 | EUR | GBR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00423 | hp1 | a0001 | c0001 | t0003 | g0191 | EAS | CHS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0298 | EAS | CHS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | CHS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0257 | EAS | CHS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00544 | hp2 | a0001 | c0001 | t0003 | g0211 | EAS | CHS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00609 | hp2 | a0001 | c0013 | t0002 | g0091 | EAS | CHS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0174 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0292 | EAS | CHS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00673 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | CHS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0056 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0176 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0325 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01069 | hp2 | a0001 | c0001 | t0003 | g0216 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01070 | hp1 | a0001 | c0001 | t0003 | g0220 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01081 | hp2 | a0001 | c0001 | t0004 | g0318 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0252 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01109 | hp1 | a0001 | c0001 | t0003 | g0228 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0043 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0284 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01175 | hp1 | a0001 | c0012 | t0001 | g0121 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0226 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0225 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0073 | AMR | PUR | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0280 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0195 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0302 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0254 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01261 | hp1 | a0001 | c0001 | t0011 | g0242 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0153 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0031 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0120 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0173 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0194 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0175 | EUR | IBS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | IBS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0172 | EUR | IBS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0213 | EUR | IBS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0200 | EUR | IBS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0107 | EUR | IBS | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01891 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0162 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0275 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01952 | hp2 | a0001 | c0001 | t0002 | g0168 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0276 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0287 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0229 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02040 | hp1 | a0003 | c0014 | t0002 | g0255 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02040 | hp2 | a0001 | c0001 | t0003 | g0177 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02055 | hp1 | a0001 | c0001 | t0004 | g0324 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0182 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0281 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0261 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02132 | hp1 | a0002 | c0005 | t0003 | g0207 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0290 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0277 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0028 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0256 | EAS | CDX | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CDX | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0042 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0169 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02280 | hp1 | a0004 | c0008 | t0001 | g0093 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02300 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | PEL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02451 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0327 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02523 | hp2 | a0001 | c0001 | t0003 | g0179 | EAS | KHV | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0166 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0206 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02615 | hp1 | a0001 | c0004 | t0001 | g0046 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0139 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0319 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0151 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02647 | hp1 | a0001 | c0001 | t0004 | g0316 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0326 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02683 | hp1 | a0001 | c0001 | t0003 | g0224 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0283 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02717 | hp1 | a0001 | c0001 | t0007 | g0321 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0065 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0279 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02809 | hp2 | a0001 | c0003 | t0001 | g0126 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02886 | hp2 | a0001 | c0001 | t0013 | g0123 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0103 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02896 | hp1 | a0001 | c0004 | t0001 | g0047 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0128 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0315 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0132 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0080 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0314 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0125 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0138 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0323 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03225 | hp1 | a0001 | c0004 | t0001 | g0076 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03225 | hp2 | a0001 | c0003 | t0001 | g0135 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0222 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0129 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03453 | hp2 | a0001 | c0001 | t0004 | g0320 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0143 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03490 | hp1 | a0001 | c0001 | t0002 | g0264 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0300 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03491 | hp2 | a0001 | c0006 | t0001 | g0001 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03492 | hp2 | a0001 | c0006 | t0001 | g0001 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ESN | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0329 | AFR | GWD | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03579 | hp2 | a0001 | c0001 | t0005 | g0147 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0278 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0297 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0022 | SAS | BEB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0202 | SAS | BEB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03927 | hp1 | a0001 | c0001 | t0010 | g0152 | SAS | BEB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | BEB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0041 | SAS | BEB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0024 | SAS | STU | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | STU | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0018 | SAS | BEB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0293 | SAS | BEB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | STU | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG04199 | hp2 | a0007 | c0015 | t0003 | g0227 | SAS | STU | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0282 | SAS | STU | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0087 | SAS | STU | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0303 | SAS | STU | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | STU | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0214 | AFR | YRI | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0322 | AFR | YRI | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18906 | hp1 | a0001 | c0002 | t0001 | g0160 | AFR | YRI | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0155 | AFR | YRI | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0246 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0238 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0294 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0048 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18950 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0310 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18954 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18962 | hp1 | a0001 | c0001 | t0006 | g0212 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18963 | hp2 | a0001 | c0001 | t0003 | g0209 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0205 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18965 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18966 | hp1 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18968 | hp1 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18968 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0248 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0270 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18971 | hp1 | a0001 | c0001 | t0003 | g0192 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18971 | hp2 | a0001 | c0001 | t0009 | g0020 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0262 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18974 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18974 | hp2 | a0001 | c0001 | t0008 | g0233 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18975 | hp2 | a0001 | c0001 | t0003 | g0309 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18978 | hp2 | a0006 | c0011 | t0002 | g0304 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18979 | hp2 | a0002 | c0005 | t0003 | g0186 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18981 | hp2 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18987 | hp2 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18988 | hp2 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18989 | hp2 | a0008 | c0007 | t0002 | g0288 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18992 | hp1 | a0001 | c0001 | t0006 | g0178 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0308 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18994 | hp2 | a0001 | c0010 | t0001 | g0002 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0193 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18999 | hp1 | a0001 | c0001 | t0006 | g0217 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19001 | hp1 | a0001 | c0001 | t0002 | g0295 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19001 | hp2 | a0001 | c0001 | t0003 | g0188 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0219 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0243 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19011 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | LWK | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0075 | AFR | LWK | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0208 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19054 | hp2 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19057 | hp2 | a0001 | c0001 | t0002 | g0272 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0269 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19064 | hp1 | a0001 | c0001 | t0002 | g0235 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0307 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19065 | hp2 | a0001 | c0001 | t0008 | g0234 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0241 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0271 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0187 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19077 | hp1 | a0001 | c0001 | t0002 | g0260 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19077 | hp2 | a0001 | c0001 | t0003 | g0311 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0268 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19086 | hp1 | a0001 | c0001 | t0003 | g0183 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0305 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19087 | hp2 | a0001 | c0001 | t0002 | g0253 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19240 | hp1 | a0001 | c0001 | t0005 | g0141 | AFR | YRI | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | YRI | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ASW | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0063 | AFR | ASW | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0286 | EUR | TSI | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA20805 | hp1 | a0005 | c0009 | t0003 | g0210 | EUR | TSI | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0312 | EUR | TSI | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA20905 | hp1 | a0001 | c0001 | t0003 | g0231 | SAS | GIH | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | GIH | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01123 | hp1 | a0001 | c0001 | t0002 | g0289 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG01123 | hp2 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02486 | hp1 | a0001 | c0001 | t0004 | g0317 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02559 | hp1 | a0001 | c0001 | t0002 | g0165 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG02559 | hp2 | a0001 | c0001 | t0005 | g0142 | AFR | ACB | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0313 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0328 | AFR | USA | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | USA | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA20300 | hp1 | a0001 | c0002 | t0001 | g0127 | AFR | USA | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0251 | AFR | USA | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0170 | AFR | LWK | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0012 | g0113 | REF | REF | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0150 | REF | REF | BTAF1_chr10_91918770_92036437 | BTAF1 | chr10 | 91918770 | 92036437 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:91942450
|
T | A | 1 | a0008 | 1 | NA18989.hp2 | missense_variant | MODERATE | c.282T>A | p.Asp94Glu | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/38 | 589/8361 | 282/5550 | 94/1849 | chr10 | 91942450 | ||
chr10:91951543
|
G | T | 1 | a0007 | 1 | HG04199.hp2 | missense_variant | MODERATE | c.541G>T | p.Ala181Ser | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/38 | 848/8361 | 541/5550 | 181/1849 | chr10 | 91951543 | ||
chr10:91989160
|
A | G | 1 | a0003 | 1 | HG02040.hp1 | missense_variant | MODERATE | c.2434A>G | p.Thr812Ala | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/38 | 2741/8361 | 2434/5550 | 812/1849 | chr10 | 91989160 | ||
chr10:91989541
|
T | C | 1 | a0002 | 2 | HG02132.hp1 NA18979.hp2 |
missense_variant | MODERATE | c.2815T>C | p.Cys939Arg | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/38 | 3122/8361 | 2815/5550 | 939/1849 | chr10 | 91989541 | ||
chr10:91994538
|
G | GAAATCGA others(17): Show |
1 | a0006 | 1 | NA18978.hp2 | disruptive_inframe_insertion | MODERATE | c.3206_3207insTCGAAA others(18): Show |
p.Gly1068_Lys1069ins others(24): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/38 | 3514/8361 | 3207/5550 | 1069/1849 | INFO_REALIGN_3_PRIME | chr10 | 91994538 | |
chr10:92011337
|
T | A | 1 | a0004 | 1 | HG02280.hp1 | missense_variant | MODERATE | c.4233T>A | p.Asn1411Lys | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/38 | 4540/8361 | 4233/5550 | 1411/1849 | chr10 | 92011337 | ||
chr10:92011338
|
G | T | 1 | a0004 | 1 | HG02280.hp1 | stop_gained | HIGH | c.4234G>T | p.Gly1412* | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/38 | 4541/8361 | 4234/5550 | 1412/1849 | chr10 | 92011338 | ||
chr10:92018895
|
A | G | 1 | a0005 | 1 | NA20805.hp1 | missense_variant | MODERATE | c.4823A>G | p.His1608Arg | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/38 | 5130/8361 | 4823/5550 | 1608/1849 | chr10 | 92018895 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:91960040
|
C | T | 1 | a0001c0004 | 3 | HG02615.hp1 HG02896.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.1149C>T | p.Asn383Asn | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/38 | 1456/8361 | 1149/5550 | 383/1849 | chr10 | 91960040 | ||
chr10:91989291
|
A | G | 1 | a0001c0013 | 1 | HG00609.hp2 | synonymous_variant | LOW | c.2565A>G | p.Arg855Arg | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/38 | 2872/8361 | 2565/5550 | 855/1849 | chr10 | 91989291 | ||
chr10:91989346
|
T | C | 1 | a0001c0003 | 3 | HG02809.hp2 HG03139.hp1 HG03225.hp2 |
synonymous_variant | LOW | c.2620T>C | p.Leu874Leu | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/38 | 2927/8361 | 2620/5550 | 874/1849 | chr10 | 91989346 | ||
chr10:91992186
|
C | T | 1 | a0001c0012 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.2922C>T | p.Tyr974Tyr | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 21/38 | 3229/8361 | 2922/5550 | 974/1849 | chr10 | 91992186 | ||
chr10:92008134
|
A | G | 1 | a0001c0002 | 4 | HG02615.hp2 HG02976.hp1 NA18906.hp1 others(1): Show |
synonymous_variant | LOW | c.3672A>G | p.Pro1224Pro | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 26/38 | 3979/8361 | 3672/5550 | 1224/1849 | chr10 | 92008134 | ||
chr10:92016453
|
C | G | 1 | a0001c0010 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.4698C>G | p.Gly1566Gly | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/38 | 5005/8361 | 4698/5550 | 1566/1849 | chr10 | 92016453 | ||
chr10:92018794
|
C | T | 1 | a0001c0006 | 2 | HG03491.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.4722C>T | p.Tyr1574Tyr | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/38 | 5029/8361 | 4722/5550 | 1574/1849 | chr10 | 92018794 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:91923815
|
G | A | 1 | a0001c0001t0009 | 1 | NA18971.hp2 | 5_prime_UTR_variant | MODIFIER | c.-262G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/38 | 262 | chr10 | 91923815 | |||||
chr10:91923840
|
C | G | 1 | a0001c0001t0007 | 3 | HG02717.hp1 HG03209.hp1 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-237C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/38 | 237 | chr10 | 91923840 | |||||
chr10:91923841
|
G | A | 1 | a0001c0001t0008 | 2 | NA18974.hp2 NA19065.hp2 |
5_prime_UTR_variant | MODIFIER | c.-236G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/38 | 236 | chr10 | 91923841 | |||||
chr10:91923857
|
C | A | 1 | a0001c0001t0010 | 1 | HG03927.hp1 | 5_prime_UTR_variant | MODIFIER | c.-220C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/38 | 220 | chr10 | 91923857 | |||||
chr10:92029010
|
G | A | 1 | a0001c0001t0011 | 1 | HG01261.hp1 | 3_prime_UTR_variant | MODIFIER | c.*77G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 38/38 | 77 | chr10 | 92029010 | |||||
chr10:92029510
|
T | C | 6 | a0001c0001t0003a0001c0001t0006a0001c0001t0010others(3): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*577T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 38/38 | 577 | chr10 | 92029510 | |||||
chr10:92029679
|
C | CAT | 2 | a0001c0001t0004a0001c0001t0007 | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*754_*755dupTA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 38/38 | 756 | INFO_REALIGN_3_PRIME | chr10 | 92029679 | ||||
chr10:92029797
|
G | A | 1 | a0001c0001t0004 | 8 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*864G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 38/38 | 864 | chr10 | 92029797 | |||||
chr10:92029879
|
A | T | 1 | a0001c0001t0013 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*946A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 38/38 | 946 | chr10 | 92029879 | |||||
chr10:92029936
|
CA | C | 1 | a0001c0001t0006 | 3 | NA18962.hp1 NA18992.hp1 NA18999.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1004delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 38/38 | 1004 | chr10 | 92029936 | |||||
chr10:92030649
|
A | AAGTC | 6 | a0001c0001t0003a0001c0001t0006a0001c0001t0010others(3): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1719_*1722dupTCAG | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 38/38 | 1723 | INFO_REALIGN_3_PRIME | chr10 | 92030649 | ||||
chr10:92030748
|
A | G | 6 | a0001c0001t0003a0001c0001t0006a0001c0001t0010others(3): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
3_prime_UTR_variant | MODIFIER | c.*1815A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 38/38 | 1815 | chr10 | 92030748 | |||||
chr10:92030757
|
A | G | 1 | a0001c0001t0005 | 4 | HG02559.hp2 HG03486.hp2 HG03579.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1824A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 38/38 | 1824 | chr10 | 92030757 | |||||
chr10:92030766
|
A | G | 9 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(6): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
3_prime_UTR_variant | MODIFIER | c.*1833A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 38/38 | 1833 | chr10 | 92030766 | |||||
chr10:92031259
|
C | A | 1 | a0001c0001t0012 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2326C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 38/38 | 2326 | chr10 | 92031259 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:91924204
|
C | G | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+114C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91924204 | ||||||
chr10:91924229
|
G | T | 13 | a0001c0001t0002g0313a0001c0001t0002g0325a0001c0001t0004g0314others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.14+139G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91924229 | ||||||
chr10:91924283
|
A | G | 1 | a0001c0001t0003g0312 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.14+193A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91924283 | ||||||
chr10:91924389
|
G | C | 90 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 90 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.14+299G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91924389 | ||||||
chr10:91925005
|
A | AT | 5 | a0001c0001t0003g0307a0001c0001t0003g0308a0001c0001t0003g0309others(2): Show | 5 | NA18952.hp1 NA18975.hp2 NA18994.hp1 others(2): Show |
intron_variant | MODIFIER | c.14+922dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91925005 | |||||
chr10:91925190
|
A | C | 76 | a0001c0001t0002g0232a0001c0001t0002g0235a0001c0001t0002g0236others(73): Show | 76 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(73): Show |
intron_variant | MODIFIER | c.14+1100A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91925190 | ||||||
chr10:91925201
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.14+1111A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91925201 | ||||||
chr10:91925273
|
T | G | 1 | a0001c0001t0002g0232 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.14+1183T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91925273 | ||||||
chr10:91925432
|
G | A | 1 | a0001c0010t0001g0002 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.14+1342G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91925432 | ||||||
chr10:91925516
|
C | CT | 12 | a0001c0001t0001g0090a0001c0001t0001g0154a0001c0001t0001g0155others(9): Show | 12 | HG01358.hp2 HG02280.hp2 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.14+1439dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91925516 | |||||
chr10:91925516
|
C | CTTTTTTT others(3): Show |
7 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0002g0237others(4): Show | 7 | NA18942.hp1 NA18950.hp1 NA18968.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+1430_14+1439dup others(10): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91925516 | |||||
chr10:91925516
|
C | CTTTTTTT others(4): Show |
82 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(79): Show | 82 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(79): Show |
intron_variant | MODIFIER | c.14+1429_14+1439dup others(11): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91925516 | |||||
chr10:91925516
|
C | CTTTTTTT others(5): Show |
12 | a0001c0001t0002g0170a0001c0001t0002g0171a0001c0001t0002g0172others(9): Show | 12 | HG00642.hp1 HG00735.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.14+1428_14+1439dup others(12): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91925516 | |||||
chr10:91925516
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0002g0306a0001c0001t0003g0177 | 2 | HG02040.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.14+1427_14+1439dup others(13): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91925516 | |||||
chr10:91925516
|
C | CTTTTTTT others(7): Show |
2 | a0001c0001t0003g0179a0001c0001t0006g0178 | 2 | HG02523.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.14+1439_14+1440ins others(14): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91925516 | |||||
chr10:91925516
|
C | CTTTTTTT others(8): Show |
43 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(40): Show | 43 | HG00423.hp1 HG00544.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.14+1439_14+1440ins others(15): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91925516 | |||||
chr10:91925516
|
C | CTTTTTTT others(9): Show |
12 | a0001c0001t0003g0220a0001c0001t0003g0221a0001c0001t0003g0222others(9): Show | 12 | HG00140.hp2 HG01070.hp1 HG01109.hp1 others(9): Show |
intron_variant | MODIFIER | c.14+1439_14+1440ins others(16): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91925516 | |||||
chr10:91925516
|
C | CTTTTTTT others(10): Show |
1 | a0001c0001t0003g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.14+1439_14+1440ins others(17): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91925516 | |||||
chr10:91925516
|
C | CTTTTTTT others(11): Show |
2 | a0001c0001t0003g0231a0001c0001t0003g0312 | 2 | NA20805.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.14+1439_14+1440ins others(18): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91925516 | |||||
chr10:91925677
|
A | G | 90 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.14+1587A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91925677 | ||||||
chr10:91925861
|
G | A | 10 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(7): Show | 10 | HG02074.hp2 NA18952.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.14+1771G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91925861 | ||||||
chr10:91926124
|
T | A | 1 | a0001c0001t0001g0003 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.14+2034T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91926124 | ||||||
chr10:91926407
|
A | G | 1 | a0001c0001t0001g0089 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.14+2317A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91926407 | ||||||
chr10:91926596
|
C | G | 1 | a0001c0001t0003g0219 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.14+2506C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91926596 | ||||||
chr10:91926682
|
A | G | 1 | a0001c0001t0002g0301 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.14+2592A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91926682 | ||||||
chr10:91927040
|
C | G | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.14+2950C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927040 | ||||||
chr10:91927094
|
C | T | 90 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 90 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.14+3004C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927094 | ||||||
chr10:91927141
|
AT | A | 253 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(250): Show | 254 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(251): Show |
intron_variant | MODIFIER | c.14+3065delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91927141 | |||||
chr10:91927184
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | NA18985.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.14+3094G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927184 | ||||||
chr10:91927195
|
A | G | 90 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 90 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.14+3105A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927195 | ||||||
chr10:91927208
|
G | C | 1 | a0002c0005t0003g0186 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.14+3118G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927208 | ||||||
chr10:91927319
|
G | A | 1 | a0001c0001t0002g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.14+3229G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927319 | ||||||
chr10:91927514
|
A | G | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.14+3424A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927514 | ||||||
chr10:91927545
|
A | T | 18 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0001g0129others(15): Show | 18 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.14+3455A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927545 | ||||||
chr10:91927617
|
C | T | 1 | a0001c0001t0013g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.14+3527C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927617 | ||||||
chr10:91927815
|
C | A | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.14+3725C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927815 | ||||||
chr10:91927816
|
A | C | 1 | a0001c0001t0002g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.14+3726A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927816 | ||||||
chr10:91927863
|
G | A | 8 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(5): Show | 8 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.14+3773G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927863 | ||||||
chr10:91927939
|
G | T | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | NA18985.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.14+3849G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927939 | ||||||
chr10:91927980
|
C | CT | 28 | a0001c0001t0001g0140a0001c0001t0001g0151a0001c0001t0002g0170others(25): Show | 28 | HG00423.hp2 HG00642.hp1 HG00673.hp1 others(25): Show |
intron_variant | MODIFIER | c.14+3909dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91927980 | |||||
chr10:91927980
|
CT | C | 72 | a0001c0001t0001g0081a0001c0001t0001g0082a0001c0001t0001g0083others(69): Show | 72 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.14+3909delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91927980 | |||||
chr10:91927980
|
CTT | C | 119 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(116): Show | 120 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.14+3908_14+3909del others(2): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91927980 | |||||
chr10:91927989
|
T | C | 2 | a0001c0001t0003g0187a0001c0001t0003g0188 | 2 | NA19001.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.14+3899T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91927989 | ||||||
chr10:91928116
|
A | AT | 103 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(100): Show | 103 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.14+4031dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91928116 | |||||
chr10:91928293
|
C | G | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.14+4203C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928293 | ||||||
chr10:91928345
|
A | G | 1 | a0001c0001t0003g0216 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.14+4255A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928345 | ||||||
chr10:91928367
|
G | A | 1 | a0001c0001t0002g0162 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.14+4277G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928367 | ||||||
chr10:91928383
|
A | G | 1 | a0001c0001t0003g0215 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.14+4293A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928383 | ||||||
chr10:91928408
|
T | G | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.14+4318T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928408 | ||||||
chr10:91928502
|
A | C | 1 | a0001c0001t0002g0291 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.14+4412A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928502 | ||||||
chr10:91928541
|
A | T | 1 | a0001c0001t0003g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.14+4451A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928541 | ||||||
chr10:91928697
|
G | A | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.14+4607G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928697 | ||||||
chr10:91928714
|
C | T | 3 | a0001c0001t0007g0321a0001c0001t0007g0322a0001c0001t0007g0323 | 3 | HG02717.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.14+4624C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928714 | ||||||
chr10:91928760
|
T | TC | 28 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(25): Show | 28 | HG00609.hp1 HG00639.hp2 HG00733.hp2 others(25): Show |
intron_variant | MODIFIER | c.14+4683dupC | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91928760 | |||||
chr10:91928760
|
T | TCC | 54 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(51): Show | 54 | HG00438.hp1 HG00544.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.14+4682_14+4683dup others(2): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91928760 | |||||
chr10:91928760
|
TCCC | T | 56 | a0001c0001t0001g0101a0001c0001t0001g0102a0001c0001t0001g0103others(53): Show | 57 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(54): Show |
intron_variant | MODIFIER | c.14+4681_14+4683del others(3): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91928760 | |||||
chr10:91928760
|
TCCCC | T | 152 | a0001c0001t0001g0120a0001c0001t0002g0162a0001c0001t0002g0165others(149): Show | 152 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(149): Show |
intron_variant | MODIFIER | c.14+4680_14+4683del others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91928760 | |||||
chr10:91928769
|
C | G | 4 | a0001c0001t0002g0162a0001c0001t0002g0167a0001c0001t0002g0168others(1): Show | 4 | HG01070.hp2 HG01928.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.14+4679C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928769 | ||||||
chr10:91928773
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.14+4683C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928773 | ||||||
chr10:91928778
|
C | A | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.14+4688C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928778 | ||||||
chr10:91928955
|
T | C | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.14+4865T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91928955 | ||||||
chr10:91929208
|
T | A | 2 | a0001c0001t0002g0246a0001c0001t0002g0247 | 2 | NA18939.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.14+5118T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91929208 | ||||||
chr10:91929240
|
A | G | 13 | a0001c0001t0002g0313a0001c0001t0002g0325a0001c0001t0004g0314others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.14+5150A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91929240 | ||||||
chr10:91929394
|
A | C | 7 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.14+5304A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91929394 | ||||||
chr10:91929512
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.14+5422A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91929512 | ||||||
chr10:91929608
|
G | T | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.14+5518G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91929608 | ||||||
chr10:91929685
|
G | T | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.14+5595G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91929685 | ||||||
chr10:91929746
|
A | G | 167 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.14+5656A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91929746 | ||||||
chr10:91929782
|
T | C | 318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(315): Show | 319 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.14+5692T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91929782 | ||||||
chr10:91929825
|
A | AT | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.14+5737dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | INFO_REALIGN_3_PRIME | chr10 | 91929825 | |||||
chr10:91929978
|
A | G | 1 | a0001c0001t0002g0290 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.15-5679A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91929978 | ||||||
chr10:91930028
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.15-5629G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91930028 | ||||||
chr10:91930067
|
A | T | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.15-5590A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91930067 | ||||||
chr10:91930613
|
A | G | 1 | a0001c0001t0002g0289 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.15-5044A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91930613 | ||||||
chr10:91930695
|
C | T | 1 | a0001c0001t0001g0118 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.15-4962C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91930695 | ||||||
chr10:91930812
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.15-4845T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91930812 | ||||||
chr10:91930814
|
G | T | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.15-4843G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91930814 | ||||||
chr10:91930861
|
T | C | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.15-4796T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91930861 | ||||||
chr10:91930874
|
A | G | 1 | a0001c0001t0001g0086 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.15-4783A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91930874 | ||||||
chr10:91931024
|
T | C | 1 | a0001c0001t0003g0180 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.15-4633T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91931024 | ||||||
chr10:91931272
|
C | A | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.15-4385C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91931272 | ||||||
chr10:91931431
|
A | G | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.15-4226A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91931431 | ||||||
chr10:91931517
|
G | A | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.15-4140G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91931517 | ||||||
chr10:91931687
|
G | A | 3 | a0001c0001t0002g0291a0001c0001t0002g0294a0001c0001t0002g0295 | 3 | NA18944.hp1 NA18965.hp2 NA19001.hp1 |
intron_variant | MODIFIER | c.15-3970G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91931687 | ||||||
chr10:91931699
|
G | A | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 137 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.15-3958G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91931699 | ||||||
chr10:91931796
|
T | C | 1 | a0001c0001t0003g0220 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.15-3861T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91931796 | ||||||
chr10:91932083
|
A | G | 103 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(100): Show | 103 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.15-3574A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91932083 | ||||||
chr10:91932101
|
T | G | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.15-3556T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91932101 | ||||||
chr10:91932186
|
C | A | 5 | a0001c0001t0003g0185a0001c0001t0003g0189a0001c0001t0003g0190others(2): Show | 5 | HG00423.hp1 HG02083.hp1 NA18950.hp2 others(2): Show |
intron_variant | MODIFIER | c.15-3471C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91932186 | ||||||
chr10:91932254
|
A | G | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.15-3403A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91932254 | ||||||
chr10:91932335
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.15-3322A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91932335 | ||||||
chr10:91932723
|
A | G | 8 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(5): Show | 8 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.15-2934A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91932723 | ||||||
chr10:91932800
|
A | G | 2 | a0001c0001t0001g0100a0001c0001t0001g0117 | 2 | HG01192.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.15-2857A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91932800 | ||||||
chr10:91933093
|
T | C | 1 | a0001c0002t0001g0160 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.15-2564T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91933093 | ||||||
chr10:91933120
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15-2537A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91933120 | ||||||
chr10:91933156
|
AAACAGTA others(13): Show |
A | 1 | a0008c0007t0002g0288 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.15-2500_15-2481del others(20): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91933156 | ||||||
chr10:91933262
|
A | G | 167 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(164): Show | 167 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.15-2395A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91933262 | ||||||
chr10:91933421
|
C | T | 1 | a0001c0001t0003g0312 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.15-2236C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91933421 | ||||||
chr10:91933446
|
C | T | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.15-2211C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91933446 | ||||||
chr10:91933548
|
G | A | 90 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.15-2109G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91933548 | ||||||
chr10:91933755
|
T | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.15-1902T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91933755 | ||||||
chr10:91933923
|
G | C | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.15-1734G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91933923 | ||||||
chr10:91933928
|
G | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0128a0001c0001t0001g0129 | 3 | HG02965.hp2 HG03453.hp1 NA18946.hp1 |
intron_variant | MODIFIER | c.15-1729G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91933928 | ||||||
chr10:91934011
|
T | C | 1 | a0001c0001t0002g0241 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.15-1646T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91934011 | ||||||
chr10:91934361
|
C | T | 1 | a0001c0001t0002g0287 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.15-1296C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91934361 | ||||||
chr10:91934799
|
G | A | 2 | a0001c0001t0002g0248a0001c0001t0002g0249 | 2 | NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.15-858G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91934799 | ||||||
chr10:91934989
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.15-668A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91934989 | ||||||
chr10:91935075
|
G | C | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.15-582G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91935075 | ||||||
chr10:91935136
|
A | T | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.15-521A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91935136 | ||||||
chr10:91935140
|
A | T | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.15-517A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91935140 | ||||||
chr10:91935284
|
A | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02698.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.15-373A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91935284 | ||||||
chr10:91935319
|
C | A | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.15-338C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91935319 | ||||||
chr10:91935553
|
C | T | 20 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(17): Show | 21 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.15-104C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91935553 | ||||||
chr10:91935604
|
G | C | 1 | a0001c0001t0003g0228 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.15-53G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91935604 | ||||||
chr10:91935645
|
T | A | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.15-12T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 1/37 | chr10 | 91935645 | ||||||
chr10:91936066
|
T | G | 1 | a0001c0001t0003g0219 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.138+286T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91936066 | ||||||
chr10:91936273
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.138+493G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91936273 | ||||||
chr10:91936320
|
C | CA | 13 | a0001c0001t0002g0313a0001c0001t0002g0325a0001c0001t0004g0314others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.138+541dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr10 | 91936320 | |||||
chr10:91936406
|
A | AGGGGAGC others(19): Show |
142 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 143 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.138+627_138+652dup others(26): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr10 | 91936406 | |||||
chr10:91936407
|
G | A | 1 | a0008c0007t0002g0288 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.138+627G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91936407 | ||||||
chr10:91936472
|
C | T | 5 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0002g0237others(2): Show | 5 | NA18942.hp1 NA18950.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.138+692C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91936472 | ||||||
chr10:91936571
|
G | A | 1 | a0004c0008t0001g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.138+791G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91936571 | ||||||
chr10:91936791
|
T | G | 1 | a0001c0001t0002g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.138+1011T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91936791 | ||||||
chr10:91936818
|
G | A | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.138+1038G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91936818 | ||||||
chr10:91936942
|
A | G | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.138+1162A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91936942 | ||||||
chr10:91937012
|
C | CT | 65 | a0001c0001t0001g0157a0001c0001t0003g0153a0001c0001t0003g0161others(62): Show | 65 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.138+1246dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr10 | 91937012 | |||||
chr10:91937113
|
G | A | 1 | a0001c0001t0002g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.138+1333G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91937113 | ||||||
chr10:91937140
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.138+1360G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91937140 | ||||||
chr10:91937206
|
G | A | 89 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 89 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.138+1426G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91937206 | ||||||
chr10:91937229
|
G | A | 90 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.138+1449G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91937229 | ||||||
chr10:91937349
|
T | C | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.138+1569T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91937349 | ||||||
chr10:91937490
|
C | T | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.138+1710C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91937490 | ||||||
chr10:91937589
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.138+1809A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91937589 | ||||||
chr10:91937779
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.138+1999T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91937779 | ||||||
chr10:91937962
|
T | A | 2 | a0001c0001t0002g0232a0008c0007t0002g0288 | 2 | HG02004.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.139-1990T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91937962 | ||||||
chr10:91938386
|
A | G | 1 | a0001c0001t0002g0286 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.139-1566A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91938386 | ||||||
chr10:91938738
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.139-1214C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91938738 | ||||||
chr10:91938942
|
A | G | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.139-1010A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91938942 | ||||||
chr10:91938946
|
A | G | 1 | a0001c0001t0002g0285 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.139-1006A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91938946 | ||||||
chr10:91938975
|
C | CA | 13 | a0001c0001t0003g0181a0001c0001t0004g0314a0001c0001t0004g0315others(10): Show | 13 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.139-963dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr10 | 91938975 | |||||
chr10:91938975
|
CA | C | 138 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 139 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(136): Show |
intron_variant | MODIFIER | c.139-963delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | INFO_REALIGN_3_PRIME | chr10 | 91938975 | |||||
chr10:91938988
|
AAGG | A | 85 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(82): Show | 85 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.139-963_139-961del others(3): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91938988 | ||||||
chr10:91938989
|
A | G | 5 | a0001c0001t0001g0059a0001c0001t0001g0080a0001c0001t0001g0157others(2): Show | 5 | HG03098.hp1 HG03486.hp2 HG03927.hp2 others(2): Show |
intron_variant | MODIFIER | c.139-963A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91938989 | ||||||
chr10:91938990
|
G | A | 74 | a0001c0001t0002g0325a0001c0001t0003g0153a0001c0001t0003g0161others(71): Show | 74 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.139-962G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91938990 | ||||||
chr10:91938991
|
G | A | 1 | a0001c0001t0003g0192 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.139-961G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91938991 | ||||||
chr10:91939689
|
C | T | 1 | a0001c0001t0002g0284 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.139-263C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91939689 | ||||||
chr10:91939892
|
C | T | 25 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(22): Show | 25 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.139-60C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 2/37 | chr10 | 91939892 | ||||||
chr10:91940198
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(7): Show | 10 | HG00544.hp1 HG01928.hp2 HG01952.hp1 others(7): Show |
intron_variant | MODIFIER | c.253+132G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91940198 | ||||||
chr10:91940233
|
T | TA | 31 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(28): Show | 31 | HG00544.hp1 HG01928.hp2 HG01952.hp1 others(28): Show |
intron_variant | MODIFIER | c.253+179dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr10 | 91940233 | |||||
chr10:91940404
|
T | A | 2 | a0001c0001t0002g0254a0001c0001t0002g0284 | 2 | HG01169.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.253+338T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91940404 | ||||||
chr10:91940510
|
T | C | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.253+444T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91940510 | ||||||
chr10:91940625
|
A | G | 1 | a0001c0001t0001g0058 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.253+559A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91940625 | ||||||
chr10:91940775
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.253+709C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91940775 | ||||||
chr10:91940898
|
C | T | 1 | a0001c0001t0003g0229 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.253+832C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91940898 | ||||||
chr10:91941176
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.253+1110T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91941176 | ||||||
chr10:91941576
|
A | C | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.254-846A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91941576 | ||||||
chr10:91941576
|
A | G | 1 | a0001c0001t0002g0253 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.254-846A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91941576 | ||||||
chr10:91941584
|
A | G | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.254-838A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91941584 | ||||||
chr10:91941686
|
C | T | 1 | a0001c0001t0003g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.254-736C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91941686 | ||||||
chr10:91941705
|
A | C | 1 | a0004c0008t0001g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.254-717A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91941705 | ||||||
chr10:91941715
|
G | A | 328 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(325): Show | 329 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(326): Show |
intron_variant | MODIFIER | c.254-707G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91941715 | ||||||
chr10:91941730
|
T | C | 1 | a0001c0010t0001g0002 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.254-692T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91941730 | ||||||
chr10:91941892
|
A | G | 1 | a0008c0007t0002g0288 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.254-530A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91941892 | ||||||
chr10:91941993
|
T | A | 1 | a0008c0007t0002g0288 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.254-429T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91941993 | ||||||
chr10:91942093
|
G | A | 1 | a0001c0001t0003g0189 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.254-329G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91942093 | ||||||
chr10:91942216
|
T | A | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.254-206T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91942216 | ||||||
chr10:91942268
|
A | G | 1 | a0001c0001t0002g0283 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.254-154A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91942268 | ||||||
chr10:91942295
|
A | AAGTTT | 7 | a0001c0001t0002g0232a0001c0001t0002g0235a0001c0001t0002g0256others(4): Show | 7 | HG02004.hp1 HG02040.hp1 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.254-127_254-126ins others(5): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91942295 | ||||||
chr10:91942295
|
A | AAGTTTGT | 37 | a0001c0001t0002g0162a0001c0001t0002g0167a0001c0001t0002g0168others(34): Show | 37 | HG00438.hp2 HG01070.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.254-127_254-126ins others(7): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91942295 | ||||||
chr10:91942295
|
A | AAGTTTGT others(2): Show |
26 | a0001c0001t0002g0163a0001c0001t0002g0173a0001c0001t0002g0239others(23): Show | 26 | HG00423.hp2 HG00609.hp2 HG00673.hp1 others(23): Show |
intron_variant | MODIFIER | c.254-127_254-126ins others(9): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91942295 | ||||||
chr10:91942295
|
A | AAGTTTGT others(4): Show |
8 | a0001c0001t0002g0164a0001c0001t0002g0170a0001c0001t0002g0278others(5): Show | 8 | HG00140.hp1 HG01123.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.254-127_254-126ins others(11): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91942295 | ||||||
chr10:91942295
|
A | AAGTTTGT others(6): Show |
2 | a0001c0001t0002g0165a0001c0001t0002g0171 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.254-127_254-126ins others(13): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91942295 | ||||||
chr10:91942295
|
A | AAGTTTGT others(8): Show |
2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG00642.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.254-127_254-126ins others(15): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91942295 | ||||||
chr10:91942295
|
A | AAGTTTGT others(10): Show |
2 | a0001c0001t0002g0172a0001c0001t0002g0176 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.254-127_254-126ins others(17): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91942295 | ||||||
chr10:91942298
|
T | G | 86 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(83): Show | 86 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.254-124T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91942298 | ||||||
chr10:91942298
|
T | TTG | 12 | a0001c0001t0001g0094a0001c0001t0001g0133a0001c0001t0001g0134others(9): Show | 12 | HG00639.hp1 HG01258.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.254-92_254-91dupGT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr10 | 91942298 | |||||
chr10:91942298
|
TTG | T | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.254-92_254-91delGT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr10 | 91942298 | |||||
chr10:91942298
|
TTGTG | T | 6 | a0001c0001t0001g0040a0001c0001t0001g0070a0001c0001t0001g0079others(3): Show | 6 | HG00438.hp1 HG02040.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.254-94_254-91delGT others(2): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr10 | 91942298 | |||||
chr10:91942298
|
TTGTGTG | T | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(158): Show | 161 | HG00140.hp2 HG00423.hp1 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.254-96_254-91delGT others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr10 | 91942298 | |||||
chr10:91942298
|
TTGTGTGT others(1): Show |
T | 3 | a0001c0001t0007g0321a0001c0001t0007g0322a0001c0001t0007g0323 | 3 | HG02717.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.254-98_254-91delGT others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr10 | 91942298 | |||||
chr10:91942298
|
TTGTGTGT others(5): Show |
T | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.254-102_254-91delG others(11): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | INFO_REALIGN_3_PRIME | chr10 | 91942298 | |||||
chr10:91942357
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.254-65T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 3/37 | chr10 | 91942357 | ||||||
chr10:91942571
|
C | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.400+3C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91942571 | ||||||
chr10:91942648
|
C | T | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.400+80C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91942648 | ||||||
chr10:91942686
|
G | A | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.400+118G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91942686 | ||||||
chr10:91942868
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.400+300C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91942868 | ||||||
chr10:91942908
|
C | G | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.400+340C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91942908 | ||||||
chr10:91942908
|
C | T | 2 | a0001c0004t0001g0046a0001c0004t0001g0047 | 2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.400+340C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91942908 | ||||||
chr10:91942962
|
A | G | 1 | a0001c0001t0003g0216 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.400+394A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91942962 | ||||||
chr10:91942978
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.400+410A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91942978 | ||||||
chr10:91943072
|
G | T | 1 | a0001c0001t0002g0303 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.400+504G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943072 | ||||||
chr10:91943238
|
T | C | 1 | a0001c0001t0003g0193 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.400+670T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943238 | ||||||
chr10:91943239
|
G | A | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.400+671G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943239 | ||||||
chr10:91943245
|
C | T | 2 | a0001c0001t0002g0237a0001c0001t0002g0238 | 2 | NA18942.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.400+677C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943245 | ||||||
chr10:91943246
|
G | A | 2 | a0001c0001t0002g0292a0001c0001t0002g0296 | 2 | HG00673.hp1 NA19011.hp1 |
intron_variant | MODIFIER | c.400+678G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943246 | ||||||
chr10:91943403
|
G | C | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.400+835G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943403 | ||||||
chr10:91943493
|
C | A | 1 | a0008c0007t0002g0288 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.400+925C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943493 | ||||||
chr10:91943500
|
G | C | 3 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0151 | 3 | HG01891.hp2 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.400+932G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943500 | ||||||
chr10:91943521
|
T | C | 1 | a0001c0001t0003g0229 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.400+953T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943521 | ||||||
chr10:91943542
|
T | A | 2 | a0001c0001t0002g0248a0001c0001t0002g0249 | 2 | NA18969.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.400+974T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943542 | ||||||
chr10:91943624
|
T | C | 1 | a0001c0001t0003g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.400+1056T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943624 | ||||||
chr10:91943868
|
T | C | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.400+1300T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943868 | ||||||
chr10:91943877
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.400+1309G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91943877 | ||||||
chr10:91944106
|
G | A | 3 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0221 | 3 | HG00140.hp2 HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.400+1538G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91944106 | ||||||
chr10:91944157
|
T | TA | 310 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(307): Show | 311 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(308): Show |
intron_variant | MODIFIER | c.400+1601dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91944157 | |||||
chr10:91944165
|
A | T | 2 | a0001c0001t0002g0165a0001c0001t0002g0171 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.400+1597A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91944165 | ||||||
chr10:91944350
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.400+1782A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91944350 | ||||||
chr10:91944426
|
C | T | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.400+1858C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91944426 | ||||||
chr10:91944605
|
A | G | 1 | a0001c0001t0002g0285 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.400+2037A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91944605 | ||||||
chr10:91944707
|
C | T | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.400+2139C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91944707 | ||||||
chr10:91944856
|
C | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.400+2288C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91944856 | ||||||
chr10:91944950
|
A | G | 12 | a0001c0001t0002g0248a0001c0001t0002g0249a0001c0001t0002g0252others(9): Show | 12 | HG00609.hp2 HG01069.hp1 HG01099.hp1 others(9): Show |
intron_variant | MODIFIER | c.400+2382A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91944950 | ||||||
chr10:91944981
|
T | C | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156 | 3 | HG02280.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.400+2413T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91944981 | ||||||
chr10:91945046
|
C | G | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.400+2478C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91945046 | ||||||
chr10:91945103
|
C | T | 1 | a0001c0001t0001g0013 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.400+2535C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91945103 | ||||||
chr10:91945274
|
G | T | 1 | a0001c0001t0003g0179 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.400+2706G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91945274 | ||||||
chr10:91945287
|
T | A | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.400+2719T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91945287 | ||||||
chr10:91945308
|
T | A | 6 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108others(3): Show | 7 | HG00733.hp1 HG01175.hp1 HG01358.hp2 others(4): Show |
intron_variant | MODIFIER | c.400+2740T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91945308 | ||||||
chr10:91945435
|
G | A | 1 | a0001c0001t0001g0024 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.400+2867G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91945435 | ||||||
chr10:91945670
|
G | C | 2 | a0001c0001t0002g0237a0001c0001t0002g0238 | 2 | NA18942.hp1 NA19054.hp2 |
intron_variant | MODIFIER | c.400+3102G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91945670 | ||||||
chr10:91945735
|
A | G | 7 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG01109.hp2 HG02257.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.400+3167A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91945735 | ||||||
chr10:91945964
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.400+3396A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91945964 | ||||||
chr10:91946075
|
T | G | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.400+3507T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91946075 | ||||||
chr10:91946178
|
G | A | 2 | a0001c0001t0004g0314a0001c0001t0004g0316 | 2 | HG02647.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.400+3610G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91946178 | ||||||
chr10:91946232
|
G | T | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.400+3664G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91946232 | ||||||
chr10:91946276
|
T | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.400+3708T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91946276 | ||||||
chr10:91946315
|
C | T | 1 | a0001c0001t0002g0173 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.400+3747C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91946315 | ||||||
chr10:91946420
|
A | G | 1 | a0001c0001t0001g0078 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.400+3852A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91946420 | ||||||
chr10:91946655
|
A | G | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.400+4087A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91946655 | ||||||
chr10:91946870
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.400+4302C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91946870 | ||||||
chr10:91946961
|
T | C | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.400+4393T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91946961 | ||||||
chr10:91947015
|
T | A | 1 | a0001c0001t0002g0162 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.401-4388T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91947015 | ||||||
chr10:91947035
|
G | T | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.401-4368G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91947035 | ||||||
chr10:91947088
|
C | T | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.401-4315C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91947088 | ||||||
chr10:91947142
|
C | G | 1 | a0001c0001t0002g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.401-4261C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91947142 | ||||||
chr10:91947226
|
T | G | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 137 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.401-4177T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91947226 | ||||||
chr10:91947297
|
A | C | 4 | a0001c0001t0005g0141a0001c0001t0005g0142a0001c0001t0005g0143others(1): Show | 4 | HG02559.hp2 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-4106A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91947297 | ||||||
chr10:91947412
|
A | C | 1 | a0001c0001t0001g0099 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.401-3991A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91947412 | ||||||
chr10:91947543
|
C | G | 90 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.401-3860C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91947543 | ||||||
chr10:91947735
|
C | CA | 183 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(180): Show | 184 | HG00423.hp2 HG00438.hp1 HG00544.hp1 others(181): Show |
intron_variant | MODIFIER | c.401-3646dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91947735 | |||||
chr10:91947735
|
C | CAA | 19 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0025others(16): Show | 19 | HG00140.hp1 HG00438.hp2 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.401-3647_401-3646d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91947735 | |||||
chr10:91947735
|
CAA | C | 17 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(14): Show | 17 | HG00639.hp1 HG02257.hp2 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.401-3647_401-3646d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91947735 | |||||
chr10:91947735
|
CAAAAAAA | C | 63 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.401-3652_401-3646d others(9): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91947735 | |||||
chr10:91947893
|
CAG | C | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.401-3508_401-3507d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91947893 | |||||
chr10:91948202
|
C | G | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.401-3201C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91948202 | ||||||
chr10:91948202
|
CCT | C | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.401-3200_401-3199d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91948202 | ||||||
chr10:91948369
|
C | CTATT | 5 | a0001c0001t0001g0080a0001c0001t0001g0099a0001c0001t0001g0105others(2): Show | 5 | HG03098.hp1 HG03209.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.401-2999_401-2996d others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91948369 | |||||
chr10:91948369
|
CTATT | C | 174 | a0001c0001t0001g0071a0001c0001t0001g0122a0001c0001t0001g0124others(171): Show | 174 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(171): Show |
intron_variant | MODIFIER | c.401-2999_401-2996d others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91948369 | |||||
chr10:91948599
|
C | T | 13 | a0001c0001t0002g0313a0001c0001t0002g0325a0001c0001t0004g0314others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.401-2804C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91948599 | ||||||
chr10:91948620
|
G | A | 3 | a0001c0001t0002g0273a0001c0001t0002g0274a0001c0013t0002g0091 | 3 | HG00609.hp2 NA18962.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.401-2783G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91948620 | ||||||
chr10:91948699
|
T | TA | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.401-2689dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91948699 | |||||
chr10:91948699
|
TA | T | 100 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(97): Show | 100 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.401-2689delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91948699 | |||||
chr10:91948875
|
G | T | 318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(315): Show | 319 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.401-2528G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91948875 | ||||||
chr10:91948992
|
G | A | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.401-2411G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91948992 | ||||||
chr10:91949174
|
T | G | 311 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(308): Show | 312 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(309): Show |
intron_variant | MODIFIER | c.401-2229T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91949174 | ||||||
chr10:91949262
|
G | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02698.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.401-2141G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91949262 | ||||||
chr10:91949279
|
G | C | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.401-2124G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91949279 | ||||||
chr10:91949355
|
C | T | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.401-2048C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91949355 | ||||||
chr10:91949526
|
T | C | 1 | a0001c0001t0001g0007 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.401-1877T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91949526 | ||||||
chr10:91949611
|
AATTTTAG others(8): Show |
A | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.401-1765_401-1751d others(17): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91949611 | |||||
chr10:91949716
|
T | A | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.401-1687T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91949716 | ||||||
chr10:91950036
|
G | T | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.401-1367G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950036 | ||||||
chr10:91950085
|
T | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.401-1318T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950085 | ||||||
chr10:91950147
|
G | GTGT | 13 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0198others(10): Show | 13 | HG00140.hp2 HG00673.hp2 HG01069.hp2 others(10): Show |
intron_variant | MODIFIER | c.401-1254_401-1253i others(5): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91950147 | |||||
chr10:91950148
|
T | TGTTG | 21 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0185others(18): Show | 21 | HG01123.hp2 HG01169.hp1 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.401-1254_401-1253i others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91950148 | |||||
chr10:91950148
|
T | TGTTGG | 24 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0183others(21): Show | 24 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.401-1254_401-1253i others(7): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91950148 | |||||
chr10:91950148
|
T | TGTTGGGG others(4): Show |
1 | a0001c0001t0003g0177 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.401-1254_401-1253i others(13): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91950148 | |||||
chr10:91950149
|
G | C | 7 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG01109.hp2 HG02257.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.401-1254G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950149 | ||||||
chr10:91950151
|
G | C | 1 | a0001c0001t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.401-1252G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950151 | ||||||
chr10:91950155
|
G | T | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.401-1248G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950155 | ||||||
chr10:91950155
|
GGGC | G | 86 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(83): Show | 86 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.401-1245_401-1243d others(5): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91950155 | |||||
chr10:91950156
|
GGC | G | 38 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0100others(35): Show | 39 | HG00733.hp1 HG00735.hp1 HG01081.hp2 others(36): Show |
intron_variant | MODIFIER | c.401-1245_401-1244d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91950156 | |||||
chr10:91950157
|
GC | G | 98 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(95): Show | 98 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.401-1245delC | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950157 | ||||||
chr10:91950158
|
C | G | 83 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0019others(80): Show | 83 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.401-1245C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950158 | ||||||
chr10:91950162
|
A | G | 204 | a0001c0001t0001g0021a0001c0001t0001g0038a0001c0001t0001g0068others(201): Show | 205 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.401-1241A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950162 | ||||||
chr10:91950168
|
G | T | 32 | a0001c0001t0003g0177a0001c0001t0003g0179a0001c0001t0003g0180others(29): Show | 32 | HG00544.hp2 HG00673.hp2 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.401-1235G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950168 | ||||||
chr10:91950197
|
C | T | 7 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(4): Show | 7 | HG00140.hp1 HG01070.hp2 HG01928.hp1 others(4): Show |
intron_variant | MODIFIER | c.401-1206C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950197 | ||||||
chr10:91950201
|
G | A | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.401-1202G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950201 | ||||||
chr10:91950216
|
G | A | 1 | a0001c0001t0003g0192 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.401-1187G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950216 | ||||||
chr10:91950346
|
C | CT | 108 | a0001c0001t0001g0062a0001c0001t0001g0079a0001c0001t0001g0084others(105): Show | 108 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.401-1044dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91950346 | |||||
chr10:91950412
|
C | T | 18 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(15): Show | 18 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.401-991C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950412 | ||||||
chr10:91950465
|
A | G | 18 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(15): Show | 18 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.401-938A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950465 | ||||||
chr10:91950654
|
G | A | 1 | a0001c0001t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.401-749G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950654 | ||||||
chr10:91950807
|
A | T | 1 | a0001c0001t0002g0271 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.401-596A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91950807 | ||||||
chr10:91950832
|
A | AT | 156 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(153): Show | 156 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(153): Show |
intron_variant | MODIFIER | c.401-553dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91950832 | |||||
chr10:91950832
|
A | ATT | 54 | a0001c0001t0001g0012a0001c0001t0001g0037a0001c0001t0001g0044others(51): Show | 55 | HG00544.hp1 HG00639.hp1 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.401-554_401-553dup others(2): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91950832 | |||||
chr10:91950832
|
A | ATTT | 6 | a0001c0001t0001g0100a0001c0001t0001g0118a0001c0001t0001g0122others(3): Show | 6 | HG00735.hp1 HG01192.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.401-555_401-553dup others(3): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91950832 | |||||
chr10:91950832
|
A | ATTTT | 10 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(7): Show | 10 | HG01081.hp2 HG02486.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.401-556_401-553dup others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | INFO_REALIGN_3_PRIME | chr10 | 91950832 | |||||
chr10:91951028
|
G | A | 1 | a0001c0001t0003g0215 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.401-375G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91951028 | ||||||
chr10:91951035
|
A | T | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.401-368A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91951035 | ||||||
chr10:91951077
|
C | T | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.401-326C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91951077 | ||||||
chr10:91951150
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.401-253A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91951150 | ||||||
chr10:91951196
|
A | T | 3 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0086 | 3 | NA18964.hp2 NA18987.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.401-207A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91951196 | ||||||
chr10:91951243
|
T | A | 7 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0109others(4): Show | 7 | HG01099.hp2 HG01496.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.401-160T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91951243 | ||||||
chr10:91951264
|
T | G | 1 | a0001c0001t0002g0306 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.401-139T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91951264 | ||||||
chr10:91951399
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | splice_region_variant&intron_variant | LOW | c.401-4A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 4/37 | chr10 | 91951399 | ||||||
chr10:91951756
|
C | T | 2 | a0001c0001t0002g0274a0001c0013t0002g0091 | 2 | HG00609.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.564+190C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91951756 | ||||||
chr10:91951918
|
AGATAT | A | 3 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0221 | 3 | HG00140.hp2 HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.564+357_564+361del others(5): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | INFO_REALIGN_3_PRIME | chr10 | 91951918 | |||||
chr10:91952030
|
A | G | 2 | a0001c0001t0002g0254a0001c0001t0002g0284 | 2 | HG01169.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.564+464A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91952030 | ||||||
chr10:91952160
|
T | TTGTG | 12 | a0001c0001t0002g0313a0001c0001t0004g0314a0001c0001t0004g0315others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.564+612_564+615dup others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | INFO_REALIGN_3_PRIME | chr10 | 91952160 | |||||
chr10:91952160
|
TTG | T | 89 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 89 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.564+614_564+615del others(2): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | INFO_REALIGN_3_PRIME | chr10 | 91952160 | |||||
chr10:91952162
|
G | T | 1 | a0001c0001t0001g0011 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.564+596G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91952162 | ||||||
chr10:91952182
|
A | G | 4 | a0001c0001t0001g0149a0001c0001t0002g0264a0001c0001t0002g0279others(1): Show | 4 | HG02735.hp1 HG03041.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.564+616A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91952182 | ||||||
chr10:91952184
|
A | T | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 144 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.564+618A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91952184 | ||||||
chr10:91952260
|
G | A | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.564+694G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91952260 | ||||||
chr10:91952306
|
C | T | 1 | a0001c0003t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.564+740C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91952306 | ||||||
chr10:91952442
|
G | A | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.564+876G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91952442 | ||||||
chr10:91952488
|
C | G | 2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG00639.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.564+922C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91952488 | ||||||
chr10:91952760
|
T | C | 7 | a0001c0001t0003g0161a0001c0001t0003g0196a0001c0001t0003g0197others(4): Show | 7 | HG01069.hp2 HG01123.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.565-977T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91952760 | ||||||
chr10:91952869
|
A | G | 1 | a0001c0001t0003g0222 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.565-868A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91952869 | ||||||
chr10:91952903
|
ATGGGCAG others(13): Show |
A | 1 | a0001c0001t0002g0277 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.565-828_565-809del others(20): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | INFO_REALIGN_3_PRIME | chr10 | 91952903 | |||||
chr10:91953316
|
T | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 89 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.565-421T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91953316 | ||||||
chr10:91953606
|
A | G | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.565-131A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91953606 | ||||||
chr10:91953648
|
T | G | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.565-89T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 5/37 | chr10 | 91953648 | ||||||
chr10:91954001
|
T | G | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.701+128T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91954001 | ||||||
chr10:91954050
|
A | G | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.701+177A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91954050 | ||||||
chr10:91954242
|
G | C | 1 | a0001c0001t0002g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.701+369G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91954242 | ||||||
chr10:91954411
|
T | G | 1 | a0001c0001t0001g0120 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.701+538T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91954411 | ||||||
chr10:91954538
|
TA | T | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.701+675delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | INFO_REALIGN_3_PRIME | chr10 | 91954538 | |||||
chr10:91954625
|
G | A | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.701+752G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91954625 | ||||||
chr10:91954662
|
A | G | 4 | a0001c0001t0005g0141a0001c0001t0005g0142a0001c0001t0005g0143others(1): Show | 4 | HG02559.hp2 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.701+789A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91954662 | ||||||
chr10:91954759
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.701+886T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91954759 | ||||||
chr10:91954809
|
C | A | 1 | a0001c0001t0002g0271 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.701+936C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91954809 | ||||||
chr10:91954825
|
C | T | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.701+952C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91954825 | ||||||
chr10:91954868
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.701+995A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91954868 | ||||||
chr10:91954958
|
G | A | 1 | a0001c0001t0003g0180 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.701+1085G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91954958 | ||||||
chr10:91954981
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.701+1108A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91954981 | ||||||
chr10:91955166
|
A | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.701+1293A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91955166 | ||||||
chr10:91955173
|
T | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 89 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.701+1300T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91955173 | ||||||
chr10:91955195
|
C | G | 8 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(5): Show | 8 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.701+1322C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91955195 | ||||||
chr10:91955437
|
GTA | G | 4 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG02280.hp2 HG03516.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.702-1085_702-1084d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | INFO_REALIGN_3_PRIME | chr10 | 91955437 | |||||
chr10:91955689
|
T | C | 2 | a0001c0001t0002g0241a0001c0001t0002g0246 | 2 | NA18939.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.702-839T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91955689 | ||||||
chr10:91955719
|
A | C | 1 | a0001c0001t0001g0022 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.702-809A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91955719 | ||||||
chr10:91955743
|
A | G | 1 | a0001c0001t0002g0264 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.702-785A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91955743 | ||||||
chr10:91956177
|
A | G | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.702-351A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91956177 | ||||||
chr10:91956254
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.702-274A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91956254 | ||||||
chr10:91956339
|
T | G | 1 | a0001c0001t0002g0275 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.702-189T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 6/37 | chr10 | 91956339 | ||||||
chr10:91956834
|
T | C | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 145 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.831+177T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 7/37 | chr10 | 91956834 | ||||||
chr10:91956922
|
C | T | 1 | a0001c0004t0001g0046 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.831+265C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 7/37 | chr10 | 91956922 | ||||||
chr10:91957027
|
A | G | 90 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.832-198A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 7/37 | chr10 | 91957027 | ||||||
chr10:91957075
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0056 | 3 | HG00733.hp2 HG00738.hp1 HG03710.hp2 |
intron_variant | MODIFIER | c.832-150T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 7/37 | chr10 | 91957075 | ||||||
chr10:91957142
|
G | C | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 323 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(320): Show |
intron_variant | MODIFIER | c.832-83G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 7/37 | chr10 | 91957142 | ||||||
chr10:91957432
|
C | T | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.900+139C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 8/37 | chr10 | 91957432 | ||||||
chr10:91957510
|
T | G | 1 | a0001c0001t0001g0056 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.900+217T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 8/37 | chr10 | 91957510 | ||||||
chr10:91957630
|
T | A | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.900+337T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 8/37 | chr10 | 91957630 | ||||||
chr10:91957675
|
A | G | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.900+382A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 8/37 | chr10 | 91957675 | ||||||
chr10:91957733
|
A | C | 2 | a0001c0001t0005g0141a0001c0001t0005g0142 | 2 | HG02559.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.900+440A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 8/37 | chr10 | 91957733 | ||||||
chr10:91958087
|
C | T | 1 | a0001c0001t0003g0190 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.900+794C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 8/37 | chr10 | 91958087 | ||||||
chr10:91958106
|
T | C | 1 | a0001c0001t0002g0258 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.900+813T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 8/37 | chr10 | 91958106 | ||||||
chr10:91958122
|
C | T | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.900+829C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 8/37 | chr10 | 91958122 | ||||||
chr10:91958427
|
C | T | 1 | a0001c0001t0002g0300 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.901-638C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 8/37 | chr10 | 91958427 | ||||||
chr10:91958559
|
G | A | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.901-506G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 8/37 | chr10 | 91958559 | ||||||
chr10:91958703
|
G | A | 311 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(308): Show | 312 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(309): Show |
intron_variant | MODIFIER | c.901-362G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 8/37 | chr10 | 91958703 | ||||||
chr10:91959028
|
A | G | 6 | a0001c0001t0002g0244a0001c0001t0002g0262a0001c0001t0002g0263others(3): Show | 6 | HG00423.hp2 NA18946.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.901-37A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 8/37 | chr10 | 91959028 | ||||||
chr10:91959330
|
G | T | 90 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.990+176G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959330 | ||||||
chr10:91959510
|
T | C | 91 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(88): Show | 91 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(88): Show |
intron_variant | MODIFIER | c.991-275T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959510 | ||||||
chr10:91959706
|
T | C | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.991-79T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959706 | ||||||
chr10:91959718
|
A | ATG | 4 | a0001c0001t0003g0211a0001c0001t0003g0225a0001c0001t0003g0228others(1): Show | 4 | HG00544.hp2 HG01109.hp1 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.991-45_991-44dupGT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959718 | |||||
chr10:91959718
|
A | ATGTG | 42 | a0001c0001t0003g0161a0001c0001t0003g0177a0001c0001t0003g0181others(39): Show | 42 | HG00140.hp2 HG00423.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.991-47_991-44dupGT others(2): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959718 | |||||
chr10:91959718
|
A | ATGTGTG | 13 | a0001c0001t0003g0179a0001c0001t0003g0180a0001c0001t0003g0196others(10): Show | 13 | HG01069.hp2 HG01123.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.991-49_991-44dupGT others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959718 | |||||
chr10:91959732
|
GTGTGTGT others(7): Show |
G | 1 | a0001c0001t0002g0286 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.991-51_991-38delGT others(12): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959732 | |||||
chr10:91959738
|
GTGTATA | G | 7 | a0001c0001t0002g0245a0001c0001t0002g0258a0001c0001t0002g0266others(4): Show | 7 | HG01169.hp2 HG02027.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.991-45_991-40delGT others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959738 | |||||
chr10:91959738
|
GTGTATAT others(1): Show |
G | 52 | a0001c0001t0002g0165a0001c0001t0002g0171a0001c0001t0002g0172others(49): Show | 52 | HG00438.hp2 HG00609.hp2 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.991-45_991-38delGT others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959738 | |||||
chr10:91959738
|
GTGTATAT others(3): Show |
G | 5 | a0001c0001t0002g0244a0001c0001t0002g0262a0001c0001t0002g0263others(2): Show | 5 | HG00423.hp2 NA18946.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.991-45_991-36delGT others(8): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959738 | |||||
chr10:91959740
|
G | A | 1 | a0001c0001t0005g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.991-45G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959740 | ||||||
chr10:91959740
|
G | GTGTGTGT others(3): Show |
1 | a0001c0001t0003g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.991-44_991-43insGT others(8): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959740 | |||||
chr10:91959740
|
GTA | G | 12 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.991-15_991-14delAT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959740 | |||||
chr10:91959740
|
GTATA | G | 5 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0134others(2): Show | 5 | HG02257.hp2 HG02622.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.991-17_991-14delAT others(2): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959740 | |||||
chr10:91959740
|
GTATATA | G | 14 | a0001c0001t0001g0130a0001c0001t0001g0154a0001c0001t0001g0155others(11): Show | 14 | HG01070.hp2 HG01255.hp1 HG01928.hp1 others(11): Show |
intron_variant | MODIFIER | c.991-19_991-14delAT others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959740 | |||||
chr10:91959740
|
GTATATAT others(1): Show |
G | 67 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0043others(64): Show | 68 | HG00140.hp1 HG00639.hp1 HG00673.hp1 others(65): Show |
intron_variant | MODIFIER | c.991-21_991-14delAT others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959740 | |||||
chr10:91959740
|
GTATATAT others(3): Show |
G | 73 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(70): Show | 73 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(70): Show |
intron_variant | MODIFIER | c.991-23_991-14delAT others(8): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959740 | |||||
chr10:91959740
|
GTATATAT others(5): Show |
G | 9 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0048others(6): Show | 9 | HG02886.hp1 NA18939.hp2 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.991-25_991-14delAT others(10): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959740 | |||||
chr10:91959740
|
GTATATAT others(7): Show |
G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.991-27_991-14delAT others(12): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | INFO_REALIGN_3_PRIME | chr10 | 91959740 | |||||
chr10:91959742
|
A | G | 57 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(54): Show | 57 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.991-43A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959742 | ||||||
chr10:91959744
|
A | G | 25 | a0001c0001t0003g0185a0001c0001t0003g0189a0001c0001t0003g0190others(22): Show | 25 | HG00423.hp1 HG00544.hp2 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.991-41A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959744 | ||||||
chr10:91959746
|
A | G | 13 | a0001c0001t0003g0223a0001c0001t0004g0314a0001c0001t0004g0315others(10): Show | 13 | HG01081.hp2 HG02055.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.991-39A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959746 | ||||||
chr10:91959748
|
A | G | 15 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(12): Show | 15 | HG01081.hp2 HG02055.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.991-37A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959748 | ||||||
chr10:91959750
|
A | G | 54 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0043others(51): Show | 55 | HG00733.hp1 HG00735.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.991-35A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959750 | ||||||
chr10:91959752
|
A | G | 18 | a0001c0001t0001g0036a0001c0001t0001g0041a0001c0001t0001g0061others(15): Show | 18 | HG02486.hp2 HG02572.hp2 HG02615.hp1 others(15): Show |
intron_variant | MODIFIER | c.991-33A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959752 | ||||||
chr10:91959754
|
A | G | 4 | a0001c0001t0001g0072a0001c0001t0006g0178a0001c0001t0006g0212others(1): Show | 4 | HG02886.hp1 NA18962.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.991-31A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959754 | ||||||
chr10:91959756
|
A | G | 5 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0006g0178others(2): Show | 5 | HG02895.hp1 HG03540.hp1 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.991-29A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959756 | ||||||
chr10:91959774
|
T | C | 18 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(15): Show | 18 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.991-11T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 9/37 | chr10 | 91959774 | ||||||
chr10:91959962
|
C | T | 1 | a0001c0001t0003g0206 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1087-16C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 10/37 | chr10 | 91959962 | ||||||
chr10:91960350
|
G | A | 8 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(5): Show | 8 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1263+196G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91960350 | ||||||
chr10:91960387
|
T | C | 21 | a0001c0001t0003g0153a0001c0001t0003g0185a0001c0001t0003g0189others(18): Show | 21 | HG00423.hp1 HG00642.hp2 HG01070.hp1 others(18): Show |
intron_variant | MODIFIER | c.1263+233T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91960387 | ||||||
chr10:91960407
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1263+253C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91960407 | ||||||
chr10:91960441
|
C | T | 18 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(15): Show | 18 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1263+287C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91960441 | ||||||
chr10:91960587
|
G | GT | 141 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 142 | HG00438.hp1 HG00609.hp1 HG00639.hp1 others(139): Show |
intron_variant | MODIFIER | c.1263+449dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | INFO_REALIGN_3_PRIME | chr10 | 91960587 | |||||
chr10:91960639
|
A | G | 1 | a0001c0001t0002g0172 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1263+485A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91960639 | ||||||
chr10:91960662
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1263+508A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91960662 | ||||||
chr10:91960842
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1263+688T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91960842 | ||||||
chr10:91960979
|
C | T | 1 | a0001c0001t0003g0191 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1263+825C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91960979 | ||||||
chr10:91961213
|
G | C | 11 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0131others(8): Show | 11 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.1263+1059G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91961213 | ||||||
chr10:91961251
|
C | A | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1263+1097C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91961251 | ||||||
chr10:91961268
|
A | G | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1263+1114A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91961268 | ||||||
chr10:91961450
|
CT | C | 245 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(242): Show | 246 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(243): Show |
intron_variant | MODIFIER | c.1264-1075delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | INFO_REALIGN_3_PRIME | chr10 | 91961450 | |||||
chr10:91961466
|
C | T | 311 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(308): Show | 312 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(309): Show |
intron_variant | MODIFIER | c.1264-1072C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91961466 | ||||||
chr10:91961484
|
A | G | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1264-1054A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91961484 | ||||||
chr10:91961632
|
C | T | 2 | a0001c0001t0002g0241a0001c0001t0002g0246 | 2 | NA18939.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.1264-906C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91961632 | ||||||
chr10:91961657
|
A | G | 2 | a0001c0001t0002g0278a0001c0001t0002g0287 | 2 | HG02015.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.1264-881A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91961657 | ||||||
chr10:91961886
|
G | A | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1264-652G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91961886 | ||||||
chr10:91961949
|
C | T | 107 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(104): Show | 107 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.1264-589C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91961949 | ||||||
chr10:91962203
|
A | G | 1 | a0001c0002t0001g0160 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1264-335A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91962203 | ||||||
chr10:91962263
|
T | A | 1 | a0001c0001t0001g0021 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.1264-275T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91962263 | ||||||
chr10:91962277
|
G | C | 1 | a0001c0001t0002g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1264-261G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91962277 | ||||||
chr10:91962306
|
ATAGT | A | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1264-228_1264-225d others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | INFO_REALIGN_3_PRIME | chr10 | 91962306 | |||||
chr10:91962314
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | NA18944.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1264-224G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91962314 | ||||||
chr10:91962442
|
A | G | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1264-96A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91962442 | ||||||
chr10:91962475
|
A | G | 1 | a0001c0001t0002g0247 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1264-63A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 11/37 | chr10 | 91962475 | ||||||
chr10:91962694
|
T | G | 1 | a0001c0001t0003g0230 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1404+16T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | chr10 | 91962694 | ||||||
chr10:91962814
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1404+136G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | chr10 | 91962814 | ||||||
chr10:91962926
|
T | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1404+248T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | chr10 | 91962926 | ||||||
chr10:91962994
|
G | T | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1404+316G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | chr10 | 91962994 | ||||||
chr10:91963002
|
A | T | 2 | a0001c0001t0003g0203a0001c0001t0003g0208 | 2 | NA18988.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1404+324A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | chr10 | 91963002 | ||||||
chr10:91963018
|
C | T | 3 | a0001c0001t0007g0321a0001c0001t0007g0322a0001c0001t0007g0323 | 3 | HG02717.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1404+340C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | chr10 | 91963018 | ||||||
chr10:91963294
|
C | G | 1 | a0001c0001t0001g0118 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1404+616C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | chr10 | 91963294 | ||||||
chr10:91963418
|
C | CA | 182 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(179): Show | 182 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(179): Show |
intron_variant | MODIFIER | c.1405-641dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | INFO_REALIGN_3_PRIME | chr10 | 91963418 | |||||
chr10:91963418
|
C | CAA | 10 | a0001c0001t0001g0005a0001c0001t0002g0262a0001c0001t0002g0282others(7): Show | 10 | HG01081.hp2 HG01261.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1405-642_1405-641d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | INFO_REALIGN_3_PRIME | chr10 | 91963418 | |||||
chr10:91963418
|
CA | C | 9 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(6): Show | 9 | HG01109.hp1 HG01243.hp1 HG01255.hp2 others(6): Show |
intron_variant | MODIFIER | c.1405-641delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | INFO_REALIGN_3_PRIME | chr10 | 91963418 | |||||
chr10:91963457
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1405-620G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | chr10 | 91963457 | ||||||
chr10:91963476
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1405-601G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | chr10 | 91963476 | ||||||
chr10:91963568
|
C | A | 1 | a0001c0003t0001g0125 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1405-509C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | chr10 | 91963568 | ||||||
chr10:91963706
|
T | G | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1405-371T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | chr10 | 91963706 | ||||||
chr10:91964067
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1405-10G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 12/37 | chr10 | 91964067 | ||||||
chr10:91964444
|
C | T | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1529+243C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91964444 | ||||||
chr10:91964509
|
G | A | 18 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(15): Show | 18 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.1529+308G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91964509 | ||||||
chr10:91964552
|
A | G | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156 | 3 | HG02280.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.1529+351A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91964552 | ||||||
chr10:91964710
|
A | G | 318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(315): Show | 319 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.1529+509A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91964710 | ||||||
chr10:91964783
|
C | T | 2 | a0001c0001t0005g0143a0001c0001t0005g0147 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1529+582C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91964783 | ||||||
chr10:91964831
|
G | C | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1529+630G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91964831 | ||||||
chr10:91964868
|
A | G | 1 | a0007c0015t0003g0227 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.1529+667A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91964868 | ||||||
chr10:91964886
|
A | G | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1529+685A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91964886 | ||||||
chr10:91964909
|
T | G | 1 | a0001c0001t0001g0040 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1529+708T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91964909 | ||||||
chr10:91965182
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1529+981G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91965182 | ||||||
chr10:91965412
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1529+1211A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91965412 | ||||||
chr10:91965590
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1530-1047C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91965590 | ||||||
chr10:91965591
|
G | A | 4 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG02280.hp2 HG02809.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.1530-1046G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91965591 | ||||||
chr10:91965719
|
A | G | 4 | a0001c0001t0003g0200a0001c0001t0003g0213a0001c0001t0003g0218others(1): Show | 4 | HG01516.hp2 HG01517.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1530-918A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91965719 | ||||||
chr10:91965721
|
A | T | 4 | a0001c0001t0003g0200a0001c0001t0003g0213a0001c0001t0003g0218others(1): Show | 4 | HG01516.hp2 HG01517.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.1530-916A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91965721 | ||||||
chr10:91965730
|
A | T | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1530-907A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91965730 | ||||||
chr10:91965756
|
A | G | 2 | a0001c0001t0001g0073a0001c0001t0001g0080 | 2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1530-881A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91965756 | ||||||
chr10:91966162
|
T | C | 1 | a0003c0014t0002g0255 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1530-475T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91966162 | ||||||
chr10:91966200
|
A | C | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1530-437A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91966200 | ||||||
chr10:91966333
|
C | T | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1530-304C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91966333 | ||||||
chr10:91966353
|
A | G | 1 | a0001c0001t0002g0252 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1530-284A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91966353 | ||||||
chr10:91966393
|
A | T | 1 | a0001c0001t0001g0041 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1530-244A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91966393 | ||||||
chr10:91966480
|
G | T | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1530-157G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91966480 | ||||||
chr10:91966550
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1530-87C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91966550 | ||||||
chr10:91966593
|
T | C | 1 | a0001c0001t0002g0256 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.1530-44T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91966593 | ||||||
chr10:91966597
|
A | G | 1 | a0001c0001t0002g0286 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1530-40A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 13/37 | chr10 | 91966597 | ||||||
chr10:91966809
|
A | C | 12 | a0001c0001t0002g0325a0001c0001t0004g0314a0001c0001t0004g0315others(9): Show | 12 | HG00738.hp2 HG01081.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1650+52A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91966809 | ||||||
chr10:91967395
|
C | T | 1 | a0001c0001t0013g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1650+638C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91967395 | ||||||
chr10:91967526
|
C | A | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1650+769C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91967526 | ||||||
chr10:91967768
|
T | C | 1 | a0001c0001t0003g0185 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1650+1011T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91967768 | ||||||
chr10:91967824
|
C | A | 94 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0086others(91): Show | 94 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.1650+1067C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91967824 | ||||||
chr10:91967859
|
A | G | 171 | a0001c0001t0001g0049a0001c0001t0001g0051a0001c0001t0001g0086others(168): Show | 171 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(168): Show |
intron_variant | MODIFIER | c.1650+1102A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91967859 | ||||||
chr10:91967862
|
C | A | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.1650+1105C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91967862 | ||||||
chr10:91967862
|
C | G | 1 | a0001c0001t0002g0301 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1650+1105C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91967862 | ||||||
chr10:91968201
|
ATCCT | A | 3 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0151 | 3 | HG01891.hp2 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1650+1452_1650+145 others(8): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91968201 | |||||
chr10:91968404
|
T | C | 1 | a0003c0014t0002g0255 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1650+1647T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91968404 | ||||||
chr10:91968539
|
A | G | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02698.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1650+1782A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91968539 | ||||||
chr10:91969040
|
A | AT | 7 | a0001c0001t0001g0005a0001c0001t0001g0023a0001c0001t0001g0089others(4): Show | 7 | HG01192.hp2 HG02074.hp1 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1650+2301dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91969040 | |||||
chr10:91969096
|
C | T | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02698.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1650+2339C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91969096 | ||||||
chr10:91969200
|
C | T | 2 | a0001c0001t0003g0187a0001c0001t0003g0188 | 2 | NA19001.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.1650+2443C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91969200 | ||||||
chr10:91969201
|
C | G | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1650+2444C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91969201 | ||||||
chr10:91969217
|
G | A | 1 | a0001c0001t0003g0209 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1650+2460G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91969217 | ||||||
chr10:91969578
|
T | C | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 144 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.1650+2821T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91969578 | ||||||
chr10:91969769
|
A | G | 1 | a0001c0001t0007g0322 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1650+3012A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91969769 | ||||||
chr10:91969962
|
G | GA | 6 | a0001c0001t0001g0124a0001c0001t0001g0134a0001c0001t0001g0326others(3): Show | 6 | HG02257.hp2 HG02451.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.1650+3219dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91969962 | |||||
chr10:91969962
|
GA | G | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1650+3219delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91969962 | |||||
chr10:91969979
|
C | T | 26 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(23): Show | 26 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1650+3222C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91969979 | ||||||
chr10:91969980
|
G | A | 1 | a0001c0001t0001g0329 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1650+3223G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91969980 | ||||||
chr10:91970015
|
A | T | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1650+3258A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91970015 | ||||||
chr10:91970025
|
A | T | 1 | a0001c0001t0005g0142 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1650+3268A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91970025 | ||||||
chr10:91970085
|
A | AT | 304 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(301): Show | 305 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(302): Show |
intron_variant | MODIFIER | c.1650+3340dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91970085 | |||||
chr10:91970232
|
T | C | 311 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(308): Show | 312 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(309): Show |
intron_variant | MODIFIER | c.1650+3475T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91970232 | ||||||
chr10:91970241
|
T | C | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1650+3484T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91970241 | ||||||
chr10:91970301
|
C | T | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1650+3544C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91970301 | ||||||
chr10:91970483
|
G | A | 1 | a0001c0001t0001g0014 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1650+3726G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91970483 | ||||||
chr10:91970587
|
C | A | 2 | a0001c0001t0001g0073a0001c0001t0001g0080 | 2 | HG01243.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.1650+3830C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91970587 | ||||||
chr10:91970723
|
A | G | 3 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0221 | 3 | HG00140.hp2 HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.1650+3966A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91970723 | ||||||
chr10:91970735
|
A | T | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.1650+3978A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91970735 | ||||||
chr10:91970835
|
C | T | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1650+4078C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91970835 | ||||||
chr10:91971153
|
T | C | 3 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0001t0002g0176 | 3 | HG00735.hp2 HG01433.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.1650+4396T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971153 | ||||||
chr10:91971188
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1650+4431A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971188 | ||||||
chr10:91971436
|
T | C | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1650+4679T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971436 | ||||||
chr10:91971469
|
CT | C | 241 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(238): Show | 242 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(239): Show |
intron_variant | MODIFIER | c.1650+4732delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91971469 | |||||
chr10:91971469
|
CTT | C | 68 | a0001c0001t0001g0011a0001c0001t0001g0045a0001c0001t0001g0052others(65): Show | 68 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.1650+4731_1650+473 others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91971469 | |||||
chr10:91971575
|
C | T | 1 | a0001c0001t0003g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1650+4818C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971575 | ||||||
chr10:91971612
|
C | T | 1 | a0001c0001t0002g0268 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1650+4855C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971612 | ||||||
chr10:91971621
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0109 | 2 | HG01496.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.1650+4864G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971621 | ||||||
chr10:91971629
|
G | A | 1 | a0001c0001t0002g0295 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1650+4872G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971629 | ||||||
chr10:91971629
|
G | C | 1 | a0001c0001t0002g0172 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1650+4872G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971629 | ||||||
chr10:91971634
|
A | G | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1650+4877A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971634 | ||||||
chr10:91971720
|
C | T | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1650+4963C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971720 | ||||||
chr10:91971838
|
AT | A | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1650+5092delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91971838 | |||||
chr10:91971860
|
A | G | 90 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.1650+5103A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971860 | ||||||
chr10:91971893
|
A | C | 1 | a0001c0001t0002g0303 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1650+5136A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971893 | ||||||
chr10:91971936
|
TG | T | 22 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(19): Show | 23 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.1650+5180delG | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91971936 | ||||||
chr10:91972183
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1650+5426A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91972183 | ||||||
chr10:91972256
|
T | A | 1 | a0001c0001t0002g0292 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1650+5499T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91972256 | ||||||
chr10:91972268
|
T | C | 1 | a0001c0002t0001g0132 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1650+5511T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91972268 | ||||||
chr10:91972522
|
G | A | 1 | a0001c0001t0002g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1650+5765G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91972522 | ||||||
chr10:91972529
|
T | C | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1650+5772T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91972529 | ||||||
chr10:91972984
|
T | A | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1650+6227T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91972984 | ||||||
chr10:91973162
|
G | A | 1 | a0001c0001t0003g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1650+6405G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91973162 | ||||||
chr10:91973229
|
TAGAC | T | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1650+6475_1650+647 others(8): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91973229 | |||||
chr10:91973570
|
A | T | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1650+6813A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91973570 | ||||||
chr10:91973587
|
G | A | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1650+6830G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91973587 | ||||||
chr10:91973670
|
C | T | 4 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 4 | HG02895.hp1 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-6784C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91973670 | ||||||
chr10:91973686
|
C | T | 1 | a0001c0001t0001g0086 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1651-6768C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91973686 | ||||||
chr10:91973903
|
C | CA | 207 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 208 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(205): Show |
intron_variant | MODIFIER | c.1651-6531dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91973903 | |||||
chr10:91973903
|
C | CAA | 11 | a0001c0001t0001g0015a0001c0001t0001g0029a0001c0001t0001g0050others(8): Show | 11 | HG00639.hp2 HG01515.hp1 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.1651-6532_1651-653 others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91973903 | |||||
chr10:91974005
|
C | A | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1651-6449C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91974005 | ||||||
chr10:91974598
|
C | T | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.1651-5856C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91974598 | ||||||
chr10:91974612
|
G | A | 8 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(5): Show | 8 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1651-5842G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91974612 | ||||||
chr10:91974895
|
A | G | 1 | a0001c0001t0001g0103 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1651-5559A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91974895 | ||||||
chr10:91974965
|
G | C | 22 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(19): Show | 22 | HG00544.hp2 HG00673.hp2 HG02027.hp2 others(19): Show |
intron_variant | MODIFIER | c.1651-5489G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91974965 | ||||||
chr10:91975009
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1651-5445A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91975009 | ||||||
chr10:91975015
|
C | T | 1 | a0001c0001t0002g0241 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.1651-5439C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91975015 | ||||||
chr10:91975613
|
C | G | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1651-4841C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91975613 | ||||||
chr10:91975669
|
A | G | 1 | a0001c0001t0002g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1651-4785A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91975669 | ||||||
chr10:91975723
|
T | A | 1 | a0001c0001t0001g0083 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1651-4731T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91975723 | ||||||
chr10:91975758
|
A | G | 1 | a0001c0001t0003g0189 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1651-4696A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91975758 | ||||||
chr10:91976432
|
G | C | 1 | a0001c0001t0002g0257 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1651-4022G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91976432 | ||||||
chr10:91976550
|
A | G | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1651-3904A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91976550 | ||||||
chr10:91976596
|
G | A | 1 | a0001c0001t0003g0198 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1651-3858G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91976596 | ||||||
chr10:91976648
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.1651-3806A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91976648 | ||||||
chr10:91976682
|
A | G | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1651-3772A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91976682 | ||||||
chr10:91976733
|
C | T | 1 | a0001c0001t0003g0231 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1651-3721C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91976733 | ||||||
chr10:91976802
|
C | G | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.1651-3652C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91976802 | ||||||
chr10:91976991
|
T | A | 1 | a0001c0001t0004g0314 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1651-3463T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91976991 | ||||||
chr10:91977042
|
G | A | 4 | a0001c0001t0003g0225a0001c0001t0003g0226a0001c0001t0003g0230others(1): Show | 4 | HG00642.hp2 HG01175.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.1651-3412G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91977042 | ||||||
chr10:91977188
|
C | G | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1651-3266C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91977188 | ||||||
chr10:91977557
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1651-2897A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91977557 | ||||||
chr10:91977782
|
A | T | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1651-2672A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91977782 | ||||||
chr10:91977813
|
C | T | 2 | a0001c0001t0003g0231a0001c0001t0003g0312 | 2 | NA20805.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.1651-2641C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91977813 | ||||||
chr10:91978160
|
C | T | 3 | a0001c0002t0001g0132a0001c0002t0001g0139a0001c0002t0001g0160 | 3 | HG02615.hp2 HG02976.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1651-2294C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91978160 | ||||||
chr10:91978208
|
A | T | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1651-2246A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91978208 | ||||||
chr10:91978301
|
A | G | 1 | a0001c0001t0013g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1651-2153A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91978301 | ||||||
chr10:91978332
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1651-2122C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91978332 | ||||||
chr10:91978366
|
G | T | 1 | a0001c0001t0001g0018 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1651-2088G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91978366 | ||||||
chr10:91978441
|
T | C | 2 | a0001c0001t0003g0153a0001c0001t0010g0152 | 2 | HG01261.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1651-2013T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91978441 | ||||||
chr10:91978509
|
TAAG | T | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1651-1942_1651-194 others(7): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91978509 | |||||
chr10:91978814
|
G | GT | 51 | a0001c0001t0003g0153a0001c0001t0003g0177a0001c0001t0003g0179others(48): Show | 51 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.1651-1618dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91978814 | |||||
chr10:91978814
|
G | GTT | 12 | a0001c0001t0003g0161a0001c0001t0003g0183a0001c0001t0003g0197others(9): Show | 12 | HG01109.hp1 HG01123.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.1651-1619_1651-161 others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91978814 | |||||
chr10:91978814
|
G | GTTTT | 6 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(3): Show | 6 | HG01081.hp2 HG02486.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.1651-1621_1651-161 others(8): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91978814 | |||||
chr10:91978814
|
GT | G | 29 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0035others(26): Show | 29 | HG00438.hp2 HG01081.hp1 HG01243.hp1 others(26): Show |
intron_variant | MODIFIER | c.1651-1618delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91978814 | |||||
chr10:91978814
|
GTT | G | 127 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0006others(124): Show | 128 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(125): Show |
intron_variant | MODIFIER | c.1651-1619_1651-161 others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91978814 | |||||
chr10:91978814
|
GTTT | G | 88 | a0001c0001t0001g0005a0001c0001t0001g0041a0001c0001t0001g0062others(85): Show | 88 | HG00140.hp1 HG00423.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.1651-1620_1651-161 others(7): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | INFO_REALIGN_3_PRIME | chr10 | 91978814 | |||||
chr10:91978855
|
A | G | 5 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0001t0002g0174others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.1651-1599A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91978855 | ||||||
chr10:91978878
|
A | G | 1 | a0001c0001t0002g0290 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1651-1576A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91978878 | ||||||
chr10:91978893
|
T | A | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.1651-1561T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91978893 | ||||||
chr10:91978950
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1651-1504C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91978950 | ||||||
chr10:91979331
|
A | G | 2 | a0001c0001t0002g0301a0001c0001t0002g0306 | 2 | NA18999.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.1651-1123A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91979331 | ||||||
chr10:91979590
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1651-864A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91979590 | ||||||
chr10:91980184
|
T | C | 2 | a0001c0001t0002g0264a0001c0001t0002g0279 | 2 | HG02735.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1651-270T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91980184 | ||||||
chr10:91980289
|
T | G | 3 | a0001c0001t0001g0065a0001c0001t0001g0155a0001c0002t0001g0139 | 3 | HG02615.hp2 HG02723.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1651-165T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 14/37 | chr10 | 91980289 | ||||||
chr10:91980672
|
T | C | 89 | a0001c0001t0002g0162a0001c0001t0002g0165a0001c0001t0002g0166others(86): Show | 89 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.1755+114T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 15/37 | chr10 | 91980672 | ||||||
chr10:91980764
|
T | G | 1 | a0001c0001t0002g0273 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1755+206T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 15/37 | chr10 | 91980764 | ||||||
chr10:91981182
|
A | T | 1 | a0001c0001t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1756-461A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 15/37 | chr10 | 91981182 | ||||||
chr10:91981208
|
A | C | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.1756-435A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 15/37 | chr10 | 91981208 | ||||||
chr10:91981216
|
T | C | 26 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(23): Show | 26 | HG00639.hp2 HG00733.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.1756-427T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 15/37 | chr10 | 91981216 | ||||||
chr10:91981292
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1756-351T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 15/37 | chr10 | 91981292 | ||||||
chr10:91981419
|
T | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1756-224T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 15/37 | chr10 | 91981419 | ||||||
chr10:91981439
|
A | T | 1 | a0001c0001t0001g0010 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1756-204A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 15/37 | chr10 | 91981439 | ||||||
chr10:91981902
|
G | A | 1 | a0001c0001t0001g0019 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1905+110G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 16/37 | chr10 | 91981902 | ||||||
chr10:91982041
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1906-42A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 16/37 | chr10 | 91982041 | ||||||
chr10:91982052
|
T | A | 1 | a0001c0006t0001g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1906-31T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 16/37 | chr10 | 91982052 | ||||||
chr10:91982067
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1906-16T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 16/37 | chr10 | 91982067 | ||||||
chr10:91982460
|
A | G | 1 | a0001c0001t0001g0146 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2049-127A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 17/37 | chr10 | 91982460 | ||||||
chr10:91983183
|
T | C | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2223+422T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 18/37 | chr10 | 91983183 | ||||||
chr10:91983292
|
A | G | 1 | a0001c0001t0001g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.2223+531A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 18/37 | chr10 | 91983292 | ||||||
chr10:91983395
|
A | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2223+634A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 18/37 | chr10 | 91983395 | ||||||
chr10:91983415
|
G | C | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2223+654G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 18/37 | chr10 | 91983415 | ||||||
chr10:91983631
|
T | A | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2224-570T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 18/37 | chr10 | 91983631 | ||||||
chr10:91983697
|
A | G | 136 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 137 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.2224-504A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 18/37 | chr10 | 91983697 | ||||||
chr10:91983742
|
G | A | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2224-459G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 18/37 | chr10 | 91983742 | ||||||
chr10:91983793
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2224-408T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 18/37 | chr10 | 91983793 | ||||||
chr10:91983891
|
A | AT | 98 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(95): Show | 98 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.2224-296dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chr10 | 91983891 | |||||
chr10:91983891
|
A | ATT | 11 | a0001c0001t0002g0258a0001c0001t0004g0314a0001c0001t0004g0315others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2224-297_2224-296d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 18/37 | INFO_REALIGN_3_PRIME | chr10 | 91983891 | |||||
chr10:91984109
|
A | G | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2224-92A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 18/37 | chr10 | 91984109 | ||||||
chr10:91984710
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2427+306A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91984710 | ||||||
chr10:91984716
|
T | G | 88 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(85): Show | 88 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(85): Show |
intron_variant | MODIFIER | c.2427+312T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91984716 | ||||||
chr10:91984860
|
A | G | 1 | a0001c0001t0013g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2427+456A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91984860 | ||||||
chr10:91984909
|
T | A | 5 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | HG01243.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.2427+505T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91984909 | ||||||
chr10:91984915
|
C | T | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2427+511C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91984915 | ||||||
chr10:91984988
|
A | T | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2427+584A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91984988 | ||||||
chr10:91985185
|
G | A | 2 | a0001c0002t0001g0139a0001c0002t0001g0160 | 2 | HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.2427+781G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91985185 | ||||||
chr10:91985228
|
A | G | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 323 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(320): Show |
intron_variant | MODIFIER | c.2427+824A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91985228 | ||||||
chr10:91985273
|
G | A | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2427+869G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91985273 | ||||||
chr10:91985294
|
G | GTT | 4 | a0001c0001t0005g0141a0001c0001t0005g0142a0001c0001t0005g0143others(1): Show | 4 | HG02559.hp2 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2427+891_2427+892d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | INFO_REALIGN_3_PRIME | chr10 | 91985294 | |||||
chr10:91985295
|
T | TTA | 102 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(99): Show | 102 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.2427+905_2427+906d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | INFO_REALIGN_3_PRIME | chr10 | 91985295 | |||||
chr10:91985377
|
G | C | 4 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 4 | HG02895.hp1 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.2427+973G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91985377 | ||||||
chr10:91985527
|
G | C | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2427+1123G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91985527 | ||||||
chr10:91985954
|
T | C | 4 | a0001c0001t0003g0229a0001c0001t0006g0178a0001c0001t0006g0212others(1): Show | 4 | HG02027.hp2 NA18962.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.2427+1550T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91985954 | ||||||
chr10:91986004
|
T | G | 1 | a0001c0001t0003g0184 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.2427+1600T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91986004 | ||||||
chr10:91986035
|
T | A | 65 | a0001c0001t0001g0084a0001c0001t0003g0153a0001c0001t0003g0161others(62): Show | 65 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.2427+1631T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91986035 | ||||||
chr10:91986132
|
G | GT | 17 | a0001c0001t0001g0124a0001c0001t0001g0128a0001c0001t0001g0129others(14): Show | 17 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.2427+1729dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | INFO_REALIGN_3_PRIME | chr10 | 91986132 | |||||
chr10:91986238
|
C | T | 4 | a0001c0001t0005g0141a0001c0001t0005g0142a0001c0001t0005g0143others(1): Show | 4 | HG02559.hp2 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2427+1834C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91986238 | ||||||
chr10:91986254
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2427+1850A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91986254 | ||||||
chr10:91986549
|
GT | G | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.2427+2153delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | INFO_REALIGN_3_PRIME | chr10 | 91986549 | |||||
chr10:91986663
|
A | G | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.2427+2259A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91986663 | ||||||
chr10:91986837
|
C | T | 65 | a0001c0001t0001g0084a0001c0001t0003g0153a0001c0001t0003g0161others(62): Show | 65 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.2428-2317C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91986837 | ||||||
chr10:91986984
|
A | T | 1 | a0001c0001t0002g0171 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2428-2170A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91986984 | ||||||
chr10:91987026
|
A | G | 1 | a0001c0001t0003g0180 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2428-2128A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987026 | ||||||
chr10:91987073
|
A | G | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2428-2081A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987073 | ||||||
chr10:91987112
|
C | CT | 116 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 116 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(113): Show |
intron_variant | MODIFIER | c.2428-2024dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | INFO_REALIGN_3_PRIME | chr10 | 91987112 | |||||
chr10:91987112
|
CT | C | 190 | a0001c0001t0001g0084a0001c0001t0001g0097a0001c0001t0001g0098others(187): Show | 191 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(188): Show |
intron_variant | MODIFIER | c.2428-2024delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | INFO_REALIGN_3_PRIME | chr10 | 91987112 | |||||
chr10:91987192
|
CAT | C | 8 | a0001c0001t0001g0025a0001c0001t0001g0037a0001c0001t0001g0048others(5): Show | 8 | NA18939.hp2 NA18946.hp1 NA18966.hp2 others(5): Show |
intron_variant | MODIFIER | c.2428-1961_2428-196 others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987192 | ||||||
chr10:91987299
|
T | C | 169 | a0001c0001t0001g0084a0001c0001t0002g0162a0001c0001t0002g0163others(166): Show | 169 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(166): Show |
intron_variant | MODIFIER | c.2428-1855T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987299 | ||||||
chr10:91987351
|
T | C | 2 | a0001c0001t0002g0165a0001c0001t0002g0171 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2428-1803T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987351 | ||||||
chr10:91987355
|
T | C | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2428-1799T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987355 | ||||||
chr10:91987369
|
G | A | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2428-1785G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987369 | ||||||
chr10:91987396
|
T | C | 2 | a0001c0001t0002g0240a0001c0001t0002g0290 | 2 | HG02132.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.2428-1758T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987396 | ||||||
chr10:91987477
|
GGTC | G | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2428-1676_2428-167 others(7): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987477 | ||||||
chr10:91987488
|
A | C | 1 | a0001c0006t0001g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.2428-1666A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987488 | ||||||
chr10:91987503
|
A | G | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.2428-1651A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987503 | ||||||
chr10:91987559
|
A | G | 1 | a0001c0001t0003g0224 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.2428-1595A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987559 | ||||||
chr10:91987779
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2428-1375A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91987779 | ||||||
chr10:91988082
|
C | T | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.2428-1072C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91988082 | ||||||
chr10:91988151
|
A | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0120a0001c0012t0001g0121 | 3 | HG00733.hp1 HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.2428-1003A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91988151 | ||||||
chr10:91988267
|
A | G | 1 | a0001c0001t0002g0246 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2428-887A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91988267 | ||||||
chr10:91988363
|
G | A | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2428-791G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91988363 | ||||||
chr10:91988506
|
A | G | 20 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(17): Show | 21 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(18): Show |
intron_variant | MODIFIER | c.2428-648A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 19/37 | chr10 | 91988506 | ||||||
chr10:91989609
|
G | A | 1 | a0001c0001t0003g0180 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.2854+29G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91989609 | ||||||
chr10:91989623
|
T | G | 7 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0109others(4): Show | 7 | HG01099.hp2 HG01496.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.2854+43T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91989623 | ||||||
chr10:91989648
|
G | T | 1 | a0001c0001t0002g0252 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.2854+68G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91989648 | ||||||
chr10:91989678
|
T | C | 7 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2854+98T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91989678 | ||||||
chr10:91989747
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2854+167A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91989747 | ||||||
chr10:91989821
|
A | T | 2 | a0001c0001t0002g0241a0001c0001t0002g0246 | 2 | NA18939.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2854+241A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91989821 | ||||||
chr10:91989829
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2854+249C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91989829 | ||||||
chr10:91989940
|
T | C | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2854+360T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91989940 | ||||||
chr10:91990190
|
TA | T | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2854+612delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91990190 | |||||
chr10:91990454
|
A | G | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2854+874A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91990454 | ||||||
chr10:91990586
|
G | A | 4 | a0001c0001t0005g0141a0001c0001t0005g0142a0001c0001t0005g0143others(1): Show | 4 | HG02559.hp2 HG03486.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2854+1006G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91990586 | ||||||
chr10:91990708
|
G | A | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2854+1128G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91990708 | ||||||
chr10:91990741
|
T | C | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2854+1161T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91990741 | ||||||
chr10:91990839
|
G | A | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2854+1259G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91990839 | ||||||
chr10:91990885
|
T | G | 108 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(105): Show | 108 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(105): Show |
intron_variant | MODIFIER | c.2855-1234T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91990885 | ||||||
chr10:91991042
|
C | T | 1 | a0001c0001t0003g0215 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2855-1077C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991042 | ||||||
chr10:91991096
|
A | T | 1 | a0001c0001t0009g0020 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2855-1023A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991096 | ||||||
chr10:91991200
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.2855-919C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991200 | ||||||
chr10:91991265
|
A | AAT | 64 | a0001c0001t0002g0250a0001c0001t0002g0266a0001c0001t0003g0153others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.2855-850_2855-849d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATAAATA others(25): Show |
1 | a0001c0001t0002g0237 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2855-851_2855-850i others(34): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATAAATA others(27): Show |
1 | a0001c0001t0002g0238 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2855-851_2855-850i others(36): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATAAA others(35): Show |
1 | a0003c0014t0002g0255 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2855-827_2855-826i others(44): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(23): Show |
1 | a0001c0001t0003g0229 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2855-849_2855-848i others(32): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(39): Show |
1 | a0001c0001t0002g0263 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2855-849_2855-848i others(48): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(1): Show |
3 | a0001c0001t0002g0171a0001c0001t0002g0272a0001c0001t0002g0302 | 3 | HG01257.hp2 HG01891.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.2855-849_2855-848i others(10): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(3): Show |
1 | a0001c0001t0002g0278 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2855-849_2855-848i others(12): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(27): Show |
1 | a0001c0001t0002g0243 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2855-849_2855-848i others(36): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(11): Show |
2 | a0001c0001t0002g0176a0001c0001t0002g0290 | 2 | HG00735.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.2855-849_2855-848i others(20): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(13): Show |
2 | a0001c0001t0002g0244a0001c0001t0002g0300 | 2 | HG03491.hp1 NA18946.hp2 |
intron_variant | MODIFIER | c.2855-849_2855-848i others(22): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(15): Show |
1 | a0001c0001t0002g0283 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.2855-849_2855-848i others(24): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(17): Show |
3 | a0001c0001t0002g0172a0001c0001t0002g0235a0001c0001t0002g0270 | 3 | HG01516.hp1 NA18970.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.2855-849_2855-848i others(26): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(19): Show |
4 | a0001c0001t0002g0246a0001c0001t0002g0252a0001c0001t0002g0281others(1): Show | 4 | HG01099.hp1 HG01123.hp1 HG02083.hp2 others(1): Show |
intron_variant | MODIFIER | c.2855-849_2855-848i others(28): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(21): Show |
12 | a0001c0001t0002g0173a0001c0001t0002g0236a0001c0001t0002g0245others(9): Show | 12 | HG00423.hp2 HG01433.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.2855-849_2855-848i others(30): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(23): Show |
7 | a0001c0001t0002g0170a0001c0001t0002g0249a0001c0001t0002g0264others(4): Show | 7 | HG01169.hp2 HG01978.hp1 HG02015.hp2 others(4): Show |
intron_variant | MODIFIER | c.2855-849_2855-848i others(32): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(25): Show |
12 | a0001c0001t0002g0162a0001c0001t0002g0165a0001c0001t0002g0167others(9): Show | 12 | HG00642.hp1 HG01070.hp2 HG01515.hp1 others(9): Show |
intron_variant | MODIFIER | c.2855-849_2855-848i others(34): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(27): Show |
2 | a0001c0001t0002g0241a0001c0001t0002g0258 | 2 | NA18981.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2855-849_2855-848i others(36): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(29): Show |
6 | a0001c0001t0002g0169a0001c0001t0002g0247a0001c0001t0002g0254others(3): Show | 6 | HG01258.hp1 HG02148.hp1 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.2855-849_2855-848i others(38): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(31): Show |
3 | a0001c0001t0002g0303a0001c0001t0008g0233a0001c0013t0002g0091 | 3 | HG00609.hp2 HG04228.hp1 NA18974.hp2 |
intron_variant | MODIFIER | c.2855-849_2855-848i others(40): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(33): Show |
1 | a0001c0001t0002g0257 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.2855-849_2855-848i others(42): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
A | AATATATA others(45): Show |
1 | a0001c0001t0002g0265 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2855-849_2855-848i others(54): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
AATATAAA others(3): Show |
A | 1 | a0001c0001t0002g0286 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.2855-848_2855-839d others(12): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991265
|
AATATAAA others(9): Show |
A | 3 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0166 | 3 | HG00140.hp1 HG02602.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.2855-848_2855-833d others(18): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991265 | |||||
chr10:91991271
|
A | AAT | 37 | a0001c0001t0001g0003a0001c0001t0001g0024a0001c0001t0001g0042others(34): Show | 38 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.2855-828_2855-827d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991271 | |||||
chr10:91991271
|
A | AATATAAA others(51): Show |
1 | a0001c0001t0002g0294 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.2855-843_2855-842i others(60): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991271 | |||||
chr10:91991271
|
A | AATATAAA others(35): Show |
2 | a0001c0001t0002g0292a0001c0001t0002g0295 | 2 | HG00673.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.2855-843_2855-842i others(44): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991271 | |||||
chr10:91991271
|
A | AATATAAA others(39): Show |
1 | a0001c0001t0002g0296 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.2855-843_2855-842i others(48): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991271 | |||||
chr10:91991271
|
A | AATATAAA others(51): Show |
1 | a0001c0001t0002g0291 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.2855-843_2855-842i others(60): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991271 | |||||
chr10:91991271
|
A | AATATATA others(31): Show |
2 | a0001c0001t0002g0232a0001c0001t0002g0261 | 2 | HG02004.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.2855-827_2855-826i others(40): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991271 | |||||
chr10:91991271
|
A | AATATATA others(33): Show |
1 | a0008c0007t0002g0288 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.2855-827_2855-826i others(42): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991271 | |||||
chr10:91991271
|
A | AATATATA others(35): Show |
1 | a0001c0001t0002g0256 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.2855-827_2855-826i others(44): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991271 | |||||
chr10:91991271
|
A | AATATATA others(39): Show |
1 | a0006c0011t0002g0304 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.2855-827_2855-826i others(48): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991271 | |||||
chr10:91991271
|
A | T | 85 | a0001c0001t0002g0162a0001c0001t0002g0165a0001c0001t0002g0167others(82): Show | 85 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(82): Show |
intron_variant | MODIFIER | c.2855-848A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991271 | ||||||
chr10:91991277
|
T | A | 1 | a0001c0001t0007g0322 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2855-842T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991277 | ||||||
chr10:91991279
|
T | TATATAA | 3 | a0001c0001t0003g0194a0001c0001t0003g0195a0001c0001t0003g0221 | 3 | HG00140.hp2 HG01255.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.2855-835_2855-834i others(8): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(5): Show |
1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2855-831_2855-830i others(14): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(29): Show |
1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2855-829_2855-828i others(38): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(79): Show |
1 | a0001c0001t0007g0323 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2855-827_2855-826i others(88): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(79): Show |
1 | a0001c0001t0007g0321 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2855-827_2855-826i others(88): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(17): Show |
33 | a0001c0001t0003g0153a0001c0001t0003g0180a0001c0001t0003g0181others(30): Show | 33 | HG00423.hp1 HG00544.hp2 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.2855-827_2855-826i others(26): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(19): Show |
18 | a0001c0001t0003g0161a0001c0001t0003g0177a0001c0001t0003g0179others(15): Show | 18 | HG01069.hp2 HG01070.hp1 HG01123.hp2 others(15): Show |
intron_variant | MODIFIER | c.2855-827_2855-826i others(28): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(85): Show |
1 | a0001c0001t0007g0322 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2855-827_2855-826i others(94): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(21): Show |
2 | a0001c0001t0003g0201a0001c0001t0003g0307 | 2 | NA19007.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.2855-827_2855-826i others(30): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(23): Show |
2 | a0001c0001t0003g0205a0001c0001t0003g0214 | 2 | NA18522.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.2855-827_2855-826i others(32): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(25): Show |
1 | a0001c0001t0003g0311 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.2855-827_2855-826i others(34): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(27): Show |
3 | a0001c0001t0006g0178a0001c0001t0006g0212a0001c0001t0006g0217 | 3 | NA18962.hp1 NA18992.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.2855-827_2855-826i others(36): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(35): Show |
1 | a0001c0001t0003g0225 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.2855-827_2855-826i others(44): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(125): Show |
1 | a0001c0001t0004g0314 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2855-828_2855-827i others(134): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(121): Show |
1 | a0001c0001t0004g0316 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2855-830_2855-829i others(130): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(115): Show |
1 | a0001c0001t0004g0320 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2855-832_2855-831i others(124): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(115): Show |
1 | a0001c0001t0004g0317 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.2855-832_2855-831i others(124): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(123): Show |
1 | a0001c0001t0004g0315 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2855-832_2855-831i others(132): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(125): Show |
1 | a0001c0001t0004g0324 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2855-832_2855-831i others(134): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(121): Show |
1 | a0001c0001t0004g0318 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2855-832_2855-831i others(130): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991279
|
T | TATATATA others(123): Show |
1 | a0001c0001t0004g0319 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2855-832_2855-831i others(132): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991279 | |||||
chr10:91991291
|
T | TATATATA others(3): Show |
1 | a0001c0001t0002g0297 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2855-827_2855-826i others(12): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991291 | |||||
chr10:91991291
|
T | TATATATA others(23): Show |
1 | a0001c0001t0002g0293 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2855-827_2855-826i others(32): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991291 | |||||
chr10:91991291
|
T | TATATATA others(25): Show |
1 | a0001c0001t0002g0282 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2855-827_2855-826i others(34): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991291 | |||||
chr10:91991291
|
T | TATATATA others(33): Show |
1 | a0001c0001t0002g0299 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.2855-827_2855-826i others(42): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991291 | |||||
chr10:91991292
|
A | ATATATAT others(12): Show |
1 | a0001c0001t0011g0242 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.2855-827_2855-826i others(21): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991292 | ||||||
chr10:91991292
|
A | ATATATAT others(22): Show |
1 | a0001c0001t0002g0280 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2855-827_2855-826i others(31): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991292 | ||||||
chr10:91991502
|
G | A | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2855-617G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991502 | ||||||
chr10:91991521
|
C | T | 1 | a0001c0001t0002g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.2855-598C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991521 | ||||||
chr10:91991669
|
C | A | 1 | a0001c0001t0002g0236 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.2855-450C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991669 | ||||||
chr10:91991775
|
A | G | 3 | a0001c0001t0001g0326a0001c0001t0001g0328a0001c0001t0001g0329 | 3 | HG02647.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2855-344A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991775 | ||||||
chr10:91991777
|
G | A | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.2855-342G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991777 | ||||||
chr10:91991785
|
GTGTGTGT others(27): Show |
G | 1 | a0001c0001t0001g0117 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2855-332_2855-299d others(36): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991785 | |||||
chr10:91991789
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2855-328_2855-317d others(14): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991789 | |||||
chr10:91991789
|
GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2855-328_2855-313d others(18): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991789 | |||||
chr10:91991789
|
GTGTGTGT others(11): Show |
G | 14 | a0001c0001t0002g0325a0001c0001t0003g0177a0001c0001t0003g0179others(11): Show | 14 | HG00738.hp2 HG01081.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.2855-328_2855-311d others(20): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991789 | |||||
chr10:91991789
|
GTGTGTGT others(13): Show |
G | 61 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0180others(58): Show | 61 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.2855-328_2855-309d others(22): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991789 | |||||
chr10:91991789
|
GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0004g0319 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2855-328_2855-301d others(30): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991789 | |||||
chr10:91991791
|
GTGTGTGT others(3): Show |
G | 2 | a0001c0001t0002g0262a0001c0001t0002g0270 | 2 | NA18970.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.2855-326_2855-317d others(12): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991791 | |||||
chr10:91991791
|
GTGTGTGT others(5): Show |
G | 24 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(21): Show | 24 | HG00140.hp1 HG01070.hp2 HG01169.hp2 others(21): Show |
intron_variant | MODIFIER | c.2855-326_2855-315d others(14): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991791 | |||||
chr10:91991791
|
GTGTGTGT others(7): Show |
G | 63 | a0001c0001t0002g0165a0001c0001t0002g0171a0001c0001t0002g0173others(60): Show | 63 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(60): Show |
intron_variant | MODIFIER | c.2855-326_2855-313d others(16): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991791 | |||||
chr10:91991791
|
GTGTGTGT others(9): Show |
G | 1 | a0001c0001t0002g0303 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.2855-326_2855-311d others(18): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991791 | |||||
chr10:91991793
|
G | GTA | 3 | a0001c0001t0001g0092a0001c0001t0001g0096a0004c0008t0001g0093 | 3 | HG01243.hp1 HG02280.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2855-325_2855-324i others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991793 | |||||
chr10:91991793
|
G | GTATATAT others(3): Show |
1 | a0001c0001t0013g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2855-325_2855-324i others(12): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991793 | |||||
chr10:91991793
|
GTGTGTAT others(17): Show |
G | 133 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(130): Show | 134 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.2855-324_2855-301d others(26): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991793 | |||||
chr10:91991795
|
G | A | 6 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.2855-324G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991795 | ||||||
chr10:91991795
|
GTGTATAT others(17): Show |
G | 2 | a0001c0001t0001g0014a0001c0001t0001g0100 | 2 | HG01192.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.2855-322_2855-299d others(26): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991795 | |||||
chr10:91991797
|
G | A | 7 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2855-322G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991797 | ||||||
chr10:91991797
|
G | GTGTATAT others(7): Show |
1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2855-321_2855-320i others(16): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991797 | |||||
chr10:91991830
|
T | C | 14 | a0001c0001t0002g0170a0001c0001t0002g0256a0001c0001t0002g0313others(11): Show | 14 | HG00738.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.2855-289T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991830 | ||||||
chr10:91991832
|
T | C | 305 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(302): Show | 306 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(303): Show |
intron_variant | MODIFIER | c.2855-287T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991832 | ||||||
chr10:91991832
|
T | TATATATA others(5): Show |
1 | a0001c0001t0005g0147 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2855-286_2855-285i others(14): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991832 | |||||
chr10:91991832
|
T | TATATATA others(11): Show |
1 | a0001c0001t0005g0142 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2855-286_2855-285i others(20): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991832 | |||||
chr10:91991832
|
T | TATATATA others(17): Show |
1 | a0001c0001t0001g0155 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2855-286_2855-285i others(26): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991832 | |||||
chr10:91991832
|
T | TATATATA others(17): Show |
1 | a0001c0001t0005g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.2855-286_2855-285i others(26): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991832 | |||||
chr10:91991832
|
T | TATATATA others(19): Show |
1 | a0001c0001t0001g0154 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2855-286_2855-285i others(28): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991832 | |||||
chr10:91991832
|
T | TATATATA others(21): Show |
1 | a0001c0001t0001g0156 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2855-286_2855-285i others(30): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991832 | |||||
chr10:91991838
|
C | CACACACA others(1): Show |
4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.2855-280_2855-279i others(10): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | INFO_REALIGN_3_PRIME | chr10 | 91991838 | |||||
chr10:91991838
|
C | T | 306 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(303): Show | 307 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(304): Show |
intron_variant | MODIFIER | c.2855-281C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 20/37 | chr10 | 91991838 | ||||||
chr10:91992317
|
GT | G | 74 | a0001c0001t0001g0110a0001c0001t0001g0154a0001c0001t0001g0155others(71): Show | 74 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.3045+23delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 21/37 | INFO_REALIGN_3_PRIME | chr10 | 91992317 | |||||
chr10:91992350
|
A | G | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.3045+41A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 21/37 | chr10 | 91992350 | ||||||
chr10:91992465
|
G | A | 6 | a0001c0001t0003g0220a0001c0001t0003g0222a0001c0001t0003g0224others(3): Show | 6 | HG01070.hp1 HG01109.hp1 HG02683.hp1 others(3): Show |
intron_variant | MODIFIER | c.3045+156G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 21/37 | chr10 | 91992465 | ||||||
chr10:91992501
|
A | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3045+192A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 21/37 | chr10 | 91992501 | ||||||
chr10:91992556
|
A | G | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.3045+247A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 21/37 | chr10 | 91992556 | ||||||
chr10:91993160
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3046-534A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 21/37 | chr10 | 91993160 | ||||||
chr10:91993223
|
T | C | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3046-471T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 21/37 | chr10 | 91993223 | ||||||
chr10:91993347
|
C | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3046-347C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 21/37 | chr10 | 91993347 | ||||||
chr10:91993375
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3046-319T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 21/37 | chr10 | 91993375 | ||||||
chr10:91993380
|
G | A | 1 | a0001c0001t0003g0211 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.3046-314G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 21/37 | chr10 | 91993380 | ||||||
chr10:91993388
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3046-306A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 21/37 | chr10 | 91993388 | ||||||
chr10:91994299
|
C | CA | 16 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(13): Show | 16 | HG01081.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.3200-222dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chr10 | 91994299 | |||||
chr10:91994299
|
CA | C | 65 | a0001c0001t0002g0274a0001c0001t0003g0153a0001c0001t0003g0161others(62): Show | 65 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.3200-222delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 22/37 | INFO_REALIGN_3_PRIME | chr10 | 91994299 | |||||
chr10:91994340
|
G | A | 62 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(59): Show | 62 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(59): Show |
intron_variant | MODIFIER | c.3200-195G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 22/37 | chr10 | 91994340 | ||||||
chr10:91994406
|
G | A | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.3200-129G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 22/37 | chr10 | 91994406 | ||||||
chr10:91994413
|
A | T | 1 | a0006c0011t0002g0304 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3200-122A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 22/37 | chr10 | 91994413 | ||||||
chr10:91994534
|
G | T | 1 | a0006c0011t0002g0304 | 1 | NA18978.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.3200-1G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 22/37 | chr10 | 91994534 | ||||||
chr10:91994759
|
T | C | 1 | a0006c0011t0002g0304 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3309+115T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91994759 | ||||||
chr10:91994786
|
T | G | 91 | a0001c0001t0001g0022a0001c0001t0002g0162a0001c0001t0002g0163others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.3309+142T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91994786 | ||||||
chr10:91994912
|
G | T | 1 | a0001c0001t0002g0175 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.3309+268G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91994912 | ||||||
chr10:91995000
|
A | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3309+356A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995000 | ||||||
chr10:91995046
|
A | G | 1 | a0006c0011t0002g0304 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3309+402A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995046 | ||||||
chr10:91995068
|
A | G | 1 | a0006c0011t0002g0304 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3309+424A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995068 | ||||||
chr10:91995095
|
T | A | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3309+451T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995095 | ||||||
chr10:91995098
|
A | G | 1 | a0006c0011t0002g0304 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3309+454A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995098 | ||||||
chr10:91995115
|
T | C | 1 | a0006c0011t0002g0304 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.3309+471T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995115 | ||||||
chr10:91995143
|
G | A | 1 | a0001c0001t0003g0215 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.3309+499G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995143 | ||||||
chr10:91995383
|
T | C | 2 | a0001c0004t0001g0046a0001c0004t0001g0047 | 2 | HG02615.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3309+739T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995383 | ||||||
chr10:91995442
|
C | T | 1 | a0001c0001t0002g0172 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.3309+798C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995442 | ||||||
chr10:91995637
|
C | T | 1 | a0001c0001t0001g0075 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.3310-732C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995637 | ||||||
chr10:91995688
|
A | G | 1 | a0001c0001t0002g0173 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3310-681A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995688 | ||||||
chr10:91995844
|
GTGCTGTT others(4): Show |
G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3310-512_3310-502d others(13): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | INFO_REALIGN_3_PRIME | chr10 | 91995844 | |||||
chr10:91995855
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.3310-514A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995855 | ||||||
chr10:91995905
|
G | A | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3310-464G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 23/37 | chr10 | 91995905 | ||||||
chr10:91996730
|
T | G | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.3511+160T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 24/37 | chr10 | 91996730 | ||||||
chr10:91996803
|
T | C | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.3511+233T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 24/37 | chr10 | 91996803 | ||||||
chr10:91996808
|
A | G | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.3511+238A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 24/37 | chr10 | 91996808 | ||||||
chr10:91996979
|
A | G | 1 | a0001c0001t0001g0116 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3511+409A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 24/37 | chr10 | 91996979 | ||||||
chr10:91997126
|
ACT | A | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.3512-474_3512-473d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 24/37 | INFO_REALIGN_3_PRIME | chr10 | 91997126 | |||||
chr10:91997562
|
G | A | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3512-41G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 24/37 | chr10 | 91997562 | ||||||
chr10:91998127
|
CA | C | 306 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(303): Show | 307 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(304): Show |
intron_variant | MODIFIER | c.3660+392delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 91998127 | |||||
chr10:91998141
|
A | G | 4 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0104others(1): Show | 4 | HG02895.hp1 HG03516.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.3660+390A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91998141 | ||||||
chr10:91998322
|
TA | T | 63 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.3660+579delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 91998322 | |||||
chr10:91998534
|
G | C | 1 | a0001c0001t0001g0038 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.3660+783G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91998534 | ||||||
chr10:91998545
|
G | A | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156 | 3 | HG02280.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3660+794G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91998545 | ||||||
chr10:91998551
|
C | T | 7 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0043others(4): Show | 7 | HG01109.hp2 HG02257.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.3660+800C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91998551 | ||||||
chr10:91998628
|
A | G | 1 | a0001c0001t0004g0319 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3660+877A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91998628 | ||||||
chr10:91998687
|
A | G | 3 | a0001c0001t0001g0079a0001c0004t0001g0046a0001c0004t0001g0047 | 3 | HG02615.hp1 HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3660+936A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91998687 | ||||||
chr10:91998932
|
A | G | 168 | a0001c0001t0001g0101a0001c0001t0002g0162a0001c0001t0002g0163others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.3660+1181A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91998932 | ||||||
chr10:91999029
|
C | T | 1 | a0001c0001t0003g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3660+1278C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91999029 | ||||||
chr10:91999062
|
C | CA | 91 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0028others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.3660+1329dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 91999062 | |||||
chr10:91999062
|
C | CAA | 6 | a0001c0001t0002g0173a0001c0001t0002g0253a0001c0001t0002g0282others(3): Show | 6 | HG01433.hp2 HG03710.hp1 HG04184.hp2 others(3): Show |
intron_variant | MODIFIER | c.3660+1328_3660+132 others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 91999062 | |||||
chr10:91999062
|
CA | C | 29 | a0001c0001t0001g0095a0001c0001t0001g0097a0001c0001t0001g0098others(26): Show | 30 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.3660+1329delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 91999062 | |||||
chr10:91999154
|
T | TAAATACT others(25): Show |
1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3660+1434_3660+143 others(36): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 91999154 | |||||
chr10:91999475
|
A | T | 10 | a0001c0001t0003g0180a0001c0001t0003g0181a0001c0001t0003g0182others(7): Show | 10 | HG02074.hp2 NA18952.hp1 NA18954.hp1 others(7): Show |
intron_variant | MODIFIER | c.3660+1724A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91999475 | ||||||
chr10:91999650
|
C | G | 2 | a0002c0005t0003g0186a0002c0005t0003g0207 | 2 | HG02132.hp1 NA18979.hp2 |
intron_variant | MODIFIER | c.3660+1899C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91999650 | ||||||
chr10:91999760
|
T | C | 92 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(89): Show | 92 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.3660+2009T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91999760 | ||||||
chr10:91999903
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3660+2152A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91999903 | ||||||
chr10:91999915
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3660+2164A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 91999915 | ||||||
chr10:92000236
|
C | T | 1 | a0001c0001t0003g0189 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.3660+2485C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92000236 | ||||||
chr10:92000465
|
G | T | 1 | a0001c0001t0001g0052 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.3660+2714G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92000465 | ||||||
chr10:92000484
|
A | G | 2 | a0001c0001t0003g0177a0001c0001t0003g0179 | 2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.3660+2733A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92000484 | ||||||
chr10:92000712
|
C | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3660+2961C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92000712 | ||||||
chr10:92001224
|
T | A | 19 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(16): Show | 19 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.3660+3473T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001224 | ||||||
chr10:92001307
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.3660+3556G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001307 | ||||||
chr10:92001480
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3660+3729A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001480 | ||||||
chr10:92001499
|
T | G | 1 | a0001c0001t0003g0218 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3660+3748T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001499 | ||||||
chr10:92001641
|
C | T | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3660+3890C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001641 | ||||||
chr10:92001667
|
A | T | 63 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.3660+3916A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001667 | ||||||
chr10:92001862
|
C | T | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3660+4111C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001862 | ||||||
chr10:92001887
|
C | T | 32 | a0001c0001t0003g0177a0001c0001t0003g0179a0001c0001t0003g0180others(29): Show | 32 | HG00544.hp2 HG00673.hp2 HG01516.hp2 others(29): Show |
intron_variant | MODIFIER | c.3660+4136C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001887 | ||||||
chr10:92001946
|
CA | C | 20 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0031others(17): Show | 20 | HG00609.hp1 HG00639.hp2 HG00642.hp1 others(17): Show |
intron_variant | MODIFIER | c.3660+4216delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92001946 | |||||
chr10:92001946
|
CAA | C | 220 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(217): Show | 221 | HG00140.hp1 HG00423.hp2 HG00438.hp1 others(218): Show |
intron_variant | MODIFIER | c.3660+4215_3660+421 others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92001946 | |||||
chr10:92001967
|
A | C | 55 | a0001c0001t0001g0101a0001c0001t0001g0110a0001c0001t0001g0130others(52): Show | 55 | HG00140.hp2 HG00544.hp2 HG00642.hp2 others(52): Show |
intron_variant | MODIFIER | c.3660+4216A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001967 | ||||||
chr10:92001968
|
CCAT | C | 4 | a0001c0001t0001g0101a0001c0001t0001g0110a0001c0001t0001g0130others(1): Show | 4 | HG01099.hp2 HG01358.hp2 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.3660+4218_3660+422 others(7): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001968 | ||||||
chr10:92001968
|
CCATATAT | C | 6 | a0001c0001t0003g0193a0001c0001t0003g0196a0001c0001t0003g0197others(3): Show | 6 | HG01123.hp2 HG01169.hp1 HG01943.hp1 others(3): Show |
intron_variant | MODIFIER | c.3660+4218_3660+422 others(11): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001968 | ||||||
chr10:92001968
|
CCATATAT others(2): Show |
C | 45 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(42): Show | 45 | HG00140.hp2 HG00544.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.3660+4218_3660+422 others(13): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001968 | ||||||
chr10:92001969
|
CAT | C | 37 | a0001c0001t0001g0050a0001c0001t0001g0097a0001c0001t0001g0098others(34): Show | 38 | HG00733.hp1 HG00738.hp2 HG01175.hp1 others(35): Show |
intron_variant | MODIFIER | c.3660+4234_3660+423 others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92001969 | |||||
chr10:92001969
|
CATATAT | C | 4 | a0001c0001t0003g0202a0001c0001t0003g0208a0001c0001t0003g0311others(1): Show | 4 | HG03831.hp2 NA18979.hp2 NA19054.hp1 others(1): Show |
intron_variant | MODIFIER | c.3660+4230_3660+423 others(10): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92001969 | |||||
chr10:92001969
|
CATATATA others(1): Show |
C | 7 | a0001c0001t0003g0181a0001c0001t0003g0191a0001c0001t0003g0209others(4): Show | 7 | HG00423.hp1 HG01109.hp1 HG02055.hp2 others(4): Show |
intron_variant | MODIFIER | c.3660+4228_3660+423 others(12): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92001969 | |||||
chr10:92001977
|
T | C | 1 | a0001c0001t0002g0174 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3660+4226T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001977 | ||||||
chr10:92001977
|
TATATATA others(15): Show |
T | 1 | a0001c0001t0003g0223 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3660+4228_3660+424 others(26): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92001977 | |||||
chr10:92001981
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0031a0001c0001t0001g0032 | 3 | HG01358.hp1 HG01361.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.3660+4230T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001981 | ||||||
chr10:92001981
|
T | TAC | 15 | a0001c0001t0001g0026a0001c0001t0001g0036a0001c0001t0001g0040others(12): Show | 15 | HG00438.hp1 HG00733.hp2 HG00738.hp1 others(12): Show |
intron_variant | MODIFIER | c.3660+4231_3660+423 others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92001981 | |||||
chr10:92001983
|
T | C | 86 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(83): Show | 86 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(83): Show |
intron_variant | MODIFIER | c.3660+4232T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001983 | ||||||
chr10:92001983
|
T | TAC | 3 | a0001c0001t0001g0079a0001c0004t0001g0046a0001c0004t0001g0047 | 3 | HG02615.hp1 HG02818.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.3660+4233_3660+423 others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92001983 | |||||
chr10:92001983
|
TATACACA others(3): Show |
T | 1 | a0001c0001t0002g0164 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3660+4234_3660+424 others(14): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92001983 | |||||
chr10:92001983
|
TATACACA others(5): Show |
T | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3660+4234_3660+424 others(16): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92001983 | |||||
chr10:92001985
|
T | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(115): Show | 118 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(115): Show |
intron_variant | MODIFIER | c.3660+4234T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001985 | ||||||
chr10:92001985
|
TACACAC | T | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3660+4259_3660+426 others(10): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92001985 | |||||
chr10:92001987
|
C | T | 2 | a0001c0001t0002g0170a0001c0001t0002g0172 | 2 | HG01516.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3660+4236C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001987 | ||||||
chr10:92001989
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3660+4238C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001989 | ||||||
chr10:92001991
|
C | T | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3660+4240C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92001991 | ||||||
chr10:92002006
|
ACACACAC others(3): Show |
A | 90 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0165others(87): Show | 90 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.3660+4257_3660+426 others(14): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92002006 | |||||
chr10:92002009
|
CACACACT others(6): Show |
C | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156 | 3 | HG02280.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3660+4260_3660+427 others(17): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92002009 | |||||
chr10:92002016
|
T | A | 1 | a0001c0001t0002g0164 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.3660+4265T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002016 | ||||||
chr10:92002223
|
G | A | 3 | a0001c0001t0001g0326a0001c0001t0001g0328a0001c0001t0001g0329 | 3 | HG02647.hp2 HG03540.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.3660+4472G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002223 | ||||||
chr10:92002238
|
T | C | 5 | a0001c0001t0001g0061a0001c0001t0001g0063a0001c0001t0001g0064others(2): Show | 5 | HG02486.hp2 HG02723.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.3660+4487T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002238 | ||||||
chr10:92002413
|
G | A | 5 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0001t0002g0174others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.3660+4662G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002413 | ||||||
chr10:92002422
|
G | A | 63 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.3660+4671G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002422 | ||||||
chr10:92002450
|
C | T | 1 | a0001c0001t0002g0267 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.3660+4699C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002450 | ||||||
chr10:92002461
|
G | T | 89 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 89 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.3660+4710G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002461 | ||||||
chr10:92002493
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3660+4742A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002493 | ||||||
chr10:92002551
|
A | G | 1 | a0001c0001t0002g0235 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3660+4800A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002551 | ||||||
chr10:92002664
|
A | G | 2 | a0001c0001t0002g0264a0001c0001t0002g0279 | 2 | HG02735.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.3660+4913A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002664 | ||||||
chr10:92002819
|
C | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3660+5068C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002819 | ||||||
chr10:92002834
|
C | T | 10 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0043others(7): Show | 10 | HG01109.hp2 HG02257.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.3660+5083C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002834 | ||||||
chr10:92002843
|
T | G | 2 | a0001c0001t0002g0165a0001c0001t0002g0171 | 2 | HG01891.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.3660+5092T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002843 | ||||||
chr10:92002897
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3660+5146C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002897 | ||||||
chr10:92002967
|
G | A | 1 | a0001c0001t0004g0314 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3661-5156G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92002967 | ||||||
chr10:92003118
|
T | C | 1 | a0001c0001t0002g0260 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.3661-5005T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92003118 | ||||||
chr10:92003155
|
C | CA | 310 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(307): Show | 311 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(308): Show |
intron_variant | MODIFIER | c.3661-4953dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92003155 | |||||
chr10:92003155
|
C | CAA | 6 | a0001c0001t0001g0015a0001c0001t0001g0090a0001c0001t0001g0136others(3): Show | 6 | HG01358.hp2 HG03041.hp2 NA18963.hp1 others(3): Show |
intron_variant | MODIFIER | c.3661-4954_3661-495 others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92003155 | |||||
chr10:92003335
|
C | G | 7 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.3661-4788C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92003335 | ||||||
chr10:92003440
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3661-4683A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92003440 | ||||||
chr10:92003485
|
T | C | 1 | a0001c0001t0002g0253 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3661-4638T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92003485 | ||||||
chr10:92003509
|
T | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 89 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.3661-4614T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92003509 | ||||||
chr10:92003580
|
A | T | 105 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(102): Show | 105 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.3661-4543A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92003580 | ||||||
chr10:92003804
|
T | C | 1 | a0001c0001t0002g0270 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.3661-4319T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92003804 | ||||||
chr10:92003908
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.3661-4215C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92003908 | ||||||
chr10:92003909
|
G | A | 1 | a0001c0001t0002g0247 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3661-4214G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92003909 | ||||||
chr10:92004151
|
C | T | 1 | a0001c0001t0003g0223 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.3661-3972C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92004151 | ||||||
chr10:92004232
|
T | C | 1 | a0004c0008t0001g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3661-3891T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92004232 | ||||||
chr10:92004237
|
C | T | 13 | a0001c0001t0002g0313a0001c0001t0002g0325a0001c0001t0004g0314others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.3661-3886C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92004237 | ||||||
chr10:92004359
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3661-3764A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92004359 | ||||||
chr10:92004384
|
T | A | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.3661-3739T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92004384 | ||||||
chr10:92004639
|
A | G | 19 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(16): Show | 19 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.3661-3484A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92004639 | ||||||
chr10:92004687
|
T | TCTTAAAC others(7): Show |
1 | a0001c0001t0001g0078 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3661-3433_3661-342 others(18): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92004687 | |||||
chr10:92004724
|
G | A | 284 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(281): Show | 284 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(281): Show |
intron_variant | MODIFIER | c.3661-3399G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92004724 | ||||||
chr10:92004734
|
G | A | 11 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0131others(8): Show | 11 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.3661-3389G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92004734 | ||||||
chr10:92004849
|
T | C | 3 | a0001c0001t0001g0108a0001c0001t0001g0120a0001c0012t0001g0121 | 3 | HG00733.hp1 HG01175.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.3661-3274T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92004849 | ||||||
chr10:92004853
|
A | T | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3661-3270A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92004853 | ||||||
chr10:92005021
|
G | A | 2 | a0001c0001t0002g0313a0001c0001t0002g0325 | 2 | HG00738.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.3661-3102G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92005021 | ||||||
chr10:92005164
|
G | A | 14 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0131others(11): Show | 14 | HG00639.hp1 HG01433.hp1 HG02647.hp1 others(11): Show |
intron_variant | MODIFIER | c.3661-2959G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92005164 | ||||||
chr10:92005236
|
G | GT | 90 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(87): Show | 90 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(87): Show |
intron_variant | MODIFIER | c.3661-2880dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92005236 | |||||
chr10:92005244
|
G | T | 65 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(62): Show | 66 | HG00639.hp1 HG00733.hp1 HG00735.hp1 others(63): Show |
intron_variant | MODIFIER | c.3661-2879G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92005244 | ||||||
chr10:92005318
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3661-2805A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92005318 | ||||||
chr10:92005430
|
A | G | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.3661-2693A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92005430 | ||||||
chr10:92005619
|
T | A | 1 | a0001c0001t0002g0282 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3661-2504T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92005619 | ||||||
chr10:92005781
|
CTT | C | 63 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(60): Show | 63 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.3661-2339_3661-233 others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92005781 | |||||
chr10:92005844
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.3661-2279T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92005844 | ||||||
chr10:92006075
|
A | G | 2 | a0001c0001t0002g0172a0001c0001t0002g0176 | 2 | HG00735.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.3661-2048A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92006075 | ||||||
chr10:92006090
|
G | T | 4 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG02280.hp2 HG03516.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.3661-2033G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92006090 | ||||||
chr10:92006558
|
C | A | 63 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.3661-1565C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92006558 | ||||||
chr10:92007019
|
G | A | 1 | a0001c0001t0002g0245 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3661-1104G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92007019 | ||||||
chr10:92007026
|
T | A | 1 | a0001c0001t0002g0280 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.3661-1097T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92007026 | ||||||
chr10:92007056
|
A | T | 1 | a0001c0001t0001g0080 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3661-1067A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92007056 | ||||||
chr10:92007210
|
C | CT | 60 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0001t0001g0017others(57): Show | 60 | HG00673.hp1 HG01169.hp2 HG01175.hp2 others(57): Show |
intron_variant | MODIFIER | c.3661-887dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92007210 | |||||
chr10:92007210
|
C | CTT | 6 | a0001c0001t0001g0100a0001c0001t0001g0106a0001c0001t0001g0114others(3): Show | 6 | HG01192.hp2 HG01515.hp2 HG02155.hp1 others(3): Show |
intron_variant | MODIFIER | c.3661-888_3661-887d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92007210 | |||||
chr10:92007210
|
C | CTTT | 16 | a0001c0001t0001g0097a0001c0001t0001g0102a0001c0001t0001g0103others(13): Show | 17 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.3661-889_3661-887d others(5): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92007210 | |||||
chr10:92007210
|
C | CTTTT | 8 | a0001c0001t0001g0098a0001c0001t0001g0099a0001c0001t0001g0101others(5): Show | 8 | HG01496.hp1 HG02155.hp2 HG02698.hp2 others(5): Show |
intron_variant | MODIFIER | c.3661-890_3661-887d others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92007210 | |||||
chr10:92007210
|
CT | C | 18 | a0001c0001t0001g0092a0001c0001t0001g0096a0001c0001t0001g0328others(15): Show | 18 | HG00642.hp1 HG00735.hp2 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.3661-887delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92007210 | |||||
chr10:92007210
|
CTT | C | 8 | a0001c0001t0001g0095a0001c0001t0002g0325a0001c0001t0004g0315others(5): Show | 8 | HG00738.hp2 HG01081.hp2 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.3661-888_3661-887d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | INFO_REALIGN_3_PRIME | chr10 | 92007210 | |||||
chr10:92007240
|
A | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.3661-883A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92007240 | ||||||
chr10:92007249
|
C | T | 63 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.3661-874C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92007249 | ||||||
chr10:92007392
|
T | C | 1 | a0001c0001t0001g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.3661-731T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92007392 | ||||||
chr10:92007512
|
C | G | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3661-611C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92007512 | ||||||
chr10:92007789
|
C | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3661-334C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92007789 | ||||||
chr10:92007969
|
T | C | 1 | a0001c0002t0001g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3661-154T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92007969 | ||||||
chr10:92007994
|
T | A | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3661-129T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92007994 | ||||||
chr10:92008040
|
G | A | 92 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(89): Show | 92 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.3661-83G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 25/37 | chr10 | 92008040 | ||||||
chr10:92008323
|
C | T | 2 | a0001c0001t0002g0313a0001c0006t0001g0001 | 3 | HG03471.hp1 HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.3813+48C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 26/37 | chr10 | 92008323 | ||||||
chr10:92008337
|
T | TG | 143 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 144 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.3813+70dupG | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 26/37 | INFO_REALIGN_3_PRIME | chr10 | 92008337 | |||||
chr10:92008339
|
G | C | 63 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.3813+64G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 26/37 | chr10 | 92008339 | ||||||
chr10:92008381
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3813+106T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 26/37 | chr10 | 92008381 | ||||||
chr10:92008456
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3813+181A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 26/37 | chr10 | 92008456 | ||||||
chr10:92008480
|
A | G | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3813+205A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 26/37 | chr10 | 92008480 | ||||||
chr10:92008510
|
G | GT | 103 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(100): Show | 103 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(100): Show |
intron_variant | MODIFIER | c.3813+252dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 26/37 | INFO_REALIGN_3_PRIME | chr10 | 92008510 | |||||
chr10:92008510
|
G | GTT | 10 | a0001c0001t0001g0017a0001c0001t0001g0028a0001c0001t0001g0050others(7): Show | 10 | HG02148.hp2 HG02280.hp2 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.3813+251_3813+252d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 26/37 | INFO_REALIGN_3_PRIME | chr10 | 92008510 | |||||
chr10:92008605
|
C | T | 105 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(102): Show | 105 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.3814-224C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 26/37 | chr10 | 92008605 | ||||||
chr10:92009374
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | NA18944.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.4103+166C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 28/37 | chr10 | 92009374 | ||||||
chr10:92009397
|
A | T | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.4103+189A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 28/37 | chr10 | 92009397 | ||||||
chr10:92009742
|
A | G | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 145 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.4103+534A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 28/37 | chr10 | 92009742 | ||||||
chr10:92009788
|
G | A | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4103+580G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 28/37 | chr10 | 92009788 | ||||||
chr10:92009827
|
A | C | 1 | a0001c0001t0003g0206 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.4103+619A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 28/37 | chr10 | 92009827 | ||||||
chr10:92009864
|
A | G | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.4103+656A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 28/37 | chr10 | 92009864 | ||||||
chr10:92010027
|
G | C | 3 | a0001c0001t0001g0015a0001c0001t0001g0016a0001c0010t0001g0002 | 3 | NA18944.hp2 NA18963.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.4103+819G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 28/37 | chr10 | 92010027 | ||||||
chr10:92010092
|
GA | G | 6 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4103+893delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 28/37 | INFO_REALIGN_3_PRIME | chr10 | 92010092 | |||||
chr10:92010728
|
T | A | 1 | a0004c0008t0001g0093 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4104-345T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 28/37 | chr10 | 92010728 | ||||||
chr10:92010881
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4104-192C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 28/37 | chr10 | 92010881 | ||||||
chr10:92011011
|
T | C | 19 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(16): Show | 19 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.4104-62T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 28/37 | chr10 | 92011011 | ||||||
chr10:92011161
|
AT | A | 6 | a0001c0001t0001g0117a0001c0001t0001g0155a0001c0001t0002g0167others(3): Show | 6 | HG01070.hp2 HG02896.hp2 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.4181+21delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 29/37 | INFO_REALIGN_3_PRIME | chr10 | 92011161 | |||||
chr10:92011200
|
C | G | 19 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(16): Show | 19 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.4181+50C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 29/37 | chr10 | 92011200 | ||||||
chr10:92011432
|
A | T | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4311+17A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92011432 | ||||||
chr10:92011435
|
T | A | 92 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(89): Show | 92 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.4311+20T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92011435 | ||||||
chr10:92011440
|
T | A | 1 | a0001c0001t0001g0031 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.4311+25T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92011440 | ||||||
chr10:92011532
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.4311+117T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92011532 | ||||||
chr10:92011776
|
T | C | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4311+361T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92011776 | ||||||
chr10:92011856
|
A | T | 1 | a0001c0001t0002g0173 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4311+441A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92011856 | ||||||
chr10:92011919
|
T | A | 1 | a0001c0001t0001g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4311+504T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92011919 | ||||||
chr10:92011987
|
G | T | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4311+572G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92011987 | ||||||
chr10:92012070
|
TCTCCCTC others(9): Show |
T | 1 | a0001c0001t0001g0092 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4311+664_4311+679d others(18): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012070 | |||||
chr10:92012079
|
T | TTCCC | 4 | a0001c0001t0001g0326a0001c0001t0001g0327a0001c0001t0001g0328others(1): Show | 4 | HG02451.hp2 HG02647.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.4311+677_4311+680d others(6): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012079 | |||||
chr10:92012103
|
T | C | 1 | a0001c0001t0001g0066 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4311+688T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012103 | ||||||
chr10:92012149
|
C | G | 1 | a0001c0001t0002g0251 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.4311+734C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012149 | ||||||
chr10:92012156
|
T | TCCTCC | 7 | a0001c0001t0004g0315a0001c0001t0004g0316a0001c0001t0004g0317others(4): Show | 7 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.4311+746_4311+750d others(7): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012156 | |||||
chr10:92012169
|
T | TCCTCCCC others(69): Show |
1 | a0001c0001t0002g0274 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.4311+761_4311+762i others(78): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012169 | |||||
chr10:92012169
|
T | TCCTCCCC others(347): Show |
1 | a0001c0001t0001g0117 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4311+761_4311+762i others(356): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012169 | |||||
chr10:92012179
|
C | CCCTCCCC others(169): Show |
3 | a0001c0001t0001g0146a0001c0001t0001g0149a0001c0001t0013g0123 | 3 | HG02886.hp2 HG03041.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(178): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCCCC others(238): Show |
5 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | HG01243.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(247): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCCCC others(195): Show |
1 | a0001c0001t0001g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(204): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCCCC others(159): Show |
3 | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0151 | 3 | HG01891.hp2 HG02630.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(168): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCCCC others(347): Show |
1 | a0001c0001t0001g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(356): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCCCC others(280): Show |
1 | a0001c0001t0001g0100 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(289): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCCCC others(293): Show |
1 | a0001c0001t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(302): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCCCC others(308): Show |
3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02698.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(317): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCCCC others(259): Show |
1 | a0001c0001t0001g0118 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(268): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCCCC others(272): Show |
13 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(10): Show | 13 | HG00733.hp1 HG01099.hp2 HG01175.hp1 others(10): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(281): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCCCC others(285): Show |
1 | a0001c0001t0001g0109 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(294): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCCCC others(285): Show |
1 | a0001c0001t0001g0111 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(294): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCCCC others(272): Show |
1 | a0001c0006t0001g0001 | 2 | HG03491.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(281): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(4): Show |
58 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(55): Show | 58 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(13): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(213): Show |
1 | a0001c0013t0002g0091 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(222): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(185): Show |
1 | a0001c0001t0002g0236 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(194): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(198): Show |
2 | a0001c0001t0002g0235a0001c0001t0002g0239 | 2 | NA18950.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(207): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(210): Show |
2 | a0001c0001t0002g0286a0001c0001t0002g0302 | 2 | HG01257.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(219): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(182): Show |
8 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0257others(5): Show | 8 | HG00438.hp2 HG02148.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(191): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(182): Show |
1 | a0001c0001t0002g0260 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(191): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(195): Show |
34 | a0001c0001t0002g0232a0001c0001t0002g0237a0001c0001t0002g0238others(31): Show | 34 | HG00423.hp2 HG00673.hp1 HG01258.hp1 others(31): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(204): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(208): Show |
1 | a0001c0001t0002g0245 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(217): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(221): Show |
1 | a0008c0007t0002g0288 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(230): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(208): Show |
7 | a0001c0001t0002g0248a0001c0001t0002g0251a0001c0001t0002g0252others(4): Show | 7 | HG01069.hp1 HG01099.hp1 HG01123.hp1 others(4): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(217): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(221): Show |
1 | a0001c0001t0002g0300 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(230): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(234): Show |
1 | a0001c0001t0002g0273 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(243): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(259): Show |
1 | a0001c0001t0011g0242 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(268): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(246): Show |
1 | a0001c0001t0002g0261 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(255): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(182): Show |
2 | a0001c0001t0002g0278a0001c0001t0002g0287 | 2 | HG02015.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(191): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012179
|
C | CCCTCTCC others(172): Show |
1 | a0001c0001t0002g0294 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(181): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012179 | |||||
chr10:92012180
|
C | CCTCCCCT others(251): Show |
1 | a0001c0001t0001g0010 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(260): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012180 | |||||
chr10:92012181
|
C | CTCCCCT | 5 | a0001c0001t0001g0102a0001c0001t0005g0141a0001c0001t0005g0142others(2): Show | 5 | HG02559.hp2 HG03486.hp2 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(8): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(230): Show |
1 | a0001c0001t0001g0052 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(239): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(267): Show |
3 | a0001c0001t0007g0321a0001c0001t0007g0322a0001c0001t0007g0323 | 3 | HG02717.hp1 HG03209.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(276): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(239): Show |
7 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(4): Show | 7 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(248): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(252): Show |
1 | a0001c0001t0004g0319 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(261): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(248): Show |
1 | a0001c0001t0001g0015 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(257): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(183): Show |
1 | a0001c0003t0001g0135 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(192): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(259): Show |
3 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0067 | 3 | HG01952.hp1 HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(268): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(241): Show |
2 | a0001c0001t0001g0012a0001c0001t0001g0013 | 2 | HG00544.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(250): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(255): Show |
1 | a0001c0001t0001g0024 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(264): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(254): Show |
1 | a0001c0001t0001g0033 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(263): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(223): Show |
1 | a0001c0001t0001g0006 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(232): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(236): Show |
40 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(37): Show | 40 | HG00609.hp1 HG00639.hp2 HG00733.hp2 others(37): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(245): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(249): Show |
1 | a0001c0001t0001g0040 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(258): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(249): Show |
5 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0081others(2): Show | 5 | HG04184.hp1 NA18942.hp2 NA19000.hp1 others(2): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(258): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(262): Show |
1 | a0001c0001t0001g0082 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(271): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(235): Show |
1 | a0001c0001t0001g0035 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(244): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(283): Show |
1 | a0001c0001t0001g0329 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(292): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(283): Show |
1 | a0001c0001t0001g0326 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(292): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(282): Show |
1 | a0001c0001t0001g0328 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(291): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(259): Show |
1 | a0001c0001t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(268): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(241): Show |
4 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(1): Show | 4 | HG02280.hp2 HG03516.hp1 NA18906.hp2 others(1): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(250): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(232): Show |
1 | a0001c0001t0001g0080 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(241): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(254): Show |
2 | a0001c0001t0001g0072a0001c0004t0001g0076 | 2 | HG02886.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(263): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(267): Show |
2 | a0001c0001t0001g0043a0001c0001t0001g0045 | 2 | HG01109.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(276): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(249): Show |
5 | a0001c0001t0001g0003a0001c0001t0001g0042a0001c0001t0001g0044others(2): Show | 5 | HG02257.hp1 HG02965.hp1 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(258): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(218): Show |
1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(227): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(231): Show |
13 | a0001c0001t0001g0022a0001c0001t0001g0041a0001c0001t0001g0061others(10): Show | 13 | HG02486.hp2 HG02615.hp1 HG02723.hp2 others(10): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(240): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(257): Show |
2 | a0001c0001t0001g0062a0001c0001t0001g0075 | 2 | HG02572.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(266): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(182): Show |
10 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0131others(7): Show | 10 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(7): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(191): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(195): Show |
6 | a0001c0001t0001g0124a0001c0001t0001g0134a0001c0002t0001g0127others(3): Show | 6 | HG02257.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(204): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(267): Show |
1 | a0001c0001t0001g0158 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(276): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(187): Show |
1 | a0001c0001t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(196): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(195): Show |
1 | a0001c0001t0001g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(204): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(279): Show |
2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(288): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(226): Show |
1 | a0001c0001t0001g0073 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(235): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(241): Show |
1 | a0001c0001t0001g0086 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(250): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCCCCTC others(234): Show |
1 | a0001c0001t0001g0050 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(243): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(196): Show |
1 | a0001c0001t0002g0167 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(205): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(162): Show |
1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(171): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(58): Show |
1 | a0001c0001t0003g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(67): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(221): Show |
1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(230): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(182): Show |
2 | a0001c0001t0002g0243a0001c0001t0002g0258 | 2 | NA18981.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(191): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(182): Show |
4 | a0001c0001t0002g0269a0001c0001t0002g0270a0001c0001t0002g0272others(1): Show | 4 | NA18970.hp1 NA18985.hp2 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(191): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(195): Show |
6 | a0001c0001t0002g0162a0001c0001t0002g0168a0001c0001t0002g0169others(3): Show | 6 | HG01928.hp1 HG01952.hp2 HG02273.hp2 others(3): Show |
intron_variant | MODIFIER | c.4311+766_4311+767i others(204): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(265): Show |
1 | a0001c0001t0002g0173 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(274): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(239): Show |
2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG00642.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(248): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(195): Show |
2 | a0001c0001t0002g0241a0001c0001t0002g0246 | 2 | NA18939.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(204): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(265): Show |
1 | a0001c0001t0002g0176 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(274): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(278): Show |
1 | a0001c0001t0002g0172 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(287): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(234): Show |
1 | a0001c0001t0002g0171 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(243): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(208): Show |
1 | a0002c0005t0003g0186 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(217): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(216): Show |
2 | a0001c0001t0003g0193a0001c0001t0003g0229 | 2 | HG02027.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.4311+766_4311+767i others(225): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(224): Show |
1 | a0001c0001t0003g0218 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(233): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(239): Show |
1 | a0001c0001t0002g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(248): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(139): Show |
1 | a0001c0001t0002g0164 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(148): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(152): Show |
1 | a0001c0001t0002g0163 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.4311+766_4311+767i others(161): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | CTCTCCTC others(152): Show |
1 | a0001c0001t0002g0166 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4311+766_4311+767i others(161): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012181
|
C | T | 1 | a0001c0001t0002g0274 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.4311+766C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012181 | ||||||
chr10:92012182
|
C | CTCCCTCC others(251): Show |
1 | a0001c0001t0001g0066 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4311+767_4311+768i others(260): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012182 | ||||||
chr10:92012182
|
C | T | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 155 | HG00140.hp1 HG00438.hp1 HG00544.hp1 others(152): Show |
intron_variant | MODIFIER | c.4311+767C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012182 | ||||||
chr10:92012192
|
C | T | 5 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | HG01243.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4311+777C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012192 | ||||||
chr10:92012194
|
T | C | 5 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(2): Show | 5 | HG01243.hp1 HG02280.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.4311+779T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012194 | ||||||
chr10:92012195
|
T | C | 71 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(68): Show | 71 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(68): Show |
intron_variant | MODIFIER | c.4311+780T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012195 | ||||||
chr10:92012195
|
T | TCTCCC | 8 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0130others(5): Show | 8 | HG02257.hp2 HG02572.hp1 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.4311+800_4311+804d others(7): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012195 | |||||
chr10:92012197
|
T | TCTCCCCT others(284): Show |
1 | a0001c0001t0001g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4311+783_4311+784i others(293): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012197 | |||||
chr10:92012200
|
C | CCTCCCCT others(1): Show |
24 | a0001c0001t0001g0071a0001c0001t0001g0097a0001c0001t0001g0098others(21): Show | 25 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(22): Show |
intron_variant | MODIFIER | c.4311+792_4311+793i others(10): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012200 | |||||
chr10:92012209
|
C | CTCCCCTC others(143): Show |
1 | a0001c0001t0005g0141 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.4311+794_4311+795i others(152): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012209 | ||||||
chr10:92012210
|
C | T | 61 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(58): Show | 61 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.4311+795C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012210 | ||||||
chr10:92012211
|
C | T | 105 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(102): Show | 105 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(102): Show |
intron_variant | MODIFIER | c.4311+796C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012211 | ||||||
chr10:92012215
|
C | T | 58 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(55): Show | 58 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.4311+800C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012215 | ||||||
chr10:92012220
|
T | C | 17 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(14): Show | 17 | HG00639.hp1 HG01243.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.4311+805T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012220 | ||||||
chr10:92012220
|
T | TCCCCTCC others(21): Show |
1 | a0001c0001t0013g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4311+829_4311+830i others(30): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012220 | |||||
chr10:92012222
|
C | CCCTCCCC others(132): Show |
1 | a0001c0001t0005g0142 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.4311+817_4311+818i others(141): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012222 | |||||
chr10:92012222
|
C | CCCTCCCC others(130): Show |
2 | a0001c0001t0005g0143a0001c0001t0005g0147 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.4311+817_4311+818i others(139): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012222 | |||||
chr10:92012222
|
C | T | 13 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0131others(10): Show | 13 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(10): Show |
intron_variant | MODIFIER | c.4311+807C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012222 | ||||||
chr10:92012223
|
C | T | 1 | a0001c0013t0002g0091 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4311+808C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012223 | ||||||
chr10:92012225
|
T | C | 1 | a0001c0013t0002g0091 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4311+810T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012225 | ||||||
chr10:92012227
|
C | CCTCCTCC others(139): Show |
1 | a0001c0001t0002g0274 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.4311+813_4311+814i others(148): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012227 | |||||
chr10:92012228
|
C | CCTCCCCT others(20): Show |
12 | a0001c0001t0002g0291a0001c0001t0004g0314a0001c0001t0004g0315others(9): Show | 12 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.4311+824_4311+825i others(29): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012228 | |||||
chr10:92012228
|
C | T | 1 | a0001c0013t0002g0091 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.4311+813C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012228 | ||||||
chr10:92012233
|
C | CCCTCTAT others(10): Show |
1 | a0001c0001t0002g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4311+819_4311+820i others(19): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCCCT others(20): Show |
1 | a0001c0001t0002g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4311+830_4311+831i others(29): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCCCT others(218): Show |
1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4311+829_4311+830i others(227): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(233): Show |
1 | a0001c0001t0003g0187 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.4311+822_4311+823i others(242): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(212): Show |
1 | a0001c0001t0003g0189 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.4311+822_4311+823i others(221): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(224): Show |
3 | a0001c0001t0003g0201a0001c0001t0003g0231a0002c0005t0003g0207 | 3 | HG02132.hp1 NA19007.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.4311+822_4311+823i others(233): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(211): Show |
20 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0190others(17): Show | 20 | HG00423.hp1 HG00642.hp2 HG01069.hp2 others(17): Show |
intron_variant | MODIFIER | c.4311+822_4311+823i others(220): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(224): Show |
1 | a0001c0001t0003g0226 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4311+822_4311+823i others(233): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(233): Show |
1 | a0001c0001t0006g0212 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4311+822_4311+823i others(242): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(224): Show |
2 | a0001c0001t0003g0177a0001c0001t0003g0179 | 2 | HG02040.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.4311+822_4311+823i others(233): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(234): Show |
1 | a0001c0001t0003g0209 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4311+822_4311+823i others(243): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(232): Show |
22 | a0001c0001t0003g0181a0001c0001t0003g0182a0001c0001t0003g0183others(19): Show | 22 | HG00140.hp2 HG00544.hp2 HG00673.hp2 others(19): Show |
intron_variant | MODIFIER | c.4311+822_4311+823i others(241): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(219): Show |
1 | a0001c0001t0003g0180 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4311+822_4311+823i others(228): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(242): Show |
1 | a0001c0001t0003g0192 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4311+822_4311+823i others(251): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(183): Show |
1 | a0001c0001t0003g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4311+822_4311+823i others(192): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012233
|
C | CCTCCTCC others(245): Show |
4 | a0001c0001t0003g0195a0001c0001t0003g0200a0001c0001t0003g0213others(1): Show | 4 | HG01255.hp2 HG01516.hp2 HG01517.hp1 others(1): Show |
intron_variant | MODIFIER | c.4311+822_4311+823i others(254): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012233 | |||||
chr10:92012238
|
CCTCCCCC others(3): Show |
C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.4311+825_4311+834d others(12): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012238 | |||||
chr10:92012240
|
T | C | 14 | a0001c0001t0002g0278a0001c0001t0002g0291a0001c0001t0004g0314others(11): Show | 14 | HG00609.hp2 HG01081.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.4311+825T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012240 | ||||||
chr10:92012240
|
T | TCCCCCTG others(21): Show |
4 | a0001c0001t0003g0193a0001c0001t0003g0218a0001c0001t0003g0229others(1): Show | 4 | HG02027.hp2 HG02055.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.4311+830_4311+831i others(30): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012240 | |||||
chr10:92012243
|
C | CCCCCT | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(184): Show | 188 | HG00140.hp2 HG00423.hp1 HG00438.hp1 others(185): Show |
intron_variant | MODIFIER | c.4311+851_4311+855d others(7): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012243 | |||||
chr10:92012243
|
C | CCCCCTCC others(3): Show |
10 | a0001c0001t0001g0042a0001c0001t0001g0043a0001c0001t0001g0044others(7): Show | 10 | HG01109.hp2 HG02257.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.4311+846_4311+855d others(12): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012243 | |||||
chr10:92012243
|
C | CCCTCTAT others(27): Show |
1 | a0001c0001t0002g0253 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.4311+830_4311+831i others(36): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012243 | |||||
chr10:92012243
|
C | CCCTCTAT others(26): Show |
4 | a0001c0001t0002g0168a0001c0001t0002g0293a0001c0001t0002g0303others(1): Show | 4 | HG01261.hp1 HG01952.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.4311+830_4311+831i others(35): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012243 | |||||
chr10:92012243
|
C | CCCTCTAT others(25): Show |
81 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(78): Show | 81 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.4311+830_4311+831i others(34): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012243 | |||||
chr10:92012243
|
C | CCCTCTAT others(30): Show |
1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4311+830_4311+831i others(39): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012243 | |||||
chr10:92012243
|
C | T | 17 | a0001c0001t0002g0278a0001c0001t0002g0291a0001c0001t0004g0314others(14): Show | 17 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.4311+828C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012243 | ||||||
chr10:92012271
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4311+856T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012271 | ||||||
chr10:92012521
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4311+1106G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012521 | ||||||
chr10:92012552
|
A | G | 4 | a0001c0001t0001g0073a0001c0001t0001g0080a0001c0001t0006g0217others(1): Show | 4 | HG01243.hp2 HG03098.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.4312-1115A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012552 | ||||||
chr10:92012585
|
G | A | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 323 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(320): Show |
intron_variant | MODIFIER | c.4312-1082G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012585 | ||||||
chr10:92012602
|
C | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4312-1065C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012602 | ||||||
chr10:92012652
|
T | A | 4 | a0001c0001t0003g0200a0001c0001t0003g0213a0001c0001t0003g0218others(1): Show | 4 | HG01516.hp2 HG01517.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.4312-1015T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012652 | ||||||
chr10:92012653
|
C | A | 4 | a0001c0001t0003g0200a0001c0001t0003g0213a0001c0001t0003g0218others(1): Show | 4 | HG01516.hp2 HG01517.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.4312-1014C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012653 | ||||||
chr10:92012770
|
C | CA | 96 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 96 | HG00544.hp1 HG00609.hp1 HG00639.hp2 others(93): Show |
intron_variant | MODIFIER | c.4312-877dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012770 | |||||
chr10:92012770
|
C | CAA | 59 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(56): Show | 60 | HG00438.hp1 HG00733.hp1 HG00733.hp2 others(57): Show |
intron_variant | MODIFIER | c.4312-878_4312-877d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012770 | |||||
chr10:92012770
|
CA | C | 79 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0002g0162others(76): Show | 79 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.4312-877delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012770 | |||||
chr10:92012770
|
CAA | C | 48 | a0001c0001t0002g0163a0001c0001t0002g0164a0001c0001t0002g0166others(45): Show | 48 | HG00140.hp1 HG00735.hp2 HG01069.hp1 others(45): Show |
intron_variant | MODIFIER | c.4312-878_4312-877d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012770 | |||||
chr10:92012800
|
TATAATTA others(8): Show |
T | 1 | a0001c0001t0002g0274 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.4312-865_4312-851d others(17): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | INFO_REALIGN_3_PRIME | chr10 | 92012800 | |||||
chr10:92012840
|
C | T | 1 | a0001c0001t0001g0102 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4312-827C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012840 | ||||||
chr10:92012902
|
A | T | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4312-765A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92012902 | ||||||
chr10:92013102
|
A | T | 1 | a0001c0001t0001g0069 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4312-565A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92013102 | ||||||
chr10:92013147
|
G | A | 1 | a0001c0001t0003g0209 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.4312-520G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92013147 | ||||||
chr10:92013266
|
T | C | 1 | a0001c0001t0002g0300 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4312-401T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92013266 | ||||||
chr10:92013424
|
G | C | 1 | a0001c0001t0002g0300 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.4312-243G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92013424 | ||||||
chr10:92013496
|
G | T | 3 | a0001c0001t0003g0201a0002c0005t0003g0186a0002c0005t0003g0207 | 3 | HG02132.hp1 NA18979.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.4312-171G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92013496 | ||||||
chr10:92013554
|
T | G | 1 | a0001c0001t0002g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.4312-113T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92013554 | ||||||
chr10:92013592
|
C | T | 1 | a0001c0001t0001g0087 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.4312-75C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92013592 | ||||||
chr10:92013634
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4312-33A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 30/37 | chr10 | 92013634 | ||||||
chr10:92014035
|
G | A | 5 | a0001c0001t0003g0196a0001c0001t0003g0197a0001c0001t0003g0198others(2): Show | 5 | HG01069.hp2 HG01123.hp2 HG01169.hp1 others(2): Show |
splice_region_variant&intron_variant | LOW | c.4584+6G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92014035 | ||||||
chr10:92014060
|
G | T | 18 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(15): Show | 18 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.4584+31G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92014060 | ||||||
chr10:92014165
|
G | A | 318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(315): Show | 319 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.4584+136G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92014165 | ||||||
chr10:92014295
|
C | T | 1 | a0001c0003t0001g0126 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4584+266C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92014295 | ||||||
chr10:92014314
|
G | A | 89 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 89 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.4584+285G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92014314 | ||||||
chr10:92014321
|
G | A | 1 | a0001c0001t0001g0138 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4584+292G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92014321 | ||||||
chr10:92014335
|
C | G | 1 | a0001c0001t0002g0250 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4584+306C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92014335 | ||||||
chr10:92014492
|
G | A | 1 | a0001c0001t0002g0269 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.4584+463G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92014492 | ||||||
chr10:92014614
|
A | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.4584+585A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92014614 | ||||||
chr10:92015019
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.4584+990A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92015019 | ||||||
chr10:92015025
|
TTGTGCAG others(16): Show |
T | 1 | a0001c0001t0003g0185 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4584+997_4584+1019 others(26): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92015025 | ||||||
chr10:92015032
|
G | T | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4584+1003G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92015032 | ||||||
chr10:92015194
|
G | T | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.4585-1146G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92015194 | ||||||
chr10:92015239
|
C | T | 7 | a0001c0001t0003g0161a0001c0001t0003g0196a0001c0001t0003g0197others(4): Show | 7 | HG01069.hp2 HG01123.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.4585-1101C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92015239 | ||||||
chr10:92015263
|
C | G | 2 | a0001c0001t0001g0103a0001c0001t0001g0104 | 2 | HG02895.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.4585-1077C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92015263 | ||||||
chr10:92015384
|
A | G | 1 | a0001c0010t0001g0002 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.4585-956A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92015384 | ||||||
chr10:92015616
|
A | G | 91 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(88): Show | 91 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(88): Show |
intron_variant | MODIFIER | c.4585-724A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92015616 | ||||||
chr10:92015620
|
G | GA | 26 | a0001c0001t0001g0003a0001c0001t0001g0041a0001c0001t0001g0042others(23): Show | 26 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(23): Show |
intron_variant | MODIFIER | c.4585-713dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | INFO_REALIGN_3_PRIME | chr10 | 92015620 | |||||
chr10:92015728
|
G | A | 4 | a0001c0001t0002g0275a0001c0001t0002g0276a0001c0001t0002g0280others(1): Show | 4 | HG01069.hp1 HG01255.hp1 HG01943.hp2 others(1): Show |
intron_variant | MODIFIER | c.4585-612G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92015728 | ||||||
chr10:92015884
|
G | T | 2 | a0001c0001t0002g0278a0001c0001t0002g0287 | 2 | HG02015.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.4585-456G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92015884 | ||||||
chr10:92016011
|
A | G | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.4585-329A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92016011 | ||||||
chr10:92016064
|
A | G | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4585-276A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92016064 | ||||||
chr10:92016087
|
G | A | 3 | a0001c0003t0001g0125a0001c0003t0001g0126a0001c0003t0001g0135 | 3 | HG02809.hp2 HG03139.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4585-253G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92016087 | ||||||
chr10:92016130
|
A | G | 1 | a0001c0001t0002g0265 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.4585-210A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92016130 | ||||||
chr10:92016196
|
G | A | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.4585-144G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92016196 | ||||||
chr10:92016291
|
A | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.4585-49A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 32/37 | chr10 | 92016291 | ||||||
chr10:92016483
|
C | CT | 88 | a0001c0001t0001g0052a0001c0001t0002g0162a0001c0001t0002g0163others(85): Show | 88 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.4710+31dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr10 | 92016483 | |||||
chr10:92016500
|
A | G | 19 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(16): Show | 19 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.4710+35A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92016500 | ||||||
chr10:92016549
|
G | C | 1 | a0001c0001t0001g0051 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4710+84G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92016549 | ||||||
chr10:92016550
|
C | G | 1 | a0001c0001t0001g0051 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.4710+85C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92016550 | ||||||
chr10:92016559
|
A | G | 1 | a0001c0001t0002g0325 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4710+94A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92016559 | ||||||
chr10:92016747
|
A | G | 1 | a0001c0001t0001g0119 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4710+282A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92016747 | ||||||
chr10:92016814
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4710+349G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92016814 | ||||||
chr10:92017107
|
C | A | 1 | a0001c0001t0013g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4710+642C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92017107 | ||||||
chr10:92017110
|
T | C | 1 | a0001c0001t0002g0297 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4710+645T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92017110 | ||||||
chr10:92017145
|
T | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4710+680T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92017145 | ||||||
chr10:92017198
|
G | A | 3 | a0001c0001t0002g0265a0001c0001t0002g0266a0001c0001t0002g0267 | 3 | HG02135.hp2 NA18954.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.4710+733G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92017198 | ||||||
chr10:92017367
|
A | T | 1 | a0001c0001t0003g0180 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.4710+902A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92017367 | ||||||
chr10:92017458
|
G | A | 1 | a0001c0001t0003g0226 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.4710+993G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92017458 | ||||||
chr10:92017560
|
G | T | 5 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0001t0002g0174others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.4710+1095G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92017560 | ||||||
chr10:92017593
|
C | A | 7 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0033others(4): Show | 7 | HG00733.hp2 HG00738.hp1 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.4710+1128C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92017593 | ||||||
chr10:92017739
|
G | T | 1 | a0001c0001t0003g0185 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4711-1044G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92017739 | ||||||
chr10:92017768
|
C | T | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4711-1015C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92017768 | ||||||
chr10:92018062
|
G | T | 19 | a0001c0001t0001g0122a0001c0001t0001g0124a0001c0001t0001g0128others(16): Show | 19 | HG00639.hp1 HG01433.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.4711-721G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92018062 | ||||||
chr10:92018158
|
A | C | 1 | a0001c0001t0001g0038 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4711-625A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92018158 | ||||||
chr10:92018512
|
A | C | 89 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(86): Show | 89 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(86): Show |
intron_variant | MODIFIER | c.4711-271A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92018512 | ||||||
chr10:92018575
|
C | T | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.4711-208C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92018575 | ||||||
chr10:92018576
|
G | A | 2 | a0001c0001t0003g0153a0001c0001t0010g0152 | 2 | HG01261.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.4711-207G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | chr10 | 92018576 | ||||||
chr10:92018675
|
G | GAAAGGCA others(4): Show |
1 | a0001c0001t0003g0185 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4711-104_4711-94du others(12): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr10 | 92018675 | |||||
chr10:92018763
|
CT | C | 63 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.4711-11delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 33/37 | INFO_REALIGN_3_PRIME | chr10 | 92018763 | |||||
chr10:92019114
|
T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0134 | 2 | HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.4863+179T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92019114 | ||||||
chr10:92019158
|
A | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.4863+223A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92019158 | ||||||
chr10:92019239
|
A | G | 1 | a0001c0001t0003g0179 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.4863+304A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92019239 | ||||||
chr10:92019450
|
A | C | 3 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156 | 3 | HG02280.hp2 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.4863+515A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92019450 | ||||||
chr10:92019774
|
T | C | 1 | a0001c0001t0002g0240 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.4863+839T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92019774 | ||||||
chr10:92019891
|
G | GT | 270 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(267): Show | 270 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(267): Show |
intron_variant | MODIFIER | c.4863+971dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr10 | 92019891 | |||||
chr10:92019891
|
G | GTT | 37 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0097others(34): Show | 38 | HG00733.hp1 HG00735.hp1 HG01081.hp2 others(35): Show |
intron_variant | MODIFIER | c.4863+970_4863+971d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr10 | 92019891 | |||||
chr10:92019893
|
T | G | 1 | a0001c0001t0013g0123 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.4863+958T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92019893 | ||||||
chr10:92020110
|
C | CT | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.4863+1177dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr10 | 92020110 | |||||
chr10:92020117
|
A | T | 1 | a0001c0001t0001g0038 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.4863+1182A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92020117 | ||||||
chr10:92020195
|
T | G | 1 | a0001c0001t0002g0276 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4863+1260T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92020195 | ||||||
chr10:92020213
|
G | A | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.4863+1278G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92020213 | ||||||
chr10:92020286
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.4863+1351A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92020286 | ||||||
chr10:92020353
|
C | G | 1 | a0001c0002t0001g0127 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4863+1418C>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92020353 | ||||||
chr10:92020447
|
T | G | 1 | a0001c0001t0002g0271 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.4863+1512T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92020447 | ||||||
chr10:92020461
|
A | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.4863+1526A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92020461 | ||||||
chr10:92020505
|
T | C | 1 | a0001c0001t0002g0282 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.4863+1570T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92020505 | ||||||
chr10:92020524
|
G | A | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.4863+1589G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92020524 | ||||||
chr10:92020601
|
A | G | 2 | a0001c0001t0003g0200a0001c0001t0003g0213 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.4863+1666A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92020601 | ||||||
chr10:92020714
|
G | A | 1 | a0001c0001t0004g0318 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.4863+1779G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92020714 | ||||||
chr10:92021017
|
G | T | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.4863+2082G>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021017 | ||||||
chr10:92021099
|
T | A | 1 | a0001c0001t0003g0185 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4863+2164T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021099 | ||||||
chr10:92021345
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.4863+2410C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021345 | ||||||
chr10:92021382
|
A | G | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | HG00642.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.4863+2447A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021382 | ||||||
chr10:92021385
|
T | G | 1 | a0001c0001t0005g0143 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4863+2450T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021385 | ||||||
chr10:92021427
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | NA18944.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.4863+2492G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021427 | ||||||
chr10:92021652
|
T | C | 312 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(309): Show | 313 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(310): Show |
intron_variant | MODIFIER | c.4863+2717T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021652 | ||||||
chr10:92021678
|
A | G | 28 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(25): Show | 29 | HG00733.hp1 HG00735.hp1 HG01099.hp2 others(26): Show |
intron_variant | MODIFIER | c.4863+2743A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021678 | ||||||
chr10:92021699
|
G | A | 13 | a0001c0001t0002g0313a0001c0001t0002g0325a0001c0001t0004g0314others(10): Show | 13 | HG00738.hp2 HG01081.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.4863+2764G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021699 | ||||||
chr10:92021735
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4863+2800A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021735 | ||||||
chr10:92021746
|
G | A | 2 | a0001c0001t0001g0124a0001c0001t0001g0134 | 2 | HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.4863+2811G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021746 | ||||||
chr10:92021765
|
C | T | 5 | a0001c0001t0002g0235a0001c0001t0002g0236a0001c0001t0002g0237others(2): Show | 5 | NA18942.hp1 NA18950.hp1 NA18968.hp2 others(2): Show |
intron_variant | MODIFIER | c.4863+2830C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021765 | ||||||
chr10:92021961
|
A | G | 1 | a0001c0001t0001g0117 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4864-2795A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92021961 | ||||||
chr10:92022123
|
G | A | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4864-2633G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92022123 | ||||||
chr10:92022169
|
C | T | 168 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(165): Show | 168 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(165): Show |
intron_variant | MODIFIER | c.4864-2587C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92022169 | ||||||
chr10:92022746
|
A | C | 2 | a0001c0001t0001g0105a0001c0001t0001g0119 | 2 | HG02717.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.4864-2010A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92022746 | ||||||
chr10:92022753
|
C | T | 1 | a0001c0001t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4864-2003C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92022753 | ||||||
chr10:92022788
|
A | G | 90 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(87): Show | 90 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.4864-1968A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92022788 | ||||||
chr10:92022903
|
A | G | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.4864-1853A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92022903 | ||||||
chr10:92023034
|
C | A | 1 | a0001c0001t0001g0011 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4864-1722C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92023034 | ||||||
chr10:92023138
|
G | A | 1 | a0001c0001t0001g0013 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.4864-1618G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92023138 | ||||||
chr10:92023221
|
A | G | 7 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.4864-1535A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92023221 | ||||||
chr10:92023437
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4864-1319C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92023437 | ||||||
chr10:92023510
|
C | T | 1 | a0001c0001t0001g0071 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4864-1246C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92023510 | ||||||
chr10:92023529
|
C | T | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.4864-1227C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92023529 | ||||||
chr10:92023552
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4864-1204C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92023552 | ||||||
chr10:92023672
|
A | T | 8 | a0001c0001t0001g0154a0001c0001t0001g0155a0001c0001t0001g0156others(5): Show | 8 | HG02280.hp2 HG02451.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.4864-1084A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92023672 | ||||||
chr10:92023776
|
C | T | 1 | a0001c0001t0002g0232 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.4864-980C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92023776 | ||||||
chr10:92023791
|
A | G | 11 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0131others(8): Show | 11 | HG00639.hp1 HG01433.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.4864-965A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92023791 | ||||||
chr10:92023863
|
A | T | 1 | a0001c0001t0001g0105 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4864-893A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92023863 | ||||||
chr10:92023920
|
G | C | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4864-836G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92023920 | ||||||
chr10:92024062
|
A | G | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.4864-694A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92024062 | ||||||
chr10:92024297
|
T | G | 2 | a0001c0001t0003g0203a0001c0001t0003g0208 | 2 | NA18988.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.4864-459T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92024297 | ||||||
chr10:92024461
|
G | C | 1 | a0001c0001t0003g0214 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4864-295G>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92024461 | ||||||
chr10:92024511
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4864-245C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | chr10 | 92024511 | ||||||
chr10:92024731
|
A | AGTTTTTT others(1): Show |
63 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(60): Show | 63 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.4864-24_4864-17dup others(8): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr10 | 92024731 | |||||
chr10:92024731
|
A | AGTTTTTT others(3): Show |
1 | a0001c0001t0002g0165 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4864-17_4864-16ins others(10): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr10 | 92024731 | |||||
chr10:92024732
|
G | GTTTTTTT others(2): Show |
14 | a0001c0001t0002g0174a0001c0001t0002g0313a0001c0001t0002g0325others(11): Show | 14 | HG00642.hp1 HG00738.hp2 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.4864-17_4864-16ins others(9): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr10 | 92024732 | |||||
chr10:92024732
|
G | GTTTTTTT others(3): Show |
85 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(82): Show | 85 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(82): Show |
intron_variant | MODIFIER | c.4864-17_4864-16ins others(10): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr10 | 92024732 | |||||
chr10:92024732
|
G | GTTTTTTT others(4): Show |
4 | a0001c0001t0002g0171a0001c0001t0002g0245a0001c0001t0002g0250others(1): Show | 4 | HG01891.hp1 HG02027.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.4864-17_4864-16ins others(11): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr10 | 92024732 | |||||
chr10:92024732
|
GT | G | 6 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(3): Show | 6 | HG01243.hp1 HG02280.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.4864-10delT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 34/37 | INFO_REALIGN_3_PRIME | chr10 | 92024732 | |||||
chr10:92025005
|
T | C | 3 | a0001c0001t0001g0114a0001c0001t0001g0115a0001c0001t0001g0116 | 3 | HG02698.hp2 HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.5075+38T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025005 | ||||||
chr10:92025113
|
C | A | 311 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(308): Show | 312 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(309): Show |
intron_variant | MODIFIER | c.5075+146C>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025113 | ||||||
chr10:92025122
|
T | A | 2 | a0001c0001t0001g0053a0001c0001t0001g0059 | 2 | HG02698.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.5075+155T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025122 | ||||||
chr10:92025181
|
A | G | 11 | a0001c0001t0004g0314a0001c0001t0004g0315a0001c0001t0004g0316others(8): Show | 11 | HG01081.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.5075+214A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025181 | ||||||
chr10:92025442
|
T | A | 16 | a0001c0001t0001g0006a0001c0001t0001g0028a0001c0001t0001g0029others(13): Show | 16 | HG01070.hp1 HG01358.hp1 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.5075+475T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025442 | ||||||
chr10:92025443
|
T | A | 220 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(217): Show | 220 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(217): Show |
intron_variant | MODIFIER | c.5075+476T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025443 | ||||||
chr10:92025443
|
TA | T | 7 | a0001c0001t0001g0092a0001c0001t0001g0094a0001c0001t0001g0095others(4): Show | 7 | HG01243.hp1 HG02280.hp1 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.5075+486delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr10 | 92025443 | |||||
chr10:92025444
|
A | T | 57 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(54): Show | 58 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(55): Show |
intron_variant | MODIFIER | c.5075+477A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025444 | ||||||
chr10:92025445
|
A | T | 44 | a0001c0001t0001g0097a0001c0001t0001g0099a0001c0001t0001g0101others(41): Show | 45 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(42): Show |
intron_variant | MODIFIER | c.5075+478A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025445 | ||||||
chr10:92025446
|
A | T | 2 | a0001c0001t0001g0102a0001c0001t0001g0158 | 2 | HG03516.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.5075+479A>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025446 | ||||||
chr10:92025501
|
G | A | 1 | a0001c0001t0001g0148 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.5075+534G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025501 | ||||||
chr10:92025528
|
T | C | 104 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(101): Show | 104 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.5075+561T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025528 | ||||||
chr10:92025533
|
G | A | 1 | a0001c0001t0002g0301 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.5075+566G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025533 | ||||||
chr10:92025678
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5075+711A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92025678 | ||||||
chr10:92025810
|
C | CA | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(122): Show | 126 | HG00423.hp1 HG00438.hp1 HG00544.hp1 others(123): Show |
intron_variant | MODIFIER | c.5076-760dupA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr10 | 92025810 | |||||
chr10:92025810
|
C | CAA | 35 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(32): Show | 35 | HG00609.hp1 HG00738.hp1 HG01109.hp2 others(32): Show |
intron_variant | MODIFIER | c.5076-761_5076-760d others(4): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr10 | 92025810 | |||||
chr10:92025810
|
CA | C | 79 | a0001c0001t0001g0146a0001c0001t0002g0162a0001c0001t0002g0164others(76): Show | 79 | HG00140.hp1 HG00140.hp2 HG00423.hp2 others(76): Show |
intron_variant | MODIFIER | c.5076-760delA | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | INFO_REALIGN_3_PRIME | chr10 | 92025810 | |||||
chr10:92026074
|
C | T | 1 | a0001c0001t0003g0187 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.5076-518C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92026074 | ||||||
chr10:92026399
|
A | C | 318 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(315): Show | 319 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(316): Show |
intron_variant | MODIFIER | c.5076-193A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92026399 | ||||||
chr10:92026564
|
T | C | 1 | a0001c0001t0003g0161 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5076-28T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 35/37 | chr10 | 92026564 | ||||||
chr10:92026800
|
A | C | 64 | a0001c0001t0003g0153a0001c0001t0003g0161a0001c0001t0003g0177others(61): Show | 64 | HG00140.hp2 HG00423.hp1 HG00544.hp2 others(61): Show |
intron_variant | MODIFIER | c.5235+49A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 36/37 | chr10 | 92026800 | ||||||
chr10:92027480
|
A | AT | 144 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 145 | HG00438.hp1 HG00544.hp1 HG00609.hp1 others(142): Show |
intron_variant | MODIFIER | c.5406+191dupT | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chr10 | 92027480 | |||||
chr10:92027511
|
T | A | 1 | a0001c0001t0002g0170 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5406+211T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | chr10 | 92027511 | ||||||
chr10:92027530
|
C | T | 3 | a0001c0001t0002g0273a0001c0001t0002g0274a0001c0013t0002g0091 | 3 | HG00609.hp2 NA18962.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.5406+230C>T | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | chr10 | 92027530 | ||||||
chr10:92027667
|
A | G | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5406+367A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | chr10 | 92027667 | ||||||
chr10:92027677
|
T | G | 322 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(319): Show | 323 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(320): Show |
intron_variant | MODIFIER | c.5406+377T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | chr10 | 92027677 | ||||||
chr10:92027917
|
T | C | 1 | a0001c0001t0003g0205 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.5406+617T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | chr10 | 92027917 | ||||||
chr10:92027972
|
G | A | 1 | a0001c0001t0001g0057 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.5406+672G>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | chr10 | 92027972 | ||||||
chr10:92028056
|
T | A | 1 | a0001c0001t0001g0097 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.5407-734T>A | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | chr10 | 92028056 | ||||||
chr10:92028056
|
T | C | 1 | a0001c0001t0002g0313 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.5407-734T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | chr10 | 92028056 | ||||||
chr10:92028133
|
A | C | 1 | a0001c0001t0003g0194 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.5407-657A>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | chr10 | 92028133 | ||||||
chr10:92028464
|
T | G | 1 | a0001c0001t0001g0012 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.5407-326T>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | chr10 | 92028464 | ||||||
chr10:92028495
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.5407-295T>C | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | chr10 | 92028495 | ||||||
chr10:92028521
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5407-269A>G | BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | chr10 | 92028521 | ||||||
chr10:92028759
|
A | ATT | 96 | a0001c0001t0002g0162a0001c0001t0002g0163a0001c0001t0002g0164others(93): Show | 96 | HG00140.hp1 HG00423.hp2 HG00438.hp2 others(93): Show |
intron_variant | MODIFIER | c.5407-18_5407-17dup others(2): Show |
BTAF1 | ENSG00000095564.15 | transcript | ENST00000265990.12 | protein_coding | 37/37 | INFO_REALIGN_3_PRIME | chr10 | 92028759 |