geneid | 79870 |
---|---|
ensemblid | ENSG00000164929.17 |
hgncid | 14333 |
symbol | BAALC |
name | BAALC binder of MAP3K1 and KLF4 |
refseq_nuc | NM_024812.3 |
refseq_prot | NP_079088.1 |
ensembl_nuc | ENST00000309982.10 |
ensembl_prot | ENSP00000312457.5 |
mane_status | MANE Select |
chr | chr8 |
start | 103140725 |
end | 103230305 |
strand | + |
ver | v1.2 |
region | chr8:103140725-103230305 |
region5000 | chr8:103135725-103235305 |
regionname0 | BAALC_chr8_103140725_103230305 |
regionname5000 | BAALC_chr8_103135725_103235305 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 145 | 323 | 71 | 62 | 130 | 16 | 42 | 96 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0002 | 0/0 | 145 | 9 | 9 | 0 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 438 | 317 | 69 | 62 | 128 | 14 | 42 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
c0002 | 0/0 | 438 | 5 | 5 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
c0003 | 0/0 | 438 | 5 | 1 | 0 | 2 | 2 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
c0004 | 0/0 | 438 | 4 | 4 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
c0005 | 0/0 | 438 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2380 | 153 | 25 | 30 | 67 | 7 | 23 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0002 | 0/1 | 2377 | 72 | 14 | 11 | 38 | 1 | 7 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0003 | 0/0 | 2380 | 25 | 10 | 3 | 2 | 4 | 6 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0004 | 0/0 | 2380 | 14 | 0 | 0 | 14 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0005 | 0/0 | 2380 | 11 | 7 | 1 | 0 | 1 | 2 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0006 | 0/0 | 2380 | 11 | 5 | 4 | 0 | 1 | 1 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0007 | 0/0 | 2377 | 9 | 0 | 9 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0008 | 0/0 | 2380 | 6 | 3 | 3 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0009 | 0/0 | 2380 | 5 | 1 | 0 | 2 | 2 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0010 | 0/0 | 2377 | 5 | 5 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0011 | 0/0 | 2380 | 4 | 0 | 0 | 4 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0012 | 0/0 | 2380 | 2 | 0 | 0 | 0 | 0 | 2 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0013 | 0/0 | 2380 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0014 | 0/0 | 2380 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0015 | 0/0 | 2380 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0016 | 0/0 | 2380 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0017 | 0/0 | 2380 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0018 | 0/0 | 2380 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0019 | 0/0 | 2380 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0020 | 0/0 | 2380 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0021 | 0/0 | 2380 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0022 | 0/0 | 2380 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0023 | 0/0 | 2377 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
t0024 | 0/0 | 2380 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0013 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0016 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0217 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 438 | 317 | 69 | 62 | 128 | 14 | 42 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0003 | 0/0 | 438 | 5 | 1 | 0 | 2 | 2 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0005 | 0/0 | 438 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0002c0002 | 0/0 | 438 | 5 | 5 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0002c0004 | 0/0 | 438 | 4 | 4 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 2817 | 153 | 25 | 30 | 67 | 7 | 23 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0002 | 0/1 | 2814 | 72 | 14 | 11 | 38 | 1 | 7 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0003 | 0/0 | 2817 | 16 | 1 | 3 | 2 | 4 | 6 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0004 | 0/0 | 2817 | 14 | 0 | 0 | 14 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0005 | 0/0 | 2817 | 11 | 7 | 1 | 0 | 1 | 2 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0006 | 0/0 | 2817 | 11 | 5 | 4 | 0 | 1 | 1 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0007 | 0/0 | 2814 | 9 | 0 | 9 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0008 | 0/0 | 2817 | 6 | 3 | 3 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0010 | 0/0 | 2814 | 5 | 5 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0011 | 0/0 | 2817 | 4 | 0 | 0 | 4 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0012 | 0/0 | 2817 | 2 | 0 | 0 | 0 | 0 | 2 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0013 | 0/0 | 2817 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0014 | 0/0 | 2817 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0015 | 0/0 | 2817 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0016 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0017 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0018 | 0/0 | 2817 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0019 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0020 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0021 | 0/0 | 2817 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0022 | 0/0 | 2817 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0001t0024 | 0/0 | 2817 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0003t0009 | 0/0 | 2817 | 5 | 1 | 0 | 2 | 2 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0001c0005t0023 | 0/0 | 2814 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0002c0002t0003 | 0/0 | 2817 | 5 | 5 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
a0002c0004t0003 | 0/0 | 2817 | 4 | 4 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | copy fasta | chr8 | 103135725 | 103235305 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0014 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0180 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0027 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0030 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0217 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0028 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0029 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0004g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0004g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0004g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0004g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0004g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0005g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0005g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0005g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0005g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0005g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0005g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0005g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0005g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0006g0031 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0006g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0006g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0006g0047 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0006g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0006g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0006g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0006g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0007g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0007g0025 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0007g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0007g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0007g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0007g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0008g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0008g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0008g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0008g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0008g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0008g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0010g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0010g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0010g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0010g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0011g0002 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0012g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0012g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0013g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0013g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0014g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0014g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0015g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0015g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0016g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0017g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0018g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0019g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0020g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0021g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0022g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0001t0024g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0003t0009g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0003t0009g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0003t0009g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0003t0009g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0003t0009g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0001c0005t0023g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0002c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0002c0002t0003g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0002c0002t0003g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0002c0002t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0002c0002t0003g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
a0002c0004t0003g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0005 | g0098 | EUR | GBR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00099 | hp2 | a0001 | c0003 | t0009 | g0260 | EUR | GBR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00140 | hp1 | a0001 | c0001 | t0006 | g0031 | EUR | GBR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0141 | EUR | GBR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0018 | EUR | FIN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0106 | EUR | FIN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0121 | EUR | FIN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0231 | EUR | FIN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0187 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00438 | hp1 | a0001 | c0001 | t0004 | g0114 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00642 | hp2 | a0001 | c0001 | t0007 | g0006 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0029 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00741 | hp1 | a0001 | c0001 | t0008 | g0081 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0093 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0062 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0078 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01106 | hp1 | a0001 | c0001 | t0021 | g0147 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01109 | hp1 | a0001 | c0001 | t0008 | g0261 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01109 | hp2 | a0001 | c0001 | t0007 | g0208 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0166 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0030 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01175 | hp1 | a0001 | c0001 | t0003 | g0118 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01192 | hp2 | a0001 | c0001 | t0007 | g0203 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01255 | hp1 | a0001 | c0001 | t0006 | g0031 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01256 | hp1 | a0001 | c0001 | t0006 | g0032 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01257 | hp1 | a0001 | c0001 | t0007 | g0025 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0028 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0032 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01258 | hp2 | a0001 | c0001 | t0007 | g0025 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0216 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01346 | hp2 | a0001 | c0001 | t0007 | g0006 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01358 | hp1 | a0001 | c0001 | t0005 | g0126 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01358 | hp2 | a0001 | c0001 | t0008 | g0276 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01433 | hp1 | a0001 | c0001 | t0007 | g0006 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0290 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01496 | hp1 | a0001 | c0001 | t0006 | g0272 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01515 | hp1 | a0001 | c0001 | t0003 | g0117 | EUR | IBS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0168 | EUR | IBS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01517 | hp1 | a0001 | c0001 | t0003 | g0049 | EUR | IBS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0116 | EUR | IBS | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0281 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0240 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01891 | hp1 | a0002 | c0004 | t0003 | g0001 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01928 | hp2 | a0001 | c0001 | t0007 | g0060 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0222 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0056 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0223 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02015 | hp2 | a0001 | c0001 | t0003 | g0232 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02055 | hp1 | a0001 | c0001 | t0024 | g0282 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0077 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02056 | hp1 | a0001 | c0001 | t0002 | g0043 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02080 | hp1 | a0001 | c0001 | t0019 | g0188 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0069 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0112 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0124 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0133 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02148 | hp2 | a0001 | c0001 | t0007 | g0210 | AMR | PEL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0015 | EAS | CDX | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CDX | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | CDX | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | CDX | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02258 | hp1 | a0001 | c0005 | t0023 | g0038 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02280 | hp2 | a0001 | c0001 | t0010 | g0278 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0252 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02523 | hp1 | a0001 | c0001 | t0022 | g0185 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | KHV | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02572 | hp1 | a0001 | c0003 | t0009 | g0262 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0246 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0095 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0274 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02615 | hp1 | a0001 | c0001 | t0014 | g0284 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0238 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02630 | hp1 | a0001 | c0001 | t0010 | g0287 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02630 | hp2 | a0001 | c0001 | t0010 | g0089 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0275 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02717 | hp1 | a0001 | c0001 | t0015 | g0158 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0286 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0230 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0047 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02809 | hp1 | a0001 | c0001 | t0010 | g0249 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02809 | hp2 | a0001 | c0001 | t0017 | g0040 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0003 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0254 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02886 | hp1 | a0001 | c0001 | t0020 | g0013 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0080 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0008 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0244 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02970 | hp1 | a0001 | c0001 | t0015 | g0243 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02976 | hp1 | a0001 | c0001 | t0006 | g0151 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02976 | hp2 | a0001 | c0001 | t0005 | g0247 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03017 | hp1 | a0001 | c0001 | t0018 | g0016 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03017 | hp2 | a0001 | c0001 | t0012 | g0197 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03130 | hp1 | a0002 | c0004 | t0003 | g0001 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03130 | hp2 | a0001 | c0001 | t0002 | g0241 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03139 | hp1 | a0001 | c0001 | t0008 | g0239 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03195 | hp1 | a0001 | c0001 | t0006 | g0153 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03195 | hp2 | a0001 | c0001 | t0013 | g0277 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03209 | hp1 | a0001 | c0001 | t0005 | g0250 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0033 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03239 | hp2 | a0001 | c0001 | t0005 | g0285 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0074 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0003 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03486 | hp1 | a0001 | c0001 | t0002 | g0253 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03486 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | MSL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03491 | hp2 | a0001 | c0001 | t0012 | g0248 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03516 | hp1 | a0001 | c0001 | t0014 | g0157 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03516 | hp2 | a0002 | c0002 | t0003 | g0073 | AFR | ESN | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03540 | hp1 | a0001 | c0001 | t0010 | g0088 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03540 | hp2 | a0001 | c0001 | t0013 | g0279 | AFR | GWD | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0288 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03669 | hp1 | a0001 | c0001 | t0003 | g0036 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0136 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0044 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0092 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03704 | hp2 | a0001 | c0001 | t0003 | g0237 | SAS | PJL | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0048 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03831 | hp2 | a0001 | c0001 | t0003 | g0233 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0028 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0115 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0059 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0181 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG04184 | hp1 | a0001 | c0001 | t0005 | g0234 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0108 | SAS | BEB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0024 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0134 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0053 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG04228 | hp2 | a0001 | c0001 | t0003 | g0174 | SAS | STU | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18522 | hp1 | a0002 | c0004 | t0003 | g0001 | AFR | YRI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0163 | AFR | YRI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | CHB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0183 | EAS | CHB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18906 | hp1 | a0001 | c0001 | t0005 | g0127 | AFR | YRI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18906 | hp2 | a0001 | c0001 | t0008 | g0156 | AFR | YRI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18943 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18946 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0200 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18959 | hp1 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0195 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18965 | hp1 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18965 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18967 | hp1 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18967 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18983 | hp1 | a0001 | c0003 | t0009 | g0257 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0107 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18989 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0196 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18995 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18999 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19055 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0194 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19060 | hp1 | a0001 | c0003 | t0009 | g0258 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19062 | hp1 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19066 | hp2 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0201 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19082 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19085 | hp2 | a0001 | c0001 | t0016 | g0173 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19088 | hp1 | a0001 | c0001 | t0011 | g0002 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0068 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | YRI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA19240 | hp2 | a0002 | c0002 | t0003 | g0131 | AFR | YRI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA20129 | hp1 | a0002 | c0004 | t0003 | g0001 | AFR | ASW | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA20129 | hp2 | a0001 | c0001 | t0005 | g0242 | AFR | ASW | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0029 | EUR | TSI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA20752 | hp2 | a0001 | c0003 | t0009 | g0259 | EUR | TSI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0207 | EUR | TSI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0289 | SAS | GIH | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA20905 | hp2 | a0001 | c0001 | t0003 | g0236 | SAS | GIH | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0273 | AMR | CLM | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02486 | hp1 | a0002 | c0002 | t0003 | g0291 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG02559 | hp2 | a0002 | c0002 | t0003 | g0039 | AFR | ACB | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG06807 | hp1 | a0001 | c0001 | t0003 | g0235 | AFR | USA | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0280 | AFR | USA | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0012 | EAS | JPT | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA20300 | hp1 | a0002 | c0002 | t0003 | g0283 | AFR | USA | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | USA | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0217 | REF | REF | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0180 | REF | REF | BAALC_chr8_103135725_103235305 | BAALC | chr8 | 103135725 | 103235305 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:103228047
|
G | C | 1 | a0002 | 9 | HG01891.hp1 HG02486.hp1 HG02559.hp2 others(6): Show |
missense_variant | MODERATE | c.386G>C | p.Ser129Thr | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 559/2817 | 386/438 | 129/145 | chr8 | 103228047 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:103140909
|
C | T | 1 | a0001c0003 | 5 | HG00099.hp2 HG02572.hp1 NA18983.hp1 others(2): Show |
synonymous_variant | LOW | c.12C>T | p.Gly4Gly | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/3 | 185/2817 | 12/438 | 4/145 | chr8 | 103140909 | ||
chr8:103141056
|
G | A | 2 | a0001c0005a0002c0004 | 5 | HG01891.hp1 HG02258.hp1 HG03130.hp1 others(2): Show |
splice_region_variant&synonymous_variant | LOW | c.159G>A | p.Ser53Ser | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/3 | 332/2817 | 159/438 | 53/145 | chr8 | 103141056 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:103140800
|
C | A | 1 | a0001c0003t0009 | 5 | HG00099.hp2 HG02572.hp1 NA18983.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-98C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/3 | 98 | chr8 | 103140800 | |||||
chr8:103140845
|
G | A | 1 | a0001c0001t0011 | 4 | NA18965.hp2 NA18989.hp2 NA19066.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-53G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/3 | 53 | chr8 | 103140845 | |||||
chr8:103228226
|
A | G | 1 | a0001c0001t0010 | 5 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*127A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 127 | chr8 | 103228226 | |||||
chr8:103228310
|
T | G | 1 | a0001c0001t0016 | 1 | NA19085.hp2 | 3_prime_UTR_variant | MODIFIER | c.*211T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 211 | chr8 | 103228310 | |||||
chr8:103228419
|
T | A | 1 | a0001c0001t0017 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*320T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 320 | chr8 | 103228419 | |||||
chr8:103228448
|
G | A | 1 | a0001c0001t0012 | 2 | HG03017.hp2 HG03491.hp2 |
3_prime_UTR_variant | MODIFIER | c.*349G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 349 | chr8 | 103228448 | |||||
chr8:103228677
|
C | T | 1 | a0001c0001t0024 | 1 | HG02055.hp1 | 3_prime_UTR_variant | MODIFIER | c.*578C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 578 | chr8 | 103228677 | |||||
chr8:103228924
|
C | T | 2 | a0001c0001t0006a0001c0001t0015 | 13 | HG00140.hp1 HG01255.hp1 HG01256.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*825C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 825 | chr8 | 103228924 | |||||
chr8:103229050
|
C | G | 1 | a0001c0005t0023 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*951C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 951 | chr8 | 103229050 | |||||
chr8:103229418
|
G | A | 1 | a0001c0001t0007 | 9 | HG00642.hp2 HG01109.hp2 HG01192.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1319G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1319 | chr8 | 103229418 | |||||
chr8:103229518
|
T | C | 1 | a0001c0001t0015 | 2 | HG02717.hp1 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1419T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1419 | chr8 | 103229518 | |||||
chr8:103229538
|
A | C | 2 | a0001c0001t0005a0001c0001t0012 | 13 | HG00099.hp1 HG01358.hp1 HG01884.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1439A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1439 | chr8 | 103229538 | |||||
chr8:103229599
|
T | C | 1 | a0001c0001t0018 | 1 | HG03017.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1500T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1500 | chr8 | 103229599 | |||||
chr8:103229730
|
C | T | 1 | a0001c0001t0008 | 6 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1631C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1631 | chr8 | 103229730 | |||||
chr8:103229766
|
A | G | 1 | a0001c0001t0021 | 1 | HG01106.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1667A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1667 | chr8 | 103229766 | |||||
chr8:103229766
|
A | T | 6 | a0001c0001t0003a0001c0001t0006a0001c0001t0015others(3): Show | 39 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1667A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1667 | chr8 | 103229766 | |||||
chr8:103229781
|
C | T | 1 | a0001c0001t0014 | 2 | HG02615.hp1 HG03516.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1682C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1682 | chr8 | 103229781 | |||||
chr8:103229924
|
A | C | 2 | a0001c0001t0008a0001c0001t0013 | 8 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1825A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 1825 | chr8 | 103229924 | |||||
chr8:103230111
|
G | A | 1 | a0001c0001t0019 | 1 | HG02080.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2012G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 2012 | chr8 | 103230111 | |||||
chr8:103230152
|
G | A | 1 | a0001c0001t0022 | 1 | HG02523.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2053G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 2053 | chr8 | 103230152 | |||||
chr8:103230198
|
GCTA | G | 4 | a0001c0001t0002a0001c0001t0007a0001c0001t0010others(1): Show | 87 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*2102_*2104delACT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 2102 | INFO_REALIGN_3_PRIME | chr8 | 103230198 | ||||
chr8:103230223
|
C | T | 1 | a0001c0001t0020 | 1 | HG02886.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2124C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 2124 | chr8 | 103230223 | |||||
chr8:103230242
|
T | C | 1 | a0001c0001t0004 | 14 | HG00438.hp1 HG02132.hp2 HG02155.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2143T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 3/3 | 2143 | chr8 | 103230242 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:103141127
|
G | A | 4 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0034others(1): Show | 7 | HG02109.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+70G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141127 | ||||||
chr8:103141195
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+138G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141195 | ||||||
chr8:103141291
|
A | G | 1 | a0002c0002t0003g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+234A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141291 | ||||||
chr8:103141321
|
G | T | 22 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(19): Show | 24 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.160+264G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141321 | ||||||
chr8:103141440
|
C | T | 6 | a0001c0001t0001g0265a0001c0001t0001g0266a0001c0001t0001g0268others(3): Show | 6 | NA18939.hp1 NA18982.hp1 NA19007.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+383C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141440 | ||||||
chr8:103141454
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033 | 4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+397C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141454 | ||||||
chr8:103141455
|
G | A | 7 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(4): Show | 9 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+398G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141455 | ||||||
chr8:103141659
|
C | A | 1 | a0001c0001t0003g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.160+602C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141659 | ||||||
chr8:103141737
|
A | G | 22 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(19): Show | 24 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(21): Show |
intron_variant | MODIFIER | c.160+680A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141737 | ||||||
chr8:103141922
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.160+865G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141922 | ||||||
chr8:103141927
|
G | C | 4 | a0001c0001t0017g0040a0001c0005t0023g0038a0002c0002t0003g0039others(1): Show | 7 | HG01891.hp1 HG02258.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+870G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103141927 | ||||||
chr8:103142053
|
T | C | 3 | a0001c0001t0001g0041a0001c0001t0002g0043a0001c0001t0003g0042 | 3 | HG02040.hp2 HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.160+996T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142053 | ||||||
chr8:103142168
|
G | A | 1 | a0001c0001t0006g0033 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.160+1111G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142168 | ||||||
chr8:103142300
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.160+1243T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142300 | ||||||
chr8:103142350
|
C | T | 1 | a0001c0001t0001g0264 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.160+1293C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142350 | ||||||
chr8:103142462
|
C | G | 1 | a0001c0001t0001g0263 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.160+1405C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142462 | ||||||
chr8:103142485
|
T | G | 156 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(153): Show | 173 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(170): Show |
intron_variant | MODIFIER | c.160+1428T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142485 | ||||||
chr8:103142737
|
T | C | 157 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(154): Show | 174 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(171): Show |
intron_variant | MODIFIER | c.160+1680T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142737 | ||||||
chr8:103142971
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033 | 4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+1914C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142971 | ||||||
chr8:103142983
|
C | G | 1 | a0002c0002t0003g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+1926C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103142983 | ||||||
chr8:103143137
|
G | T | 1 | a0001c0003t0009g0262 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160+2080G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143137 | ||||||
chr8:103143211
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0045 | 5 | HG02129.hp1 NA18960.hp2 NA18993.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+2154G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143211 | ||||||
chr8:103143220
|
G | A | 1 | a0002c0002t0003g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+2163G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143220 | ||||||
chr8:103143358
|
C | T | 1 | a0001c0001t0008g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+2301C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143358 | ||||||
chr8:103143427
|
A | G | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+2370A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143427 | ||||||
chr8:103143435
|
G | A | 1 | a0002c0002t0003g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+2378G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143435 | ||||||
chr8:103143484
|
T | C | 1 | a0001c0001t0003g0174 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.160+2427T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143484 | ||||||
chr8:103143624
|
C | T | 73 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(70): Show | 82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.160+2567C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143624 | ||||||
chr8:103143731
|
G | C | 1 | a0001c0001t0002g0175 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.160+2674G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143731 | ||||||
chr8:103143768
|
C | T | 73 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(70): Show | 82 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.160+2711C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143768 | ||||||
chr8:103143773
|
C | G | 5 | a0001c0003t0009g0257a0001c0003t0009g0258a0001c0003t0009g0259others(2): Show | 5 | HG00099.hp2 HG02572.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+2716C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143773 | ||||||
chr8:103143810
|
C | G | 8 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0002g0286others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+2753C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143810 | ||||||
chr8:103143913
|
C | G | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0263others(1): Show | 4 | HG00438.hp2 HG02165.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+2856C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143913 | ||||||
chr8:103143984
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.160+2927C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103143984 | ||||||
chr8:103144231
|
T | C | 6 | a0001c0003t0009g0257a0001c0003t0009g0258a0001c0003t0009g0259others(3): Show | 6 | HG00099.hp2 HG02486.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+3174T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144231 | ||||||
chr8:103144238
|
A | G | 23 | a0001c0001t0001g0035a0001c0001t0001g0271a0001c0001t0001g0273others(20): Show | 25 | HG00140.hp1 HG01123.hp2 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.160+3181A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144238 | ||||||
chr8:103144266
|
T | G | 7 | a0001c0001t0001g0281a0001c0001t0008g0276a0001c0001t0008g0280others(4): Show | 7 | HG01358.hp2 HG01884.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+3209T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144266 | ||||||
chr8:103144300
|
T | C | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.160+3243T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144300 | ||||||
chr8:103144375
|
A | G | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.160+3318A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144375 | ||||||
chr8:103144422
|
A | T | 1 | a0001c0001t0002g0253 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.160+3365A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144422 | ||||||
chr8:103144496
|
G | A | 15 | a0001c0001t0001g0035a0001c0001t0001g0288a0001c0001t0001g0289others(12): Show | 15 | HG00099.hp2 HG01243.hp2 HG01433.hp2 others(12): Show |
intron_variant | MODIFIER | c.160+3439G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144496 | ||||||
chr8:103144599
|
A | C | 5 | a0001c0003t0009g0257a0001c0003t0009g0258a0001c0003t0009g0259others(2): Show | 5 | HG00099.hp2 HG02572.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+3542A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144599 | ||||||
chr8:103144645
|
G | A | 4 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0034others(1): Show | 7 | HG02109.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+3588G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144645 | ||||||
chr8:103144646
|
C | T | 34 | a0001c0001t0001g0044a0001c0001t0001g0228a0001c0001t0001g0230others(31): Show | 37 | HG00323.hp2 HG00738.hp1 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.160+3589C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144646 | ||||||
chr8:103144739
|
C | A | 172 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(169): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.160+3682C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144739 | ||||||
chr8:103144802
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118 | 3 | HG01175.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.160+3745C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144802 | ||||||
chr8:103144852
|
T | C | 1 | a0001c0001t0002g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.160+3795T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144852 | ||||||
chr8:103144869
|
A | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033 | 4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+3812A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144869 | ||||||
chr8:103144930
|
C | A | 4 | a0001c0001t0002g0003a0001c0001t0002g0008a0001c0001t0002g0034others(1): Show | 7 | HG02109.hp2 HG02818.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+3873C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144930 | ||||||
chr8:103144946
|
G | A | 178 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(175): Show | 201 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.160+3889G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103144946 | ||||||
chr8:103145046
|
T | C | 19 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0051others(16): Show | 21 | HG01070.hp2 HG01192.hp1 HG01517.hp1 others(18): Show |
intron_variant | MODIFIER | c.160+3989T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145046 | ||||||
chr8:103145180
|
T | C | 2 | a0001c0005t0023g0038a0002c0004t0003g0001 | 5 | HG01891.hp1 HG02258.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+4123T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145180 | ||||||
chr8:103145232
|
C | G | 5 | a0001c0003t0009g0257a0001c0003t0009g0258a0001c0003t0009g0259others(2): Show | 5 | HG00099.hp2 HG02572.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+4175C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145232 | ||||||
chr8:103145303
|
A | G | 192 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(189): Show | 217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.160+4246A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145303 | ||||||
chr8:103145430
|
GA | G | 8 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0002g0286others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+4374delA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145430 | ||||||
chr8:103145492
|
G | A | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.160+4435G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145492 | ||||||
chr8:103145586
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.160+4529T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145586 | ||||||
chr8:103145632
|
A | C | 3 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033 | 4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+4575A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145632 | ||||||
chr8:103145901
|
T | G | 8 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0002g0286others(5): Show | 8 | HG01433.hp2 HG02615.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+4844T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103145901 | ||||||
chr8:103146048
|
T | C | 3 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033 | 4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+4991T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146048 | ||||||
chr8:103146061
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.160+5004T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146061 | ||||||
chr8:103146238
|
G | A | 1 | a0002c0002t0003g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.160+5181G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146238 | ||||||
chr8:103146491
|
T | C | 1 | a0001c0001t0002g0177 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.160+5434T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146491 | ||||||
chr8:103146498
|
A | T | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+5441A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146498 | ||||||
chr8:103146548
|
T | C | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | NA18953.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.160+5491T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146548 | ||||||
chr8:103146560
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+5503T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146560 | ||||||
chr8:103146890
|
T | G | 87 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(84): Show | 99 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.160+5833T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103146890 | ||||||
chr8:103146946
|
C | CT | 87 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0011others(84): Show | 99 | HG00099.hp1 HG00280.hp2 HG00438.hp1 others(96): Show |
intron_variant | MODIFIER | c.160+5890dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103146946 | |||||
chr8:103147225
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.160+6168A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147225 | ||||||
chr8:103147357
|
C | T | 114 | a0001c0001t0001g0044a0001c0001t0001g0176a0001c0001t0001g0178others(111): Show | 130 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.160+6300C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147357 | ||||||
chr8:103147484
|
C | T | 6 | a0001c0001t0002g0043a0001c0001t0004g0110a0001c0001t0004g0111others(3): Show | 6 | HG00438.hp1 HG02056.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+6427C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147484 | ||||||
chr8:103147486
|
G | A | 210 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(207): Show | 241 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(238): Show |
intron_variant | MODIFIER | c.160+6429G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147486 | ||||||
chr8:103147556
|
G | T | 114 | a0001c0001t0001g0044a0001c0001t0001g0176a0001c0001t0001g0178others(111): Show | 130 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.160+6499G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147556 | ||||||
chr8:103147655
|
T | C | 1 | a0001c0001t0001g0064 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.160+6598T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147655 | ||||||
chr8:103147669
|
A | G | 114 | a0001c0001t0001g0044a0001c0001t0001g0176a0001c0001t0001g0178others(111): Show | 130 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.160+6612A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147669 | ||||||
chr8:103147701
|
G | T | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+6644G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147701 | ||||||
chr8:103147751
|
G | A | 1 | a0001c0001t0008g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+6694G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147751 | ||||||
chr8:103147761
|
C | G | 1 | a0001c0001t0005g0252 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.160+6704C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147761 | ||||||
chr8:103147769
|
C | T | 1 | a0002c0002t0003g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+6712C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147769 | ||||||
chr8:103147831
|
C | G | 2 | a0001c0001t0017g0040a0002c0002t0003g0039 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.160+6774C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147831 | ||||||
chr8:103147915
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033 | 4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+6858G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147915 | ||||||
chr8:103147928
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033 | 4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+6871G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103147928 | ||||||
chr8:103148045
|
C | G | 3 | a0001c0001t0001g0226a0001c0001t0002g0007a0001c0001t0002g0227 | 5 | NA18943.hp1 NA18957.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+6988C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148045 | ||||||
chr8:103148050
|
G | A | 3 | a0001c0001t0001g0226a0001c0001t0002g0007a0001c0001t0002g0227 | 5 | NA18943.hp1 NA18957.hp1 NA19004.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+6993G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148050 | ||||||
chr8:103148281
|
T | C | 114 | a0001c0001t0001g0044a0001c0001t0001g0176a0001c0001t0001g0178others(111): Show | 130 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.160+7224T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148281 | ||||||
chr8:103148336
|
T | C | 1 | a0001c0001t0003g0049 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.160+7279T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148336 | ||||||
chr8:103148495
|
C | T | 114 | a0001c0001t0001g0044a0001c0001t0001g0176a0001c0001t0001g0178others(111): Show | 130 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.160+7438C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148495 | ||||||
chr8:103148511
|
T | C | 2 | a0001c0001t0017g0040a0002c0002t0003g0039 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.160+7454T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148511 | ||||||
chr8:103148723
|
G | A | 3 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0002g0229 | 3 | HG01993.hp1 HG02735.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.160+7666G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148723 | ||||||
chr8:103148744
|
G | T | 9 | a0001c0001t0001g0176a0001c0001t0001g0281a0001c0001t0008g0261others(6): Show | 9 | HG01109.hp1 HG01167.hp2 HG01358.hp2 others(6): Show |
intron_variant | MODIFIER | c.160+7687G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148744 | ||||||
chr8:103148833
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+7776C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148833 | ||||||
chr8:103148906
|
G | A | 5 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0051others(2): Show | 7 | NA18955.hp2 NA18959.hp1 NA18963.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+7849G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148906 | ||||||
chr8:103148938
|
A | G | 114 | a0001c0001t0001g0044a0001c0001t0001g0176a0001c0001t0001g0178others(111): Show | 130 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.160+7881A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103148938 | ||||||
chr8:103149040
|
G | A | 4 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0066others(1): Show | 6 | HG01099.hp2 HG01261.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+7983G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103149040 | ||||||
chr8:103149170
|
TC | T | 292 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(289): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.160+8119delC | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103149170 | |||||
chr8:103149315
|
A | G | 2 | a0001c0001t0001g0281a0001c0001t0024g0282 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.160+8258A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103149315 | ||||||
chr8:103149530
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.160+8473C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103149530 | ||||||
chr8:103149573
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.160+8516G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103149573 | ||||||
chr8:103149604
|
G | A | 1 | a0001c0003t0009g0262 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.160+8547G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103149604 | ||||||
chr8:103149777
|
C | T | 3 | a0001c0001t0001g0116a0001c0001t0003g0117a0001c0001t0003g0118 | 3 | HG01175.hp1 HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.160+8720C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103149777 | ||||||
chr8:103150147
|
T | C | 95 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(92): Show | 105 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(102): Show |
intron_variant | MODIFIER | c.160+9090T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150147 | ||||||
chr8:103150221
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.160+9164A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150221 | ||||||
chr8:103150252
|
G | A | 77 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0176others(74): Show | 88 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.160+9195G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150252 | ||||||
chr8:103150280
|
A | G | 1 | a0001c0001t0002g0225 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.160+9223A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150280 | ||||||
chr8:103150333
|
C | CTG | 84 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0178others(81): Show | 100 | HG00140.hp1 HG00408.hp2 HG00438.hp2 others(97): Show |
intron_variant | MODIFIER | c.160+9294_160+9295d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103150333 | |||||
chr8:103150333
|
C | CTGTGTGT others(3): Show |
2 | a0001c0003t0009g0260a0001c0003t0009g0262 | 2 | HG00099.hp2 HG02572.hp1 |
intron_variant | MODIFIER | c.160+9286_160+9295d others(12): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103150333 | |||||
chr8:103150351
|
GTC | G | 83 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(80): Show | 92 | HG00140.hp2 HG00280.hp1 HG00408.hp1 others(89): Show |
intron_variant | MODIFIER | c.160+9296_160+9297d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103150351 | |||||
chr8:103150353
|
C | G | 123 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0001g0070others(120): Show | 139 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.160+9296C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150353 | ||||||
chr8:103150383
|
C | CTG | 76 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0176others(73): Show | 87 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
intron_variant | MODIFIER | c.160+9341_160+9342d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103150383 | |||||
chr8:103150440
|
G | C | 1 | a0001c0001t0002g0184 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.160+9383G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150440 | ||||||
chr8:103150691
|
G | A | 72 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(69): Show | 81 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(78): Show |
intron_variant | MODIFIER | c.160+9634G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150691 | ||||||
chr8:103150751
|
C | T | 9 | a0001c0001t0001g0035a0001c0001t0001g0288a0001c0001t0001g0289others(6): Show | 9 | HG01243.hp2 HG01433.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+9694C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150751 | ||||||
chr8:103150842
|
C | T | 5 | a0001c0003t0009g0257a0001c0003t0009g0258a0001c0003t0009g0259others(2): Show | 5 | HG00099.hp2 HG02572.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+9785C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103150842 | ||||||
chr8:103151004
|
A | T | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(87): Show | 99 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.160+9947A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151004 | ||||||
chr8:103151019
|
AT | A | 108 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(105): Show | 119 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(116): Show |
intron_variant | MODIFIER | c.160+9978delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103151019 | |||||
chr8:103151019
|
ATT | A | 102 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0001g0070others(99): Show | 118 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(115): Show |
intron_variant | MODIFIER | c.160+9977_160+9978d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103151019 | |||||
chr8:103151141
|
C | T | 1 | a0001c0001t0005g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.160+10084C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151141 | ||||||
chr8:103151142
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.160+10085C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151142 | ||||||
chr8:103151209
|
A | G | 214 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(211): Show | 245 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(242): Show |
intron_variant | MODIFIER | c.160+10152A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151209 | ||||||
chr8:103151252
|
C | T | 2 | a0001c0001t0017g0040a0002c0002t0003g0039 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.160+10195C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151252 | ||||||
chr8:103151409
|
A | G | 4 | a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0168others(1): Show | 4 | HG00639.hp1 HG00642.hp1 HG01168.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+10352A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151409 | ||||||
chr8:103151531
|
T | C | 118 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0001g0070others(115): Show | 134 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.160+10474T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151531 | ||||||
chr8:103151694
|
T | C | 85 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(82): Show | 94 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(91): Show |
intron_variant | MODIFIER | c.160+10637T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151694 | ||||||
chr8:103151758
|
T | TA | 172 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0013others(169): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.160+10712dupA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103151758 | |||||
chr8:103151782
|
C | T | 141 | a0001c0001t0001g0035a0001c0001t0001g0044a0001c0001t0001g0069others(138): Show | 163 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.160+10725C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151782 | ||||||
chr8:103151934
|
C | T | 118 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0001g0070others(115): Show | 134 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(131): Show |
intron_variant | MODIFIER | c.160+10877C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151934 | ||||||
chr8:103151973
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+10916C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103151973 | ||||||
chr8:103152035
|
C | T | 1 | a0001c0001t0002g0222 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.160+10978C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152035 | ||||||
chr8:103152172
|
GA | G | 3 | a0001c0001t0001g0041a0001c0001t0002g0043a0001c0001t0003g0042 | 3 | HG02040.hp2 HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.160+11117delA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103152172 | |||||
chr8:103152198
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.160+11141C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152198 | ||||||
chr8:103152543
|
C | T | 1 | a0001c0001t0001g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.160+11486C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152543 | ||||||
chr8:103152603
|
C | T | 118 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0001g0070others(115): Show | 136 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(133): Show |
intron_variant | MODIFIER | c.160+11546C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152603 | ||||||
chr8:103152629
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.160+11572G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152629 | ||||||
chr8:103152636
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.160+11579G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152636 | ||||||
chr8:103152862
|
C | T | 5 | a0001c0001t0001g0020a0001c0001t0001g0170a0001c0001t0001g0171others(2): Show | 6 | NA18960.hp1 NA18969.hp1 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+11805C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103152862 | ||||||
chr8:103153554
|
C | T | 93 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(90): Show | 103 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.160+12497C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153554 | ||||||
chr8:103153555
|
G | A | 217 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(214): Show | 248 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.160+12498G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153555 | ||||||
chr8:103153743
|
C | T | 1 | a0001c0001t0002g0275 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.160+12686C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153743 | ||||||
chr8:103153797
|
A | T | 76 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0176others(73): Show | 89 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.160+12740A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153797 | ||||||
chr8:103153805
|
C | T | 1 | a0002c0002t0003g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+12748C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153805 | ||||||
chr8:103153845
|
A | G | 1 | a0001c0001t0002g0221 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.160+12788A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153845 | ||||||
chr8:103153941
|
C | T | 3 | a0001c0001t0001g0041a0001c0001t0002g0043a0001c0001t0003g0042 | 3 | HG02040.hp2 HG02056.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.160+12884C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153941 | ||||||
chr8:103153952
|
C | A | 2 | a0001c0001t0017g0040a0002c0002t0003g0039 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.160+12895C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153952 | ||||||
chr8:103153990
|
T | A | 1 | a0001c0001t0001g0170 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.160+12933T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103153990 | ||||||
chr8:103154182
|
C | T | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+13125C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154182 | ||||||
chr8:103154273
|
G | A | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+13216G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154273 | ||||||
chr8:103154311
|
T | G | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0257others(4): Show | 7 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+13254T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154311 | ||||||
chr8:103154518
|
C | T | 102 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(99): Show | 114 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.160+13461C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154518 | ||||||
chr8:103154672
|
C | T | 1 | a0001c0001t0001g0270 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.160+13615C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154672 | ||||||
chr8:103154674
|
G | GC | 292 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(289): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.160+13620dupC | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103154674 | |||||
chr8:103154920
|
C | CTATA | 3 | a0001c0001t0001g0251a0001c0001t0010g0088a0001c0001t0010g0089 | 3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+13880_160+1388 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103154920 | |||||
chr8:103154920
|
CTA | C | 94 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(91): Show | 104 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(101): Show |
intron_variant | MODIFIER | c.160+13882_160+1388 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103154920 | |||||
chr8:103154920
|
CTATATA | C | 76 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0176others(73): Show | 89 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.160+13878_160+1388 others(10): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103154920 | |||||
chr8:103154939
|
T | A | 76 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0176others(73): Show | 89 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.160+13882T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154939 | ||||||
chr8:103154948
|
T | G | 4 | a0001c0001t0001g0125a0001c0001t0005g0124a0001c0001t0005g0126others(1): Show | 4 | HG00738.hp2 HG01358.hp1 HG02145.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+13891T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154948 | ||||||
chr8:103154955
|
T | G | 44 | a0001c0001t0001g0044a0001c0001t0001g0228a0001c0001t0001g0230others(41): Show | 48 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.160+13898T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103154955 | ||||||
chr8:103155132
|
C | T | 1 | a0001c0001t0010g0249 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.160+14075C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155132 | ||||||
chr8:103155173
|
T | C | 78 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0176others(75): Show | 91 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.160+14116T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155173 | ||||||
chr8:103155318
|
CTAATG | C | 75 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0176others(72): Show | 86 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.160+14266_160+1427 others(9): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103155318 | |||||
chr8:103155393
|
A | G | 1 | a0001c0001t0008g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+14336A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155393 | ||||||
chr8:103155548
|
G | A | 2 | a0001c0001t0017g0040a0002c0002t0003g0039 | 2 | HG02559.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.160+14491G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155548 | ||||||
chr8:103155564
|
C | T | 1 | a0001c0001t0008g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+14507C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155564 | ||||||
chr8:103155808
|
T | A | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+14751T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155808 | ||||||
chr8:103155999
|
A | G | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.160+14942A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103155999 | ||||||
chr8:103156206
|
A | T | 2 | a0001c0001t0002g0219a0001c0001t0002g0220 | 2 | NA18948.hp2 NA18987.hp1 |
intron_variant | MODIFIER | c.160+15149A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156206 | ||||||
chr8:103156417
|
C | T | 1 | a0001c0001t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.160+15360C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156417 | ||||||
chr8:103156418
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0010g0088a0001c0001t0010g0089 | 3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+15361G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156418 | ||||||
chr8:103156523
|
G | A | 1 | a0001c0001t0002g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.160+15466G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156523 | ||||||
chr8:103156620
|
A | G | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+15563A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156620 | ||||||
chr8:103156637
|
C | T | 126 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0001g0070others(123): Show | 145 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(142): Show |
intron_variant | MODIFIER | c.160+15580C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156637 | ||||||
chr8:103156737
|
G | A | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+15680G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156737 | ||||||
chr8:103156779
|
G | C | 1 | a0001c0001t0001g0128 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.160+15722G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156779 | ||||||
chr8:103156792
|
C | T | 10 | a0001c0001t0001g0035a0001c0001t0001g0288a0001c0001t0001g0289others(7): Show | 11 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.160+15735C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156792 | ||||||
chr8:103156945
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.160+15888C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156945 | ||||||
chr8:103156965
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.160+15908C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103156965 | ||||||
chr8:103157053
|
A | G | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+15996A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157053 | ||||||
chr8:103157125
|
T | TAC | 8 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0005g0124others(5): Show | 8 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+16093_160+1609 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103157125 | |||||
chr8:103157125
|
TAC | T | 5 | a0001c0001t0001g0251a0001c0001t0008g0261a0001c0001t0010g0088others(2): Show | 5 | HG01109.hp1 HG02486.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+16093_160+1609 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103157125 | |||||
chr8:103157125
|
TACAC | T | 134 | a0001c0001t0001g0035a0001c0001t0001g0044a0001c0001t0001g0069others(131): Show | 155 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.160+16091_160+1609 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103157125 | |||||
chr8:103157235
|
A | T | 1 | a0001c0001t0003g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.160+16178A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157235 | ||||||
chr8:103157300
|
C | T | 3 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033 | 4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+16243C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157300 | ||||||
chr8:103157315
|
C | CTA | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+16272_160+1627 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103157315 | |||||
chr8:103157353
|
C | T | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+16296C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157353 | ||||||
chr8:103157450
|
G | A | 1 | a0002c0002t0003g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+16393G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157450 | ||||||
chr8:103157612
|
G | A | 138 | a0001c0001t0001g0035a0001c0001t0001g0044a0001c0001t0001g0069others(135): Show | 160 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.160+16555G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157612 | ||||||
chr8:103157833
|
G | T | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.160+16776G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157833 | ||||||
chr8:103157840
|
G | T | 10 | a0001c0001t0001g0035a0001c0001t0001g0288a0001c0001t0001g0289others(7): Show | 11 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(8): Show |
intron_variant | MODIFIER | c.160+16783G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157840 | ||||||
chr8:103157901
|
G | A | 1 | a0001c0001t0002g0238 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.160+16844G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157901 | ||||||
chr8:103157981
|
A | G | 1 | a0001c0001t0012g0248 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.160+16924A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103157981 | ||||||
chr8:103158126
|
G | A | 1 | a0001c0001t0008g0239 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.160+17069G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103158126 | ||||||
chr8:103158296
|
C | T | 1 | a0001c0001t0010g0249 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.160+17239C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103158296 | ||||||
chr8:103158392
|
G | A | 3 | a0001c0001t0001g0251a0001c0001t0010g0088a0001c0001t0010g0089 | 3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+17335G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103158392 | ||||||
chr8:103158649
|
C | T | 67 | a0001c0001t0001g0069a0001c0001t0001g0070a0001c0001t0001g0178others(64): Show | 78 | HG00408.hp2 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.160+17592C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103158649 | ||||||
chr8:103158685
|
A | AATAC | 90 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0017others(87): Show | 100 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(97): Show |
intron_variant | MODIFIER | c.160+17654_160+1765 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103158685 | |||||
chr8:103158725
|
G | A | 138 | a0001c0001t0001g0035a0001c0001t0001g0044a0001c0001t0001g0069others(135): Show | 160 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.160+17668G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103158725 | ||||||
chr8:103158786
|
C | T | 3 | a0001c0001t0005g0124a0001c0001t0005g0126a0001c0001t0005g0127 | 3 | HG01358.hp1 HG02145.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.160+17729C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103158786 | ||||||
chr8:103159005
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.160+17948A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159005 | ||||||
chr8:103159028
|
C | A | 128 | a0001c0001t0001g0044a0001c0001t0001g0069a0001c0001t0001g0070others(125): Show | 149 | HG00140.hp1 HG00323.hp2 HG00408.hp2 others(146): Show |
intron_variant | MODIFIER | c.160+17971C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159028 | ||||||
chr8:103159261
|
A | G | 2 | a0001c0001t0001g0069a0001c0001t0001g0070 | 2 | HG02132.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.160+18204A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159261 | ||||||
chr8:103159347
|
G | A | 2 | a0001c0003t0009g0257a0001c0003t0009g0258 | 2 | NA18983.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.160+18290G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159347 | ||||||
chr8:103159387
|
T | C | 9 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0002g0286others(6): Show | 10 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.160+18330T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159387 | ||||||
chr8:103159469
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+18412T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159469 | ||||||
chr8:103159658
|
C | T | 92 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(89): Show | 102 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(99): Show |
intron_variant | MODIFIER | c.160+18601C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159658 | ||||||
chr8:103159724
|
G | T | 7 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0002g0286others(4): Show | 8 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+18667G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159724 | ||||||
chr8:103159739
|
C | T | 2 | a0001c0001t0008g0276a0001c0001t0008g0280 | 2 | HG01358.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.160+18682C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159739 | ||||||
chr8:103159816
|
G | A | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0257others(4): Show | 7 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+18759G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159816 | ||||||
chr8:103159908
|
G | T | 2 | a0001c0001t0003g0236a0001c0001t0003g0237 | 2 | HG03704.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.160+18851G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159908 | ||||||
chr8:103159920
|
A | G | 82 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(79): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.160+18863A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159920 | ||||||
chr8:103159964
|
T | C | 1 | a0001c0001t0001g0009 | 2 | NA18960.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.160+18907T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103159964 | ||||||
chr8:103160043
|
C | T | 82 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(79): Show | 91 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.160+18986C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160043 | ||||||
chr8:103160134
|
C | T | 5 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0254others(2): Show | 5 | HG02486.hp2 HG02572.hp2 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+19077C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160134 | ||||||
chr8:103160300
|
G | A | 1 | a0001c0001t0014g0284 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160+19243G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160300 | ||||||
chr8:103160706
|
A | C | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0257others(4): Show | 7 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+19649A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160706 | ||||||
chr8:103160783
|
C | G | 5 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033others(2): Show | 9 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+19726C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160783 | ||||||
chr8:103160784
|
C | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033others(2): Show | 9 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+19727C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160784 | ||||||
chr8:103160785
|
A | G | 5 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033others(2): Show | 9 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+19728A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103160785 | ||||||
chr8:103161054
|
C | T | 220 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(217): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.160+19997C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103161054 | ||||||
chr8:103161280
|
C | CT | 43 | a0001c0001t0001g0044a0001c0001t0001g0228a0001c0001t0001g0230others(40): Show | 47 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.160+20233dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103161280 | |||||
chr8:103161398
|
T | A | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+20341T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103161398 | ||||||
chr8:103161416
|
C | G | 15 | a0001c0001t0001g0035a0001c0001t0001g0288a0001c0001t0001g0289others(12): Show | 20 | HG01243.hp2 HG01256.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.160+20359C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103161416 | ||||||
chr8:103161929
|
G | A | 3 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033 | 4 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+20872G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103161929 | ||||||
chr8:103161959
|
T | TTTTTG | 143 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(140): Show | 163 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(160): Show |
intron_variant | MODIFIER | c.160+20906_160+2090 others(9): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103161959 | |||||
chr8:103162160
|
C | T | 1 | a0001c0003t0009g0260 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.160+21103C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162160 | ||||||
chr8:103162174
|
C | T | 142 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(139): Show | 162 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(159): Show |
intron_variant | MODIFIER | c.160+21117C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162174 | ||||||
chr8:103162221
|
G | A | 53 | a0001c0001t0001g0035a0001c0001t0001g0044a0001c0001t0001g0228others(50): Show | 58 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.160+21164G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162221 | ||||||
chr8:103162237
|
C | A | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+21180C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162237 | ||||||
chr8:103162375
|
T | G | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.160+21318T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162375 | ||||||
chr8:103162431
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160+21374G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162431 | ||||||
chr8:103162465
|
C | G | 220 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(217): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.160+21408C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162465 | ||||||
chr8:103162473
|
C | A | 1 | a0001c0001t0008g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+21416C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162473 | ||||||
chr8:103162535
|
A | G | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | NA18948.hp2 NA18987.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.160+21478A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162535 | ||||||
chr8:103162620
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.160+21563G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162620 | ||||||
chr8:103162679
|
C | T | 1 | a0001c0001t0002g0048 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.160+21622C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162679 | ||||||
chr8:103162729
|
G | A | 4 | a0001c0001t0001g0255a0001c0001t0001g0256a0001c0001t0001g0263others(1): Show | 4 | HG00438.hp2 HG02165.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+21672G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103162729 | ||||||
chr8:103162756
|
TTAA | T | 220 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(217): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.160+21706_160+2170 others(7): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103162756 | |||||
chr8:103163055
|
C | T | 1 | a0002c0002t0003g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+21998C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163055 | ||||||
chr8:103163081
|
A | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0163a0001c0001t0002g0164 | 3 | HG02451.hp2 HG03486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.160+22024A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163081 | ||||||
chr8:103163168
|
A | G | 2 | a0001c0001t0002g0216a0001c0001t0002g0217 | 2 | HG01261.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.160+22111A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163168 | ||||||
chr8:103163253
|
C | A | 4 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0045others(1): Show | 6 | HG02129.hp1 NA18960.hp2 NA18993.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+22196C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163253 | ||||||
chr8:103163254
|
G | A | 1 | a0001c0001t0002g0074 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.160+22197G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163254 | ||||||
chr8:103163337
|
C | T | 1 | a0001c0001t0001g0162 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.160+22280C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163337 | ||||||
chr8:103163348
|
C | T | 66 | a0001c0001t0001g0035a0001c0001t0001g0044a0001c0001t0001g0062others(63): Show | 77 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(74): Show |
intron_variant | MODIFIER | c.160+22291C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163348 | ||||||
chr8:103163495
|
C | T | 1 | a0001c0001t0002g0175 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.160+22438C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163495 | ||||||
chr8:103163532
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.160+22475G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163532 | ||||||
chr8:103163592
|
C | T | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+22535C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163592 | ||||||
chr8:103163595
|
A | G | 1 | a0001c0001t0008g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+22538A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163595 | ||||||
chr8:103163633
|
A | C | 7 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0257others(4): Show | 7 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+22576A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163633 | ||||||
chr8:103163879
|
A | G | 7 | a0001c0001t0001g0281a0001c0001t0008g0276a0001c0001t0008g0280others(4): Show | 7 | HG01358.hp2 HG01884.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+22822A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103163879 | ||||||
chr8:103164026
|
C | T | 1 | a0002c0002t0003g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+22969C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164026 | ||||||
chr8:103164158
|
A | G | 15 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0001g0244others(12): Show | 15 | HG01993.hp1 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.160+23101A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164158 | ||||||
chr8:103164172
|
T | G | 60 | a0001c0001t0001g0035a0001c0001t0001g0044a0001c0001t0001g0062others(57): Show | 70 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.160+23115T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164172 | ||||||
chr8:103164237
|
G | A | 3 | a0001c0001t0002g0218a0001c0001t0002g0219a0001c0001t0002g0220 | 3 | NA18948.hp2 NA18987.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.160+23180G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164237 | ||||||
chr8:103164340
|
A | G | 220 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(217): Show | 251 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(248): Show |
intron_variant | MODIFIER | c.160+23283A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164340 | ||||||
chr8:103164372
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.160+23315G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164372 | ||||||
chr8:103164408
|
C | T | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+23351C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164408 | ||||||
chr8:103164805
|
C | T | 5 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(2): Show | 6 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+23748C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164805 | ||||||
chr8:103164929
|
C | G | 1 | a0001c0001t0002g0290 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.160+23872C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164929 | ||||||
chr8:103164931
|
C | T | 1 | a0001c0001t0014g0284 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160+23874C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164931 | ||||||
chr8:103164938
|
AG | A | 3 | a0001c0001t0001g0251a0001c0001t0010g0088a0001c0001t0010g0089 | 3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+23883delG | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103164938 | |||||
chr8:103164978
|
C | T | 15 | a0001c0001t0001g0044a0001c0001t0002g0030a0001c0001t0003g0028others(12): Show | 18 | HG00323.hp2 HG00738.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.160+23921C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103164978 | ||||||
chr8:103165103
|
T | A | 15 | a0001c0001t0001g0044a0001c0001t0002g0030a0001c0001t0003g0028others(12): Show | 18 | HG00323.hp2 HG00738.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.160+24046T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103165103 | ||||||
chr8:103165188
|
A | G | 1 | a0001c0001t0006g0032 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.160+24131A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103165188 | ||||||
chr8:103165424
|
C | T | 1 | a0001c0001t0001g0215 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.160+24367C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103165424 | ||||||
chr8:103165708
|
C | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0160a0001c0001t0001g0161 | 4 | HG02080.hp2 NA18955.hp1 NA18991.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+24651C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103165708 | ||||||
chr8:103165883
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.160+24826G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103165883 | ||||||
chr8:103166104
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.160+25047C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166104 | ||||||
chr8:103166105
|
G | A | 1 | a0001c0001t0008g0239 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.160+25048G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166105 | ||||||
chr8:103166112
|
G | A | 1 | a0001c0001t0006g0272 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.160+25055G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166112 | ||||||
chr8:103166153
|
C | T | 10 | a0001c0001t0002g0030a0001c0001t0003g0028a0001c0001t0003g0029others(7): Show | 13 | HG00738.hp1 HG01168.hp1 HG01169.hp2 others(10): Show |
intron_variant | MODIFIER | c.160+25096C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166153 | ||||||
chr8:103166243
|
C | A | 1 | a0001c0001t0022g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.160+25186C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166243 | ||||||
chr8:103166269
|
C | T | 2 | a0001c0001t0001g0067a0001c0001t0002g0222 | 2 | HG01261.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.160+25212C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166269 | ||||||
chr8:103166277
|
C | T | 3 | a0001c0001t0001g0251a0001c0001t0010g0088a0001c0001t0010g0089 | 3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+25220C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166277 | ||||||
chr8:103166349
|
A | C | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+25292A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166349 | ||||||
chr8:103166377
|
A | G | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | NA18964.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.160+25320A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166377 | ||||||
chr8:103166674
|
G | A | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+25617G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166674 | ||||||
chr8:103166708
|
T | C | 1 | a0001c0001t0001g0053 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.160+25651T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103166708 | ||||||
chr8:103167277
|
A | G | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0259others(1): Show | 4 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+26220A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167277 | ||||||
chr8:103167344
|
C | T | 3 | a0001c0001t0005g0247a0001c0001t0005g0250a0001c0001t0012g0248 | 3 | HG02976.hp2 HG03209.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.160+26287C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167344 | ||||||
chr8:103167361
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.160+26304A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167361 | ||||||
chr8:103167558
|
T | C | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+26501T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167558 | ||||||
chr8:103167721
|
T | C | 3 | a0001c0001t0008g0261a0001c0005t0023g0038a0002c0004t0003g0001 | 6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+26664T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167721 | ||||||
chr8:103167723
|
A | T | 89 | a0001c0001t0001g0037a0001c0001t0001g0067a0001c0001t0001g0069others(86): Show | 102 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.160+26666A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167723 | ||||||
chr8:103167794
|
T | C | 3 | a0001c0001t0008g0261a0001c0005t0023g0038a0002c0004t0003g0001 | 6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+26737T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167794 | ||||||
chr8:103167886
|
A | C | 93 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(90): Show | 109 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.160+26829A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167886 | ||||||
chr8:103167900
|
G | T | 1 | a0001c0001t0001g0212 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.160+26843G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167900 | ||||||
chr8:103167921
|
G | A | 1 | a0001c0001t0001g0050 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.160+26864G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167921 | ||||||
chr8:103167935
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.160+26878T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103167935 | ||||||
chr8:103168110
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.160+27053C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168110 | ||||||
chr8:103168132
|
T | C | 1 | a0001c0001t0001g0265 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.160+27075T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168132 | ||||||
chr8:103168233
|
G | A | 85 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(82): Show | 97 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(94): Show |
intron_variant | MODIFIER | c.160+27176G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168233 | ||||||
chr8:103168237
|
T | C | 16 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0074others(13): Show | 16 | HG01884.hp2 HG01993.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+27180T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168237 | ||||||
chr8:103168269
|
G | T | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.160+27212G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168269 | ||||||
chr8:103168273
|
G | A | 56 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0017others(53): Show | 62 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(59): Show |
intron_variant | MODIFIER | c.160+27216G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168273 | ||||||
chr8:103168511
|
G | GT | 3 | a0001c0001t0008g0261a0001c0005t0023g0038a0002c0004t0003g0001 | 6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+27467dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103168511 | |||||
chr8:103168511
|
GT | G | 86 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(83): Show | 99 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(96): Show |
intron_variant | MODIFIER | c.160+27467delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103168511 | |||||
chr8:103168515
|
T | G | 17 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0074others(14): Show | 17 | HG01884.hp2 HG01993.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.160+27458T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168515 | ||||||
chr8:103168694
|
C | T | 16 | a0001c0001t0001g0044a0001c0001t0001g0230a0001c0001t0002g0030others(13): Show | 19 | HG00323.hp2 HG00738.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.160+27637C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168694 | ||||||
chr8:103168772
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(81): Show | 95 | HG00140.hp2 HG00280.hp1 HG00323.hp1 others(92): Show |
intron_variant | MODIFIER | c.160+27715G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168772 | ||||||
chr8:103168813
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.160+27756T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168813 | ||||||
chr8:103168855
|
G | C | 2 | a0001c0001t0001g0281a0001c0001t0024g0282 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.160+27798G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168855 | ||||||
chr8:103168980
|
A | T | 215 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(212): Show | 246 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.160+27923A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103168980 | ||||||
chr8:103169093
|
GTTA | G | 16 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0074others(13): Show | 16 | HG01884.hp2 HG01993.hp1 HG02451.hp1 others(13): Show |
intron_variant | MODIFIER | c.160+28050_160+2805 others(7): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103169093 | |||||
chr8:103169191
|
A | G | 2 | a0001c0001t0005g0252a0001c0001t0010g0249 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.160+28134A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169191 | ||||||
chr8:103169423
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.160+28366G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169423 | ||||||
chr8:103169669
|
A | C | 26 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0288others(23): Show | 29 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(26): Show |
intron_variant | MODIFIER | c.160+28612A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169669 | ||||||
chr8:103169674
|
C | A | 1 | a0001c0001t0001g0179 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.160+28617C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169674 | ||||||
chr8:103169736
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.160+28679C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169736 | ||||||
chr8:103169737
|
G | A | 1 | a0001c0001t0001g0170 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.160+28680G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169737 | ||||||
chr8:103169922
|
C | A | 1 | a0001c0001t0001g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.160+28865C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169922 | ||||||
chr8:103169922
|
C | G | 1 | a0001c0001t0002g0034 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.160+28865C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169922 | ||||||
chr8:103169943
|
C | T | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+28886C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103169943 | ||||||
chr8:103170005
|
T | G | 1 | a0001c0001t0014g0284 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160+28948T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170005 | ||||||
chr8:103170145
|
T | C | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0259others(1): Show | 4 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+29088T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170145 | ||||||
chr8:103170235
|
C | CT | 16 | a0001c0001t0001g0046a0001c0001t0001g0086a0001c0001t0001g0101others(13): Show | 19 | HG00741.hp2 HG01109.hp1 HG01256.hp1 others(16): Show |
intron_variant | MODIFIER | c.160+29191dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103170235 | |||||
chr8:103170235
|
CT | C | 11 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(8): Show | 12 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.160+29191delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103170235 | |||||
chr8:103170260
|
G | T | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+29203G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170260 | ||||||
chr8:103170438
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.160+29381A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170438 | ||||||
chr8:103170468
|
T | G | 55 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 62 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.160+29411T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170468 | ||||||
chr8:103170578
|
G | A | 5 | a0001c0001t0002g0074a0001c0001t0002g0238a0001c0001t0002g0241others(2): Show | 5 | HG01884.hp2 HG02615.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+29521G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170578 | ||||||
chr8:103170619
|
C | T | 69 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0070others(66): Show | 80 | HG00438.hp2 HG00544.hp1 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.160+29562C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170619 | ||||||
chr8:103170691
|
G | A | 1 | a0001c0001t0002g0196 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.160+29634G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170691 | ||||||
chr8:103170796
|
G | A | 3 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0094 | 5 | NA18943.hp2 NA18953.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+29739G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170796 | ||||||
chr8:103170892
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.160+29835T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170892 | ||||||
chr8:103170977
|
C | T | 153 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0044others(150): Show | 177 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(174): Show |
intron_variant | MODIFIER | c.160+29920C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103170977 | ||||||
chr8:103171066
|
C | T | 1 | a0001c0001t0001g0115 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.160+30009C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171066 | ||||||
chr8:103171070
|
T | C | 5 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033others(2): Show | 6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+30013T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171070 | ||||||
chr8:103171072
|
A | G | 5 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033others(2): Show | 6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.160+30015A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171072 | ||||||
chr8:103171195
|
A | G | 55 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0063others(52): Show | 62 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.160+30138A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171195 | ||||||
chr8:103171228
|
GGACA | G | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+30174_160+3017 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171228 | |||||
chr8:103171231
|
CAGAA | C | 145 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0044others(142): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.160+30185_160+3018 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171231 | |||||
chr8:103171283
|
A | AAGAG | 36 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0063others(33): Show | 41 | HG00099.hp2 HG00323.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.160+30230_160+3023 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171283 | |||||
chr8:103171283
|
A | G | 19 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0003others(16): Show | 21 | HG01884.hp2 HG01993.hp1 HG02451.hp1 others(18): Show |
intron_variant | MODIFIER | c.160+30226A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171283 | ||||||
chr8:103171340
|
AAGG | A | 6 | a0001c0001t0001g0271a0001c0001t0001g0273a0001c0001t0001g0274others(3): Show | 7 | HG00140.hp1 HG01123.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.160+30288_160+3029 others(7): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171340 | |||||
chr8:103171346
|
G | A | 31 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0063others(28): Show | 35 | HG00099.hp2 HG00323.hp2 HG00639.hp2 others(32): Show |
intron_variant | MODIFIER | c.160+30289G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171346 | ||||||
chr8:103171380
|
G | C | 4 | a0001c0001t0005g0242a0001c0001t0005g0247a0001c0001t0005g0250others(1): Show | 4 | HG02976.hp2 HG03209.hp1 HG03491.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+30323G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171380 | ||||||
chr8:103171385
|
A | AGAGGAAG others(9): Show |
145 | a0001c0001t0001g0037a0001c0001t0001g0044a0001c0001t0001g0062others(142): Show | 165 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(162): Show |
intron_variant | MODIFIER | c.160+30342_160+3034 others(20): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171385 | |||||
chr8:103171390
|
A | AAGGAAGG others(5): Show |
11 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0271others(8): Show | 16 | HG00140.hp1 HG01070.hp1 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.160+30342_160+3034 others(16): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171390 | |||||
chr8:103171404
|
A | G | 7 | a0001c0001t0001g0035a0001c0001t0001g0271a0001c0001t0001g0273others(4): Show | 8 | HG00140.hp1 HG01123.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+30347A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171404 | ||||||
chr8:103171413
|
A | G | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+30356A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171413 | ||||||
chr8:103171424
|
GA | G | 149 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0037others(146): Show | 173 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.160+30371delA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171424 | |||||
chr8:103171424
|
GAAAAT | G | 7 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0002g0286others(4): Show | 8 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.160+30372_160+3037 others(9): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171424 | |||||
chr8:103171429
|
T | G | 149 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0037others(146): Show | 173 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(170): Show |
intron_variant | MODIFIER | c.160+30372T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171429 | ||||||
chr8:103171433
|
A | G | 156 | a0001c0001t0001g0017a0001c0001t0001g0035a0001c0001t0001g0037others(153): Show | 181 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(178): Show |
intron_variant | MODIFIER | c.160+30376A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171433 | ||||||
chr8:103171467
|
AAAAG | A | 4 | a0001c0001t0001g0017a0001c0001t0008g0261a0001c0005t0023g0038others(1): Show | 8 | HG01070.hp1 HG01071.hp2 HG01109.hp1 others(5): Show |
intron_variant | MODIFIER | c.160+30420_160+3042 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103171467 | |||||
chr8:103171628
|
C | T | 105 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(102): Show | 118 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(115): Show |
intron_variant | MODIFIER | c.160+30571C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171628 | ||||||
chr8:103171708
|
G | C | 23 | a0001c0001t0001g0044a0001c0001t0001g0230a0001c0001t0002g0008others(20): Show | 27 | HG00323.hp2 HG00738.hp1 HG01168.hp1 others(24): Show |
intron_variant | MODIFIER | c.160+30651G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171708 | ||||||
chr8:103171956
|
C | T | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.160+30899C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171956 | ||||||
chr8:103171998
|
G | A | 1 | a0001c0001t0001g0045 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.160+30941G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103171998 | ||||||
chr8:103172184
|
CT | C | 116 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(113): Show | 133 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.160+31137delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103172184 | |||||
chr8:103172334
|
T | C | 3 | a0001c0001t0001g0251a0001c0001t0010g0088a0001c0001t0010g0089 | 3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.160+31277T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172334 | ||||||
chr8:103172391
|
C | CT | 22 | a0001c0001t0001g0020a0001c0001t0001g0050a0001c0001t0001g0061others(19): Show | 24 | HG00438.hp1 HG00544.hp2 HG01168.hp1 others(21): Show |
intron_variant | MODIFIER | c.160+31357dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103172391 | |||||
chr8:103172391
|
CT | C | 78 | a0001c0001t0001g0062a0001c0001t0001g0067a0001c0001t0001g0069others(75): Show | 90 | HG00140.hp1 HG00408.hp1 HG00438.hp2 others(87): Show |
intron_variant | MODIFIER | c.160+31357delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103172391 | |||||
chr8:103172391
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0014g0284 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.160+31347_160+3135 others(15): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103172391 | |||||
chr8:103172406
|
T | C | 8 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0002g0286others(5): Show | 9 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.160+31349T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172406 | ||||||
chr8:103172423
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.160+31366G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172423 | ||||||
chr8:103172482
|
T | A | 155 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0044others(152): Show | 179 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(176): Show |
intron_variant | MODIFIER | c.160+31425T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172482 | ||||||
chr8:103172495
|
G | A | 1 | a0001c0001t0012g0197 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.160+31438G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172495 | ||||||
chr8:103172527
|
G | A | 16 | a0001c0001t0001g0044a0001c0001t0001g0230a0001c0001t0002g0030others(13): Show | 19 | HG00323.hp2 HG00738.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.160+31470G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172527 | ||||||
chr8:103172618
|
C | A | 1 | a0001c0001t0002g0107 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.160+31561C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172618 | ||||||
chr8:103172733
|
T | C | 6 | a0001c0001t0001g0013a0001c0001t0001g0075a0001c0001t0001g0076others(3): Show | 6 | HG02055.hp2 HG02280.hp1 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+31676T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172733 | ||||||
chr8:103172837
|
A | G | 1 | a0002c0002t0003g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.160+31780A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172837 | ||||||
chr8:103172859
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.160+31802T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103172859 | ||||||
chr8:103173022
|
C | T | 113 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(110): Show | 130 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.160+31965C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103173022 | ||||||
chr8:103173517
|
A | T | 114 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(111): Show | 131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.160+32460A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103173517 | ||||||
chr8:103173894
|
C | T | 2 | a0001c0001t0005g0252a0001c0001t0010g0249 | 2 | HG02451.hp1 HG02809.hp1 |
intron_variant | MODIFIER | c.160+32837C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103173894 | ||||||
chr8:103173895
|
G | A | 1 | a0001c0001t0008g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.160+32838G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103173895 | ||||||
chr8:103173983
|
G | A | 107 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(104): Show | 120 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.160+32926G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103173983 | ||||||
chr8:103174058
|
C | T | 1 | a0001c0001t0001g0061 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.160+33001C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103174058 | ||||||
chr8:103174172
|
G | A | 4 | a0001c0001t0001g0271a0001c0001t0002g0275a0001c0001t0006g0031others(1): Show | 5 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+33115G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103174172 | ||||||
chr8:103174216
|
G | A | 1 | a0001c0001t0001g0037 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.160+33159G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103174216 | ||||||
chr8:103174260
|
C | CA | 30 | a0001c0001t0001g0093a0001c0001t0001g0134a0001c0001t0001g0135others(27): Show | 34 | HG00323.hp2 HG00609.hp1 HG00738.hp1 others(31): Show |
intron_variant | MODIFIER | c.160+33219dupA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103174260 | |||||
chr8:103174260
|
C | CAAA | 8 | a0001c0001t0001g0281a0001c0001t0002g0207a0001c0001t0002g0217others(5): Show | 9 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.160+33217_160+3321 others(7): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103174260 | |||||
chr8:103174260
|
C | CAAAA | 94 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(91): Show | 107 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.160+33216_160+3321 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103174260 | |||||
chr8:103174260
|
C | CAAAAA | 7 | a0001c0001t0001g0181a0001c0001t0001g0251a0001c0001t0002g0184others(4): Show | 7 | HG01255.hp2 HG02630.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.160+33215_160+3321 others(9): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103174260 | |||||
chr8:103174791
|
T | C | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+33734T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103174791 | ||||||
chr8:103174809
|
G | A | 3 | a0001c0001t0002g0286a0001c0001t0002g0290a0001c0001t0006g0032 | 4 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.160+33752G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103174809 | ||||||
chr8:103174914
|
A | G | 4 | a0001c0001t0001g0271a0001c0001t0002g0275a0001c0001t0006g0031others(1): Show | 5 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+33857A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103174914 | ||||||
chr8:103175017
|
TC | T | 3 | a0001c0001t0001g0020a0001c0001t0001g0171a0001c0001t0002g0172 | 4 | NA18969.hp1 NA18980.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.160+33962delC | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103175017 | |||||
chr8:103175443
|
T | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(104): Show | 120 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.160+34386T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103175443 | ||||||
chr8:103175667
|
G | A | 1 | a0001c0001t0002g0199 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.160+34610G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103175667 | ||||||
chr8:103175740
|
G | A | 114 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(111): Show | 131 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.160+34683G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103175740 | ||||||
chr8:103175750
|
G | A | 5 | a0001c0001t0002g0074a0001c0001t0002g0238a0001c0001t0002g0241others(2): Show | 5 | HG01884.hp2 HG02615.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+34693G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103175750 | ||||||
chr8:103175768
|
G | C | 152 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0062others(149): Show | 176 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(173): Show |
intron_variant | MODIFIER | c.160+34711G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103175768 | ||||||
chr8:103176260
|
C | A | 4 | a0001c0001t0001g0271a0001c0001t0002g0275a0001c0001t0006g0031others(1): Show | 5 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+35203C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176260 | ||||||
chr8:103176362
|
C | A | 106 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(103): Show | 119 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.160+35305C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176362 | ||||||
chr8:103176363
|
C | A | 5 | a0001c0001t0002g0199a0001c0001t0004g0110a0001c0001t0004g0111others(2): Show | 5 | HG02132.hp2 HG02615.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.160+35306C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176363 | ||||||
chr8:103176378
|
C | T | 1 | a0001c0001t0005g0242 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.160+35321C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176378 | ||||||
chr8:103176488
|
G | A | 6 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0257others(3): Show | 6 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+35431G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176488 | ||||||
chr8:103176551
|
G | T | 4 | a0001c0001t0001g0271a0001c0001t0002g0275a0001c0001t0006g0031others(1): Show | 5 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+35494G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176551 | ||||||
chr8:103176573
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0075others(7): Show | 10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.160+35516C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176573 | ||||||
chr8:103176621
|
C | T | 1 | a0001c0001t0001g0035 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.160+35564C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176621 | ||||||
chr8:103176629
|
G | A | 7 | a0001c0001t0001g0271a0001c0001t0002g0275a0001c0001t0006g0031others(4): Show | 11 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.160+35572G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176629 | ||||||
chr8:103176646
|
C | T | 1 | a0001c0001t0002g0229 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.160+35589C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176646 | ||||||
chr8:103176754
|
C | G | 3 | a0001c0001t0008g0261a0001c0005t0023g0038a0002c0004t0003g0001 | 6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+35697C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176754 | ||||||
chr8:103176768
|
G | A | 3 | a0001c0001t0008g0261a0001c0005t0023g0038a0002c0004t0003g0001 | 6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+35711G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176768 | ||||||
chr8:103176834
|
G | A | 4 | a0001c0001t0001g0271a0001c0001t0002g0275a0001c0001t0006g0031others(1): Show | 5 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(2): Show |
intron_variant | MODIFIER | c.160+35777G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176834 | ||||||
chr8:103176894
|
G | A | 6 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0257others(3): Show | 6 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.160+35837G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176894 | ||||||
chr8:103176916
|
C | A | 106 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(103): Show | 119 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.160+35859C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103176916 | ||||||
chr8:103177150
|
T | C | 42 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0230others(39): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-35769T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177150 | ||||||
chr8:103177167
|
TTTG | T | 45 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0230others(42): Show | 56 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(53): Show |
intron_variant | MODIFIER | c.161-35731_161-3572 others(7): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103177167 | |||||
chr8:103177180
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.161-35739T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177180 | ||||||
chr8:103177184
|
TG | T | 4 | a0001c0001t0001g0176a0001c0001t0001g0254a0001c0001t0008g0276others(1): Show | 4 | HG01167.hp2 HG01358.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-35734delG | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177184 | ||||||
chr8:103177193
|
G | GT | 41 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0102others(38): Show | 43 | HG00280.hp2 HG00438.hp1 HG01167.hp2 others(40): Show |
intron_variant | MODIFIER | c.161-35713dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103177193 | |||||
chr8:103177193
|
G | GTT | 64 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0070others(61): Show | 75 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.161-35714_161-3571 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103177193 | |||||
chr8:103177193
|
G | T | 1 | a0001c0001t0014g0284 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.161-35726G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177193 | ||||||
chr8:103177193
|
GT | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0075a0001c0001t0001g0076others(7): Show | 13 | HG01109.hp1 HG01891.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.161-35713delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103177193 | |||||
chr8:103177193
|
GTT | G | 42 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0230others(39): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-35714_161-3571 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103177193 | |||||
chr8:103177197
|
T | A | 42 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0230others(39): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-35722T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177197 | ||||||
chr8:103177213
|
A | G | 151 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0062others(148): Show | 175 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(172): Show |
intron_variant | MODIFIER | c.161-35706A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177213 | ||||||
chr8:103177235
|
G | A | 42 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0230others(39): Show | 50 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-35684G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177235 | ||||||
chr8:103177273
|
C | A | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.161-35646C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177273 | ||||||
chr8:103177461
|
A | C | 2 | a0001c0001t0015g0158a0001c0001t0015g0243 | 2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-35458A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177461 | ||||||
chr8:103177482
|
C | T | 18 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(15): Show | 20 | HG00280.hp2 HG00438.hp1 HG01884.hp1 others(17): Show |
intron_variant | MODIFIER | c.161-35437C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177482 | ||||||
chr8:103177483
|
G | A | 1 | a0001c0001t0001g0072 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.161-35436G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177483 | ||||||
chr8:103177533
|
G | A | 19 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0074others(16): Show | 22 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-35386G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177533 | ||||||
chr8:103177886
|
T | C | 1 | a0001c0001t0001g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.161-35033T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177886 | ||||||
chr8:103177913
|
C | T | 3 | a0001c0001t0008g0261a0001c0005t0023g0038a0002c0004t0003g0001 | 6 | HG01109.hp1 HG01891.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-35006C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177913 | ||||||
chr8:103177945
|
A | G | 7 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033others(4): Show | 8 | HG02109.hp2 HG02717.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-34974A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103177945 | ||||||
chr8:103178047
|
G | A | 1 | a0001c0001t0008g0239 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-34872G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178047 | ||||||
chr8:103178178
|
G | C | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.161-34741G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178178 | ||||||
chr8:103178219
|
G | A | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0259others(1): Show | 4 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-34700G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178219 | ||||||
chr8:103178228
|
G | T | 1 | a0001c0001t0014g0284 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.161-34691G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178228 | ||||||
chr8:103178299
|
C | G | 1 | a0002c0004t0003g0001 | 4 | HG01891.hp1 HG03130.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-34620C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178299 | ||||||
chr8:103178317
|
G | A | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0259others(1): Show | 4 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-34602G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178317 | ||||||
chr8:103178453
|
G | T | 6 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0257others(3): Show | 6 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-34466G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178453 | ||||||
chr8:103178515
|
A | T | 1 | a0001c0001t0004g0112 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.161-34404A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178515 | ||||||
chr8:103178691
|
T | A | 3 | a0001c0001t0001g0251a0001c0001t0010g0088a0001c0001t0010g0089 | 3 | HG02630.hp2 HG02886.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.161-34228T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178691 | ||||||
chr8:103178750
|
A | G | 156 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0062others(153): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.161-34169A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178750 | ||||||
chr8:103178794
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.161-34125C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178794 | ||||||
chr8:103178798
|
G | A | 1 | a0001c0001t0005g0242 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161-34121G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178798 | ||||||
chr8:103178849
|
T | C | 128 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0063others(125): Show | 146 | HG00099.hp2 HG00280.hp2 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.161-34070T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178849 | ||||||
chr8:103178862
|
C | CA | 24 | a0001c0001t0001g0005a0001c0001t0001g0064a0001c0001t0001g0094others(21): Show | 30 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.161-34042dupA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103178862 | |||||
chr8:103178862
|
CA | C | 24 | a0001c0001t0001g0013a0001c0001t0001g0050a0001c0001t0001g0051others(21): Show | 24 | HG00741.hp1 HG00741.hp2 HG01099.hp2 others(21): Show |
intron_variant | MODIFIER | c.161-34042delA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103178862 | |||||
chr8:103178877
|
AG | A | 89 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(86): Show | 102 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(99): Show |
intron_variant | MODIFIER | c.161-34041delG | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178877 | ||||||
chr8:103178878
|
G | A | 65 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0176others(62): Show | 73 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.161-34041G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103178878 | ||||||
chr8:103179086
|
A | G | 1 | a0001c0001t0001g0191 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.161-33833A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179086 | ||||||
chr8:103179205
|
A | C | 6 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0257others(3): Show | 6 | HG00099.hp2 HG01070.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.161-33714A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179205 | ||||||
chr8:103179263
|
T | TTAG | 5 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033others(2): Show | 6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-33652_161-3365 others(7): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103179263 | |||||
chr8:103179275
|
G | A | 5 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033others(2): Show | 6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-33644G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179275 | ||||||
chr8:103179360
|
C | T | 2 | a0001c0001t0002g0003a0002c0002t0003g0039 | 4 | HG02559.hp2 HG02818.hp1 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-33559C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179360 | ||||||
chr8:103179495
|
C | T | 6 | a0001c0001t0001g0035a0001c0001t0001g0176a0001c0001t0001g0254others(3): Show | 6 | HG01167.hp2 HG01243.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-33424C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179495 | ||||||
chr8:103179496
|
G | A | 2 | a0001c0001t0015g0158a0001c0001t0015g0243 | 2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-33423G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179496 | ||||||
chr8:103179641
|
C | T | 1 | a0001c0001t0001g0045 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.161-33278C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179641 | ||||||
chr8:103179659
|
A | T | 2 | a0001c0001t0001g0288a0001c0001t0001g0289 | 2 | HG03654.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.161-33260A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179659 | ||||||
chr8:103179675
|
A | G | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.161-33244A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179675 | ||||||
chr8:103179753
|
C | T | 1 | a0001c0001t0008g0239 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-33166C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179753 | ||||||
chr8:103179754
|
G | A | 91 | a0001c0001t0001g0035a0001c0001t0001g0037a0001c0001t0001g0067others(88): Show | 104 | HG00280.hp2 HG00408.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.161-33165G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179754 | ||||||
chr8:103179894
|
G | A | 2 | a0001c0001t0015g0158a0001c0001t0015g0243 | 2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-33025G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103179894 | ||||||
chr8:103180115
|
G | A | 3 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0246 | 3 | HG02486.hp2 HG02572.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.161-32804G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180115 | ||||||
chr8:103180159
|
A | G | 1 | a0001c0001t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.161-32760A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180159 | ||||||
chr8:103180189
|
A | G | 5 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033others(2): Show | 6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-32730A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180189 | ||||||
chr8:103180248
|
A | G | 1 | a0002c0002t0003g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.161-32671A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180248 | ||||||
chr8:103180306
|
T | C | 67 | a0001c0001t0001g0067a0001c0001t0001g0069a0001c0001t0001g0070others(64): Show | 78 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(75): Show |
intron_variant | MODIFIER | c.161-32613T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180306 | ||||||
chr8:103180523
|
T | C | 5 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033others(2): Show | 6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-32396T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180523 | ||||||
chr8:103180670
|
A | T | 1 | a0001c0001t0001g0145 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.161-32249A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103180670 | ||||||
chr8:103181043
|
G | A | 2 | a0001c0001t0004g0194a0001c0001t0004g0200 | 2 | NA18957.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.161-31876G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181043 | ||||||
chr8:103181075
|
AAG | A | 22 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0003others(19): Show | 27 | HG01109.hp1 HG01884.hp2 HG01891.hp1 others(24): Show |
intron_variant | MODIFIER | c.161-31836_161-3183 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103181075 | |||||
chr8:103181088
|
C | A | 1 | a0001c0001t0001g0005 | 3 | NA18953.hp2 NA18964.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.161-31831C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181088 | ||||||
chr8:103181116
|
A | G | 1 | a0001c0001t0002g0290 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.161-31803A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181116 | ||||||
chr8:103181231
|
C | G | 16 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0074others(13): Show | 16 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.161-31688C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181231 | ||||||
chr8:103181256
|
G | A | 6 | a0001c0001t0001g0079a0001c0001t0002g0008a0001c0001t0002g0034others(3): Show | 7 | HG02109.hp2 HG02559.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-31663G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181256 | ||||||
chr8:103181312
|
G | A | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.161-31607G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181312 | ||||||
chr8:103181415
|
T | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0075others(7): Show | 10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-31504T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181415 | ||||||
chr8:103181417
|
T | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0075others(7): Show | 10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-31502T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181417 | ||||||
chr8:103181421
|
A | G | 10 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0075others(7): Show | 10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-31498A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181421 | ||||||
chr8:103181423
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-31496C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181423 | ||||||
chr8:103181424
|
A | T | 2 | a0002c0002t0003g0073a0002c0004t0003g0001 | 5 | HG01891.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-31495A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181424 | ||||||
chr8:103181428
|
C | A | 1 | a0001c0001t0001g0191 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.161-31491C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181428 | ||||||
chr8:103181459
|
G | A | 2 | a0001c0001t0015g0158a0001c0001t0015g0243 | 2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-31460G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181459 | ||||||
chr8:103181461
|
TG | T | 27 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0050others(24): Show | 30 | HG01099.hp1 HG01123.hp2 HG01517.hp2 others(27): Show |
intron_variant | MODIFIER | c.161-31453delG | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103181461 | |||||
chr8:103181523
|
T | C | 15 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0074others(12): Show | 15 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.161-31396T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181523 | ||||||
chr8:103181524
|
G | A | 15 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0002g0074others(12): Show | 15 | HG01884.hp2 HG02451.hp1 HG02486.hp2 others(12): Show |
intron_variant | MODIFIER | c.161-31395G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181524 | ||||||
chr8:103181582
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.161-31337T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181582 | ||||||
chr8:103181619
|
G | A | 10 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0075others(7): Show | 10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-31300G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181619 | ||||||
chr8:103181768
|
G | T | 5 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0006g0033others(2): Show | 6 | HG02109.hp2 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-31151G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181768 | ||||||
chr8:103181770
|
T | C | 76 | a0001c0001t0001g0035a0001c0001t0001g0065a0001c0001t0001g0067others(73): Show | 88 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(85): Show |
intron_variant | MODIFIER | c.161-31149T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181770 | ||||||
chr8:103181785
|
A | C | 1 | a0001c0001t0002g0003 | 3 | HG02818.hp1 HG03098.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.161-31134A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181785 | ||||||
chr8:103181847
|
T | C | 4 | a0001c0001t0008g0261a0002c0002t0003g0039a0002c0002t0003g0073others(1): Show | 7 | HG01109.hp1 HG01891.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-31072T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181847 | ||||||
chr8:103181922
|
G | A | 144 | a0001c0001t0001g0013a0001c0001t0001g0035a0001c0001t0001g0062others(141): Show | 166 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.161-30997G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103181922 | ||||||
chr8:103182112
|
G | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 5 | HG00408.hp2 HG02080.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-30807G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182112 | ||||||
chr8:103182129
|
C | T | 1 | a0001c0001t0013g0279 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.161-30790C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182129 | ||||||
chr8:103182407
|
G | A | 74 | a0001c0001t0001g0035a0001c0001t0001g0065a0001c0001t0001g0067others(71): Show | 86 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.161-30512G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182407 | ||||||
chr8:103182570
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.161-30349A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182570 | ||||||
chr8:103182623
|
A | T | 7 | a0001c0001t0002g0286a0001c0001t0002g0290a0001c0001t0005g0247others(4): Show | 8 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-30296A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182623 | ||||||
chr8:103182685
|
G | A | 1 | a0001c0001t0001g0288 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.161-30234G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182685 | ||||||
chr8:103182745
|
A | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(141): Show | 168 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(165): Show |
intron_variant | MODIFIER | c.161-30174A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182745 | ||||||
chr8:103182752
|
C | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0075others(7): Show | 10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-30167C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182752 | ||||||
chr8:103182753
|
G | T | 1 | a0002c0002t0003g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.161-30166G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182753 | ||||||
chr8:103182857
|
A | G | 48 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(45): Show | 55 | HG00099.hp1 HG01099.hp2 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.161-30062A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182857 | ||||||
chr8:103182877
|
C | T | 169 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(166): Show | 196 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(193): Show |
intron_variant | MODIFIER | c.161-30042C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182877 | ||||||
chr8:103182993
|
A | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0259 | 3 | HG01070.hp2 HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.161-29926A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103182993 | ||||||
chr8:103183052
|
T | C | 1 | a0001c0001t0004g0183 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.161-29867T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183052 | ||||||
chr8:103183118
|
C | T | 2 | a0001c0001t0015g0158a0001c0001t0015g0243 | 2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-29801C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183118 | ||||||
chr8:103183258
|
G | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0259 | 3 | HG01070.hp2 HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.161-29661G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183258 | ||||||
chr8:103183294
|
C | T | 16 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(13): Show | 18 | HG00280.hp2 HG00438.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-29625C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183294 | ||||||
chr8:103183328
|
C | A | 1 | a0001c0001t0008g0261 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.161-29591C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183328 | ||||||
chr8:103183489
|
G | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(19): Show | 25 | HG00099.hp1 HG01106.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.161-29430G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183489 | ||||||
chr8:103183522
|
C | T | 7 | a0001c0001t0002g0286a0001c0001t0002g0290a0001c0001t0005g0247others(4): Show | 8 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-29397C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183522 | ||||||
chr8:103183602
|
G | A | 29 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(26): Show | 35 | HG00099.hp1 HG01106.hp2 HG01884.hp2 others(32): Show |
intron_variant | MODIFIER | c.161-29317G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183602 | ||||||
chr8:103183911
|
C | T | 71 | a0001c0001t0001g0035a0001c0001t0001g0065a0001c0001t0001g0067others(68): Show | 83 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.161-29008C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183911 | ||||||
chr8:103183936
|
G | A | 41 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(38): Show | 47 | HG00099.hp1 HG01099.hp2 HG01106.hp2 others(44): Show |
intron_variant | MODIFIER | c.161-28983G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103183936 | ||||||
chr8:103184014
|
G | C | 10 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0075others(7): Show | 10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-28905G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184014 | ||||||
chr8:103184057
|
G | C | 4 | a0001c0001t0001g0125a0001c0001t0002g0275a0001c0001t0006g0031others(1): Show | 5 | HG00140.hp1 HG00738.hp2 HG01255.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-28862G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184057 | ||||||
chr8:103184281
|
C | T | 48 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(45): Show | 55 | HG00099.hp1 HG01099.hp2 HG01106.hp2 others(52): Show |
intron_variant | MODIFIER | c.161-28638C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184281 | ||||||
chr8:103184363
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0190 | 2 | HG02071.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.161-28556C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184363 | ||||||
chr8:103184485
|
T | C | 167 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(164): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.161-28434T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184485 | ||||||
chr8:103184514
|
G | C | 23 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(20): Show | 28 | HG00280.hp2 HG00438.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.161-28405G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184514 | ||||||
chr8:103184667
|
G | T | 10 | a0001c0001t0001g0013a0001c0001t0001g0066a0001c0001t0001g0075others(7): Show | 10 | HG01099.hp2 HG02055.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-28252G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184667 | ||||||
chr8:103184688
|
A | T | 71 | a0001c0001t0001g0035a0001c0001t0001g0065a0001c0001t0001g0067others(68): Show | 83 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(80): Show |
intron_variant | MODIFIER | c.161-28231A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184688 | ||||||
chr8:103184822
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0259 | 3 | HG01070.hp2 HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.161-28097G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184822 | ||||||
chr8:103184874
|
C | T | 1 | a0001c0001t0001g0245 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.161-28045C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184874 | ||||||
chr8:103184993
|
A | G | 167 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(164): Show | 194 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(191): Show |
intron_variant | MODIFIER | c.161-27926A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103184993 | ||||||
chr8:103185011
|
C | T | 16 | a0001c0001t0001g0230a0001c0001t0003g0028a0001c0001t0003g0029others(13): Show | 18 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.161-27908C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185011 | ||||||
chr8:103185049
|
C | T | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-27870C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185049 | ||||||
chr8:103185211
|
A | G | 1 | a0002c0002t0003g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.161-27708A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185211 | ||||||
chr8:103185407
|
C | T | 5 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0257others(2): Show | 5 | HG01070.hp2 HG01192.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-27512C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185407 | ||||||
chr8:103185463
|
T | A | 6 | a0001c0001t0001g0065a0001c0001t0002g0022a0001c0001t0002g0023others(3): Show | 8 | HG00609.hp2 HG01069.hp1 HG01071.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-27456T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185463 | ||||||
chr8:103185466
|
T | G | 7 | a0001c0001t0002g0286a0001c0001t0002g0290a0001c0001t0005g0247others(4): Show | 8 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(5): Show |
intron_variant | MODIFIER | c.161-27453T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185466 | ||||||
chr8:103185467
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0003t0009g0259 | 3 | HG01070.hp2 HG01192.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.161-27452G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185467 | ||||||
chr8:103185713
|
G | A | 166 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0014others(163): Show | 193 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(190): Show |
intron_variant | MODIFIER | c.161-27206G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185713 | ||||||
chr8:103185822
|
A | C | 2 | a0001c0001t0002g0213a0001c0001t0002g0214 | 2 | NA18964.hp1 NA18991.hp2 |
intron_variant | MODIFIER | c.161-27097A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103185822 | ||||||
chr8:103186153
|
T | A | 1 | a0001c0001t0001g0136 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.161-26766T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186153 | ||||||
chr8:103186199
|
C | T | 1 | a0001c0001t0001g0017 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.161-26720C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186199 | ||||||
chr8:103186206
|
G | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0102 | 2 | NA18982.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.161-26713G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186206 | ||||||
chr8:103186273
|
C | T | 3 | a0001c0001t0003g0049a0001c0001t0003g0117a0001c0001t0003g0118 | 3 | HG01175.hp1 HG01515.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.161-26646C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186273 | ||||||
chr8:103186294
|
G | A | 1 | a0001c0001t0010g0249 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.161-26625G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186294 | ||||||
chr8:103186349
|
G | A | 1 | a0002c0002t0003g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.161-26570G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186349 | ||||||
chr8:103186441
|
T | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(19): Show | 25 | HG00099.hp1 HG01106.hp2 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.161-26478T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186441 | ||||||
chr8:103186468
|
G | A | 1 | a0001c0001t0002g0201 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.161-26451G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186468 | ||||||
chr8:103186838
|
T | C | 1 | a0002c0002t0003g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.161-26081T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186838 | ||||||
chr8:103186963
|
T | G | 1 | a0001c0001t0005g0242 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.161-25956T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186963 | ||||||
chr8:103186989
|
T | C | 1 | a0001c0005t0023g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-25930T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103186989 | ||||||
chr8:103187046
|
G | A | 4 | a0001c0001t0001g0251a0001c0001t0010g0088a0001c0001t0010g0089others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-25873G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187046 | ||||||
chr8:103187058
|
T | C | 1 | a0001c0001t0002g0022 | 2 | HG01069.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.161-25861T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187058 | ||||||
chr8:103187121
|
G | A | 28 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(25): Show | 32 | HG00099.hp1 HG01106.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.161-25798G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187121 | ||||||
chr8:103187187
|
T | C | 3 | a0001c0001t0002g0275a0001c0001t0006g0031a0001c0001t0006g0272 | 4 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-25732T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187187 | ||||||
chr8:103187349
|
T | A | 1 | a0001c0001t0005g0252 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.161-25570T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187349 | ||||||
chr8:103187405
|
A | G | 116 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(113): Show | 134 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.161-25514A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187405 | ||||||
chr8:103187558
|
T | C | 21 | a0001c0001t0001g0230a0001c0001t0002g0092a0001c0001t0003g0028others(18): Show | 26 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.161-25361T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187558 | ||||||
chr8:103187566
|
G | T | 20 | a0001c0001t0001g0230a0001c0001t0003g0028a0001c0001t0003g0029others(17): Show | 25 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(22): Show |
intron_variant | MODIFIER | c.161-25353G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187566 | ||||||
chr8:103187573
|
G | A | 47 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(44): Show | 56 | HG00099.hp1 HG00099.hp2 HG00438.hp1 others(53): Show |
intron_variant | MODIFIER | c.161-25346G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187573 | ||||||
chr8:103187626
|
T | G | 1 | a0001c0001t0002g0043 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.161-25293T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187626 | ||||||
chr8:103187689
|
C | T | 47 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(44): Show | 55 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.161-25230C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187689 | ||||||
chr8:103187757
|
C | G | 2 | a0001c0001t0006g0031a0001c0001t0006g0272 | 3 | HG00140.hp1 HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.161-25162C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187757 | ||||||
chr8:103187777
|
G | A | 26 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(23): Show | 28 | HG00280.hp2 HG00438.hp1 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.161-25142G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103187777 | ||||||
chr8:103188391
|
G | A | 2 | a0002c0002t0003g0131a0002c0002t0003g0283 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.161-24528G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188391 | ||||||
chr8:103188435
|
G | A | 39 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(36): Show | 47 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(44): Show |
intron_variant | MODIFIER | c.161-24484G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188435 | ||||||
chr8:103188598
|
G | A | 1 | a0001c0005t0023g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-24321G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188598 | ||||||
chr8:103188678
|
T | C | 1 | a0001c0001t0017g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.161-24241T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188678 | ||||||
chr8:103188680
|
A | G | 1 | a0001c0001t0008g0239 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.161-24239A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188680 | ||||||
chr8:103188764
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.161-24155G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188764 | ||||||
chr8:103188798
|
G | A | 1 | a0001c0001t0002g0021 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.161-24121G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188798 | ||||||
chr8:103188806
|
T | C | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG02258.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.161-24113T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188806 | ||||||
chr8:103188921
|
G | A | 41 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(38): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-23998G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103188921 | ||||||
chr8:103189173
|
C | T | 91 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0230others(88): Show | 108 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(105): Show |
intron_variant | MODIFIER | c.161-23746C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189173 | ||||||
chr8:103189291
|
T | G | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-23628T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189291 | ||||||
chr8:103189325
|
C | T | 41 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(38): Show | 50 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.161-23594C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189325 | ||||||
chr8:103189330
|
C | T | 1 | a0001c0001t0007g0060 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.161-23589C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189330 | ||||||
chr8:103189450
|
A | G | 1 | a0001c0001t0017g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.161-23469A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189450 | ||||||
chr8:103189507
|
G | A | 1 | a0001c0001t0007g0060 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.161-23412G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189507 | ||||||
chr8:103189581
|
T | C | 1 | a0001c0001t0001g0146 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.161-23338T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189581 | ||||||
chr8:103189702
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.161-23217G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189702 | ||||||
chr8:103189733
|
G | C | 1 | a0001c0001t0001g0091 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.161-23186G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189733 | ||||||
chr8:103189784
|
T | C | 21 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(18): Show | 23 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-23135T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189784 | ||||||
chr8:103189850
|
G | T | 4 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG01069.hp2 HG01123.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-23069G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189850 | ||||||
chr8:103189873
|
C | T | 2 | a0001c0001t0002g0177a0001c0001t0002g0184 | 2 | HG01255.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.161-23046C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103189873 | ||||||
chr8:103190170
|
T | C | 2 | a0001c0001t0013g0277a0001c0001t0013g0279 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.161-22749T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190170 | ||||||
chr8:103190197
|
G | A | 93 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0226others(90): Show | 110 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(107): Show |
intron_variant | MODIFIER | c.161-22722G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190197 | ||||||
chr8:103190413
|
T | C | 1 | a0001c0001t0001g0085 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.161-22506T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190413 | ||||||
chr8:103190750
|
A | G | 4 | a0001c0001t0001g0093a0001c0001t0001g0096a0001c0001t0001g0097others(1): Show | 4 | HG01069.hp2 HG01123.hp1 HG01167.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-22169A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190750 | ||||||
chr8:103190839
|
G | A | 4 | a0001c0001t0001g0019a0001c0001t0001g0160a0001c0001t0001g0161others(1): Show | 5 | HG00408.hp2 HG02080.hp2 NA18955.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-22080G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190839 | ||||||
chr8:103190861
|
C | T | 1 | a0001c0001t0002g0107 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.161-22058C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190861 | ||||||
chr8:103190921
|
C | T | 1 | a0001c0001t0003g0036 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.161-21998C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190921 | ||||||
chr8:103190986
|
A | G | 5 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0045others(2): Show | 7 | HG02129.hp1 NA18957.hp1 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-21933A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103190986 | ||||||
chr8:103191012
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.161-21907A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103191012 | ||||||
chr8:103191196
|
TA | T | 79 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(76): Show | 96 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(93): Show |
intron_variant | MODIFIER | c.161-21710delA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103191196 | |||||
chr8:103191292
|
G | A | 1 | a0001c0005t0023g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-21627G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103191292 | ||||||
chr8:103191436
|
C | A | 2 | a0001c0001t0004g0110a0001c0001t0004g0111 | 2 | NA19054.hp1 NA19062.hp1 |
intron_variant | MODIFIER | c.161-21483C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103191436 | ||||||
chr8:103191507
|
G | C | 4 | a0001c0001t0015g0158a0001c0001t0015g0243a0002c0002t0003g0073others(1): Show | 7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-21412G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103191507 | ||||||
chr8:103191911
|
C | T | 25 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(22): Show | 32 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.161-21008C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103191911 | ||||||
chr8:103192115
|
G | A | 2 | a0002c0002t0003g0073a0002c0004t0003g0001 | 5 | HG01891.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-20804G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192115 | ||||||
chr8:103192209
|
C | G | 142 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(139): Show | 168 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(165): Show |
intron_variant | MODIFIER | c.161-20710C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192209 | ||||||
chr8:103192426
|
C | T | 53 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0002g0007others(50): Show | 65 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.161-20493C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192426 | ||||||
chr8:103192473
|
A | G | 12 | a0001c0001t0001g0206a0001c0001t0002g0026a0001c0001t0002g0027others(9): Show | 14 | HG00544.hp1 NA18946.hp2 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.161-20446A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192473 | ||||||
chr8:103192533
|
TAGTC | T | 21 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(18): Show | 23 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-20382_161-2037 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103192533 | |||||
chr8:103192578
|
T | C | 15 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0238others(12): Show | 15 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-20341T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192578 | ||||||
chr8:103192630
|
C | T | 53 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0002g0007others(50): Show | 65 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.161-20289C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192630 | ||||||
chr8:103192648
|
A | G | 53 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0002g0007others(50): Show | 65 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.161-20271A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192648 | ||||||
chr8:103192775
|
A | G | 143 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(140): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.161-20144A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103192775 | ||||||
chr8:103193011
|
G | C | 1 | a0001c0001t0001g0055 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.161-19908G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193011 | ||||||
chr8:103193033
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.161-19886A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193033 | ||||||
chr8:103193203
|
T | C | 53 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0002g0007others(50): Show | 65 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.161-19716T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193203 | ||||||
chr8:103193291
|
C | A | 1 | a0001c0001t0001g0087 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.161-19628C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193291 | ||||||
chr8:103193535
|
G | A | 39 | a0001c0001t0001g0230a0001c0001t0002g0003a0001c0001t0002g0074others(36): Show | 44 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.161-19384G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193535 | ||||||
chr8:103193677
|
G | A | 15 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0238others(12): Show | 15 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-19242G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193677 | ||||||
chr8:103193766
|
T | G | 3 | a0001c0001t0001g0152a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | HG01243.hp1 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.161-19153T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193766 | ||||||
chr8:103193780
|
A | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0003t0009g0259 | 3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.161-19139A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193780 | ||||||
chr8:103193885
|
C | A | 39 | a0001c0001t0001g0230a0001c0001t0002g0003a0001c0001t0002g0074others(36): Show | 44 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.161-19034C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103193885 | ||||||
chr8:103194056
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0003t0009g0259 | 3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.161-18863G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194056 | ||||||
chr8:103194093
|
T | A | 1 | a0001c0001t0001g0051 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.161-18826T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194093 | ||||||
chr8:103194141
|
C | A | 2 | a0001c0003t0009g0257a0001c0003t0009g0258 | 2 | NA18983.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.161-18778C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194141 | ||||||
chr8:103194370
|
GTCTTT | G | 19 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(16): Show | 21 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-18543_161-1853 others(9): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103194370 | |||||
chr8:103194587
|
G | T | 1 | a0001c0005t0023g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-18332G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194587 | ||||||
chr8:103194604
|
T | C | 290 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(287): Show | 329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.161-18315T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194604 | ||||||
chr8:103194697
|
A | C | 1 | a0001c0001t0002g0205 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.161-18222A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194697 | ||||||
chr8:103194751
|
G | A | 2 | a0002c0002t0003g0131a0002c0002t0003g0283 | 2 | NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.161-18168G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194751 | ||||||
chr8:103194784
|
A | G | 2 | a0001c0001t0014g0157a0001c0001t0014g0284 | 2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.161-18135A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194784 | ||||||
chr8:103194861
|
G | A | 2 | a0001c0001t0014g0157a0001c0001t0014g0284 | 2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.161-18058G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194861 | ||||||
chr8:103194891
|
C | T | 1 | a0001c0001t0002g0092 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.161-18028C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103194891 | ||||||
chr8:103195073
|
T | G | 1 | a0001c0001t0003g0174 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.161-17846T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195073 | ||||||
chr8:103195185
|
C | T | 1 | a0001c0003t0009g0259 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.161-17734C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195185 | ||||||
chr8:103195223
|
A | G | 21 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(18): Show | 25 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.161-17696A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195223 | ||||||
chr8:103195331
|
G | A | 7 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0006g0090others(4): Show | 8 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-17588G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195331 | ||||||
chr8:103195353
|
C | T | 39 | a0001c0001t0001g0230a0001c0001t0002g0003a0001c0001t0002g0074others(36): Show | 44 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(41): Show |
intron_variant | MODIFIER | c.161-17566C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195353 | ||||||
chr8:103195460
|
C | T | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-17459C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195460 | ||||||
chr8:103195561
|
A | T | 20 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(17): Show | 22 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-17358A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195561 | ||||||
chr8:103195625
|
C | T | 4 | a0001c0001t0001g0063a0001c0001t0001g0132a0001c0001t0001g0133others(1): Show | 4 | HG00140.hp2 HG00639.hp2 HG01192.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-17294C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195625 | ||||||
chr8:103195680
|
A | G | 2 | a0001c0001t0013g0277a0001c0001t0013g0279 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.161-17239A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195680 | ||||||
chr8:103195711
|
A | C | 47 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(44): Show | 56 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.161-17208A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195711 | ||||||
chr8:103195880
|
C | G | 5 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0238others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-17039C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103195880 | ||||||
chr8:103196004
|
A | T | 20 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(17): Show | 22 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-16915A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196004 | ||||||
chr8:103196009
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.161-16910T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196009 | ||||||
chr8:103196047
|
G | T | 1 | a0001c0001t0002g0214 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.161-16872G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196047 | ||||||
chr8:103196102
|
T | C | 145 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(142): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.161-16817T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196102 | ||||||
chr8:103196735
|
T | A | 101 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(98): Show | 122 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(119): Show |
intron_variant | MODIFIER | c.161-16184T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196735 | ||||||
chr8:103196789
|
G | A | 21 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(18): Show | 25 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.161-16130G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196789 | ||||||
chr8:103196838
|
C | T | 1 | a0001c0001t0008g0156 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.161-16081C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196838 | ||||||
chr8:103196918
|
C | T | 1 | a0001c0001t0012g0197 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.161-16001C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196918 | ||||||
chr8:103196947
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.161-15972C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103196947 | ||||||
chr8:103197077
|
A | G | 2 | a0001c0001t0001g0129a0001c0001t0001g0251 | 2 | HG02451.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.161-15842A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197077 | ||||||
chr8:103197093
|
G | A | 19 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(16): Show | 21 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-15826G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197093 | ||||||
chr8:103197204
|
T | C | 5 | a0001c0001t0008g0081a0001c0001t0008g0156a0001c0001t0008g0239others(2): Show | 5 | HG00741.hp1 HG01358.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-15715T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197204 | ||||||
chr8:103197237
|
GT | G | 7 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0006g0090others(4): Show | 8 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-15678delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103197237 | |||||
chr8:103197456
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.161-15463G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197456 | ||||||
chr8:103197525
|
T | C | 2 | a0001c0001t0002g0021a0001c0001t0002g0211 | 3 | HG02683.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.161-15394T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197525 | ||||||
chr8:103197589
|
G | T | 4 | a0001c0001t0015g0158a0001c0001t0015g0243a0002c0002t0003g0073others(1): Show | 7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-15330G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197589 | ||||||
chr8:103197649
|
A | G | 10 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0238others(7): Show | 10 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-15270A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103197649 | ||||||
chr8:103198033
|
G | A | 2 | a0001c0001t0006g0031a0001c0001t0006g0272 | 3 | HG00140.hp1 HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.161-14886G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198033 | ||||||
chr8:103198139
|
A | G | 3 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0003t0009g0259 | 3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.161-14780A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198139 | ||||||
chr8:103198175
|
A | G | 1 | a0001c0001t0001g0076 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.161-14744A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198175 | ||||||
chr8:103198271
|
T | C | 24 | a0001c0001t0001g0230a0001c0001t0002g0003a0001c0001t0002g0092others(21): Show | 29 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(26): Show |
intron_variant | MODIFIER | c.161-14648T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198271 | ||||||
chr8:103198378
|
A | G | 7 | a0001c0001t0001g0143a0001c0001t0001g0265a0001c0001t0001g0266others(4): Show | 7 | NA18939.hp1 NA18982.hp1 NA18987.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-14541A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198378 | ||||||
chr8:103198464
|
G | A | 26 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(23): Show | 33 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.161-14455G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198464 | ||||||
chr8:103198529
|
T | C | 2 | a0001c0001t0006g0031a0001c0001t0006g0272 | 3 | HG00140.hp1 HG01255.hp1 HG01496.hp1 |
intron_variant | MODIFIER | c.161-14390T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198529 | ||||||
chr8:103198550
|
A | ATG | 22 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(19): Show | 24 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.161-14361_161-1436 others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103198550 | |||||
chr8:103198573
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-14346C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198573 | ||||||
chr8:103198749
|
C | CA | 9 | a0001c0001t0001g0004a0001c0001t0001g0065a0001c0001t0001g0104others(6): Show | 11 | HG00609.hp1 HG01496.hp2 HG01975.hp2 others(8): Show |
intron_variant | MODIFIER | c.161-14157dupA | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103198749 | |||||
chr8:103198842
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.161-14077C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198842 | ||||||
chr8:103198843
|
G | A | 20 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(17): Show | 22 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.161-14076G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103198843 | ||||||
chr8:103199090
|
T | C | 7 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0006g0090others(4): Show | 8 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-13829T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199090 | ||||||
chr8:103199125
|
C | T | 4 | a0001c0001t0010g0088a0001c0001t0010g0089a0001c0001t0010g0249others(1): Show | 4 | HG02630.hp1 HG02630.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-13794C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199125 | ||||||
chr8:103199177
|
T | G | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-13742T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199177 | ||||||
chr8:103199181
|
G | C | 1 | a0001c0001t0001g0193 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.161-13738G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199181 | ||||||
chr8:103199238
|
A | T | 1 | a0001c0001t0001g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.161-13681A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199238 | ||||||
chr8:103199241
|
G | T | 1 | a0001c0001t0001g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.161-13678G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199241 | ||||||
chr8:103199243
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.161-13676A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199243 | ||||||
chr8:103199527
|
AATTG | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0003t0009g0259 | 3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.161-13383_161-1338 others(8): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103199527 | |||||
chr8:103199548
|
G | A | 2 | a0001c0001t0010g0088a0001c0001t0010g0089 | 2 | HG02630.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.161-13371G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199548 | ||||||
chr8:103199655
|
C | CT | 7 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0006g0090others(4): Show | 8 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.161-13253dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103199655 | |||||
chr8:103199665
|
T | C | 1 | a0001c0005t0023g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.161-13254T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199665 | ||||||
chr8:103199679
|
C | G | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-13240C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199679 | ||||||
chr8:103199755
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.161-13164C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199755 | ||||||
chr8:103199786
|
T | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0056a0001c0001t0001g0288 | 3 | HG02004.hp1 HG03654.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.161-13133T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199786 | ||||||
chr8:103199795
|
T | TC | 292 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(289): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.161-13124_161-1312 others(5): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199795 | ||||||
chr8:103199798
|
T | C | 292 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(289): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.161-13121T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199798 | ||||||
chr8:103199802
|
T | C | 292 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(289): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.161-13117T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199802 | ||||||
chr8:103199803
|
C | T | 292 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(289): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.161-13116C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199803 | ||||||
chr8:103199821
|
T | A | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.161-13098T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199821 | ||||||
chr8:103199890
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.161-13029T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199890 | ||||||
chr8:103199982
|
A | G | 54 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0226others(51): Show | 66 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(63): Show |
intron_variant | MODIFIER | c.161-12937A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103199982 | ||||||
chr8:103200066
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.161-12853C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200066 | ||||||
chr8:103200268
|
A | G | 1 | a0001c0001t0004g0103 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.161-12651A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200268 | ||||||
chr8:103200483
|
A | C | 1 | a0001c0001t0005g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.161-12436A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200483 | ||||||
chr8:103200538
|
C | A | 21 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(18): Show | 23 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-12381C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200538 | ||||||
chr8:103200617
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.161-12302T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200617 | ||||||
chr8:103200803
|
C | T | 1 | a0001c0001t0005g0250 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.161-12116C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200803 | ||||||
chr8:103200964
|
C | T | 1 | a0001c0001t0012g0248 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.161-11955C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103200964 | ||||||
chr8:103201029
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0065 | 4 | HG01496.hp2 HG01975.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-11890G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201029 | ||||||
chr8:103201277
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0003t0009g0259 | 3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.161-11642C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201277 | ||||||
chr8:103201299
|
A | T | 3 | a0001c0001t0001g0170a0001c0001t0001g0189a0001c0001t0001g0190 | 3 | HG02071.hp2 NA18948.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.161-11620A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201299 | ||||||
chr8:103201458
|
C | T | 21 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(18): Show | 23 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.161-11461C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201458 | ||||||
chr8:103201470
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.161-11449C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201470 | ||||||
chr8:103201500
|
A | G | 3 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0264 | 3 | HG00438.hp2 HG02165.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.161-11419A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201500 | ||||||
chr8:103201661
|
T | C | 8 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0006g0047others(5): Show | 9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-11258T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201661 | ||||||
chr8:103201963
|
T | A | 1 | a0001c0001t0001g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.161-10956T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103201963 | ||||||
chr8:103202240
|
A | G | 2 | a0001c0001t0001g0265a0001c0001t0001g0269 | 2 | NA19007.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.161-10679A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202240 | ||||||
chr8:103202302
|
C | A | 1 | a0001c0001t0001g0136 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.161-10617C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202302 | ||||||
chr8:103202419
|
A | C | 5 | a0001c0001t0005g0124a0001c0001t0005g0126a0001c0001t0005g0127others(2): Show | 5 | HG01358.hp1 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-10500A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202419 | ||||||
chr8:103202527
|
C | G | 1 | a0001c0001t0001g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.161-10392C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202527 | ||||||
chr8:103202601
|
A | G | 2 | a0001c0001t0014g0157a0001c0001t0014g0284 | 2 | HG02615.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.161-10318A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202601 | ||||||
chr8:103202674
|
C | T | 53 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0002g0007others(50): Show | 65 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.161-10245C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202674 | ||||||
chr8:103202728
|
G | A | 1 | a0001c0001t0002g0227 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.161-10191G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202728 | ||||||
chr8:103202753
|
G | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG00639.hp2 HG01192.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.161-10166G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202753 | ||||||
chr8:103202815
|
C | T | 8 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0006g0047others(5): Show | 9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-10104C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103202815 | ||||||
chr8:103203191
|
C | T | 1 | a0001c0001t0002g0220 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.161-9728C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203191 | ||||||
chr8:103203197
|
A | G | 1 | a0001c0001t0001g0017 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.161-9722A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203197 | ||||||
chr8:103203219
|
C | T | 1 | a0001c0001t0003g0232 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.161-9700C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203219 | ||||||
chr8:103203238
|
T | C | 158 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(155): Show | 185 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(182): Show |
intron_variant | MODIFIER | c.161-9681T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203238 | ||||||
chr8:103203306
|
G | A | 1 | a0001c0001t0011g0002 | 4 | NA18965.hp2 NA18989.hp2 NA19066.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-9613G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203306 | ||||||
chr8:103203355
|
T | C | 8 | a0001c0001t0003g0028a0001c0001t0003g0036a0001c0001t0003g0049others(5): Show | 9 | HG01175.hp1 HG01257.hp2 HG01515.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-9564T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203355 | ||||||
chr8:103203428
|
G | A | 19 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(16): Show | 21 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-9491G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103203428 | ||||||
chr8:103203812
|
CTTTA | C | 19 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(16): Show | 21 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-9101_161-9098d others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103203812 | |||||
chr8:103204021
|
C | A | 19 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(16): Show | 21 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-8898C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103204021 | ||||||
chr8:103204046
|
A | T | 1 | a0001c0001t0002g0229 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.161-8873A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103204046 | ||||||
chr8:103204128
|
A | C | 4 | a0001c0001t0005g0124a0001c0001t0005g0126a0001c0001t0005g0127others(1): Show | 4 | HG01358.hp1 HG02145.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.161-8791A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103204128 | ||||||
chr8:103204506
|
T | A | 5 | a0001c0001t0008g0081a0001c0001t0008g0156a0001c0001t0008g0239others(2): Show | 5 | HG00741.hp1 HG01358.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-8413T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103204506 | ||||||
chr8:103204518
|
C | T | 53 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0002g0007others(50): Show | 65 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.161-8401C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103204518 | ||||||
chr8:103204610
|
G | T | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-8309G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103204610 | ||||||
chr8:103205538
|
T | TGATA | 7 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0106others(4): Show | 7 | HG00280.hp2 HG01884.hp2 NA18953.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-7365_161-7362d others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr8 | 103205538 | |||||
chr8:103205570
|
A | G | 3 | a0001c0001t0006g0031a0001c0001t0006g0047a0001c0001t0006g0272 | 4 | HG00140.hp1 HG01255.hp1 HG01496.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-7349A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103205570 | ||||||
chr8:103205711
|
A | G | 21 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(18): Show | 25 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.161-7208A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103205711 | ||||||
chr8:103205725
|
C | T | 23 | a0001c0001t0001g0230a0001c0001t0002g0003a0001c0001t0002g0092others(20): Show | 28 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.161-7194C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103205725 | ||||||
chr8:103205816
|
G | A | 1 | a0001c0001t0001g0146 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.161-7103G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103205816 | ||||||
chr8:103206004
|
G | T | 5 | a0001c0001t0005g0124a0001c0001t0005g0126a0001c0001t0005g0127others(2): Show | 5 | HG01358.hp1 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-6915G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206004 | ||||||
chr8:103206110
|
T | C | 6 | a0001c0001t0005g0124a0001c0001t0005g0126a0001c0001t0005g0127others(3): Show | 6 | HG01358.hp1 HG02145.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.161-6809T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206110 | ||||||
chr8:103206215
|
T | C | 97 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0001g0230others(94): Show | 114 | HG00323.hp2 HG00408.hp1 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.161-6704T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206215 | ||||||
chr8:103206499
|
C | T | 5 | a0001c0001t0001g0016a0001c0001t0001g0115a0001c0001t0001g0134others(2): Show | 5 | HG03017.hp1 HG03704.hp1 HG03834.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-6420C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206499 | ||||||
chr8:103206590
|
G | T | 53 | a0001c0001t0001g0202a0001c0001t0001g0206a0001c0001t0002g0007others(50): Show | 65 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.161-6329G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206590 | ||||||
chr8:103206618
|
G | T | 5 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0238others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-6301G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206618 | ||||||
chr8:103206855
|
T | C | 4 | a0001c0001t0015g0158a0001c0001t0015g0243a0002c0002t0003g0073others(1): Show | 7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-6064T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103206855 | ||||||
chr8:103207207
|
C | A | 19 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(16): Show | 21 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.161-5712C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103207207 | ||||||
chr8:103207283
|
C | T | 5 | a0001c0001t0002g0246a0001c0001t0006g0077a0002c0002t0003g0131others(2): Show | 5 | HG02055.hp2 HG02486.hp1 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-5636C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103207283 | ||||||
chr8:103207301
|
A | G | 7 | a0001c0001t0001g0067a0001c0001t0001g0170a0001c0001t0001g0178others(4): Show | 7 | HG01261.hp1 HG02071.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-5618A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103207301 | ||||||
chr8:103207490
|
T | C | 1 | a0001c0001t0002g0199 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.161-5429T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103207490 | ||||||
chr8:103207533
|
G | T | 8 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0006g0047others(5): Show | 9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-5386G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103207533 | ||||||
chr8:103207895
|
A | G | 21 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(18): Show | 25 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.161-5024A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103207895 | ||||||
chr8:103208028
|
C | G | 1 | a0001c0001t0002g0224 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.161-4891C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208028 | ||||||
chr8:103208031
|
A | G | 2 | a0001c0001t0013g0277a0001c0001t0013g0279 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.161-4888A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208031 | ||||||
chr8:103208081
|
C | G | 1 | a0001c0001t0005g0247 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.161-4838C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208081 | ||||||
chr8:103208178
|
C | T | 3 | a0002c0002t0003g0131a0002c0002t0003g0283a0002c0002t0003g0291 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.161-4741C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208178 | ||||||
chr8:103208212
|
G | A | 15 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0238others(12): Show | 15 | HG02055.hp2 HG02280.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.161-4707G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208212 | ||||||
chr8:103208407
|
G | A | 1 | a0001c0001t0002g0172 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.161-4512G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208407 | ||||||
chr8:103208478
|
G | T | 22 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(19): Show | 24 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.161-4441G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208478 | ||||||
chr8:103208586
|
G | A | 1 | a0001c0001t0016g0173 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.161-4333G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208586 | ||||||
chr8:103208691
|
G | A | 5 | a0001c0001t0008g0081a0001c0001t0008g0156a0001c0001t0008g0239others(2): Show | 5 | HG00741.hp1 HG01358.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.161-4228G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208691 | ||||||
chr8:103208766
|
C | T | 2 | a0001c0001t0015g0158a0001c0001t0015g0243 | 2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.161-4153C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208766 | ||||||
chr8:103208769
|
G | C | 1 | a0001c0001t0019g0188 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.161-4150G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208769 | ||||||
chr8:103208854
|
G | C | 8 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0006g0047others(5): Show | 9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-4065G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208854 | ||||||
chr8:103208873
|
A | G | 1 | a0001c0001t0002g0107 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.161-4046A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208873 | ||||||
chr8:103208891
|
G | A | 264 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(261): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.161-4028G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208891 | ||||||
chr8:103208909
|
A | G | 38 | a0001c0001t0001g0230a0001c0001t0002g0003a0001c0001t0002g0074others(35): Show | 43 | HG00323.hp2 HG00738.hp1 HG01175.hp1 others(40): Show |
intron_variant | MODIFIER | c.161-4010A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103208909 | ||||||
chr8:103209046
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.161-3873C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209046 | ||||||
chr8:103209149
|
A | T | 5 | a0001c0001t0005g0124a0001c0001t0005g0126a0001c0001t0005g0127others(2): Show | 5 | HG01358.hp1 HG02145.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.161-3770A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209149 | ||||||
chr8:103209267
|
G | A | 1 | a0001c0001t0006g0077 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.161-3652G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209267 | ||||||
chr8:103209276
|
G | A | 8 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0006g0047others(5): Show | 9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-3643G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209276 | ||||||
chr8:103209312
|
C | T | 2 | a0001c0001t0002g0246a0001c0001t0006g0077 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.161-3607C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209312 | ||||||
chr8:103209358
|
C | T | 3 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0003t0009g0259 | 3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.161-3561C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209358 | ||||||
chr8:103209359
|
G | A | 7 | a0001c0001t0002g0003a0001c0001t0002g0092a0001c0001t0002g0164others(4): Show | 10 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-3560G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209359 | ||||||
chr8:103209498
|
A | T | 2 | a0001c0001t0001g0041a0001c0001t0001g0215 | 2 | HG02040.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.161-3421A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209498 | ||||||
chr8:103209797
|
T | C | 40 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(37): Show | 44 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(41): Show |
intron_variant | MODIFIER | c.161-3122T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209797 | ||||||
chr8:103209896
|
C | A | 1 | a0001c0001t0001g0181 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.161-3023C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209896 | ||||||
chr8:103209903
|
G | T | 1 | a0001c0001t0002g0207 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.161-3016G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103209903 | ||||||
chr8:103210052
|
C | T | 8 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0006g0047others(5): Show | 9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-2867C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210052 | ||||||
chr8:103210101
|
G | A | 8 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0006g0047others(5): Show | 9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.161-2818G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210101 | ||||||
chr8:103210116
|
T | C | 4 | a0001c0001t0015g0158a0001c0001t0015g0243a0002c0002t0003g0073others(1): Show | 7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.161-2803T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210116 | ||||||
chr8:103210418
|
A | G | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.161-2501A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210418 | ||||||
chr8:103210500
|
C | T | 4 | a0001c0001t0002g0123a0001c0001t0002g0154a0001c0001t0002g0205others(1): Show | 4 | HG00408.hp1 HG02135.hp1 NA18980.hp1 others(1): Show |
intron_variant | MODIFIER | c.161-2419C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210500 | ||||||
chr8:103210598
|
C | T | 1 | a0001c0001t0017g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.161-2321C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210598 | ||||||
chr8:103210710
|
C | T | 37 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(34): Show | 41 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.161-2209C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210710 | ||||||
chr8:103210795
|
A | G | 1 | a0001c0001t0001g0141 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.161-2124A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210795 | ||||||
chr8:103210831
|
T | C | 1 | a0001c0001t0017g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.161-2088T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210831 | ||||||
chr8:103210988
|
T | G | 19 | a0001c0001t0002g0003a0001c0001t0002g0074a0001c0001t0002g0080others(16): Show | 22 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(19): Show |
intron_variant | MODIFIER | c.161-1931T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103210988 | ||||||
chr8:103211215
|
C | G | 1 | a0001c0001t0001g0168 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.161-1704C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211215 | ||||||
chr8:103211336
|
G | T | 153 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(150): Show | 179 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(176): Show |
intron_variant | MODIFIER | c.161-1583G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211336 | ||||||
chr8:103211337
|
A | T | 1 | a0001c0001t0002g0192 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.161-1582A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211337 | ||||||
chr8:103211448
|
C | T | 10 | a0001c0001t0001g0035a0001c0001t0001g0071a0001c0001t0001g0072others(7): Show | 10 | HG01243.hp2 HG01884.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.161-1471C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211448 | ||||||
chr8:103211512
|
T | C | 1 | a0001c0001t0001g0166 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.161-1407T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211512 | ||||||
chr8:103211514
|
C | A | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.161-1405C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211514 | ||||||
chr8:103211686
|
C | A | 1 | a0001c0001t0016g0173 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.161-1233C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211686 | ||||||
chr8:103211693
|
G | T | 7 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0238others(4): Show | 7 | HG02055.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.161-1226G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211693 | ||||||
chr8:103211888
|
G | A | 36 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(33): Show | 40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.161-1031G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103211888 | ||||||
chr8:103212286
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.161-633A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103212286 | ||||||
chr8:103212412
|
C | A | 1 | a0001c0001t0001g0189 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.161-507C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103212412 | ||||||
chr8:103212412
|
C | T | 1 | a0001c0001t0001g0064 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.161-507C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103212412 | ||||||
chr8:103212560
|
G | A | 12 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0238others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.161-359G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103212560 | ||||||
chr8:103212909
|
C | T | 2 | a0001c0001t0002g0246a0001c0001t0006g0077 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.161-10C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 1/2 | chr8 | 103212909 | ||||||
chr8:103213250
|
C | T | 3 | a0001c0001t0006g0090a0001c0001t0006g0151a0001c0001t0006g0153 | 3 | HG02976.hp1 HG03139.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.327+165C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213250 | ||||||
chr8:103213308
|
T | C | 38 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(35): Show | 42 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.327+223T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213308 | ||||||
chr8:103213334
|
T | G | 1 | a0001c0001t0001g0063 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.327+249T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213334 | ||||||
chr8:103213422
|
T | C | 8 | a0001c0001t0006g0031a0001c0001t0006g0033a0001c0001t0006g0047others(5): Show | 9 | HG00140.hp1 HG01109.hp1 HG01255.hp1 others(6): Show |
intron_variant | MODIFIER | c.327+337T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213422 | ||||||
chr8:103213513
|
T | C | 1 | a0001c0001t0003g0042 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.327+428T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213513 | ||||||
chr8:103213516
|
A | G | 144 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(141): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.327+431A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213516 | ||||||
chr8:103213609
|
A | T | 144 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(141): Show | 169 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(166): Show |
intron_variant | MODIFIER | c.327+524A>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213609 | ||||||
chr8:103213618
|
C | T | 5 | a0001c0001t0010g0088a0001c0001t0010g0089a0001c0001t0010g0249others(2): Show | 5 | HG02280.hp2 HG02630.hp1 HG02630.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+533C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213618 | ||||||
chr8:103213695
|
G | A | 4 | a0001c0001t0015g0158a0001c0001t0015g0243a0002c0002t0003g0073others(1): Show | 7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+610G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213695 | ||||||
chr8:103213754
|
C | T | 1 | a0001c0001t0007g0025 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.327+669C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213754 | ||||||
chr8:103213831
|
C | A | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.327+746C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213831 | ||||||
chr8:103213832
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.327+747T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103213832 | ||||||
chr8:103214331
|
T | C | 1 | a0001c0001t0001g0017 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.327+1246T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103214331 | ||||||
chr8:103214379
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.327+1294C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103214379 | ||||||
chr8:103214487
|
C | A | 1 | a0001c0001t0021g0147 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.327+1402C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103214487 | ||||||
chr8:103214718
|
A | G | 146 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(143): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.327+1633A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103214718 | ||||||
chr8:103214850
|
G | A | 4 | a0001c0001t0015g0158a0001c0001t0015g0243a0002c0002t0003g0073others(1): Show | 7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+1765G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103214850 | ||||||
chr8:103215227
|
T | C | 1 | a0001c0001t0019g0188 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.327+2142T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215227 | ||||||
chr8:103215264
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0165 | 2 | HG01175.hp2 HG01346.hp1 |
intron_variant | MODIFIER | c.327+2179T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215264 | ||||||
chr8:103215318
|
T | C | 3 | a0002c0002t0003g0131a0002c0002t0003g0283a0002c0002t0003g0291 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.327+2233T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215318 | ||||||
chr8:103215432
|
G | C | 1 | a0001c0003t0009g0259 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.327+2347G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215432 | ||||||
chr8:103215486
|
AC | A | 292 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0009others(289): Show | 331 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(328): Show |
intron_variant | MODIFIER | c.327+2404delC | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103215486 | |||||
chr8:103215681
|
G | A | 5 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0238others(2): Show | 5 | HG02615.hp2 HG02895.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.327+2596G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215681 | ||||||
chr8:103215777
|
C | T | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.327+2692C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215777 | ||||||
chr8:103215803
|
A | G | 1 | a0001c0001t0003g0233 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.327+2718A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103215803 | ||||||
chr8:103216002
|
G | C | 36 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(33): Show | 40 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(37): Show |
intron_variant | MODIFIER | c.327+2917G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216002 | ||||||
chr8:103216118
|
C | T | 2 | a0001c0001t0002g0043a0001c0001t0002g0192 | 2 | HG02056.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.327+3033C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216118 | ||||||
chr8:103216121
|
C | T | 4 | a0001c0001t0015g0158a0001c0001t0015g0243a0002c0002t0003g0073others(1): Show | 7 | HG01891.hp1 HG02717.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.327+3036C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216121 | ||||||
chr8:103216362
|
C | T | 3 | a0001c0001t0015g0158a0001c0001t0015g0243a0001c0001t0017g0040 | 3 | HG02717.hp1 HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.327+3277C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216362 | ||||||
chr8:103216399
|
T | C | 3 | a0001c0001t0015g0158a0001c0001t0015g0243a0001c0001t0017g0040 | 3 | HG02717.hp1 HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.327+3314T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216399 | ||||||
chr8:103216443
|
T | C | 24 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(21): Show | 27 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.327+3358T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216443 | ||||||
chr8:103216464
|
TATTA | T | 3 | a0002c0002t0003g0131a0002c0002t0003g0283a0002c0002t0003g0291 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.327+3395_327+3398d others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103216464 | |||||
chr8:103216775
|
C | T | 2 | a0001c0001t0001g0178a0001c0001t0001g0179 | 2 | NA18953.hp1 NA18969.hp2 |
intron_variant | MODIFIER | c.327+3690C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216775 | ||||||
chr8:103216806
|
G | A | 1 | a0001c0001t0007g0203 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.327+3721G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216806 | ||||||
chr8:103216821
|
G | A | 1 | a0002c0002t0003g0283 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.327+3736G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216821 | ||||||
chr8:103216841
|
A | C | 3 | a0001c0001t0015g0158a0001c0001t0015g0243a0001c0001t0017g0040 | 3 | HG02717.hp1 HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.327+3756A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216841 | ||||||
chr8:103216950
|
A | G | 12 | a0001c0001t0002g0074a0001c0001t0002g0080a0001c0001t0002g0238others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02572.hp2 others(9): Show |
intron_variant | MODIFIER | c.327+3865A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103216950 | ||||||
chr8:103217016
|
C | A | 38 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(35): Show | 42 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.327+3931C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217016 | ||||||
chr8:103217080
|
A | G | 1 | a0001c0001t0001g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.327+3995A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217080 | ||||||
chr8:103217238
|
T | G | 1 | a0001c0001t0001g0095 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.327+4153T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217238 | ||||||
chr8:103217305
|
G | T | 38 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(35): Show | 42 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.327+4220G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217305 | ||||||
chr8:103217354
|
T | C | 3 | a0001c0001t0015g0158a0001c0001t0015g0243a0001c0001t0017g0040 | 3 | HG02717.hp1 HG02809.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.327+4269T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217354 | ||||||
chr8:103217407
|
C | T | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.327+4322C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217407 | ||||||
chr8:103217464
|
G | GT | 150 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(147): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): Show |
intron_variant | MODIFIER | c.327+4386dupT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103217464 | |||||
chr8:103217499
|
T | C | 1 | a0001c0001t0001g0148 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.327+4414T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217499 | ||||||
chr8:103217565
|
C | T | 38 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(35): Show | 42 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(39): Show |
intron_variant | MODIFIER | c.327+4480C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217565 | ||||||
chr8:103217596
|
C | T | 73 | a0001c0001t0001g0206a0001c0001t0001g0226a0001c0001t0002g0003others(70): Show | 88 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.327+4511C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103217596 | ||||||
chr8:103218039
|
A | G | 24 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(21): Show | 27 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(24): Show |
intron_variant | MODIFIER | c.327+4954A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218039 | ||||||
chr8:103218067
|
G | A | 26 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(23): Show | 32 | HG00099.hp1 HG00099.hp2 HG00741.hp1 others(29): Show |
intron_variant | MODIFIER | c.327+4982G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218067 | ||||||
chr8:103218141
|
G | T | 7 | a0001c0001t0002g0003a0001c0001t0002g0092a0001c0001t0002g0164others(4): Show | 10 | HG01256.hp1 HG01258.hp1 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.327+5056G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218141 | ||||||
chr8:103218365
|
CCA | C | 37 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(34): Show | 41 | HG00280.hp2 HG00323.hp2 HG00438.hp1 others(38): Show |
intron_variant | MODIFIER | c.327+5281_327+5282d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218365 | ||||||
chr8:103218553
|
C | G | 1 | a0001c0001t0005g0098 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.327+5468C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218553 | ||||||
chr8:103218752
|
A | G | 1 | a0001c0001t0010g0089 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.327+5667A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218752 | ||||||
chr8:103218753
|
T | C | 22 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(19): Show | 24 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(21): Show |
intron_variant | MODIFIER | c.327+5668T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218753 | ||||||
chr8:103218869
|
T | A | 3 | a0002c0002t0003g0131a0002c0002t0003g0283a0002c0002t0003g0291 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.327+5784T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218869 | ||||||
chr8:103218944
|
G | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0171 | 3 | NA18969.hp1 NA19004.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.327+5859G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103218944 | ||||||
chr8:103219025
|
G | A | 1 | a0001c0001t0017g0040 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.327+5940G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219025 | ||||||
chr8:103219106
|
G | T | 1 | a0001c0001t0001g0150 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.327+6021G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219106 | ||||||
chr8:103219230
|
G | T | 20 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(17): Show | 22 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.327+6145G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219230 | ||||||
chr8:103219716
|
C | A | 75 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0064others(72): Show | 93 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.327+6631C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219716 | ||||||
chr8:103219809
|
T | C | 56 | a0001c0001t0001g0206a0001c0001t0001g0226a0001c0001t0002g0007others(53): Show | 71 | HG00408.hp1 HG00544.hp1 HG00609.hp2 others(68): Show |
intron_variant | MODIFIER | c.327+6724T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219809 | ||||||
chr8:103219839
|
A | C | 132 | a0001c0001t0001g0005a0001c0001t0001g0014a0001c0001t0001g0037others(129): Show | 155 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(152): Show |
intron_variant | MODIFIER | c.327+6754A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219839 | ||||||
chr8:103219998
|
C | T | 1 | a0001c0001t0003g0042 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.327+6913C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103219998 | ||||||
chr8:103220145
|
G | A | 1 | a0001c0001t0015g0158 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.327+7060G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220145 | ||||||
chr8:103220290
|
G | A | 6 | a0001c0001t0008g0081a0001c0001t0008g0156a0001c0001t0008g0239others(3): Show | 6 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.327+7205G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220290 | ||||||
chr8:103220295
|
C | T | 1 | a0001c0001t0001g0105 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.327+7210C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220295 | ||||||
chr8:103220303
|
A | G | 1 | a0001c0001t0002g0154 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.327+7218A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220303 | ||||||
chr8:103220314
|
A | G | 2 | a0001c0001t0002g0008a0001c0001t0002g0034 | 3 | HG02109.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.327+7229A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220314 | ||||||
chr8:103220385
|
G | C | 1 | a0001c0001t0001g0109 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.327+7300G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220385 | ||||||
chr8:103220398
|
G | T | 2 | a0001c0001t0002g0246a0001c0001t0006g0077 | 2 | HG02055.hp2 HG02572.hp2 |
intron_variant | MODIFIER | c.327+7313G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220398 | ||||||
chr8:103220483
|
A | G | 2 | a0001c0001t0013g0277a0001c0001t0013g0279 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.327+7398A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220483 | ||||||
chr8:103220813
|
A | C | 3 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0003t0009g0259 | 3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.328-7176A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220813 | ||||||
chr8:103220927
|
G | C | 1 | a0002c0002t0003g0039 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.328-7062G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103220927 | ||||||
chr8:103221000
|
A | G | 20 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0001t0002g0008others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.328-6989A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221000 | ||||||
chr8:103221179
|
T | C | 1 | a0001c0001t0022g0185 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.328-6810T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221179 | ||||||
chr8:103221333
|
G | A | 6 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0033others(3): Show | 8 | HG00140.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-6656G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221333 | ||||||
chr8:103221462
|
T | A | 2 | a0001c0001t0002g0043a0001c0001t0002g0192 | 2 | HG02056.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.328-6527T>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221462 | ||||||
chr8:103221464
|
CT | C | 6 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0003t0009g0259others(3): Show | 6 | HG00639.hp1 HG01070.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.328-6513delT | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103221464 | |||||
chr8:103221570
|
A | G | 1 | a0001c0001t0001g0142 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.328-6419A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221570 | ||||||
chr8:103221588
|
C | T | 1 | a0001c0001t0004g0103 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.328-6401C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221588 | ||||||
chr8:103221731
|
ATCT | A | 6 | a0001c0001t0008g0081a0001c0001t0008g0156a0001c0001t0008g0239others(3): Show | 6 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.328-6253_328-6251d others(5): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103221731 | |||||
chr8:103221921
|
G | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0254 | 2 | HG02818.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.328-6068G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103221921 | ||||||
chr8:103222020
|
G | T | 1 | a0001c0001t0005g0234 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.328-5969G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222020 | ||||||
chr8:103222104
|
T | C | 27 | a0001c0001t0001g0135a0001c0001t0003g0028a0001c0001t0003g0029others(24): Show | 31 | HG00140.hp1 HG00323.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.328-5885T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222104 | ||||||
chr8:103222149
|
A | G | 20 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0001t0002g0008others(17): Show | 21 | HG00639.hp1 HG01070.hp2 HG02109.hp2 others(18): Show |
intron_variant | MODIFIER | c.328-5840A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222149 | ||||||
chr8:103222238
|
C | G | 31 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(28): Show | 33 | HG00280.hp2 HG00438.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.328-5751C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222238 | ||||||
chr8:103222266
|
A | G | 2 | a0001c0001t0015g0158a0001c0001t0015g0243 | 2 | HG02717.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.328-5723A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222266 | ||||||
chr8:103222284
|
A | G | 77 | a0001c0001t0001g0037a0001c0001t0001g0062a0001c0001t0001g0102others(74): Show | 84 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.328-5705A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222284 | ||||||
chr8:103222328
|
ACT | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0003t0009g0259 | 3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.328-5658_328-5657d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103222328 | |||||
chr8:103222769
|
A | G | 5 | a0001c0001t0001g0135a0001c0001t0001g0255a0001c0001t0001g0256others(2): Show | 5 | HG00438.hp2 HG00609.hp1 HG02165.hp1 others(2): Show |
intron_variant | MODIFIER | c.328-5220A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222769 | ||||||
chr8:103222999
|
G | A | 55 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(52): Show | 61 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.328-4990G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103222999 | ||||||
chr8:103223025
|
C | T | 3 | a0001c0001t0001g0152a0001c0001t0001g0244a0001c0001t0001g0245 | 3 | HG01243.hp1 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.328-4964C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223025 | ||||||
chr8:103223026
|
G | A | 1 | a0001c0003t0009g0258 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.328-4963G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223026 | ||||||
chr8:103223031
|
G | A | 1 | a0001c0001t0008g0276 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.328-4958G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223031 | ||||||
chr8:103223108
|
C | T | 1 | a0001c0001t0002g0225 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.328-4881C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223108 | ||||||
chr8:103223294
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.328-4695G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223294 | ||||||
chr8:103223305
|
A | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0050a0001c0001t0001g0051others(16): Show | 20 | HG01099.hp1 HG01123.hp2 HG01517.hp2 others(17): Show |
intron_variant | MODIFIER | c.328-4684A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223305 | ||||||
chr8:103223315
|
AAAAC | A | 26 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0036others(23): Show | 30 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.328-4662_328-4659d others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103223315 | |||||
chr8:103223542
|
G | A | 3 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0003t0009g0259 | 3 | HG00639.hp1 HG01070.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.328-4447G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223542 | ||||||
chr8:103223631
|
T | TTA | 57 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(54): Show | 63 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.328-4346_328-4345d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103223631 | |||||
chr8:103223665
|
A | C | 1 | a0002c0002t0003g0291 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.328-4324A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223665 | ||||||
chr8:103223703
|
C | T | 1 | a0001c0001t0002g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.328-4286C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223703 | ||||||
chr8:103223751
|
A | G | 6 | a0001c0001t0007g0006a0001c0001t0007g0025a0001c0001t0007g0060others(3): Show | 9 | HG00642.hp2 HG01109.hp2 HG01192.hp2 others(6): Show |
intron_variant | MODIFIER | c.328-4238A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223751 | ||||||
chr8:103223752
|
T | C | 1 | a0001c0001t0001g0075 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.328-4237T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223752 | ||||||
chr8:103223954
|
T | C | 2 | a0002c0002t0003g0073a0002c0004t0003g0001 | 5 | HG01891.hp1 HG03130.hp1 HG03516.hp2 others(2): Show |
intron_variant | MODIFIER | c.328-4035T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103223954 | ||||||
chr8:103224081
|
G | A | 2 | a0001c0001t0002g0205a0001c0001t0002g0209 | 2 | NA18980.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.328-3908G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224081 | ||||||
chr8:103224089
|
A | C | 13 | a0001c0001t0002g0008a0001c0001t0002g0034a0001c0001t0002g0074others(10): Show | 14 | HG02109.hp2 HG02280.hp2 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.328-3900A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224089 | ||||||
chr8:103224115
|
CTG | C | 93 | a0001c0001t0001g0062a0001c0001t0001g0169a0001c0001t0001g0206others(90): Show | 111 | HG00099.hp1 HG00408.hp1 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.328-3852_328-3851d others(4): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103224115 | |||||
chr8:103224115
|
CTGTG | C | 55 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(52): Show | 61 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.328-3854_328-3851d others(6): Show |
BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | INFO_REALIGN_3_PRIME | chr8 | 103224115 | |||||
chr8:103224157
|
T | C | 9 | a0001c0001t0005g0124a0001c0001t0005g0126a0001c0001t0005g0127others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.328-3832T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224157 | ||||||
chr8:103224430
|
G | T | 10 | a0001c0001t0008g0081a0001c0001t0008g0156a0001c0001t0008g0239others(7): Show | 10 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.328-3559G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224430 | ||||||
chr8:103224484
|
A | G | 2 | a0001c0001t0013g0277a0001c0001t0013g0279 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.328-3505A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224484 | ||||||
chr8:103224493
|
G | A | 1 | a0001c0001t0002g0026 | 2 | HG00544.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.328-3496G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224493 | ||||||
chr8:103224518
|
A | G | 26 | a0001c0001t0003g0028a0001c0001t0003g0029a0001c0001t0003g0036others(23): Show | 30 | HG00140.hp1 HG00323.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.328-3471A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224518 | ||||||
chr8:103224697
|
G | A | 54 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(51): Show | 60 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(57): Show |
intron_variant | MODIFIER | c.328-3292G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224697 | ||||||
chr8:103224754
|
G | T | 1 | a0001c0001t0001g0045 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.328-3235G>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224754 | ||||||
chr8:103224765
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.328-3224T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224765 | ||||||
chr8:103224866
|
A | G | 1 | a0001c0001t0001g0086 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.328-3123A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103224866 | ||||||
chr8:103225074
|
G | C | 1 | a0001c0001t0001g0129 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.328-2915G>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103225074 | ||||||
chr8:103225340
|
A | G | 1 | a0001c0001t0006g0047 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.328-2649A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103225340 | ||||||
chr8:103225434
|
A | C | 8 | a0001c0001t0008g0081a0001c0001t0008g0156a0001c0001t0008g0239others(5): Show | 8 | HG00741.hp1 HG01109.hp1 HG01358.hp2 others(5): Show |
intron_variant | MODIFIER | c.328-2555A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103225434 | ||||||
chr8:103225655
|
C | G | 18 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0010others(15): Show | 26 | HG00099.hp2 HG00741.hp2 HG01106.hp1 others(23): Show |
intron_variant | MODIFIER | c.328-2334C>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103225655 | ||||||
chr8:103225851
|
A | G | 9 | a0001c0001t0005g0124a0001c0001t0005g0126a0001c0001t0005g0127others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.328-2138A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103225851 | ||||||
chr8:103225954
|
A | G | 56 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(53): Show | 62 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.328-2035A>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103225954 | ||||||
chr8:103226249
|
A | C | 1 | a0001c0005t0023g0038 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.328-1740A>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103226249 | ||||||
chr8:103226409
|
C | T | 13 | a0001c0001t0005g0098a0001c0001t0005g0124a0001c0001t0005g0126others(10): Show | 13 | HG00099.hp1 HG01358.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.328-1580C>T | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103226409 | ||||||
chr8:103226438
|
C | A | 20 | a0001c0001t0001g0037a0001c0001t0001g0102a0001c0001t0001g0104others(17): Show | 22 | HG00280.hp2 HG00438.hp1 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.328-1551C>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103226438 | ||||||
chr8:103226519
|
T | C | 99 | a0001c0001t0001g0135a0001c0001t0002g0003a0001c0001t0002g0007others(96): Show | 118 | HG00140.hp1 HG00323.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.328-1470T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103226519 | ||||||
chr8:103226576
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.328-1413T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103226576 | ||||||
chr8:103226651
|
T | C | 6 | a0001c0001t0006g0031a0001c0001t0006g0032a0001c0001t0006g0033others(3): Show | 8 | HG00140.hp1 HG01255.hp1 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.328-1338T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103226651 | ||||||
chr8:103227050
|
T | C | 4 | a0001c0001t0002g0092a0001c0001t0002g0275a0001c0001t0002g0286others(1): Show | 4 | HG01433.hp2 HG02647.hp2 HG02735.hp1 others(1): Show |
intron_variant | MODIFIER | c.328-939T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227050 | ||||||
chr8:103227171
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.328-818G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227171 | ||||||
chr8:103227429
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.328-560T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227429 | ||||||
chr8:103227430
|
T | C | 2 | a0001c0003t0009g0257a0001c0003t0009g0258 | 2 | NA18983.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.328-559T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227430 | ||||||
chr8:103227630
|
T | G | 13 | a0001c0001t0005g0098a0001c0001t0005g0124a0001c0001t0005g0126others(10): Show | 13 | HG00099.hp1 HG01358.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.328-359T>G | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227630 | ||||||
chr8:103227785
|
T | C | 3 | a0002c0002t0003g0131a0002c0002t0003g0283a0002c0002t0003g0291 | 3 | HG02486.hp1 NA19240.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.328-204T>C | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227785 | ||||||
chr8:103227988
|
G | A | 1 | a0001c0001t0001g0212 | 1 | NA18971.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.328-1G>A | BAALC | ENSG00000164929.17 | transcript | ENST00000309982.10 | protein_coding | 2/2 | chr8 | 103227988 |