Item | Value |
---|---|
geneid | 63035 |
ensemblid | ENSG00000085185.16 |
hgncid | 25657 |
symbol | BCORL1 |
name | BCL6 corepressor like 1 |
refseq_nuc | NM_001379451.1 |
refseq_prot | NP_001366380.1 |
ensembl_nuc | ENST00000540052.6 |
ensembl_prot | ENSP00000437775.2 |
mane_status | MANE Select |
chr | chrX |
start | 129982635 |
end | 130058071 |
strand | + |
ver | v1.2 |
region | chrX:129982635-130058071 |
region5000 | chrX:129977635-130063071 |
regionname0 | BCORL1_chrX_129982635_130058071 |
regionname5000 | BCORL1_chrX_129977635_130063071 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1785 | 191 | 66 | 29 | 74 | 5 | 15 | 55 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0002 | 0/0 | 1785 | 5 | 0 | 5 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0003 | 0/0 | 1785 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0004 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0005 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0006 | 0/0 | 1785 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0007 | 0/0 | 1257 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0008 | 0/0 | 1785 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0009 | 0/0 | 1785 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 5358 | 155 | 36 | 27 | 72 | 5 | 13 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0002 | 0/0 | 5358 | 11 | 9 | 2 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0003 | 0/0 | 5358 | 9 | 9 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0004 | 0/0 | 5358 | 5 | 0 | 5 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0005 | 0/0 | 5358 | 4 | 4 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0006 | 0/0 | 5358 | 3 | 3 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0007 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0008 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0009 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0010 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0011 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0012 | 0/0 | 5357 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0013 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0014 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0015 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0016 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0017 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0018 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0019 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0020 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0021 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
c0022 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 2108 | 155 | 30 | 32 | 70 | 5 | 16 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0002 | 0/0 | 2108 | 26 | 24 | 2 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0003 | 0/0 | 2108 | 4 | 0 | 0 | 4 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0004 | 0/0 | 2108 | 2 | 2 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0005 | 0/0 | 2108 | 2 | 2 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0006 | 0/0 | 2108 | 2 | 2 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0007 | 0/0 | 2108 | 2 | 2 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0008 | 0/0 | 2108 | 2 | 2 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0009 | 0/0 | 2108 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0010 | 0/0 | 2108 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0011 | 0/0 | 2073 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0012 | 0/0 | 2109 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0013 | 0/0 | 2108 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0014 | 0/0 | 2108 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0015 | 0/0 | 2108 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
t0016 | 0/0 | 2110 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0008 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 5358 | 155 | 36 | 27 | 72 | 5 | 13 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0002 | 0/0 | 5358 | 11 | 9 | 2 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0003 | 0/0 | 5358 | 9 | 9 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0005 | 0/0 | 5358 | 4 | 4 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0006 | 0/0 | 5358 | 3 | 3 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0007 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0008 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0009 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0010 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0014 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0016 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0019 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0020 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0001c0022 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0002c0004 | 0/0 | 5358 | 5 | 0 | 5 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0003c0011 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0004c0018 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0005c0013 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0006c0015 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0007c0012 | 0/0 | 5357 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0008c0017 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 | |
a0009c0021 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 7465 | 141 | 28 | 26 | 67 | 5 | 13 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0001t0002 | 0/0 | 7465 | 2 | 2 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0001t0003 | 0/0 | 7465 | 3 | 0 | 0 | 3 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0001t0004 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0001t0005 | 0/0 | 7465 | 2 | 2 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0001t0007 | 0/0 | 7465 | 2 | 2 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0001t0010 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0001t0012 | 0/0 | 7466 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0001t0014 | 0/0 | 7465 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0001t0016 | 0/0 | 7467 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0002t0002 | 0/0 | 7465 | 10 | 8 | 2 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0002t0006 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0003t0002 | 0/0 | 7465 | 9 | 9 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0005t0006 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0005t0008 | 0/0 | 7465 | 2 | 2 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0005t0009 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0006t0002 | 0/0 | 7465 | 3 | 3 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0007t0001 | 0/0 | 7465 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0008t0004 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0009t0015 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0010t0003 | 0/0 | 7465 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0014t0013 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0016t0001 | 0/0 | 7465 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0019t0002 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0020t0001 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0001c0022t0001 | 0/0 | 7465 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0002c0004t0001 | 0/0 | 7465 | 5 | 0 | 5 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0003c0011t0001 | 0/0 | 7465 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0004c0018t0001 | 0/0 | 7465 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0005c0013t0001 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0006c0015t0001 | 0/0 | 7465 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0007c0012t0011 | 0/0 | 7429 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0008c0017t0001 | 0/0 | 7465 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
a0009c0021t0002 | 0/0 | 7465 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | copy fasta | chrX | 129977635 | 130063071 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0008 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0003g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0004g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0005g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0005g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0007g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0010g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0012g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0014g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0001t0016g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0002t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0002t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0002t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0002t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0002t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0002t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0002t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0002t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0002t0006g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0003t0002g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0003t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0003t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0003t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0003t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0003t0002g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0003t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0005t0006g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0005t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0005t0008g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0005t0009g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0006t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0006t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0006t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0007t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0008t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0009t0015g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0010t0003g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0014t0013g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0016t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0019t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0020t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0001c0022t0001g0024 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0002c0004t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0002c0004t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0002c0004t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0002c0004t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0002c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0003c0011t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0004c0018t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0005c0013t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0006c0015t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0007c0012t0011g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0008c0017t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
a0009c0021t0002g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | GBR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0178 | EUR | FIN | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | CHS | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | CHS | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CHS | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG00642 | hp1 | a0002 | c0004 | t0001 | g0170 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | CHS | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG00735 | hp2 | a0002 | c0004 | t0001 | g0137 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0077 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0087 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01081 | hp1 | a0001 | c0002 | t0002 | g0092 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0184 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01192 | hp1 | a0001 | c0001 | t0014 | g0085 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PUR | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | CLM | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01256 | hp1 | a0002 | c0004 | t0001 | g0171 | AMR | CLM | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | CLM | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01358 | hp1 | a0002 | c0004 | t0001 | g0049 | AMR | CLM | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0029 | AMR | CLM | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | CLM | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | CLM | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | CLM | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01496 | hp2 | a0001 | c0002 | t0002 | g0188 | AMR | CLM | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0104 | EUR | IBS | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01884 | hp1 | a0001 | c0003 | t0002 | g0055 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01891 | hp1 | a0001 | c0005 | t0009 | g0191 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0135 | AMR | PEL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01978 | hp1 | a0008 | c0017 | t0001 | g0013 | AMR | PEL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | KHV | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02055 | hp1 | a0001 | c0002 | t0002 | g0032 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | KHV | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | KHV | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | KHV | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | KHV | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02148 | hp2 | a0002 | c0004 | t0001 | g0130 | AMR | PEL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02257 | hp1 | a0001 | c0002 | t0006 | g0031 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02258 | hp1 | a0001 | c0005 | t0008 | g0139 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02280 | hp2 | a0001 | c0003 | t0002 | g0193 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0132 | AMR | PEL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02451 | hp1 | a0001 | c0009 | t0015 | g0082 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02572 | hp1 | a0001 | c0006 | t0002 | g0119 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | PJL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02615 | hp1 | a0001 | c0002 | t0002 | g0004 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02622 | hp1 | a0005 | c0013 | t0001 | g0157 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02622 | hp2 | a0001 | c0003 | t0002 | g0174 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02630 | hp1 | a0001 | c0002 | t0002 | g0056 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02630 | hp2 | a0001 | c0008 | t0004 | g0060 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02717 | hp1 | a0001 | c0003 | t0002 | g0053 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02735 | hp1 | a0003 | c0011 | t0001 | g0026 | SAS | PJL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | PJL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02809 | hp1 | a0001 | c0003 | t0002 | g0051 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02818 | hp1 | a0001 | c0003 | t0002 | g0054 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0194 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02886 | hp2 | a0001 | c0002 | t0002 | g0173 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0081 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0080 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0149 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0197 | AFR | ESN | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | ESN | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ESN | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02970 | hp1 | a0001 | c0002 | t0002 | g0156 | AFR | ESN | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0099 | AFR | GWD | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ESN | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03195 | hp1 | a0001 | c0020 | t0001 | g0125 | AFR | ESN | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03195 | hp2 | a0001 | c0001 | t0007 | g0057 | AFR | ESN | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03209 | hp1 | a0009 | c0021 | t0002 | g0007 | AFR | MSL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03225 | hp1 | a0001 | c0006 | t0002 | g0094 | AFR | MSL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0189 | AFR | MSL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03453 | hp2 | a0001 | c0006 | t0002 | g0093 | AFR | MSL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03486 | hp1 | a0001 | c0014 | t0013 | g0138 | AFR | MSL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | MSL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0200 | AFR | ESN | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03516 | hp2 | a0001 | c0005 | t0008 | g0140 | AFR | ESN | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03579 | hp1 | a0001 | c0001 | t0005 | g0058 | AFR | MSL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03688 | hp1 | a0001 | c0022 | t0001 | g0024 | SAS | STU | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0042 | SAS | BEB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | STU | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0039 | SAS | STU | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG04228 | hp1 | a0001 | c0016 | t0001 | g0067 | SAS | STU | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18522 | hp1 | a0001 | c0005 | t0006 | g0196 | AFR | YRI | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18612 | hp1 | a0001 | c0007 | t0001 | g0064 | EAS | CHB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18906 | hp2 | a0001 | c0001 | t0007 | g0059 | AFR | YRI | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18974 | hp1 | a0001 | c0001 | t0016 | g0203 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18983 | hp1 | a0004 | c0018 | t0001 | g0175 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18985 | hp1 | a0007 | c0012 | t0011 | g0043 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18986 | hp1 | a0001 | c0001 | t0003 | g0105 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18990 | hp1 | a0006 | c0015 | t0001 | g0107 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19043 | hp1 | a0001 | c0003 | t0002 | g0148 | AFR | LWK | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0108 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19082 | hp1 | a0001 | c0010 | t0003 | g0198 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19086 | hp1 | a0001 | c0001 | t0012 | g0121 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19088 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0144 | EUR | TSI | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0124 | EUR | TSI | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | GIH | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02486 | hp1 | a0001 | c0002 | t0002 | g0033 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02559 | hp1 | a0001 | c0001 | t0010 | g0050 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG02559 | hp2 | a0001 | c0003 | t0002 | g0052 | AFR | ACB | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG06807 | hp1 | a0001 | c0002 | t0002 | g0155 | AFR | USA | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
HG06807 | hp2 | a0001 | c0001 | t0005 | g0120 | AFR | USA | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | USA | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA20300 | hp2 | a0001 | c0001 | t0004 | g0061 | AFR | USA | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA21309 | hp1 | a0001 | c0003 | t0002 | g0185 | AFR | LWK | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
NA21309 | hp2 | a0001 | c0019 | t0002 | g0117 | AFR | LWK | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0008 | REF | REF | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0180 | REF | REF | BCORL1_chrX_129977635_130063071 | BCORL1 | chrX | 129977635 | 130063071 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:130013397 | G | A | 1 | a0002 | 5 | HG00642.hp1 HG00735.hp2 HG01256.hp1 others(2): Show |
missense_variant | MODERATE | c.625G>A | p.Gly209Ser | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 797/7465 | 625/5358 | 209/1785 | chrX | 130013397 | ||
chrX:130015342 | G | A | 1 | a0003 | 1 | HG02735.hp1 | missense_variant | MODERATE | c.2570G>A | p.Gly857Glu | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 2742/7465 | 2570/5358 | 857/1785 | chrX | 130015342 | ||
chrX:130015404 | A | G | 1 | a0004 | 1 | NA18983.hp1 | missense_variant | MODERATE | c.2632A>G | p.Ser878Gly | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 2804/7465 | 2632/5358 | 878/1785 | chrX | 130015404 | ||
chrX:130016031 | G | A | 1 | a0009 | 1 | HG03209.hp1 | missense_variant | MODERATE | c.3259G>A | p.Gly1087Arg | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 3431/7465 | 3259/5358 | 1087/1785 | chrX | 130016031 | ||
chrX:130020988 | C | T | 1 | a0008 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.3445C>T | p.Arg1149Trp | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/14 | 3617/7465 | 3445/5358 | 1149/1785 | chrX | 130020988 | ||
chrX:130025038 | GC | G | 1 | a0007 | 1 | NA18985.hp1 | frameshift_variant | HIGH | c.3739delC | p.Gln1247fs | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/14 | 3911/7465 | 3739/5358 | 1247/1785 | INFO_REALIGN_3_PRIME | chrX | 130025038 | |
chrX:130025365 | G | A | 1 | a0005 | 1 | HG02622.hp1 | missense_variant | MODERATE | c.4064G>A | p.Arg1355Gln | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/14 | 4236/7465 | 4064/5358 | 1355/1785 | chrX | 130025365 | ||
chrX:130051940 | G | C | 1 | a0006 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.4999G>C | p.Glu1667Gln | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/14 | 5171/7465 | 4999/5358 | 1667/1785 | chrX | 130051940 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:130013051 | C | T | 1 | a0001c0022 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.279C>T | p.Asp93Asp | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 451/7465 | 279/5358 | 93/1785 | chrX | 130013051 | ||
chrX:130013561 | G | A | 1 | a0001c0007 | 1 | NA18612.hp1 | synonymous_variant | LOW | c.789G>A | p.Pro263Pro | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 961/7465 | 789/5358 | 263/1785 | chrX | 130013561 | ||
chrX:130014218 | G | A | 2 | a0001c0008a0001c0009 | 2 | HG02451.hp1 HG02630.hp2 |
synonymous_variant | LOW | c.1446G>A | p.Pro482Pro | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 1618/7465 | 1446/5358 | 482/1785 | chrX | 130014218 | ||
chrX:130014431 | T | C | 1 | a0001c0002 | 11 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(8): Show |
synonymous_variant | LOW | c.1659T>C | p.Leu553Leu | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 1831/7465 | 1659/5358 | 553/1785 | chrX | 130014431 | ||
chrX:130014471 | C | T | 2 | a0001c0006a0009c0021 | 4 | HG02572.hp1 HG03209.hp1 HG03225.hp1 others(1): Show |
synonymous_variant | LOW | c.1699C>T | p.Leu567Leu | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 1871/7465 | 1699/5358 | 567/1785 | chrX | 130014471 | ||
chrX:130014479 | A | G | 1 | a0001c0020 | 1 | HG03195.hp1 | synonymous_variant | LOW | c.1707A>G | p.Pro569Pro | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 1879/7465 | 1707/5358 | 569/1785 | chrX | 130014479 | ||
chrX:130014680 | G | A | 1 | a0001c0010 | 1 | NA19082.hp1 | synonymous_variant | LOW | c.1908G>A | p.Pro636Pro | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 2080/7465 | 1908/5358 | 636/1785 | chrX | 130014680 | ||
chrX:130014719 | C | T | 1 | a0001c0019 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.1947C>T | p.Pro649Pro | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 2119/7465 | 1947/5358 | 649/1785 | chrX | 130014719 | ||
chrX:130015517 | T | C | 1 | a0001c0008 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.2745T>C | p.Tyr915Tyr | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 2917/7465 | 2745/5358 | 915/1785 | chrX | 130015517 | ||
chrX:130015961 | C | T | 3 | a0001c0003a0001c0006a0009c0021 | 13 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
synonymous_variant | LOW | c.3189C>T | p.Ala1063Ala | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 3361/7465 | 3189/5358 | 1063/1785 | chrX | 130015961 | ||
chrX:130016168 | C | G | 6 | a0001c0002a0001c0003a0001c0005others(3): Show | 29 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(26): Show |
synonymous_variant | LOW | c.3396C>G | p.Leu1132Leu | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/14 | 3568/7465 | 3396/5358 | 1132/1785 | chrX | 130016168 | ||
chrX:130025081 | C | T | 1 | a0001c0016 | 1 | HG04228.hp1 | synonymous_variant | LOW | c.3780C>T | p.Pro1260Pro | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/14 | 3952/7465 | 3780/5358 | 1260/1785 | chrX | 130025081 | ||
chrX:130028714 | C | T | 1 | a0001c0019 | 1 | NA21309.hp2 | synonymous_variant | LOW | c.4158C>T | p.Pro1386Pro | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/14 | 4330/7465 | 4158/5358 | 1386/1785 | chrX | 130028714 | ||
chrX:130050727 | G | A | 1 | a0001c0014 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.4851G>A | p.Ser1617Ser | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 12/14 | 5023/7465 | 4851/5358 | 1617/1785 | chrX | 130050727 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:129982638 | C | CT | 1 | a0001c0001t0016 | 1 | NA18974.hp1 | 5_prime_UTR_variant | MODIFIER | c.-166dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/14 | 22590 | INFO_REALIGN_3_PRIME | chrX | 129982638 | ||||
chrX:129982675 | G | A | 1 | a0001c0005t0009 | 1 | HG01891.hp1 | 5_prime_UTR_variant | MODIFIER | c.-132G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/14 | 22557 | chrX | 129982675 | |||||
chrX:130056208 | A | G | 1 | a0001c0009t0015 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*72A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 72 | chrX | 130056208 | |||||
chrX:130056242 | C | T | 1 | a0001c0001t0014 | 1 | HG01192.hp1 | 3_prime_UTR_variant | MODIFIER | c.*106C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 106 | chrX | 130056242 | |||||
chrX:130056410 | G | A | 1 | a0001c0005t0009 | 1 | HG01891.hp1 | 3_prime_UTR_variant | MODIFIER | c.*274G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 274 | chrX | 130056410 | |||||
chrX:130056444 | T | A | 1 | a0001c0009t0015 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*308T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 308 | chrX | 130056444 | |||||
chrX:130056754 | G | T | 1 | a0001c0005t0008 | 2 | HG02258.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*618G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 618 | chrX | 130056754 | |||||
chrX:130056795 | C | T | 1 | a0001c0014t0013 | 1 | HG03486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*659C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 659 | chrX | 130056795 | |||||
chrX:130056894 | C | T | 1 | a0001c0001t0007 | 2 | HG03195.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*758C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 758 | chrX | 130056894 | |||||
chrX:130056895 | G | A | 2 | a0001c0001t0004a0001c0008t0004 | 2 | HG02630.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*759G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 759 | chrX | 130056895 | |||||
chrX:130057132 | G | A | 1 | a0001c0001t0005 | 2 | HG03579.hp1 HG06807.hp2 |
3_prime_UTR_variant | MODIFIER | c.*996G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 996 | chrX | 130057132 | |||||
chrX:130057253 | G | A | 12 | a0001c0001t0002a0001c0001t0007a0001c0002t0002others(9): Show | 34 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1117G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 1117 | chrX | 130057253 | |||||
chrX:130057281 | C | G | 2 | a0001c0001t0003a0001c0010t0003 | 4 | NA18986.hp1 NA19068.hp1 NA19082.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1145C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 1145 | chrX | 130057281 | |||||
chrX:130057405 | G | C | 1 | a0001c0001t0010 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1269G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 1269 | chrX | 130057405 | |||||
chrX:130057440 | T | TC | 1 | a0007c0012t0011 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1308dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 1309 | INFO_REALIGN_3_PRIME | chrX | 130057440 | ||||
chrX:130057466 | C | T | 3 | a0001c0002t0006a0001c0005t0006a0001c0005t0009 | 3 | HG01891.hp1 HG02257.hp1 NA18522.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1330C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 1330 | chrX | 130057466 | |||||
chrX:130057626 | G | GA | 1 | a0001c0001t0016 | 1 | NA18974.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1500dupA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 1501 | INFO_REALIGN_3_PRIME | chrX | 130057626 | ||||
chrX:130057651 | GGAAAAAA others(29): Show |
G | 1 | a0007c0012t0011 | 1 | NA18985.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1517_*1552delAAAA others(32): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 1517 | INFO_REALIGN_3_PRIME | chrX | 130057651 | ||||
chrX:130057652 | G | GA | 1 | a0001c0001t0012 | 1 | NA19086.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1527dupA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 14/14 | 1528 | INFO_REALIGN_3_PRIME | chrX | 130057652 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chrX:129982784 | A | AG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+28dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129982784 | |||||
chrX:129982854 | C | CG | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+94dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129982854 | |||||
chrX:129982879 | A | AC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+120dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129982879 | |||||
chrX:129982907 | T | TCTCCC | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-45+147_-45+151dup others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129982907 | |||||
chrX:129982924 | A | AC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+166dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129982924 | |||||
chrX:129982960 | A | AC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+201dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129982960 | |||||
chrX:129983014 | C | CG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+254dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983014 | |||||
chrX:129983034 | C | CCG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+272_-45+273ins others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129983034 | ||||||
chrX:129983120 | T | TC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+360dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983120 | |||||
chrX:129983144 | T | TC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+386dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983144 | |||||
chrX:129983172 | A | AC | 2 | a0001c0001t0001g0202a0001c0001t0016g0203 | 2 | NA18974.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-45+415dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983172 | |||||
chrX:129983275 | T | TG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+520dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983275 | |||||
chrX:129983387 | A | AG | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+627dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983387 | |||||
chrX:129983418 | C | CT | 3 | a0001c0001t0001g0199a0001c0001t0001g0202a0001c0010t0003g0198 | 3 | NA18989.hp1 NA19055.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.-45+664dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983418 | |||||
chrX:129983418 | CT | C | 3 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003 | 3 | HG01109.hp1 HG02257.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.-45+664delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983418 | |||||
chrX:129983426 | T | TG | 43 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(40): Show | 43 | HG00408.hp1 HG00621.hp1 HG01099.hp1 others(40): Show |
intron_variant | MODIFIER | c.-45+676dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983426 | |||||
chrX:129983426 | T | TGG | 3 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0002t0002g0004 | 3 | HG02145.hp1 HG02615.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-45+675_-45+676dup others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983426 | |||||
chrX:129983426 | TG | T | 13 | a0001c0001t0001g0183a0001c0001t0001g0184a0001c0001t0001g0186others(10): Show | 13 | HG01167.hp1 HG01169.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.-45+676delG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983426 | |||||
chrX:129983426 | TGG | T | 2 | a0001c0001t0001g0197a0001c0005t0006g0196 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-45+675_-45+676del others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983426 | |||||
chrX:129983427 | G | T | 1 | a0001c0001t0002g0200 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-45+665G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129983427 | ||||||
chrX:129983436 | G | GGGC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+676_-45+677ins others(3): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983436 | |||||
chrX:129983454 | G | GT | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+694dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983454 | |||||
chrX:129983480 | T | TC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+720dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983480 | |||||
chrX:129983491 | A | AG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+733dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983491 | |||||
chrX:129983531 | C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | NA18939.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.-45+769C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129983531 | ||||||
chrX:129983565 | G | GT | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+804dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983565 | |||||
chrX:129983582 | C | CG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+824dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983582 | |||||
chrX:129983651 | A | AAG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+889_-45+890ins others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129983651 | ||||||
chrX:129983708 | G | GGC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+946_-45+947ins others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129983708 | ||||||
chrX:129983713 | C | CG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+954dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983713 | |||||
chrX:129983724 | C | CG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+964dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983724 | |||||
chrX:129983761 | C | CGG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1003_-45+1004d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983761 | |||||
chrX:129983925 | T | TC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1168dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983925 | |||||
chrX:129983982 | A | AC | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-45+1224dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983982 | |||||
chrX:129983990 | T | TC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1230dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129983990 | |||||
chrX:129984007 | G | A | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(145): Show | 148 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(145): Show |
intron_variant | MODIFIER | c.-45+1245G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129984007 | ||||||
chrX:129984052 | C | CG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1294dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984052 | |||||
chrX:129984056 | G | GA | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+1295dupA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984056 | |||||
chrX:129984063 | A | AG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1304dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984063 | |||||
chrX:129984082 | C | CG | 2 | a0001c0001t0001g0201a0001c0001t0016g0203 | 2 | NA18974.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.-45+1326dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984082 | |||||
chrX:129984112 | G | A | 1 | a0009c0021t0002g0007 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-45+1350G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129984112 | ||||||
chrX:129984115 | C | CG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1357dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984115 | |||||
chrX:129984122 | T | TG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1364dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984122 | |||||
chrX:129984151 | CG | C | 201 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(198): Show | 201 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.-45+1394delG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984151 | |||||
chrX:129984182 | G | GC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1422dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984182 | |||||
chrX:129984223 | T | TGCC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1479_-45+1481d others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984223 | |||||
chrX:129984274 | T | TC | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.-45+1515dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984274 | |||||
chrX:129984314 | G | GGA | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1552_-45+1553i others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129984314 | ||||||
chrX:129984315 | A | AG | 1 | a0001c0001t0001g0034 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.-45+1558dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984315 | |||||
chrX:129984315 | A | G | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1553A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129984315 | ||||||
chrX:129984324 | T | TC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1564dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984324 | |||||
chrX:129984333 | C | CG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1576dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984333 | |||||
chrX:129984343 | C | CG | 2 | a0001c0001t0001g0199a0001c0001t0001g0202 | 2 | NA18989.hp1 NA19055.hp1 |
intron_variant | MODIFIER | c.-45+1588dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984343 | |||||
chrX:129984347 | G | GT | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1585_-45+1586i others(3): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129984347 | ||||||
chrX:129984355 | G | GC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1598dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984355 | |||||
chrX:129984363 | C | CG | 1 | a0001c0001t0001g0142 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-45+1607dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984363 | |||||
chrX:129984380 | C | CG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1621dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984380 | |||||
chrX:129984422 | A | AG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1662dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984422 | |||||
chrX:129984445 | A | AG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1689dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984445 | |||||
chrX:129984447 | G | T | 1 | a0001c0001t0001g0141 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-45+1685G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129984447 | ||||||
chrX:129984502 | C | CG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1743dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984502 | |||||
chrX:129984507 | CAG | C | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-45+1748_-45+1749d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984507 | |||||
chrX:129984538 | G | GGA | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1776_-45+1777i others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129984538 | ||||||
chrX:129984540 | A | G | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1778A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129984540 | ||||||
chrX:129984554 | G | GA | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+1794dupA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984554 | |||||
chrX:129984573 | G | GGC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1811_-45+1812i others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129984573 | ||||||
chrX:129984584 | C | CG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1826dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984584 | |||||
chrX:129984660 | T | TG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1902dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984660 | |||||
chrX:129984729 | A | AG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+1970dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984729 | |||||
chrX:129984732 | G | GA | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+1973dupA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984732 | |||||
chrX:129984833 | G | A | 3 | a0001c0001t0001g0035a0001c0001t0001g0143a0001c0001t0001g0144 | 3 | HG01255.hp1 HG01361.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-45+2071G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129984833 | ||||||
chrX:129984848 | A | C | 1 | a0001c0014t0013g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-45+2086A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129984848 | ||||||
chrX:129984856 | A | G | 1 | a0001c0001t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-45+2094A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129984856 | ||||||
chrX:129984880 | T | TG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+2122dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129984880 | |||||
chrX:129985039 | T | C | 2 | a0001c0001t0001g0183a0001c0005t0006g0196 | 2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-45+2277T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129985039 | ||||||
chrX:129985045 | T | TC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+2284dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129985045 | |||||
chrX:129985054 | T | TG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+2294dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129985054 | |||||
chrX:129985170 | C | CG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+2408_-45+2409i others(3): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129985170 | ||||||
chrX:129985218 | T | TG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+2460dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129985218 | |||||
chrX:129985265 | G | GGAGTTTT others(59): Show |
1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+2504_-45+2505i others(68): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129985265 | |||||
chrX:129985542 | G | GC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+2782dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129985542 | |||||
chrX:129985627 | A | G | 1 | a0001c0001t0002g0200 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-45+2865A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129985627 | ||||||
chrX:129985765 | A | AAG | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+3003_-45+3004i others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129985765 | ||||||
chrX:129985998 | C | T | 2 | a0001c0001t0001g0136a0002c0004t0001g0137 | 2 | HG00735.hp2 HG01081.hp2 |
intron_variant | MODIFIER | c.-45+3236C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129985998 | ||||||
chrX:129986097 | C | T | 6 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0133others(3): Show | 6 | HG01261.hp1 HG01928.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.-45+3335C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129986097 | ||||||
chrX:129986527 | G | GA | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+3772dupA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129986527 | |||||
chrX:129986629 | G | A | 1 | a0001c0001t0010g0050 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.-45+3867G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129986629 | ||||||
chrX:129986749 | G | T | 4 | a0001c0001t0001g0129a0001c0001t0001g0192a0001c0001t0001g0194others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-45+3987G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129986749 | ||||||
chrX:129986824 | CAAAAACA others(1): Show |
C | 8 | a0001c0001t0001g0127a0001c0001t0001g0190a0001c0002t0002g0032others(5): Show | 8 | HG01496.hp2 HG01891.hp1 HG02055.hp1 others(5): Show |
intron_variant | MODIFIER | c.-45+4084_-45+4091d others(10): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129986824 | |||||
chrX:129986824 | CAAAAACA others(9): Show |
C | 1 | a0001c0001t0001g0128 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.-45+4076_-45+4091d others(18): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129986824 | |||||
chrX:129987137 | A | G | 1 | a0001c0001t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-45+4375A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129987137 | ||||||
chrX:129987552 | G | A | 1 | a0001c0001t0001g0145 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-45+4790G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129987552 | ||||||
chrX:129987555 | C | A | 3 | a0001c0001t0001g0008a0001c0001t0001g0034a0001c0001t0001g0184 | 3 | HG01169.hp2 HG01433.hp1 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.-45+4793C>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129987555 | ||||||
chrX:129987585 | A | C | 4 | a0001c0001t0001g0129a0001c0001t0001g0192a0001c0001t0001g0194others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-45+4823A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129987585 | ||||||
chrX:129987755 | GC | G | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+4995delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129987755 | |||||
chrX:129987771 | C | G | 1 | a0001c0001t0002g0200 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-45+5009C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129987771 | ||||||
chrX:129987907 | C | A | 1 | a0002c0004t0001g0130 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.-45+5145C>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129987907 | ||||||
chrX:129988249 | TA | T | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.-45+5490delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129988249 | |||||
chrX:129988268 | TC | T | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+5509delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129988268 | |||||
chrX:129988375 | C | T | 4 | a0001c0001t0001g0129a0001c0001t0001g0192a0001c0001t0001g0194others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG02280.hp2 others(1): Show |
intron_variant | MODIFIER | c.-45+5613C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129988375 | ||||||
chrX:129988403 | CT | C | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+5647delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129988403 | |||||
chrX:129988456 | C | CT | 1 | a0001c0001t0001g0126 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-45+5702dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129988456 | |||||
chrX:129988456 | CT | C | 1 | a0001c0001t0001g0036 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-45+5702delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129988456 | |||||
chrX:129988464 | T | A | 15 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0127others(12): Show | 15 | HG01884.hp1 HG02055.hp1 HG02257.hp1 others(12): Show |
intron_variant | MODIFIER | c.-45+5702T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129988464 | ||||||
chrX:129988464 | TA | T | 5 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0202others(2): Show | 5 | HG03195.hp1 NA18959.hp1 NA18974.hp1 others(2): Show |
intron_variant | MODIFIER | c.-45+5713delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129988464 | |||||
chrX:129988465 | A | T | 1 | a0001c0001t0001g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-45+5703A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129988465 | ||||||
chrX:129988553 | T | C | 3 | a0001c0001t0005g0058a0001c0001t0007g0057a0001c0001t0007g0059 | 3 | HG03195.hp2 HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-45+5791T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129988553 | ||||||
chrX:129988562 | A | AT | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+5803dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129988562 | |||||
chrX:129988700 | GT | G | 2 | a0001c0001t0004g0061a0001c0008t0004g0060 | 2 | HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-45+5942delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129988700 | |||||
chrX:129989206 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-45+6444G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129989206 | ||||||
chrX:129989302 | A | AT | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0023others(58): Show | 61 | HG00280.hp1 HG00597.hp1 HG00597.hp2 others(58): Show |
intron_variant | MODIFIER | c.-45+6565dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989302 | |||||
chrX:129989302 | A | ATT | 16 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(13): Show | 16 | HG00735.hp2 HG01167.hp1 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.-45+6564_-45+6565d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989302 | |||||
chrX:129989302 | A | ATTT | 3 | a0001c0001t0001g0006a0001c0001t0001g0194a0001c0005t0006g0196 | 3 | HG02886.hp1 NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-45+6563_-45+6565d others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989302 | |||||
chrX:129989302 | AT | A | 1 | a0001c0001t0001g0146 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.-45+6565delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989302 | |||||
chrX:129989397 | TG | T | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+6637delG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989397 | |||||
chrX:129989425 | C | T | 1 | a0003c0011t0001g0026 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-45+6663C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129989425 | ||||||
chrX:129989436 | G | A | 2 | a0001c0001t0001g0183a0001c0005t0006g0196 | 2 | HG01243.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-45+6674G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129989436 | ||||||
chrX:129989444 | C | CT | 47 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0021others(44): Show | 47 | HG00280.hp1 HG00621.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.-45+6719dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | C | CTT | 30 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0008others(27): Show | 30 | HG00140.hp1 HG00408.hp2 HG00609.hp1 others(27): Show |
intron_variant | MODIFIER | c.-45+6718_-45+6719d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | C | CTTT | 11 | a0001c0001t0001g0195a0001c0002t0002g0056a0001c0002t0002g0173others(8): Show | 11 | HG01358.hp1 HG01884.hp1 HG02148.hp1 others(8): Show |
intron_variant | MODIFIER | c.-45+6717_-45+6719d others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | C | CTTTT | 6 | a0001c0001t0001g0135a0001c0001t0001g0176a0001c0001t0001g0199others(3): Show | 6 | HG01952.hp1 HG02922.hp2 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.-45+6716_-45+6719d others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | C | CTTTTT | 2 | a0001c0001t0005g0058a0001c0001t0007g0059 | 2 | HG03579.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-45+6715_-45+6719d others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | C | CTTTTTT | 1 | a0001c0001t0001g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.-45+6714_-45+6719d others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | CT | C | 17 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(14): Show | 17 | HG00735.hp1 HG00735.hp2 HG01243.hp1 others(14): Show |
intron_variant | MODIFIER | c.-45+6719delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | CTT | C | 14 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0106others(11): Show | 14 | HG01081.hp2 HG01515.hp1 HG01934.hp1 others(11): Show |
intron_variant | MODIFIER | c.-45+6718_-45+6719d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | CTTT | C | 1 | a0001c0001t0001g0023 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-45+6717_-45+6719d others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | CTTTTTTT others(3): Show |
C | 1 | a0001c0003t0002g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-45+6710_-45+6719d others(12): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0001g0009a0001c0001t0001g0079 | 2 | NA19012.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.-45+6709_-45+6719d others(13): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | CTTTTTTT others(5): Show |
C | 36 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0014others(33): Show | 36 | HG00408.hp1 HG00738.hp1 HG01167.hp1 others(33): Show |
intron_variant | MODIFIER | c.-45+6708_-45+6719d others(14): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0001g0100 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-45+6707_-45+6719d others(15): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989444 | CTTTTTTT others(9): Show |
C | 1 | a0003c0011t0001g0026 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-45+6704_-45+6719d others(18): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989444 | |||||
chrX:129989552 | C | T | 1 | a0001c0001t0002g0200 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-45+6790C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129989552 | ||||||
chrX:129989641 | AT | A | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+6884delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989641 | |||||
chrX:129989788 | C | CT | 16 | a0001c0001t0001g0091a0001c0001t0001g0186a0001c0001t0001g0190others(13): Show | 16 | HG01496.hp2 HG01884.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.-45+7036dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989788 | |||||
chrX:129989788 | CT | C | 1 | a0001c0001t0001g0036 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-45+7036delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129989788 | |||||
chrX:129989835 | A | G | 1 | a0001c0001t0002g0200 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-45+7073A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129989835 | ||||||
chrX:129990081 | CG | C | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+7321delG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129990081 | |||||
chrX:129990088 | C | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0186 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-45+7326C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129990088 | ||||||
chrX:129990135 | TA | T | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+7375delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129990135 | |||||
chrX:129990139 | AC | A | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+7379delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129990139 | |||||
chrX:129990190 | T | C | 10 | a0001c0001t0001g0190a0001c0002t0002g0056a0001c0002t0002g0188others(7): Show | 10 | HG01496.hp2 HG01884.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.-45+7428T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129990190 | ||||||
chrX:129990263 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.-45+7501G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129990263 | ||||||
chrX:129990340 | TC | T | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+7580delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129990340 | |||||
chrX:129990461 | C | G | 3 | a0001c0001t0001g0098a0001c0001t0004g0061a0001c0008t0004g0060 | 3 | HG02615.hp2 HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-45+7699C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129990461 | ||||||
chrX:129990466 | C | T | 3 | a0001c0001t0001g0098a0001c0001t0004g0061a0001c0008t0004g0060 | 3 | HG02615.hp2 HG02630.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-45+7704C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129990466 | ||||||
chrX:129990474 | GC | G | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+7715delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129990474 | |||||
chrX:129990478 | G | A | 1 | a0001c0002t0006g0031 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-45+7716G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129990478 | ||||||
chrX:129990671 | TC | T | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+7911delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129990671 | |||||
chrX:129990798 | GT | G | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+8038delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129990798 | |||||
chrX:129990849 | T | A | 1 | a0001c0001t0001g0062 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-45+8087T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129990849 | ||||||
chrX:129990938 | AT | A | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+8178delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129990938 | |||||
chrX:129990981 | G | A | 25 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0027others(22): Show | 25 | HG00735.hp1 HG01081.hp1 HG01361.hp1 others(22): Show |
intron_variant | MODIFIER | c.-45+8219G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129990981 | ||||||
chrX:129991038 | C | T | 1 | a0001c0003t0002g0193 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-45+8276C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129991038 | ||||||
chrX:129991510 | AT | A | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+8753delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129991510 | |||||
chrX:129991557 | T | C | 35 | a0001c0001t0001g0091a0001c0001t0001g0183a0001c0001t0001g0186others(32): Show | 35 | HG01081.hp1 HG01243.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.-45+8795T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129991557 | ||||||
chrX:129991602 | A | C | 1 | a0001c0001t0001g0017 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-45+8840A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129991602 | ||||||
chrX:129991651 | C | CT | 52 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0025others(49): Show | 52 | HG00738.hp1 HG01081.hp1 HG01361.hp2 others(49): Show |
intron_variant | MODIFIER | c.-45+8913dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129991651 | |||||
chrX:129991651 | C | CTT | 3 | a0001c0001t0007g0059a0001c0002t0002g0056a0001c0019t0002g0117 | 3 | HG02630.hp1 NA18906.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.-45+8912_-45+8913d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129991651 | |||||
chrX:129991651 | C | CTTT | 1 | a0001c0002t0002g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-45+8911_-45+8913d others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129991651 | |||||
chrX:129991651 | CT | C | 4 | a0001c0001t0001g0095a0001c0001t0001g0149a0001c0001t0001g0158others(1): Show | 4 | HG01169.hp2 HG02897.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.-45+8913delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129991651 | |||||
chrX:129991651 | CTTTT | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0081 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-45+8910_-45+8913d others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129991651 | |||||
chrX:129991651 | CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-45+8903_-45+8913d others(13): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129991651 | |||||
chrX:129991824 | A | AT | 35 | a0001c0001t0001g0027a0001c0001t0001g0048a0001c0001t0001g0091others(32): Show | 35 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(32): Show |
intron_variant | MODIFIER | c.-45+9075dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129991824 | |||||
chrX:129991824 | A | ATT | 1 | a0001c0006t0002g0094 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-45+9074_-45+9075d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129991824 | |||||
chrX:129991920 | TC | T | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+9161delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129991920 | |||||
chrX:129992055 | G | A | 7 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(4): Show | 7 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.-45+9293G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129992055 | ||||||
chrX:129992153 | TG | T | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+9394delG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129992153 | |||||
chrX:129992168 | C | G | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 202 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-45+9406C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129992168 | ||||||
chrX:129992169 | G | GC | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 202 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-45+9407_-45+9408i others(3): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129992169 | ||||||
chrX:129992248 | CA | C | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+9488delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129992248 | |||||
chrX:129992373 | GC | G | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+9614delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129992373 | |||||
chrX:129992457 | A | C | 1 | a0001c0001t0001g0097 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-45+9695A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129992457 | ||||||
chrX:129992564 | T | C | 1 | a0001c0001t0001g0147 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-45+9802T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129992564 | ||||||
chrX:129992612 | T | C | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-45+9850T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129992612 | ||||||
chrX:129992627 | C | A | 1 | a0001c0001t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-45+9865C>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129992627 | ||||||
chrX:129992785 | TG | T | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+10026delG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129992785 | |||||
chrX:129992795 | T | C | 2 | a0001c0001t0001g0091a0001c0001t0001g0186 | 2 | HG02647.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-45+10033T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129992795 | ||||||
chrX:129992847 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-45+10085C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129992847 | ||||||
chrX:129992856 | A | G | 1 | a0001c0022t0001g0024 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-45+10094A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129992856 | ||||||
chrX:129992973 | AT | A | 1 | a0001c0001t0001g0202 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-45+10213delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129992973 | |||||
chrX:129993777 | AT | A | 1 | a0001c0001t0001g0036 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-45+11021delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129993777 | |||||
chrX:129993787 | T | G | 1 | a0001c0002t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-45+11025T>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129993787 | ||||||
chrX:129993930 | G | GC | 168 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(165): Show | 168 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.-45+11175dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129993930 | |||||
chrX:129994310 | T | C | 1 | a0001c0001t0001g0133 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-44-10878T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129994310 | ||||||
chrX:129994378 | G | A | 13 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(10): Show | 13 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.-44-10810G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129994378 | ||||||
chrX:129994576 | A | AG | 202 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(199): Show | 202 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(199): Show |
intron_variant | MODIFIER | c.-44-10611dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129994576 | |||||
chrX:129994800 | G | GA | 22 | a0001c0001t0001g0091a0001c0001t0001g0183a0001c0001t0001g0186others(19): Show | 22 | HG01243.hp1 HG01884.hp1 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.-44-10378dupA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129994800 | |||||
chrX:129994800 | G | GAA | 13 | a0001c0001t0002g0200a0001c0002t0002g0004a0001c0002t0002g0032others(10): Show | 13 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.-44-10379_-44-1037 others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129994800 | |||||
chrX:129994805 | A | AAC | 1 | a0001c0002t0002g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-44-10382_-44-1038 others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129994805 | |||||
chrX:129994938 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-44-10250C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129994938 | ||||||
chrX:129995101 | G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0081 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-44-10087G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129995101 | ||||||
chrX:129995225 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-44-9963C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129995225 | ||||||
chrX:129995576 | G | A | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-44-9612G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129995576 | ||||||
chrX:129995681 | C | A | 1 | a0001c0001t0014g0085 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-44-9507C>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129995681 | ||||||
chrX:129995770 | T | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.-44-9418T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129995770 | ||||||
chrX:129996089 | CA | C | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-44-9097delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129996089 | |||||
chrX:129996208 | C | T | 35 | a0001c0001t0001g0091a0001c0001t0001g0183a0001c0001t0001g0186others(32): Show | 35 | HG01081.hp1 HG01243.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.-44-8980C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129996208 | ||||||
chrX:129996570 | C | A | 1 | a0001c0001t0001g0077 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-44-8618C>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129996570 | ||||||
chrX:129996627 | T | C | 7 | a0001c0001t0001g0005a0001c0001t0001g0010a0001c0001t0001g0018others(4): Show | 7 | HG02145.hp1 HG02451.hp2 HG02895.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-8561T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129996627 | ||||||
chrX:129996673 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.-44-8515C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129996673 | ||||||
chrX:129996807 | C | T | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-44-8381C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129996807 | ||||||
chrX:129996868 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-44-8320C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129996868 | ||||||
chrX:129997011 | T | TC | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-44-8175dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129997011 | |||||
chrX:129997091 | A | AT | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-44-8094dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129997091 | |||||
chrX:129997356 | C | T | 2 | a0001c0001t0001g0090a0001c0001t0001g0118 | 2 | HG03139.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-44-7832C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129997356 | ||||||
chrX:129997460 | A | AC | 3 | a0001c0001t0001g0113a0001c0001t0001g0183a0001c0001t0002g0200 | 3 | HG01243.hp1 HG03516.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.-44-7725dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129997460 | |||||
chrX:129997574 | G | A | 37 | a0001c0001t0001g0091a0001c0001t0001g0183a0001c0001t0001g0186others(34): Show | 37 | HG01081.hp1 HG01243.hp1 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.-44-7614G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129997574 | ||||||
chrX:129997748 | C | T | 1 | a0001c0001t0001g0166 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-44-7440C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129997748 | ||||||
chrX:129997794 | C | CA | 23 | a0001c0001t0001g0027a0001c0001t0001g0045a0001c0001t0001g0048others(20): Show | 23 | HG01081.hp1 HG01261.hp1 HG01496.hp2 others(20): Show |
intron_variant | MODIFIER | c.-44-7371dupA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129997794 | |||||
chrX:129997794 | C | CAA | 4 | a0001c0001t0001g0131a0001c0002t0002g0033a0001c0002t0002g0173others(1): Show | 4 | HG01928.hp1 HG02486.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-7372_-44-7371d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129997794 | |||||
chrX:129997794 | CA | C | 1 | a0001c0001t0001g0165 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-44-7371delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129997794 | |||||
chrX:129997986 | C | CAT | 25 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0030others(22): Show | 25 | HG00140.hp1 HG00408.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.-44-7183_-44-7182d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129997986 | |||||
chrX:129997986 | C | CATAT | 9 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(6): Show | 9 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44-7185_-44-7182d others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129997986 | |||||
chrX:129997986 | C | CATATAT | 2 | a0001c0001t0001g0183a0001c0002t0006g0031 | 2 | HG01243.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-44-7187_-44-7182d others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129997986 | |||||
chrX:129997986 | C | CATATATA others(1): Show |
2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-44-7189_-44-7182d others(10): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129997986 | |||||
chrX:129998009 | A | AT | 2 | a0001c0001t0001g0039a0001c0001t0001g0113 | 2 | HG04199.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.-44-7170dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129998009 | |||||
chrX:129998098 | G | GT | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.-44-7084dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129998098 | |||||
chrX:129998168 | C | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | NA18747.hp1 NA19070.hp1 |
intron_variant | MODIFIER | c.-44-7020C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129998168 | ||||||
chrX:129998178 | G | A | 2 | a0001c0003t0002g0148a0001c0003t0002g0174 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-44-7010G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129998178 | ||||||
chrX:129998495 | C | T | 1 | a0001c0002t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-44-6693C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129998495 | ||||||
chrX:129998611 | G | A | 10 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(7): Show | 10 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-44-6577G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129998611 | ||||||
chrX:129998616 | T | A | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-44-6572T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129998616 | ||||||
chrX:129999001 | A | T | 3 | a0001c0001t0001g0163a0001c0001t0001g0166a0001c0001t0001g0179 | 3 | HG00408.hp2 HG02056.hp1 NA18948.hp1 |
intron_variant | MODIFIER | c.-44-6187A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999001 | ||||||
chrX:129999050 | AT | A | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-44-6132delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999050 | |||||
chrX:129999060 | G | GT | 29 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0012others(26): Show | 29 | HG00621.hp1 HG00673.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.-44-6112dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999060 | |||||
chrX:129999060 | GT | G | 3 | a0001c0001t0001g0009a0001c0001t0001g0124a0001c0001t0001g0183 | 3 | HG01243.hp1 NA19067.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-44-6112delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999060 | |||||
chrX:129999060 | GTT | G | 3 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059 | 3 | HG03041.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-44-6113_-44-6112d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999060 | |||||
chrX:129999060 | GTTT | G | 28 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(25): Show | 28 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.-44-6114_-44-6112d others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999060 | |||||
chrX:129999060 | GTTTT | G | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-44-6115_-44-6112d others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999060 | |||||
chrX:129999264 | CAACT | C | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-44-5921_-44-5918d others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999264 | |||||
chrX:129999297 | C | CT | 38 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0010others(35): Show | 38 | HG00140.hp1 HG00408.hp2 HG00621.hp1 others(35): Show |
intron_variant | MODIFIER | c.-44-5862dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999297 | |||||
chrX:129999297 | C | CTT | 3 | a0001c0001t0001g0112a0001c0001t0001g0116a0001c0001t0001g0135 | 3 | HG01952.hp1 HG03490.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.-44-5863_-44-5862d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999297 | |||||
chrX:129999297 | C | CTTT | 1 | a0001c0001t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.-44-5864_-44-5862d others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999297 | |||||
chrX:129999297 | CT | C | 34 | a0001c0001t0001g0009a0001c0001t0001g0015a0001c0001t0001g0021others(31): Show | 34 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.-44-5862delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999297 | |||||
chrX:129999297 | CTT | C | 5 | a0001c0001t0001g0124a0001c0001t0002g0099a0001c0001t0007g0057others(2): Show | 5 | HG02451.hp1 HG03041.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44-5863_-44-5862d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999297 | |||||
chrX:129999372 | C | A | 32 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(29): Show | 32 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.-44-5816C>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999372 | ||||||
chrX:129999377 | C | T | 5 | a0001c0001t0001g0195a0002c0004t0001g0049a0002c0004t0001g0137others(2): Show | 5 | HG00642.hp1 HG00735.hp2 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-5811C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999377 | ||||||
chrX:129999670 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-44-5518C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999670 | ||||||
chrX:129999679 | CT | C | 29 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(26): Show | 29 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-44-5504delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999679 | |||||
chrX:129999680 | T | C | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG01109.hp1 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-44-5508T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999680 | ||||||
chrX:129999682 | T | TC | 1 | a0001c0001t0001g0186 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-44-5506_-44-5505i others(3): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999682 | ||||||
chrX:129999683 | T | C | 2 | a0001c0001t0001g0012a0001c0001t0001g0186 | 2 | HG01496.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.-44-5505T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999683 | ||||||
chrX:129999684 | T | C | 8 | a0001c0001t0001g0040a0001c0001t0001g0048a0001c0001t0001g0065others(5): Show | 8 | HG02630.hp2 HG02647.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.-44-5504T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999684 | ||||||
chrX:129999684 | T | TC | 1 | a0001c0001t0001g0112 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.-44-5494dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999684 | |||||
chrX:129999684 | TC | T | 4 | a0001c0001t0001g0178a0001c0002t0002g0056a0001c0005t0008g0139others(1): Show | 4 | HG00280.hp1 HG02258.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-5494delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 129999684 | |||||
chrX:129999685 | C | T | 1 | a0001c0001t0001g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.-44-5503C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999685 | ||||||
chrX:129999691 | C | G | 29 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(26): Show | 29 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-44-5497C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999691 | ||||||
chrX:129999692 | C | G | 3 | a0001c0002t0002g0056a0001c0005t0008g0139a0001c0005t0008g0140 | 3 | HG02258.hp1 HG02630.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-44-5496C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999692 | ||||||
chrX:129999767 | C | T | 1 | a0001c0001t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-44-5421C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999767 | ||||||
chrX:129999798 | C | T | 3 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059 | 3 | HG03041.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-44-5390C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 129999798 | ||||||
chrX:130000030 | C | T | 1 | a0001c0005t0006g0196 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-44-5158C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130000030 | ||||||
chrX:130000328 | G | A | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-44-4860G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130000328 | ||||||
chrX:130000821 | T | C | 1 | a0005c0013t0001g0157 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-44-4367T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130000821 | ||||||
chrX:130000894 | C | CTGTGTG | 5 | a0001c0002t0002g0155a0001c0002t0002g0156a0001c0002t0002g0173others(2): Show | 5 | HG01496.hp2 HG02886.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-4293_-44-4292i others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130000894 | |||||
chrX:130000894 | C | CTGTGTGT others(1): Show |
2 | a0001c0002t0006g0031a0001c0009t0015g0082 | 2 | HG02257.hp1 HG02451.hp1 |
intron_variant | MODIFIER | c.-44-4293_-44-4292i others(10): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130000894 | |||||
chrX:130000894 | C | CTGTGTGT others(3): Show |
3 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0092 | 3 | HG01081.hp1 HG02055.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-44-4293_-44-4292i others(12): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130000894 | |||||
chrX:130000894 | CTTTGTGT others(1): Show |
C | 1 | a0001c0002t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-44-4292_-44-4285d others(10): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130000894 | |||||
chrX:130000896 | T | G | 10 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0092others(7): Show | 10 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.-44-4292T>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130000896 | ||||||
chrX:130000896 | T | TG | 1 | a0001c0001t0001g0029 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.-44-4292_-44-4291i others(3): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130000896 | ||||||
chrX:130000896 | T | TTG | 18 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0034others(15): Show | 18 | HG01261.hp1 HG01433.hp1 HG01928.hp1 others(15): Show |
intron_variant | MODIFIER | c.-44-4260_-44-4259d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130000896 | |||||
chrX:130000896 | T | TTGTG | 2 | a0001c0001t0001g0021a0001c0001t0001g0124 | 2 | HG01943.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-44-4262_-44-4259d others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130000896 | |||||
chrX:130000896 | TTG | T | 2 | a0001c0001t0002g0099a0001c0005t0006g0196 | 2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.-44-4260_-44-4259d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130000896 | |||||
chrX:130000896 | TTGTG | T | 19 | a0001c0001t0001g0095a0001c0001t0007g0057a0001c0001t0007g0059others(16): Show | 19 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.-44-4262_-44-4259d others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130000896 | |||||
chrX:130000930 | C | CG | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-44-4252dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130000930 | |||||
chrX:130000931 | G | A | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0118others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.-44-4257G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130000931 | ||||||
chrX:130001194 | A | G | 32 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(29): Show | 32 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.-44-3994A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130001194 | ||||||
chrX:130001251 | CG | C | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-44-3935delG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130001251 | |||||
chrX:130001486 | G | A | 3 | a0001c0005t0006g0196a0001c0005t0009g0191a0001c0009t0015g0082 | 3 | HG01891.hp1 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-44-3702G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130001486 | ||||||
chrX:130001549 | C | T | 1 | a0001c0009t0015g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-44-3639C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130001549 | ||||||
chrX:130001581 | T | C | 3 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059 | 3 | HG03041.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.-44-3607T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130001581 | ||||||
chrX:130001876 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-44-3312C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130001876 | ||||||
chrX:130001896 | T | C | 29 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(26): Show | 29 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.-44-3292T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130001896 | ||||||
chrX:130002348 | G | A | 3 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0012g0121 | 3 | NA18984.hp1 NA18994.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.-44-2840G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130002348 | ||||||
chrX:130002432 | T | TG | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-44-2751dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130002432 | |||||
chrX:130002592 | A | G | 1 | a0001c0001t0001g0044 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-44-2596A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130002592 | ||||||
chrX:130002627 | G | GC | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.-44-2561_-44-2560i others(3): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130002627 | ||||||
chrX:130002694 | G | A | 1 | a0001c0001t0001g0098 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-44-2494G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130002694 | ||||||
chrX:130002707 | A | T | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-44-2481A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130002707 | ||||||
chrX:130002799 | A | T | 1 | a0001c0002t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-44-2389A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130002799 | ||||||
chrX:130002952 | C | T | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-44-2236C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130002952 | ||||||
chrX:130003352 | C | CCTT | 1 | a0001c0009t0015g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-44-1814_-44-1812d others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130003352 | |||||
chrX:130003352 | C | CCTTCTTC others(2): Show |
2 | a0001c0003t0002g0148a0001c0003t0002g0174 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-44-1820_-44-1812d others(11): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130003352 | |||||
chrX:130003352 | CCTT | C | 1 | a0001c0001t0001g0169 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-44-1814_-44-1812d others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130003352 | |||||
chrX:130003355 | T | C | 5 | a0001c0001t0001g0039a0001c0001t0001g0048a0001c0001t0001g0066others(2): Show | 5 | HG02615.hp1 HG02738.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-1833T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130003355 | ||||||
chrX:130003374 | C | CT | 5 | a0001c0001t0001g0021a0001c0001t0001g0106a0001c0001t0001g0183others(2): Show | 5 | HG01243.hp1 HG01943.hp1 NA18966.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-1799dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130003374 | |||||
chrX:130003374 | C | CTTCT | 2 | a0001c0005t0006g0196a0001c0005t0009g0191 | 2 | HG01891.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-44-1812_-44-1811i others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130003374 | |||||
chrX:130003374 | C | CTTCTT | 9 | a0001c0002t0002g0004a0001c0002t0002g0033a0001c0002t0002g0092others(6): Show | 9 | HG01081.hp1 HG01496.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.-44-1812_-44-1811i others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130003374 | |||||
chrX:130003374 | C | CTTCTTCT | 4 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(1): Show | 4 | HG02630.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.-44-1812_-44-1811i others(9): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130003374 | |||||
chrX:130003374 | C | CTTCTTCT others(3): Show |
11 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(8): Show | 11 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.-44-1812_-44-1811i others(12): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130003374 | |||||
chrX:130003374 | CT | C | 2 | a0001c0001t0001g0018a0001c0001t0001g0202 | 2 | HG02897.hp2 NA19055.hp1 |
intron_variant | MODIFIER | c.-44-1799delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130003374 | |||||
chrX:130003375 | T | TTCTTCTT others(1): Show |
2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-44-1812_-44-1811i others(10): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130003375 | |||||
chrX:130003376 | T | TC | 1 | a0001c0002t0002g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-44-1812_-44-1811i others(3): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130003376 | ||||||
chrX:130003434 | A | G | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-44-1754A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130003434 | ||||||
chrX:130003447 | G | A | 12 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(9): Show | 12 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.-44-1741G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130003447 | ||||||
chrX:130003781 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-44-1407C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130003781 | ||||||
chrX:130003935 | G | A | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-44-1253G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130003935 | ||||||
chrX:130004197 | G | A | 16 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(13): Show | 16 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.-44-991G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130004197 | ||||||
chrX:130004241 | G | GT | 24 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(21): Show | 24 | HG00408.hp1 HG01069.hp1 HG01109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-44-926dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130004241 | |||||
chrX:130004241 | G | GTTTTT | 7 | a0001c0002t0002g0004a0001c0002t0002g0092a0001c0002t0002g0155others(4): Show | 7 | HG01081.hp1 HG01496.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.-44-930_-44-926dup others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130004241 | |||||
chrX:130004241 | G | GTTTTTT | 5 | a0001c0002t0002g0032a0001c0002t0002g0033a0001c0002t0002g0156others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-44-931_-44-926dup others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130004241 | |||||
chrX:130004241 | GT | G | 6 | a0001c0001t0001g0083a0001c0001t0001g0095a0001c0001t0001g0123others(3): Show | 6 | HG01884.hp2 HG03041.hp2 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.-44-926delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130004241 | |||||
chrX:130004249 | T | TTTTTG | 1 | a0001c0009t0015g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-44-935_-44-934ins others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130004249 | |||||
chrX:130004267 | C | T | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-44-921C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130004267 | ||||||
chrX:130004289 | G | C | 1 | a0001c0001t0007g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-44-899G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130004289 | ||||||
chrX:130004982 | A | G | 2 | a0001c0006t0002g0119a0009c0021t0002g0007 | 2 | HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-44-206A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130004982 | ||||||
chrX:130005023 | G | C | 1 | a0001c0002t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-44-165G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | chrX | 130005023 | ||||||
chrX:130005181 | TC | T | 1 | a0001c0001t0001g0015 | 1 | NA18960.hp1 | splice_region_variant&intron_variant | LOW | c.-44-3delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chrX | 130005181 | |||||
chrX:130005616 | A | AT | 13 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(10): Show | 13 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.86+309dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130005616 | |||||
chrX:130005782 | A | AT | 31 | a0001c0001t0001g0048a0001c0001t0001g0186a0001c0001t0002g0099others(28): Show | 31 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.86+480dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130005782 | |||||
chrX:130005782 | AT | A | 7 | a0001c0001t0001g0021a0001c0001t0001g0124a0001c0001t0001g0131others(4): Show | 7 | HG01261.hp1 HG01928.hp1 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.86+480delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130005782 | |||||
chrX:130006023 | T | C | 32 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(29): Show | 32 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.86+706T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130006023 | ||||||
chrX:130006115 | G | A | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.86+798G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130006115 | ||||||
chrX:130006191 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.86+874G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130006191 | ||||||
chrX:130006245 | A | G | 1 | a0001c0006t0002g0094 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.86+928A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130006245 | ||||||
chrX:130006277 | CA | C | 1 | a0001c0001t0003g0105 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.86+964delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130006277 | |||||
chrX:130006358 | AT | A | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.86+1045delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130006358 | |||||
chrX:130006363 | C | CT | 3 | a0001c0001t0001g0009a0001c0001t0001g0077a0001c0007t0001g0064 | 3 | HG00738.hp1 NA18612.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.86+1061dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130006363 | |||||
chrX:130006454 | G | A | 1 | a0001c0001t0001g0034 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.86+1137G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130006454 | ||||||
chrX:130006561 | A | G | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0118others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.86+1244A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130006561 | ||||||
chrX:130006581 | A | G | 1 | a0001c0001t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.86+1264A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130006581 | ||||||
chrX:130006655 | G | A | 6 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0081others(3): Show | 6 | HG02451.hp2 HG02895.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.86+1338G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130006655 | ||||||
chrX:130006917 | GT | G | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.86+1607delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130006917 | |||||
chrX:130007173 | GA | G | 1 | a0001c0001t0001g0015 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.86+1858delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130007173 | |||||
chrX:130007187 | AT | A | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.86+1874delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130007187 | |||||
chrX:130007366 | C | T | 1 | a0001c0001t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.86+2049C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130007366 | ||||||
chrX:130007671 | GC | G | 1 | a0001c0001t0001g0015 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.86+2356delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130007671 | |||||
chrX:130007767 | C | T | 1 | a0001c0001t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.86+2450C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130007767 | ||||||
chrX:130007771 | C | T | 1 | a0001c0002t0006g0031 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.86+2454C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130007771 | ||||||
chrX:130007773 | G | C | 1 | a0001c0001t0001g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.86+2456G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130007773 | ||||||
chrX:130008009 | C | T | 1 | a0001c0001t0001g0096 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.86+2692C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130008009 | ||||||
chrX:130008170 | T | C | 4 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0118others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.86+2853T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130008170 | ||||||
chrX:130008264 | A | AT | 19 | a0001c0001t0001g0071a0001c0001t0001g0077a0001c0001t0001g0103others(16): Show | 19 | HG00738.hp1 HG01884.hp1 HG02280.hp2 others(16): Show |
intron_variant | MODIFIER | c.86+2963dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130008264 | |||||
chrX:130008264 | A | ATT | 1 | a0001c0001t0001g0015 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.86+2962_86+2963dup others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130008264 | |||||
chrX:130008264 | AT | A | 4 | a0001c0001t0001g0066a0001c0001t0001g0136a0001c0001t0001g0164others(1): Show | 4 | HG01081.hp2 HG01243.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.86+2963delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130008264 | |||||
chrX:130008418 | C | A | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.86+3101C>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130008418 | ||||||
chrX:130008589 | T | C | 1 | a0001c0022t0001g0024 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.86+3272T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130008589 | ||||||
chrX:130008621 | C | G | 1 | a0001c0001t0014g0085 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.86+3304C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130008621 | ||||||
chrX:130008657 | C | CTATCACT others(8): Show |
1 | a0001c0001t0001g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.86+3341_86+3355dup others(15): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130008657 | |||||
chrX:130009213 | C | G | 13 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(10): Show | 13 | HG01081.hp1 HG01496.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.87-3365C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130009213 | ||||||
chrX:130009282 | C | T | 1 | a0001c0001t0001g0187 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.87-3296C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130009282 | ||||||
chrX:130009465 | G | GA | 18 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0201others(15): Show | 18 | HG00735.hp2 HG01361.hp1 HG01361.hp2 others(15): Show |
intron_variant | MODIFIER | c.87-3096dupA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130009465 | |||||
chrX:130009465 | G | GAA | 3 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059 | 3 | HG03041.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.87-3097_87-3096dup others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130009465 | |||||
chrX:130009465 | GA | G | 5 | a0001c0001t0001g0077a0001c0001t0001g0096a0001c0001t0001g0103others(2): Show | 5 | HG00738.hp1 HG01243.hp1 HG01891.hp1 others(2): Show |
intron_variant | MODIFIER | c.87-3096delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130009465 | |||||
chrX:130009472 | A | G | 5 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(2): Show | 5 | HG01109.hp1 HG02257.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.87-3106A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130009472 | ||||||
chrX:130009943 | A | G | 3 | a0001c0001t0001g0029a0001c0001t0001g0035a0001c0001t0001g0111 | 3 | HG00735.hp1 HG01361.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.87-2635A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130009943 | ||||||
chrX:130010152 | AGG | A | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.87-2424_87-2423del others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130010152 | |||||
chrX:130011002 | T | TA | 9 | a0001c0001t0001g0047a0001c0001t0001g0073a0001c0001t0001g0086others(6): Show | 9 | HG00621.hp1 HG01106.hp1 HG02027.hp1 others(6): Show |
intron_variant | MODIFIER | c.87-1543dupA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011002 | |||||
chrX:130011002 | T | TAA | 1 | a0001c0001t0001g0169 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.87-1544_87-1543dup others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011002 | |||||
chrX:130011002 | T | TAAA | 5 | a0001c0001t0001g0065a0001c0001t0001g0072a0001c0001t0001g0091others(2): Show | 5 | HG02647.hp1 HG02818.hp2 NA18906.hp1 others(2): Show |
intron_variant | MODIFIER | c.87-1545_87-1543dup others(3): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011002 | |||||
chrX:130011002 | T | TAAAA | 1 | a0001c0001t0001g0090 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.87-1546_87-1543dup others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011002 | |||||
chrX:130011002 | TA | T | 104 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 104 | HG00408.hp1 HG00408.hp2 HG00597.hp1 others(101): Show |
intron_variant | MODIFIER | c.87-1543delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011002 | |||||
chrX:130011002 | TAA | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0087others(2): Show | 5 | HG00609.hp1 HG01074.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.87-1544_87-1543del others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011002 | |||||
chrX:130011002 | TAAA | T | 1 | a0001c0005t0008g0140 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.87-1545_87-1543del others(3): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011002 | |||||
chrX:130011002 | TAAAA | T | 15 | a0001c0001t0001g0183a0001c0003t0002g0051a0001c0003t0002g0052others(12): Show | 15 | HG01243.hp1 HG01884.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.87-1546_87-1543del others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011002 | |||||
chrX:130011002 | TAAAAA | T | 3 | a0001c0003t0002g0054a0001c0005t0006g0196a0001c0005t0009g0191 | 3 | HG01891.hp1 HG02818.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.87-1547_87-1543del others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011002 | |||||
chrX:130011002 | TAAAAAAA others(1): Show |
T | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.87-1550_87-1543del others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011002 | |||||
chrX:130011002 | TAAAAAAA others(6): Show |
T | 1 | a0001c0001t0001g0158 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.87-1555_87-1543del others(13): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011002 | |||||
chrX:130011002 | TAAAAAAA others(10): Show |
T | 11 | a0001c0001t0001g0030a0001c0002t0002g0004a0001c0002t0002g0032others(8): Show | 11 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.87-1559_87-1543del others(17): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011002 | |||||
chrX:130011035 | A | G | 1 | a0001c0001t0001g0070 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.87-1543A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011035 | ||||||
chrX:130011040 | GAA | G | 1 | a0001c0001t0001g0161 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.87-1533_87-1532del others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011040 | |||||
chrX:130011102 | G | C | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.87-1476G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011102 | ||||||
chrX:130011235 | GGTT | G | 3 | a0001c0001t0001g0102a0001c0005t0008g0139a0001c0005t0008g0140 | 3 | HG02258.hp1 HG03516.hp2 NA18952.hp1 |
intron_variant | MODIFIER | c.87-1327_87-1325del others(3): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011235 | |||||
chrX:130011238 | T | G | 1 | a0001c0001t0001g0169 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.87-1340T>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011238 | ||||||
chrX:130011324 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.87-1254G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011324 | ||||||
chrX:130011570 | A | AGT | 1 | a0001c0001t0001g0179 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.87-1007_87-1006ins others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011570 | |||||
chrX:130011571 | G | GACTTT | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.87-1007_87-1006ins others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011571 | ||||||
chrX:130011571 | G | GACTTTCA others(2): Show |
134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 134 | HG00408.hp1 HG00597.hp1 HG00735.hp1 others(131): Show |
intron_variant | MODIFIER | c.87-1007_87-1006ins others(9): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011571 | ||||||
chrX:130011572 | G | C | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.87-1006G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011572 | ||||||
chrX:130011573 | G | A | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.87-1005G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011573 | ||||||
chrX:130011574 | G | GTAACTTC | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 134 | HG00408.hp1 HG00597.hp1 HG00735.hp1 others(131): Show |
intron_variant | MODIFIER | c.87-1004_87-1003ins others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011574 | ||||||
chrX:130011574 | G | T | 1 | a0001c0001t0001g0179 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.87-1004G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011574 | ||||||
chrX:130011575 | A | T | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.87-1003A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011575 | ||||||
chrX:130011576 | G | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 134 | HG00408.hp1 HG00597.hp1 HG00735.hp1 others(131): Show |
intron_variant | MODIFIER | c.87-1002G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011576 | ||||||
chrX:130011577 | G | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 134 | HG00408.hp1 HG00597.hp1 HG00735.hp1 others(131): Show |
intron_variant | MODIFIER | c.87-1001G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011577 | ||||||
chrX:130011578 | G | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 134 | HG00408.hp1 HG00597.hp1 HG00735.hp1 others(131): Show |
intron_variant | MODIFIER | c.87-1000G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011578 | ||||||
chrX:130011578 | G | GT | 1 | a0001c0001t0001g0179 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.87-1000_87-999insT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011578 | ||||||
chrX:130011578 | G | GTAA | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.87-1000_87-999insT others(2): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011578 | ||||||
chrX:130011579 | A | C | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.87-999A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011579 | ||||||
chrX:130011579 | A | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 134 | HG00408.hp1 HG00597.hp1 HG00735.hp1 others(131): Show |
intron_variant | MODIFIER | c.87-999A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011579 | ||||||
chrX:130011580 | G | T | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(132): Show | 135 | HG00408.hp1 HG00597.hp1 HG00735.hp1 others(132): Show |
intron_variant | MODIFIER | c.87-998G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011580 | ||||||
chrX:130011581 | G | C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 134 | HG00408.hp1 HG00597.hp1 HG00735.hp1 others(131): Show |
intron_variant | MODIFIER | c.87-997G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011581 | ||||||
chrX:130011598 | T | C | 34 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0002g0099others(31): Show | 34 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.87-980T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011598 | ||||||
chrX:130011603 | C | CT | 5 | a0001c0001t0001g0046a0001c0001t0001g0187a0001c0001t0001g0202others(2): Show | 5 | HG01192.hp1 HG02630.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.87-964dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chrX | 130011603 | |||||
chrX:130011688 | A | G | 1 | a0001c0001t0001g0172 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.87-890A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 2/13 | chrX | 130011688 | ||||||
chrX:130016278 | A | G | 13 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(10): Show | 13 | HG01081.hp1 HG01496.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.3441+65A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130016278 | ||||||
chrX:130016436 | T | G | 1 | a0001c0001t0003g0108 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.3441+223T>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130016436 | ||||||
chrX:130016659 | A | G | 29 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(26): Show | 29 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(26): Show |
intron_variant | MODIFIER | c.3441+446A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130016659 | ||||||
chrX:130017321 | G | A | 10 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(7): Show | 10 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.3441+1108G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130017321 | ||||||
chrX:130017371 | G | T | 2 | a0001c0001t0001g0159a0001c0001t0001g0162 | 2 | HG01106.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.3441+1158G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130017371 | ||||||
chrX:130017390 | C | T | 1 | a0001c0001t0001g0008 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.3441+1177C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130017390 | ||||||
chrX:130017606 | T | G | 13 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(10): Show | 13 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.3441+1393T>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130017606 | ||||||
chrX:130017640 | CT | C | 1 | a0001c0001t0001g0169 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.3441+1432delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chrX | 130017640 | |||||
chrX:130017646 | G | GT | 10 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(7): Show | 10 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(7): Show |
intron_variant | MODIFIER | c.3441+1446dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chrX | 130017646 | |||||
chrX:130017757 | T | C | 35 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0183others(32): Show | 35 | HG01081.hp1 HG01243.hp1 HG01496.hp2 others(32): Show |
intron_variant | MODIFIER | c.3441+1544T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130017757 | ||||||
chrX:130018481 | G | T | 1 | a0001c0009t0015g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3441+2268G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130018481 | ||||||
chrX:130018504 | TA | T | 1 | a0001c0001t0003g0105 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.3441+2297delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | INFO_REALIGN_3_PRIME | chrX | 130018504 | |||||
chrX:130018683 | C | T | 1 | a0001c0001t0001g0005 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3442-2302C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130018683 | ||||||
chrX:130018942 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3442-2043G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130018942 | ||||||
chrX:130018958 | G | A | 1 | a0001c0001t0001g0003 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.3442-2027G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130018958 | ||||||
chrX:130018965 | A | G | 1 | a0001c0001t0014g0085 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3442-2020A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130018965 | ||||||
chrX:130019279 | T | C | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.3442-1706T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130019279 | ||||||
chrX:130019779 | A | G | 1 | a0001c0001t0001g0040 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.3442-1206A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130019779 | ||||||
chrX:130020737 | G | A | 1 | a0001c0014t0013g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3442-248G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130020737 | ||||||
chrX:130020846 | T | C | 6 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0019others(3): Show | 6 | HG01496.hp1 HG01978.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.3442-139T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 4/13 | chrX | 130020846 | ||||||
chrX:130021242 | T | C | 4 | a0001c0001t0001g0129a0001c0001t0001g0184a0001c0001t0001g0192others(1): Show | 4 | HG01167.hp1 HG01169.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.3607+92T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | chrX | 130021242 | ||||||
chrX:130021373 | A | G | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.3607+223A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | chrX | 130021373 | ||||||
chrX:130021826 | C | CAGGCTAG others(18): Show |
1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3607+678_3607+702d others(27): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chrX | 130021826 | |||||
chrX:130021928 | C | G | 1 | a0002c0004t0001g0170 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3607+778C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | chrX | 130021928 | ||||||
chrX:130022024 | C | T | 12 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(9): Show | 12 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.3608-873C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | chrX | 130022024 | ||||||
chrX:130022067 | G | A | 1 | a0001c0001t0001g0113 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3608-830G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | chrX | 130022067 | ||||||
chrX:130022220 | T | TTTTC | 7 | a0001c0002t0002g0004a0001c0002t0002g0092a0001c0002t0002g0155others(4): Show | 7 | HG01081.hp1 HG01496.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.3608-661_3608-658d others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chrX | 130022220 | |||||
chrX:130022236 | C | CT | 28 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(25): Show | 28 | HG00609.hp1 HG01109.hp1 HG01261.hp1 others(25): Show |
intron_variant | MODIFIER | c.3608-632dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chrX | 130022236 | |||||
chrX:130022236 | C | CTT | 2 | a0001c0001t0001g0183a0001c0006t0002g0094 | 2 | HG01243.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3608-633_3608-632d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chrX | 130022236 | |||||
chrX:130022236 | C | CTTTCT | 3 | a0001c0002t0002g0032a0001c0002t0006g0031a0001c0005t0009g0191 | 3 | HG01891.hp1 HG02055.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.3608-658_3608-657i others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chrX | 130022236 | |||||
chrX:130022236 | CT | C | 14 | a0001c0001t0001g0023a0001c0001t0001g0037a0001c0001t0001g0083others(11): Show | 14 | HG01081.hp2 HG01256.hp1 HG01884.hp2 others(11): Show |
intron_variant | MODIFIER | c.3608-632delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chrX | 130022236 | |||||
chrX:130022236 | CTTTTT | C | 1 | a0001c0002t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3608-636_3608-632d others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chrX | 130022236 | |||||
chrX:130022236 | CTTTTTT | C | 1 | a0001c0001t0001g0165 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.3608-637_3608-632d others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chrX | 130022236 | |||||
chrX:130022236 | CTTTTTTT | C | 1 | a0001c0001t0001g0109 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.3608-638_3608-632d others(9): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chrX | 130022236 | |||||
chrX:130022236 | CTTTTTTT others(1): Show |
C | 1 | a0001c0005t0006g0196 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3608-639_3608-632d others(10): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chrX | 130022236 | |||||
chrX:130022237 | T | TTTC | 1 | a0001c0009t0015g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.3608-658_3608-657i others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chrX | 130022237 | |||||
chrX:130022245 | T | C | 1 | a0001c0002t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3608-652T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | chrX | 130022245 | ||||||
chrX:130022248 | T | C | 1 | a0001c0005t0006g0196 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3608-649T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | chrX | 130022248 | ||||||
chrX:130022346 | C | T | 2 | a0001c0003t0002g0148a0001c0003t0002g0174 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.3608-551C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | chrX | 130022346 | ||||||
chrX:130022874 | C | T | 15 | a0001c0001t0001g0183a0001c0002t0002g0004a0001c0002t0002g0032others(12): Show | 15 | HG01081.hp1 HG01243.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.3608-23C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 5/13 | chrX | 130022874 | ||||||
chrX:130023154 | T | C | 5 | a0001c0001t0001g0014a0001c0001t0001g0065a0001c0001t0001g0072others(2): Show | 5 | HG00408.hp1 NA18612.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.3688+177T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | chrX | 130023154 | ||||||
chrX:130023498 | C | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0047 | 2 | HG00621.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.3688+521C>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | chrX | 130023498 | ||||||
chrX:130023692 | A | G | 33 | a0001c0001t0001g0183a0001c0001t0002g0099a0001c0001t0007g0057others(30): Show | 33 | HG01081.hp1 HG01243.hp1 HG01496.hp2 others(30): Show |
intron_variant | MODIFIER | c.3688+715A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | chrX | 130023692 | ||||||
chrX:130023786 | T | C | 7 | a0001c0001t0001g0010a0001c0001t0001g0018a0001c0001t0001g0081others(4): Show | 7 | HG02451.hp2 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.3688+809T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | chrX | 130023786 | ||||||
chrX:130023851 | A | G | 13 | a0001c0003t0002g0051a0001c0003t0002g0052a0001c0003t0002g0053others(10): Show | 13 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.3688+874A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | chrX | 130023851 | ||||||
chrX:130024048 | G | A | 1 | a0001c0001t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3689-942G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | chrX | 130024048 | ||||||
chrX:130024068 | G | A | 1 | a0001c0001t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.3689-922G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | chrX | 130024068 | ||||||
chrX:130024226 | T | TG | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3689-759dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chrX | 130024226 | |||||
chrX:130024255 | C | T | 1 | a0001c0022t0001g0024 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.3689-735C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | chrX | 130024255 | ||||||
chrX:130024328 | C | T | 18 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(15): Show | 18 | HG01884.hp1 HG02258.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.3689-662C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | chrX | 130024328 | ||||||
chrX:130024396 | G | C | 1 | a0001c0001t0001g0089 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3689-594G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | chrX | 130024396 | ||||||
chrX:130024478 | C | T | 1 | a0001c0005t0009g0191 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.3689-512C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | chrX | 130024478 | ||||||
chrX:130024852 | C | T | 16 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(13): Show | 16 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.3689-138C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 6/13 | chrX | 130024852 | ||||||
chrX:130025412 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4078+33G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | chrX | 130025412 | ||||||
chrX:130025417 | G | A | 1 | a0001c0001t0001g0042 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4078+38G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | chrX | 130025417 | ||||||
chrX:130025427 | T | TG | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4078+51dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chrX | 130025427 | |||||
chrX:130025438 | G | A | 1 | a0001c0001t0001g0172 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.4078+59G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | chrX | 130025438 | ||||||
chrX:130026008 | G | C | 1 | a0001c0001t0001g0151 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.4078+629G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | chrX | 130026008 | ||||||
chrX:130026392 | G | A | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4078+1013G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | chrX | 130026392 | ||||||
chrX:130026722 | A | AC | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4078+1344dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chrX | 130026722 | |||||
chrX:130026794 | T | G | 1 | a0001c0001t0001g0041 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.4078+1415T>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | chrX | 130026794 | ||||||
chrX:130026905 | C | T | 2 | a0001c0002t0002g0056a0001c0009t0015g0082 | 2 | HG02451.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.4078+1526C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | chrX | 130026905 | ||||||
chrX:130027433 | G | T | 1 | a0008c0017t0001g0013 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.4079-1202G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | chrX | 130027433 | ||||||
chrX:130027895 | AC | A | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4079-737delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chrX | 130027895 | |||||
chrX:130028144 | A | C | 2 | a0001c0001t0001g0071a0001c0001t0001g0177 | 2 | NA18995.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.4079-491A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | chrX | 130028144 | ||||||
chrX:130028550 | TC | T | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4079-83delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 7/13 | INFO_REALIGN_3_PRIME | chrX | 130028550 | |||||
chrX:130028885 | G | A | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.4305+24G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130028885 | ||||||
chrX:130028992 | AG | A | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4305+134delG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130028992 | |||||
chrX:130029231 | T | A | 2 | a0001c0001t0003g0108a0001c0001t0003g0122 | 2 | NA19068.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.4305+370T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130029231 | ||||||
chrX:130029549 | G | A | 1 | a0001c0001t0001g0128 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.4305+688G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130029549 | ||||||
chrX:130029647 | T | C | 4 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(1): Show | 4 | HG02630.hp1 HG03041.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.4305+786T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130029647 | ||||||
chrX:130029649 | T | C | 11 | a0001c0001t0001g0073a0001c0001t0001g0083a0001c0001t0001g0088others(8): Show | 11 | HG01884.hp2 HG01891.hp1 HG02027.hp1 others(8): Show |
intron_variant | MODIFIER | c.4305+788T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130029649 | ||||||
chrX:130029650 | T | C | 2 | a0001c0001t0001g0023a0001c0001t0001g0101 | 2 | NA18940.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.4305+789T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130029650 | ||||||
chrX:130029651 | C | T | 4 | a0001c0001t0001g0068a0001c0001t0001g0195a0001c0006t0002g0119others(1): Show | 4 | HG01258.hp1 HG02148.hp1 HG02572.hp1 others(1): Show |
intron_variant | MODIFIER | c.4305+790C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130029651 | ||||||
chrX:130029684 | G | A | 1 | a0001c0001t0001g0104 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.4305+823G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130029684 | ||||||
chrX:130029689 | C | T | 3 | a0001c0005t0008g0139a0001c0005t0008g0140a0001c0006t0002g0093 | 3 | HG02258.hp1 HG03453.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.4305+828C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130029689 | ||||||
chrX:130029836 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.4305+975A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130029836 | ||||||
chrX:130029898 | G | GCCC | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4305+1038_4305+104 others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130029898 | |||||
chrX:130029976 | C | T | 1 | a0001c0006t0002g0093 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4305+1115C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130029976 | ||||||
chrX:130030011 | G | GC | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4305+1154dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130030011 | |||||
chrX:130030043 | T | TC | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4305+1187dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130030043 | |||||
chrX:130030149 | TG | T | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4305+1293delG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130030149 | |||||
chrX:130030182 | C | A | 1 | a0001c0001t0003g0105 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4305+1321C>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130030182 | ||||||
chrX:130030230 | C | CT | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4305+1371dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130030230 | |||||
chrX:130030298 | A | AC | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4305+1442dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130030298 | |||||
chrX:130030484 | T | C | 36 | a0001c0001t0001g0083a0001c0001t0001g0088a0001c0001t0002g0099others(33): Show | 36 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(33): Show |
intron_variant | MODIFIER | c.4305+1623T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130030484 | ||||||
chrX:130030607 | TG | T | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4305+1751delG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130030607 | |||||
chrX:130030710 | T | TC | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4305+1854dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130030710 | |||||
chrX:130030888 | CT | C | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4305+2030delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130030888 | |||||
chrX:130031006 | T | TG | 1 | a0007c0012t0011g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4305+2147dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130031006 | |||||
chrX:130031044 | G | A | 1 | a0001c0001t0001g0047 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.4305+2183G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130031044 | ||||||
chrX:130031066 | T | TC | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4305+2211dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130031066 | |||||
chrX:130031243 | G | A | 1 | a0001c0001t0001g0080 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.4305+2382G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130031243 | ||||||
chrX:130031497 | A | C | 2 | a0001c0002t0002g0032a0001c0002t0002g0033 | 2 | HG02055.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.4305+2636A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130031497 | ||||||
chrX:130031666 | T | C | 33 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(30): Show | 33 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.4306-2789T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130031666 | ||||||
chrX:130031765 | C | T | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4306-2690C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130031765 | ||||||
chrX:130031785 | AAAAC | A | 1 | a0001c0001t0001g0124 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.4306-2659_4306-265 others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130031785 | |||||
chrX:130032022 | G | GCA | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4306-2433_4306-243 others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130032022 | ||||||
chrX:130032024 | A | C | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4306-2431A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130032024 | ||||||
chrX:130032217 | G | T | 1 | a0001c0005t0009g0191 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4306-2238G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130032217 | ||||||
chrX:130032503 | C | T | 17 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(14): Show | 17 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.4306-1952C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130032503 | ||||||
chrX:130032613 | T | TC | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.4306-1841dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130032613 | |||||
chrX:130032649 | C | T | 1 | a0001c0001t0001g0008 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.4306-1806C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130032649 | ||||||
chrX:130032687 | A | T | 1 | a0001c0009t0015g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4306-1768A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130032687 | ||||||
chrX:130032731 | TTCTA | T | 8 | a0001c0002t0002g0092a0001c0002t0002g0156a0001c0002t0002g0173others(5): Show | 8 | HG01081.hp1 HG01496.hp2 HG01891.hp1 others(5): Show |
intron_variant | MODIFIER | c.4306-1722_4306-171 others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130032731 | |||||
chrX:130032731 | TTCTATTT others(1): Show |
T | 6 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(3): Show | 6 | HG02055.hp1 HG02451.hp1 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.4306-1722_4306-171 others(12): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130032731 | |||||
chrX:130032731 | TTCTATTT others(9): Show |
T | 16 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(13): Show | 16 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.4306-1722_4306-170 others(20): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130032731 | |||||
chrX:130032733 | C | CTATT | 12 | a0001c0001t0001g0069a0001c0001t0001g0132a0001c0001t0001g0141others(9): Show | 12 | HG00609.hp1 HG01256.hp1 HG02300.hp1 others(9): Show |
intron_variant | MODIFIER | c.4306-1680_4306-167 others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130032733 | |||||
chrX:130032733 | C | T | 1 | a0001c0002t0002g0155 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.4306-1722C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130032733 | ||||||
chrX:130032733 | CTATT | C | 61 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 61 | HG00408.hp2 HG00673.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.4306-1680_4306-167 others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130032733 | |||||
chrX:130032733 | CTATTTAT others(1): Show |
C | 1 | a0001c0001t0001g0096 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.4306-1684_4306-167 others(12): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130032733 | |||||
chrX:130032819 | T | A | 9 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(6): Show | 9 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.4306-1636T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130032819 | ||||||
chrX:130032884 | T | C | 31 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(28): Show | 31 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4306-1571T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130032884 | ||||||
chrX:130033063 | A | AT | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4306-1384dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130033063 | |||||
chrX:130033084 | C | CT | 18 | a0001c0001t0001g0111a0001c0002t0002g0004a0001c0002t0002g0032others(15): Show | 18 | HG00735.hp1 HG01081.hp1 HG01496.hp2 others(15): Show |
intron_variant | MODIFIER | c.4306-1356dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130033084 | |||||
chrX:130033084 | CT | C | 2 | a0001c0001t0001g0113a0001c0001t0001g0142 | 2 | NA18953.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.4306-1356delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chrX | 130033084 | |||||
chrX:130033134 | C | T | 31 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(28): Show | 31 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4306-1321C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130033134 | ||||||
chrX:130033142 | C | T | 1 | a0001c0014t0013g0138 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.4306-1313C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130033142 | ||||||
chrX:130033161 | A | G | 3 | a0001c0002t0006g0031a0001c0005t0006g0196a0001c0009t0015g0082 | 3 | HG02257.hp1 HG02451.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4306-1294A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130033161 | ||||||
chrX:130033170 | C | T | 4 | a0001c0002t0006g0031a0001c0005t0006g0196a0001c0005t0009g0191others(1): Show | 4 | HG01891.hp1 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.4306-1285C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130033170 | ||||||
chrX:130033379 | G | A | 31 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(28): Show | 31 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4306-1076G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130033379 | ||||||
chrX:130033539 | C | A | 16 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(13): Show | 16 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.4306-916C>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130033539 | ||||||
chrX:130033562 | A | G | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4306-893A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130033562 | ||||||
chrX:130034020 | T | C | 1 | a0001c0002t0002g0156 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4306-435T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130034020 | ||||||
chrX:130034102 | G | A | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4306-353G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130034102 | ||||||
chrX:130034217 | G | A | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4306-238G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130034217 | ||||||
chrX:130034334 | A | C | 1 | a0001c0001t0001g0074 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.4306-121A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 8/13 | chrX | 130034334 | ||||||
chrX:130035174 | T | A | 1 | a0001c0001t0001g0132 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.4527+498T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | chrX | 130035174 | ||||||
chrX:130035220 | G | A | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4527+544G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | chrX | 130035220 | ||||||
chrX:130035510 | CAG | C | 1 | a0001c0001t0001g0030 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.4527+837_4527+838d others(4): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chrX | 130035510 | |||||
chrX:130035596 | C | G | 16 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(13): Show | 16 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(13): Show |
intron_variant | MODIFIER | c.4527+920C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | chrX | 130035596 | ||||||
chrX:130035915 | G | A | 1 | a0001c0001t0001g0086 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.4527+1239G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | chrX | 130035915 | ||||||
chrX:130035954 | G | A | 1 | a0001c0001t0001g0025 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4527+1278G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | chrX | 130035954 | ||||||
chrX:130036262 | C | CT | 2 | a0001c0001t0001g0110a0001c0001t0003g0108 | 2 | NA18984.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.4528-1090dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chrX | 130036262 | |||||
chrX:130036329 | C | T | 15 | a0001c0001t0002g0099a0001c0001t0007g0059a0001c0003t0002g0051others(12): Show | 15 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.4528-1038C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | chrX | 130036329 | ||||||
chrX:130036427 | A | G | 1 | a0001c0005t0009g0191 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4528-940A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | chrX | 130036427 | ||||||
chrX:130036517 | T | C | 1 | a0001c0016t0001g0067 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4528-850T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | chrX | 130036517 | ||||||
chrX:130036720 | T | C | 33 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059others(30): Show | 33 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(30): Show |
intron_variant | MODIFIER | c.4528-647T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | chrX | 130036720 | ||||||
chrX:130036757 | A | G | 2 | a0001c0002t0006g0031a0001c0005t0006g0196 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4528-610A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | chrX | 130036757 | ||||||
chrX:130037006 | C | T | 10 | a0001c0001t0001g0009a0001c0001t0001g0014a0001c0001t0001g0065others(7): Show | 10 | HG00408.hp1 HG03490.hp1 HG03710.hp1 others(7): Show |
intron_variant | MODIFIER | c.4528-361C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | chrX | 130037006 | ||||||
chrX:130037008 | TGGTGGCG others(10): Show |
T | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4528-357_4528-341d others(19): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chrX | 130037008 | |||||
chrX:130037102 | C | T | 1 | a0001c0002t0002g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4528-265C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | chrX | 130037102 | ||||||
chrX:130037143 | CA | C | 1 | a0001c0001t0003g0105 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4528-214delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chrX | 130037143 | |||||
chrX:130037590 | T | C | 1 | a0001c0001t0001g0109 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.4694+57T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 10/13 | chrX | 130037590 | ||||||
chrX:130037870 | G | C | 13 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(10): Show | 13 | HG01081.hp1 HG01496.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.4694+337G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 10/13 | chrX | 130037870 | ||||||
chrX:130037911 | TAAAG | T | 1 | a0001c0001t0001g0127 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4694+380_4694+383d others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chrX | 130037911 | |||||
chrX:130038066 | C | T | 2 | a0001c0001t0001g0035a0001c0001t0001g0111 | 2 | HG00735.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.4694+533C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 10/13 | chrX | 130038066 | ||||||
chrX:130038141 | C | T | 18 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(15): Show | 18 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.4694+608C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 10/13 | chrX | 130038141 | ||||||
chrX:130038485 | CT | C | 32 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(29): Show | 32 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.4695-638delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chrX | 130038485 | |||||
chrX:130038503 | A | T | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4695-634A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 10/13 | chrX | 130038503 | ||||||
chrX:130038777 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4695-360C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 10/13 | chrX | 130038777 | ||||||
chrX:130039038 | G | A | 1 | a0001c0001t0001g0126 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.4695-99G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 10/13 | chrX | 130039038 | ||||||
chrX:130039119 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4695-18C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 10/13 | chrX | 130039119 | ||||||
chrX:130039378 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4840+96C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130039378 | ||||||
chrX:130039422 | A | G | 1 | a0001c0001t0001g0002 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.4840+140A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130039422 | ||||||
chrX:130039480 | C | T | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4840+198C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130039480 | ||||||
chrX:130039514 | C | T | 1 | a0001c0019t0002g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.4840+232C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130039514 | ||||||
chrX:130039562 | C | T | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4840+280C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130039562 | ||||||
chrX:130039840 | C | T | 1 | a0001c0001t0001g0037 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4840+558C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130039840 | ||||||
chrX:130039938 | T | A | 1 | a0001c0001t0001g0162 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.4840+656T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130039938 | ||||||
chrX:130039939 | A | G | 1 | a0001c0001t0001g0162 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.4840+657A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130039939 | ||||||
chrX:130040167 | G | A | 32 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(29): Show | 32 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.4840+885G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130040167 | ||||||
chrX:130040467 | G | GC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4840+1187dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130040467 | |||||
chrX:130040552 | G | C | 2 | a0001c0001t0001g0149a0001c0001t0001g0150 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.4840+1270G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130040552 | ||||||
chrX:130040611 | G | GC | 1 | a0001c0001t0016g0203 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.4840+1333dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130040611 | |||||
chrX:130041019 | A | G | 1 | a0001c0001t0005g0058 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.4840+1737A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130041019 | ||||||
chrX:130041278 | C | CA | 13 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(10): Show | 13 | HG01109.hp1 HG01934.hp1 HG02257.hp2 others(10): Show |
intron_variant | MODIFIER | c.4840+2018dupA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130041278 | |||||
chrX:130041278 | CA | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0083a0001c0001t0001g0087others(4): Show | 7 | HG01069.hp1 HG01074.hp1 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.4840+2018delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130041278 | |||||
chrX:130041300 | AGAG | A | 26 | a0001c0001t0002g0200a0001c0001t0007g0057a0001c0001t0007g0059others(23): Show | 26 | HG01081.hp1 HG01496.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.4840+2019_4840+202 others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130041300 | ||||||
chrX:130041301 | G | A | 3 | a0001c0002t0006g0031a0001c0006t0002g0119a0009c0021t0002g0007 | 3 | HG02257.hp1 HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4840+2019G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130041301 | ||||||
chrX:130041301 | GAGAC | G | 3 | a0001c0001t0002g0099a0001c0002t0002g0056a0001c0003t0002g0055 | 3 | HG01884.hp1 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.4840+2023_4840+202 others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130041301 | |||||
chrX:130041303 | GAC | G | 3 | a0001c0002t0006g0031a0001c0006t0002g0119a0009c0021t0002g0007 | 3 | HG02257.hp1 HG02572.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.4840+2023_4840+202 others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130041303 | |||||
chrX:130041305 | C | G | 26 | a0001c0001t0002g0200a0001c0001t0007g0057a0001c0001t0007g0059others(23): Show | 26 | HG01081.hp1 HG01496.hp2 HG01891.hp1 others(23): Show |
intron_variant | MODIFIER | c.4840+2023C>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130041305 | ||||||
chrX:130041333 | C | T | 21 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(18): Show | 21 | HG01884.hp1 HG02257.hp1 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.4840+2051C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130041333 | ||||||
chrX:130041362 | C | T | 1 | a0001c0001t0003g0105 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.4840+2080C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130041362 | ||||||
chrX:130041613 | T | C | 1 | a0001c0001t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4840+2331T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130041613 | ||||||
chrX:130041650 | G | A | 2 | a0001c0001t0001g0019a0001c0001t0001g0075 | 2 | NA18939.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.4840+2368G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130041650 | ||||||
chrX:130041817 | C | T | 1 | a0001c0002t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4840+2535C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130041817 | ||||||
chrX:130041874 | G | T | 1 | a0001c0001t0001g0183 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4840+2592G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130041874 | ||||||
chrX:130041919 | G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0115 | 2 | HG00597.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.4840+2637G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130041919 | ||||||
chrX:130042086 | T | C | 1 | a0001c0001t0001g0019 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.4840+2804T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130042086 | ||||||
chrX:130042285 | G | A | 1 | a0001c0001t0007g0057 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.4840+3003G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130042285 | ||||||
chrX:130042460 | A | G | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4840+3178A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130042460 | ||||||
chrX:130042697 | C | T | 17 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(14): Show | 17 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.4840+3415C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130042697 | ||||||
chrX:130042790 | G | A | 1 | a0001c0001t0001g0115 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.4840+3508G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130042790 | ||||||
chrX:130042802 | T | A | 2 | a0001c0001t0001g0045a0007c0012t0011g0043 | 2 | NA18967.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.4840+3520T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130042802 | ||||||
chrX:130042988 | T | TA | 171 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(168): Show | 171 | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(168): Show |
intron_variant | MODIFIER | c.4840+3714dupA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130042988 | |||||
chrX:130042988 | T | TAA | 31 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(28): Show | 31 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4840+3713_4840+371 others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130042988 | |||||
chrX:130043032 | C | CT | 12 | a0001c0001t0001g0042a0001c0001t0001g0073a0001c0002t0002g0004others(9): Show | 12 | HG01081.hp1 HG01496.hp2 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.4840+3767dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043032 | |||||
chrX:130043032 | C | CTT | 2 | a0001c0002t0006g0031a0001c0005t0006g0196 | 2 | HG02257.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4840+3766_4840+376 others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043032 | |||||
chrX:130043034 | T | C | 3 | a0001c0001t0004g0061a0001c0008t0004g0060a0004c0018t0001g0175 | 3 | HG02630.hp2 NA18983.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.4840+3752T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043034 | ||||||
chrX:130043416 | C | T | 1 | a0001c0001t0001g0077 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4840+4134C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043416 | ||||||
chrX:130043745 | G | GTT | 4 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0006t0002g0119others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.4840+4464_4840+446 others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043745 | |||||
chrX:130043746 | T | TTA | 5 | a0001c0001t0001g0068a0001c0001t0001g0132a0001c0001t0001g0165others(2): Show | 5 | HG01243.hp1 HG01258.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.4840+4502_4840+450 others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043746 | |||||
chrX:130043746 | T | TTATA | 15 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0037others(12): Show | 15 | HG00621.hp1 HG01069.hp1 HG01106.hp1 others(12): Show |
intron_variant | MODIFIER | c.4840+4500_4840+450 others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043746 | |||||
chrX:130043746 | T | TTATATA | 6 | a0001c0001t0001g0016a0001c0001t0001g0046a0001c0001t0001g0080others(3): Show | 6 | HG02896.hp2 HG02922.hp2 HG04204.hp1 others(3): Show |
intron_variant | MODIFIER | c.4840+4498_4840+450 others(10): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043746 | |||||
chrX:130043746 | T | TTATATAT others(1): Show |
4 | a0001c0001t0001g0098a0001c0001t0001g0197a0001c0001t0001g0201others(1): Show | 4 | HG02615.hp2 HG02922.hp1 HG04228.hp1 others(1): Show |
intron_variant | MODIFIER | c.4840+4496_4840+450 others(12): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043746 | |||||
chrX:130043746 | T | TTATATAT others(3): Show |
4 | a0001c0001t0001g0077a0001c0001t0001g0086a0001c0001t0001g0181others(1): Show | 4 | HG00738.hp1 HG03486.hp2 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.4840+4494_4840+450 others(14): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043746 | |||||
chrX:130043746 | T | TTATATAT others(5): Show |
8 | a0001c0001t0001g0005a0001c0001t0001g0012a0001c0001t0001g0014others(5): Show | 8 | HG00408.hp1 HG01496.hp1 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.4840+4492_4840+450 others(16): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043746 | |||||
chrX:130043746 | T | TTATATAT others(7): Show |
7 | a0001c0001t0001g0072a0001c0001t0001g0091a0001c0001t0001g0149others(4): Show | 7 | HG01192.hp1 HG01978.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.4840+4490_4840+450 others(18): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043746 | |||||
chrX:130043746 | T | TTATATAT others(11): Show |
1 | a0001c0001t0001g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4840+4486_4840+450 others(22): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043746 | |||||
chrX:130043746 | T | TTATATAT others(13): Show |
1 | a0001c0001t0010g0050 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4840+4484_4840+450 others(24): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043746 | |||||
chrX:130043746 | T | TTATATAT others(17): Show |
1 | a0001c0001t0001g0078 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.4840+4480_4840+450 others(28): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043746 | |||||
chrX:130043746 | T | TTATATAT others(23): Show |
1 | a0001c0001t0001g0038 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.4840+4474_4840+450 others(34): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043746 | |||||
chrX:130043746 | TTATATAT others(1): Show |
T | 1 | a0001c0005t0008g0140 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4840+4496_4840+450 others(12): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043746 | |||||
chrX:130043748 | A | T | 27 | a0001c0001t0007g0057a0001c0001t0007g0059a0001c0002t0002g0004others(24): Show | 27 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(24): Show |
intron_variant | MODIFIER | c.4840+4466A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043748 | ||||||
chrX:130043758 | ATATATAT others(20): Show |
A | 1 | a0002c0004t0001g0130 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.4840+4478_4840+450 others(31): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043758 | |||||
chrX:130043758 | ATATATAT others(21): Show |
A | 3 | a0002c0004t0001g0049a0002c0004t0001g0137a0002c0004t0001g0170 | 3 | HG00642.hp1 HG00735.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.4840+4478_4840+450 others(32): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043758 | |||||
chrX:130043758 | ATATATAT others(22): Show |
A | 1 | a0002c0004t0001g0171 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.4840+4478_4840+450 others(33): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043758 | |||||
chrX:130043765 | TATATATA others(12): Show |
T | 1 | a0001c0007t0001g0064 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4840+4484_4840+450 others(23): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043765 | ||||||
chrX:130043766 | ATATATAT others(17): Show |
A | 2 | a0001c0001t0001g0018a0001c0001t0001g0081 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.4840+4486_4840+450 others(28): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043766 | |||||
chrX:130043769 | T | TATATATA | 1 | a0001c0001t0001g0069 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.4840+4488_4840+449 others(11): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043769 | |||||
chrX:130043772 | A | T | 1 | a0001c0005t0006g0196 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4840+4490A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043772 | ||||||
chrX:130043773 | TA | T | 1 | a0001c0002t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4840+4492delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043773 | ||||||
chrX:130043774 | A | T | 1 | a0001c0005t0006g0196 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4840+4492A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043774 | ||||||
chrX:130043775 | TATATATA | T | 1 | a0001c0005t0008g0139 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.4840+4494_4840+450 others(11): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043775 | ||||||
chrX:130043776 | A | AT | 3 | a0001c0003t0002g0053a0001c0003t0002g0174a0001c0003t0002g0193 | 3 | HG02280.hp2 HG02622.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.4840+4495dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043776 | |||||
chrX:130043776 | A | T | 3 | a0001c0002t0002g0033a0001c0002t0006g0031a0001c0005t0006g0196 | 3 | HG02257.hp1 HG02486.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.4840+4494A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043776 | ||||||
chrX:130043778 | A | AT | 3 | a0001c0003t0002g0051a0001c0003t0002g0054a0001c0006t0002g0094 | 3 | HG02809.hp1 HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4840+4497dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043778 | |||||
chrX:130043778 | A | ATTTTTTT others(3): Show |
1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4840+4497_4840+449 others(14): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043778 | |||||
chrX:130043778 | A | T | 10 | a0001c0001t0002g0200a0001c0002t0002g0033a0001c0002t0006g0031others(7): Show | 10 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.4840+4496A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043778 | ||||||
chrX:130043778 | ATATATAT | A | 2 | a0001c0001t0001g0035a0001c0001t0001g0111 | 2 | HG00735.hp1 HG01361.hp2 |
intron_variant | MODIFIER | c.4840+4498_4840+450 others(11): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043778 | |||||
chrX:130043779 | TA | T | 1 | a0001c0002t0002g0092 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.4840+4498delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043779 | ||||||
chrX:130043780 | A | AT | 3 | a0001c0002t0002g0155a0001c0006t0002g0093a0009c0021t0002g0007 | 3 | HG03209.hp1 HG03453.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.4840+4499dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043780 | |||||
chrX:130043780 | A | ATTT | 3 | a0001c0001t0007g0057a0001c0003t0002g0052a0001c0003t0002g0055 | 3 | HG01884.hp1 HG02559.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.4840+4499_4840+450 others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043780 | |||||
chrX:130043780 | A | T | 15 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0002t0002g0033others(12): Show | 15 | HG02257.hp1 HG02280.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.4840+4498A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043780 | ||||||
chrX:130043780 | ATATATTT | A | 1 | a0001c0001t0001g0184 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4840+4500_4840+450 others(11): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043780 | |||||
chrX:130043780 | ATATATTT others(1): Show |
A | 1 | a0001c0001t0001g0158 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.4840+4500_4840+450 others(12): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043780 | |||||
chrX:130043781 | TA | T | 2 | a0001c0002t0002g0156a0001c0002t0002g0189 | 2 | HG02970.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4840+4500delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043781 | ||||||
chrX:130043782 | A | AT | 2 | a0001c0002t0002g0173a0001c0002t0002g0188 | 2 | HG01496.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.4840+4501dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043782 | |||||
chrX:130043782 | A | ATT | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4840+4501_4840+450 others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043782 | |||||
chrX:130043782 | A | ATTT | 1 | a0001c0001t0007g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4840+4501_4840+450 others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043782 | |||||
chrX:130043782 | A | ATTTT | 2 | a0001c0001t0001g0129a0001c0001t0001g0192 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.4840+4501_4840+450 others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043782 | |||||
chrX:130043782 | A | ATTTTT | 1 | a0001c0003t0002g0185 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4840+4501_4840+450 others(9): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043782 | |||||
chrX:130043782 | A | T | 22 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(19): Show | 22 | HG01081.hp1 HG01884.hp1 HG02257.hp1 others(19): Show |
intron_variant | MODIFIER | c.4840+4500A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043782 | ||||||
chrX:130043782 | ATATTT | A | 1 | a0001c0001t0001g0034 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4840+4502_4840+450 others(9): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043782 | |||||
chrX:130043782 | ATATTTT | A | 1 | a0001c0001t0001g0001 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.4840+4502_4840+450 others(10): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043782 | |||||
chrX:130043783 | TA | T | 1 | a0001c0002t0002g0032 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.4840+4502delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043783 | ||||||
chrX:130043784 | A | AT | 1 | a0001c0001t0001g0195 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.4840+4523dupT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | ATAT | 1 | a0001c0001t0001g0017 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.4840+4503_4840+450 others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | ATATATAT others(2): Show |
1 | a0001c0001t0001g0179 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.4840+4503_4840+450 others(13): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | ATATATAT others(20): Show |
1 | a0001c0001t0001g0076 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4840+4503_4840+450 others(31): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | ATATATAT others(16): Show |
1 | a0001c0001t0001g0116 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4840+4503_4840+450 others(27): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | ATATATAT others(12): Show |
1 | a0001c0020t0001g0125 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.4840+4503_4840+450 others(23): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | ATATATAT others(7): Show |
1 | a0001c0005t0009g0191 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4840+4503_4840+450 others(18): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | ATATATAT others(3): Show |
1 | a0001c0001t0001g0015 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.4840+4503_4840+450 others(14): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | ATATATTT | 1 | a0001c0001t0001g0163 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.4840+4503_4840+450 others(11): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | ATATT | 1 | a0001c0001t0001g0074 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.4840+4503_4840+450 others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | ATT | 2 | a0001c0001t0001g0101a0001c0001t0001g0141 | 2 | NA18940.hp1 NA19002.hp1 |
intron_variant | MODIFIER | c.4840+4522_4840+452 others(6): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | ATTT | 1 | a0001c0002t0002g0004 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.4840+4521_4840+452 others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | ATTTT | 1 | a0001c0001t0001g0146 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.4840+4520_4840+452 others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | A | T | 44 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0044others(41): Show | 44 | HG00140.hp1 HG00609.hp1 HG01081.hp1 others(41): Show |
intron_variant | MODIFIER | c.4840+4502A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043784 | ||||||
chrX:130043784 | AT | A | 6 | a0001c0001t0001g0008a0001c0001t0001g0011a0001c0001t0001g0127others(3): Show | 6 | HG02965.hp1 NA19004.hp1 NA19062.hp1 others(3): Show |
intron_variant | MODIFIER | c.4840+4523delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043784 | ATTT | A | 3 | a0001c0001t0001g0124a0001c0001t0003g0108a0001c0010t0003g0198 | 3 | NA19068.hp1 NA19082.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.4840+4521_4840+452 others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130043784 | |||||
chrX:130043785 | T | TA | 7 | a0001c0001t0001g0006a0001c0001t0001g0069a0001c0001t0001g0084others(4): Show | 7 | HG01261.hp1 HG01891.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.4840+4503_4840+450 others(5): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043785 | ||||||
chrX:130043785 | T | TATA | 10 | a0001c0001t0001g0002a0001c0001t0001g0021a0001c0001t0001g0039others(7): Show | 10 | HG00280.hp1 HG01943.hp1 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.4840+4503_4840+450 others(7): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043785 | ||||||
chrX:130043785 | T | TATATA | 7 | a0001c0001t0001g0027a0001c0001t0001g0075a0001c0001t0001g0128others(4): Show | 7 | HG03098.hp1 HG03492.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.4840+4503_4840+450 others(9): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043785 | ||||||
chrX:130043785 | T | TATATATA | 5 | a0001c0001t0001g0042a0001c0001t0001g0089a0001c0014t0013g0138others(2): Show | 5 | HG02735.hp1 HG03041.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.4840+4503_4840+450 others(11): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043785 | ||||||
chrX:130043785 | T | TATATATA others(2): Show |
6 | a0001c0001t0001g0019a0001c0001t0001g0022a0001c0001t0001g0083others(3): Show | 6 | HG01884.hp2 HG01928.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.4840+4503_4840+450 others(13): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043785 | ||||||
chrX:130043785 | T | TATATATA others(4): Show |
3 | a0001c0001t0001g0009a0001c0001t0001g0104a0001c0001t0001g0115 | 3 | HG00597.hp2 HG01515.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.4840+4503_4840+450 others(15): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043785 | ||||||
chrX:130043785 | T | TATATATA others(6): Show |
5 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0029others(2): Show | 5 | HG01361.hp1 HG02135.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.4840+4503_4840+450 others(17): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043785 | ||||||
chrX:130043785 | T | TATATATA others(8): Show |
6 | a0001c0001t0001g0028a0001c0001t0001g0087a0001c0001t0001g0110others(3): Show | 6 | HG01074.hp1 HG01255.hp1 NA18943.hp1 others(3): Show |
intron_variant | MODIFIER | c.4840+4503_4840+450 others(19): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043785 | ||||||
chrX:130043785 | T | TATATATA others(10): Show |
2 | a0001c0001t0001g0112a0001c0001t0001g0113 | 2 | NA18953.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.4840+4503_4840+450 others(21): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043785 | ||||||
chrX:130043785 | T | TATATATA others(12): Show |
2 | a0001c0001t0001g0096a0001c0001t0012g0121 | 2 | NA19005.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.4840+4503_4840+450 others(23): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043785 | ||||||
chrX:130043785 | T | TATATATA others(16): Show |
2 | a0001c0001t0001g0030a0001c0001t0001g0066 | 2 | HG02698.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.4840+4503_4840+450 others(27): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043785 | ||||||
chrX:130043785 | T | TATATATA others(18): Show |
1 | a0001c0001t0001g0065 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.4840+4503_4840+450 others(29): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043785 | ||||||
chrX:130043786 | T | A | 34 | a0001c0001t0001g0003a0001c0001t0001g0012a0001c0001t0001g0020others(31): Show | 34 | HG00597.hp1 HG00738.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.4840+4504T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043786 | ||||||
chrX:130043787 | T | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0011a0001c0001t0001g0019others(35): Show | 38 | HG00597.hp2 HG01074.hp1 HG01255.hp1 others(35): Show |
intron_variant | MODIFIER | c.4840+4505T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043787 | ||||||
chrX:130043788 | T | A | 11 | a0001c0001t0001g0003a0001c0001t0001g0077a0001c0001t0001g0080others(8): Show | 11 | HG00738.hp1 HG01081.hp2 HG01109.hp1 others(8): Show |
intron_variant | MODIFIER | c.4840+4506T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043788 | ||||||
chrX:130043789 | T | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0039a0001c0001t0001g0084others(8): Show | 11 | HG01891.hp2 HG01928.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.4840+4507T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043789 | ||||||
chrX:130043790 | T | A | 5 | a0001c0001t0001g0080a0001c0001t0001g0097a0001c0001t0001g0098others(2): Show | 5 | HG02615.hp2 HG02809.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.4840+4508T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043790 | ||||||
chrX:130043791 | T | A | 4 | a0001c0001t0001g0110a0001c0001t0001g0112a0001c0001t0012g0121others(1): Show | 4 | NA18974.hp1 NA18984.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.4840+4509T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043791 | ||||||
chrX:130043793 | T | A | 2 | a0001c0001t0001g0112a0001c0001t0012g0121 | 2 | NA18994.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.4840+4511T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043793 | ||||||
chrX:130043916 | C | T | 18 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(15): Show | 18 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.4840+4634C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043916 | ||||||
chrX:130043938 | T | G | 9 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(6): Show | 9 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(6): Show |
intron_variant | MODIFIER | c.4840+4656T>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043938 | ||||||
chrX:130043996 | C | A | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4840+4714C>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130043996 | ||||||
chrX:130044498 | CTCTTTTT | C | 1 | a0001c0005t0006g0196 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.4840+5222_4840+522 others(11): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130044498 | |||||
chrX:130044512 | AT | A | 4 | a0001c0001t0001g0080a0001c0001t0001g0147a0001c0001t0001g0152others(1): Show | 4 | HG01069.hp1 HG02896.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.4840+5244delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130044512 | |||||
chrX:130044663 | C | T | 31 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(28): Show | 31 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(28): Show |
intron_variant | MODIFIER | c.4840+5381C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130044663 | ||||||
chrX:130044732 | C | T | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.4840+5450C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130044732 | ||||||
chrX:130044789 | G | A | 1 | a0001c0001t0001g0165 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.4840+5507G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130044789 | ||||||
chrX:130044800 | C | T | 1 | a0001c0007t0001g0064 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4840+5518C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130044800 | ||||||
chrX:130044893 | T | A | 1 | a0001c0001t0001g0068 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.4840+5611T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130044893 | ||||||
chrX:130045459 | T | C | 34 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(31): Show | 34 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.4841-5258T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130045459 | ||||||
chrX:130045515 | G | A | 2 | a0001c0001t0001g0045a0007c0012t0011g0043 | 2 | NA18967.hp1 NA18985.hp1 |
intron_variant | MODIFIER | c.4841-5202G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130045515 | ||||||
chrX:130045527 | G | A | 32 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(29): Show | 32 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(29): Show |
intron_variant | MODIFIER | c.4841-5190G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130045527 | ||||||
chrX:130045583 | A | G | 1 | a0001c0001t0001g0072 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.4841-5134A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130045583 | ||||||
chrX:130045596 | G | T | 1 | a0001c0001t0001g0020 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.4841-5121G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130045596 | ||||||
chrX:130045711 | G | A | 18 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(15): Show | 18 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.4841-5006G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130045711 | ||||||
chrX:130045909 | C | T | 1 | a0001c0001t0001g0044 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.4841-4808C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130045909 | ||||||
chrX:130045934 | TA | T | 1 | a0001c0001t0001g0018 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.4841-4777delA | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130045934 | |||||
chrX:130046354 | C | T | 10 | a0001c0001t0001g0021a0001c0001t0001g0029a0001c0001t0001g0087others(7): Show | 10 | HG01074.hp1 HG01255.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.4841-4363C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130046354 | ||||||
chrX:130046492 | A | C | 34 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(31): Show | 34 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.4841-4225A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130046492 | ||||||
chrX:130046607 | C | T | 1 | a0001c0001t0001g0169 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.4841-4110C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130046607 | ||||||
chrX:130046639 | T | C | 34 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(31): Show | 34 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.4841-4078T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130046639 | ||||||
chrX:130046748 | G | A | 1 | a0001c0001t0001g0199 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.4841-3969G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130046748 | ||||||
chrX:130046753 | A | G | 1 | a0001c0001t0001g0167 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.4841-3964A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130046753 | ||||||
chrX:130046858 | T | C | 1 | a0001c0001t0001g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4841-3859T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130046858 | ||||||
chrX:130046863 | AC | A | 1 | a0001c0001t0001g0150 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.4841-3850delC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130046863 | |||||
chrX:130047022 | C | T | 1 | a0001c0001t0001g0095 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4841-3695C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130047022 | ||||||
chrX:130047194 | G | A | 1 | a0001c0001t0007g0059 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4841-3523G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130047194 | ||||||
chrX:130047322 | G | A | 18 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(15): Show | 18 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.4841-3395G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130047322 | ||||||
chrX:130047326 | A | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(120): Show | 123 | HG00140.hp1 HG00408.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.4841-3391A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130047326 | ||||||
chrX:130047380 | G | A | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4841-3337G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130047380 | ||||||
chrX:130047899 | A | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0088 | 2 | HG01884.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.4841-2818A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130047899 | ||||||
chrX:130048136 | C | T | 1 | a0001c0001t0001g0048 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4841-2581C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130048136 | ||||||
chrX:130048487 | G | A | 1 | a0001c0001t0001g0153 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4841-2230G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130048487 | ||||||
chrX:130048716 | CAGTA | C | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.4841-1996_4841-199 others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130048716 | |||||
chrX:130049089 | T | C | 1 | a0001c0009t0015g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4841-1628T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130049089 | ||||||
chrX:130049116 | G | C | 34 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(31): Show | 34 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.4841-1601G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130049116 | ||||||
chrX:130049345 | A | AGTTT | 2 | a0001c0019t0002g0117a0001c0022t0001g0024 | 2 | HG03688.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.4841-1347_4841-134 others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130049345 | |||||
chrX:130049345 | AGTTT | A | 17 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(14): Show | 17 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.4841-1347_4841-134 others(8): Show |
BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130049345 | |||||
chrX:130049642 | G | A | 1 | a0001c0001t0001g0103 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4841-1075G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130049642 | ||||||
chrX:130050005 | G | A | 1 | a0001c0005t0009g0191 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.4841-712G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130050005 | ||||||
chrX:130050308 | T | C | 34 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(31): Show | 34 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.4841-409T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130050308 | ||||||
chrX:130050469 | AT | A | 1 | a0001c0001t0005g0120 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4841-238delT | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chrX | 130050469 | |||||
chrX:130050496 | T | A | 1 | a0001c0009t0015g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4841-221T>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 11/13 | chrX | 130050496 | ||||||
chrX:130050901 | A | G | 34 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(31): Show | 34 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.4918+107A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 12/13 | chrX | 130050901 | ||||||
chrX:130051047 | G | A | 2 | a0001c0001t0001g0037a0001c0001t0001g0047 | 2 | HG00621.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.4918+253G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 12/13 | chrX | 130051047 | ||||||
chrX:130051344 | C | T | 1 | a0001c0009t0015g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4919-516C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 12/13 | chrX | 130051344 | ||||||
chrX:130051391 | A | G | 1 | a0001c0003t0002g0148 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.4919-469A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 12/13 | chrX | 130051391 | ||||||
chrX:130051614 | A | AG | 1 | a0001c0001t0001g0009 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.4919-240dupG | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chrX | 130051614 | |||||
chrX:130051764 | C | T | 13 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(10): Show | 13 | HG01081.hp1 HG01496.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.4919-96C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 12/13 | chrX | 130051764 | ||||||
chrX:130051766 | A | C | 1 | a0001c0002t0002g0033 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.4919-94A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 12/13 | chrX | 130051766 | ||||||
chrX:130052031 | G | C | 1 | a0006c0015t0001g0107 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.5075+15G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130052031 | ||||||
chrX:130052037 | C | T | 23 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(20): Show | 23 | HG01074.hp1 HG01109.hp1 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.5075+21C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130052037 | ||||||
chrX:130052628 | G | A | 2 | a0001c0001t0001g0012a0008c0017t0001g0013 | 2 | HG01496.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.5075+612G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130052628 | ||||||
chrX:130052803 | G | C | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5075+787G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130052803 | ||||||
chrX:130053074 | A | G | 2 | a0001c0001t0001g0018a0001c0001t0001g0081 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5075+1058A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130053074 | ||||||
chrX:130053194 | G | A | 34 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(31): Show | 34 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.5075+1178G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130053194 | ||||||
chrX:130053212 | T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0088 | 2 | HG01884.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.5075+1196T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130053212 | ||||||
chrX:130053291 | T | TC | 1 | a0001c0001t0001g0027 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.5075+1282dupC | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chrX | 130053291 | |||||
chrX:130053466 | C | T | 1 | a0001c0009t0015g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5075+1450C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130053466 | ||||||
chrX:130053539 | A | G | 1 | a0001c0001t0001g0195 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.5075+1523A>G | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130053539 | ||||||
chrX:130053559 | G | T | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5075+1543G>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130053559 | ||||||
chrX:130053636 | G | A | 1 | a0001c0001t0001g0201 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.5075+1620G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130053636 | ||||||
chrX:130053752 | G | A | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5075+1736G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130053752 | ||||||
chrX:130054078 | C | A | 1 | a0001c0009t0015g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5076-1776C>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054078 | ||||||
chrX:130054484 | A | T | 1 | a0001c0001t0001g0006 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.5076-1370A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054484 | ||||||
chrX:130054563 | G | A | 2 | a0001c0001t0001g0018a0001c0001t0001g0081 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5076-1291G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054563 | ||||||
chrX:130054564 | A | T | 2 | a0001c0001t0001g0018a0001c0001t0001g0081 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.5076-1290A>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054564 | ||||||
chrX:130054620 | T | C | 1 | a0001c0001t0001g0077 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.5076-1234T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054620 | ||||||
chrX:130054633 | C | T | 3 | a0001c0001t0002g0099a0001c0001t0007g0057a0001c0001t0007g0059 | 3 | HG03041.hp2 HG03195.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.5076-1221C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054633 | ||||||
chrX:130054634 | G | A | 3 | a0001c0001t0001g0022a0001c0001t0001g0037a0001c0001t0001g0047 | 3 | HG00621.hp1 NA18954.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.5076-1220G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054634 | ||||||
chrX:130054673 | A | C | 11 | a0001c0002t0002g0004a0001c0002t0002g0032a0001c0002t0002g0033others(8): Show | 11 | HG01081.hp1 HG01496.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.5076-1181A>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054673 | ||||||
chrX:130054771 | C | T | 1 | a0001c0002t0002g0189 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.5076-1083C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054771 | ||||||
chrX:130054783 | T | C | 34 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(31): Show | 34 | HG01081.hp1 HG01496.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.5076-1071T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054783 | ||||||
chrX:130054859 | C | T | 2 | a0001c0005t0008g0139a0001c0005t0008g0140 | 2 | HG02258.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.5076-995C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054859 | ||||||
chrX:130054932 | T | C | 1 | a0001c0008t0004g0060 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.5076-922T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054932 | ||||||
chrX:130054998 | G | A | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5076-856G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130054998 | ||||||
chrX:130055068 | G | C | 1 | a0001c0002t0002g0056 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.5076-786G>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130055068 | ||||||
chrX:130055153 | G | A | 1 | a0001c0001t0014g0085 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.5076-701G>A | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130055153 | ||||||
chrX:130055500 | C | T | 1 | a0001c0009t0015g0082 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.5076-354C>T | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130055500 | ||||||
chrX:130055752 | T | C | 17 | a0001c0001t0002g0099a0001c0001t0002g0200a0001c0001t0007g0057others(14): Show | 17 | HG01884.hp1 HG02280.hp2 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.5076-102T>C | BCORL1 | ENSG00000085185.16 | transcript | ENST00000540052.6 | protein_coding | 13/13 | chrX | 130055752 |