geneid | 57795 |
---|---|
ensemblid | ENSG00000198797.7 |
hgncid | 13746 |
symbol | BRINP2 |
name | BMP/retinoic acid inducible neural specific 2 |
refseq_nuc | NM_021165.4 |
refseq_prot | NP_066988.1 |
ensembl_nuc | ENST00000361539.5 |
ensembl_prot | ENSP00000354481.4 |
mane_status | MANE Select |
chr | chr1 |
start | 177170958 |
end | 177282422 |
strand | + |
ver | v1.2 |
region | chr1:177170958-177282422 |
region5000 | chr1:177165958-177287422 |
regionname0 | BRINP2_chr1_177170958_177282422 |
regionname5000 | BRINP2_chr1_177165958_177287422 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 783 | 174 | 40 | 40 | 68 | 5 | 20 | 47 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002 | 0/1 | 783 | 74 | 24 | 10 | 33 | 2 | 4 | 26 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0003 | 0/0 | 783 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0004 | 0/0 | 783 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0005 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0006 | 0/0 | 783 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2352 | 167 | 40 | 36 | 65 | 5 | 20 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
c0002 | 0/1 | 2352 | 69 | 19 | 10 | 33 | 2 | 4 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
c0003 | 0/0 | 2352 | 4 | 4 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
c0004 | 0/0 | 2352 | 3 | 0 | 2 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
c0005 | 0/0 | 2352 | 2 | 0 | 2 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
c0006 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
c0007 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
c0008 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
c0009 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
c0010 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
c0011 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
c0012 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1746 | 152 | 32 | 24 | 75 | 4 | 15 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0002 | 0/0 | 1748 | 42 | 9 | 4 | 23 | 2 | 4 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0003 | 0/0 | 1746 | 20 | 7 | 8 | 0 | 1 | 4 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0004 | 0/0 | 1746 | 14 | 10 | 4 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0005 | 0/0 | 1746 | 8 | 0 | 8 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0006 | 0/0 | 1746 | 2 | 0 | 1 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0007 | 0/0 | 1746 | 2 | 0 | 0 | 1 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0008 | 0/0 | 1746 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0009 | 0/0 | 1748 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0010 | 0/0 | 1748 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0011 | 0/0 | 1748 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0012 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0013 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0014 | 0/0 | 1748 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0015 | 0/0 | 1748 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0016 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0017 | 0/0 | 1746 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
t0018 | 0/0 | 1746 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2352 | 167 | 40 | 36 | 65 | 5 | 20 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0004 | 0/0 | 2352 | 3 | 0 | 2 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0005 | 0/0 | 2352 | 2 | 0 | 2 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0009 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0012 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0002 | 0/1 | 2352 | 69 | 19 | 10 | 33 | 2 | 4 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0003 | 0/0 | 2352 | 4 | 4 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0011 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0003c0007 | 0/0 | 2352 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0004c0008 | 0/0 | 2352 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0005c0010 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0006c0006 | 0/0 | 2352 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4097 | 120 | 23 | 17 | 61 | 3 | 15 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0001t0002 | 0/0 | 4099 | 2 | 2 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0001t0003 | 0/0 | 4097 | 20 | 7 | 8 | 0 | 1 | 4 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0001t0004 | 0/0 | 4097 | 8 | 6 | 2 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0001t0005 | 0/0 | 4097 | 8 | 0 | 8 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0001t0006 | 0/0 | 4097 | 2 | 0 | 1 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0001t0007 | 0/0 | 4097 | 2 | 0 | 0 | 1 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0001t0008 | 0/0 | 4097 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0001t0012 | 0/0 | 4097 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0001t0016 | 0/0 | 4097 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0001t0017 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0004t0001 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0004t0004 | 0/0 | 4097 | 2 | 0 | 2 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0005t0001 | 0/0 | 4097 | 2 | 0 | 2 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0009t0001 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0001c0012t0001 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0002t0001 | 0/1 | 4097 | 25 | 8 | 5 | 10 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0002t0002 | 0/0 | 4099 | 37 | 5 | 4 | 23 | 1 | 4 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0002t0004 | 0/0 | 4097 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0002t0009 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0002t0010 | 0/0 | 4099 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0002t0011 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0002t0013 | 0/0 | 4097 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0002t0014 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0002t0018 | 0/0 | 4097 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0003t0004 | 0/0 | 4097 | 3 | 3 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0003t0015 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0002c0011t0002 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0003c0007t0002 | 0/0 | 4099 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0004c0008t0001 | 0/0 | 4097 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0005c0010t0002 | 0/0 | 4099 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
a0006c0006t0001 | 0/0 | 4097 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | copy fasta | chr1 | 177165958 | 177287422 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0034 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0004 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0004g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0004g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0004g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0004g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0004g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0005g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0005g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0005g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0006g0014 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0006g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0007g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0007g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0008g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0008g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0012g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0016g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0001t0017g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0004t0004g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0004t0004g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0005t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0005t0001g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0009t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0001c0012t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0006 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0010 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0154 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0004g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0009g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0010g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0011g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0013g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0014g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0002t0018g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0003t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0003t0004g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0003t0004g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0003t0015g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0002c0011t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0003c0007t0002g0037 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0004c0008t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0005c0010t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
a0006c0006t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | GBR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00099 | hp2 | a0002 | c0002 | t0001 | g0006 | EUR | GBR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00280 | hp1 | a0001 | c0001 | t0006 | g0014 | EUR | FIN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0047 | EUR | FIN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00438 | hp1 | a0001 | c0001 | t0008 | g0041 | EAS | CHS | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00438 | hp2 | a0002 | c0002 | t0002 | g0074 | EAS | CHS | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | CHS | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | CHS | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00558 | hp1 | a0002 | c0002 | t0002 | g0122 | EAS | CHS | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0118 | EAS | CHS | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | CHS | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00609 | hp2 | a0002 | c0002 | t0001 | g0096 | EAS | CHS | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | CHS | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CHS | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00639 | hp1 | a0001 | c0001 | t0003 | g0092 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00733 | hp1 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00733 | hp2 | a0001 | c0001 | t0004 | g0090 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0089 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00741 | hp1 | a0001 | c0001 | t0005 | g0136 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG00741 | hp2 | a0002 | c0002 | t0001 | g0151 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01070 | hp2 | a0001 | c0004 | t0004 | g0228 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01071 | hp1 | a0001 | c0001 | t0005 | g0141 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01071 | hp2 | a0001 | c0004 | t0004 | g0230 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0088 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01099 | hp1 | a0001 | c0001 | t0003 | g0161 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01099 | hp2 | a0002 | c0002 | t0002 | g0066 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0036 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0159 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0021 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01175 | hp2 | a0001 | c0001 | t0004 | g0087 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01192 | hp1 | a0002 | c0002 | t0010 | g0181 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0162 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0103 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01243 | hp2 | a0001 | c0001 | t0005 | g0137 | AMR | PUR | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0015 | AMR | CLM | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | CLM | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01257 | hp2 | a0001 | c0001 | t0005 | g0113 | AMR | CLM | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | CLM | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0158 | AMR | CLM | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01346 | hp1 | a0002 | c0002 | t0002 | g0049 | AMR | CLM | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | CLM | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01358 | hp1 | a0001 | c0005 | t0001 | g0016 | AMR | CLM | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0009 | AMR | CLM | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | CLM | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01496 | hp2 | a0001 | c0001 | t0006 | g0190 | AMR | CLM | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01884 | hp2 | a0002 | c0002 | t0013 | g0023 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PEL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01934 | hp2 | a0001 | c0001 | t0005 | g0115 | AMR | PEL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01978 | hp2 | a0002 | c0002 | t0002 | g0163 | AMR | PEL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01993 | hp1 | a0001 | c0001 | t0005 | g0135 | AMR | PEL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG01993 | hp2 | a0001 | c0005 | t0001 | g0017 | AMR | PEL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02004 | hp1 | a0002 | c0002 | t0001 | g0120 | AMR | PEL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02055 | hp1 | a0002 | c0002 | t0014 | g0020 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0238 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02071 | hp2 | a0002 | c0002 | t0002 | g0082 | EAS | KHV | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | KHV | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | KHV | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02132 | hp2 | a0001 | c0012 | t0001 | g0084 | EAS | KHV | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02135 | hp2 | a0002 | c0002 | t0002 | g0146 | EAS | KHV | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PEL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02148 | hp2 | a0002 | c0002 | t0002 | g0126 | AMR | PEL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02165 | hp1 | a0002 | c0002 | t0002 | g0209 | EAS | CDX | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | CDX | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02257 | hp2 | a0002 | c0002 | t0002 | g0147 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0167 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02258 | hp2 | a0001 | c0001 | t0004 | g0086 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02300 | hp2 | a0001 | c0001 | t0005 | g0114 | AMR | PEL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02523 | hp1 | a0002 | c0002 | t0002 | g0075 | EAS | KHV | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | KHV | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02615 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02630 | hp1 | a0002 | c0002 | t0002 | g0233 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0220 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0165 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02723 | hp1 | a0002 | c0003 | t0015 | g0176 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0218 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0091 | SAS | PJL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0203 | SAS | PJL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02738 | hp2 | a0001 | c0001 | t0007 | g0019 | SAS | PJL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02809 | hp1 | a0002 | c0002 | t0011 | g0054 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02818 | hp1 | a0001 | c0001 | t0003 | g0217 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02886 | hp1 | a0002 | c0002 | t0009 | g0180 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02895 | hp1 | a0002 | c0003 | t0004 | g0018 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02895 | hp2 | a0001 | c0001 | t0004 | g0173 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02897 | hp2 | a0001 | c0001 | t0004 | g0174 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02922 | hp1 | a0002 | c0002 | t0002 | g0213 | AFR | ESN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0065 | AFR | ESN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | ESN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | ESN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02970 | hp1 | a0002 | c0002 | t0018 | g0179 | AFR | ESN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | ESN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03041 | hp1 | a0006 | c0006 | t0001 | g0234 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0170 | AFR | GWD | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0071 | AFR | MSL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03098 | hp2 | a0002 | c0011 | t0002 | g0232 | AFR | MSL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0240 | AFR | ESN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0200 | AFR | ESN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03139 | hp2 | a0005 | c0010 | t0002 | g0212 | AFR | ESN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03225 | hp1 | a0002 | c0003 | t0004 | g0169 | AFR | MSL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03225 | hp2 | a0002 | c0002 | t0002 | g0155 | AFR | MSL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0216 | AFR | MSL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03486 | hp2 | a0001 | c0001 | t0016 | g0182 | AFR | MSL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0085 | SAS | PJL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0004 | SAS | PJL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | ESN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0072 | AFR | ESN | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03579 | hp1 | a0002 | c0002 | t0002 | g0227 | AFR | MSL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0033 | AFR | MSL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03831 | hp2 | a0002 | c0002 | t0002 | g0148 | SAS | BEB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0045 | SAS | BEB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | BEB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0025 | SAS | STU | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | STU | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0097 | SAS | BEB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG04184 | hp2 | a0002 | c0002 | t0002 | g0116 | SAS | BEB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG04199 | hp1 | a0002 | c0002 | t0002 | g0156 | SAS | STU | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG04199 | hp2 | a0001 | c0001 | t0003 | g0093 | SAS | STU | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0060 | SAS | STU | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0208 | SAS | STU | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | YRI | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18522 | hp2 | a0002 | c0002 | t0004 | g0241 | AFR | YRI | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0121 | EAS | CHB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18906 | hp1 | a0002 | c0002 | t0001 | g0164 | AFR | YRI | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0177 | AFR | YRI | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18940 | hp1 | a0002 | c0002 | t0002 | g0111 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18941 | hp1 | a0002 | c0002 | t0002 | g0152 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18942 | hp2 | a0004 | c0008 | t0001 | g0131 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0222 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18949 | hp1 | a0002 | c0002 | t0002 | g0051 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18952 | hp1 | a0002 | c0002 | t0001 | g0225 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18960 | hp1 | a0001 | c0001 | t0007 | g0142 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18960 | hp2 | a0002 | c0002 | t0001 | g0053 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18961 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0027 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18970 | hp1 | a0002 | c0002 | t0002 | g0063 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18972 | hp1 | a0001 | c0009 | t0001 | g0026 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18973 | hp1 | a0002 | c0002 | t0002 | g0083 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18974 | hp1 | a0002 | c0002 | t0002 | g0062 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18989 | hp2 | a0001 | c0001 | t0008 | g0076 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18995 | hp2 | a0002 | c0002 | t0002 | g0112 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19001 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19005 | hp1 | a0001 | c0001 | t0017 | g0196 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19005 | hp2 | a0002 | c0002 | t0002 | g0138 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19009 | hp2 | a0002 | c0002 | t0001 | g0008 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19011 | hp2 | a0002 | c0002 | t0001 | g0224 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19030 | hp1 | a0002 | c0003 | t0004 | g0231 | AFR | LWK | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19030 | hp2 | a0001 | c0001 | t0012 | g0024 | AFR | LWK | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19055 | hp2 | a0002 | c0002 | t0002 | g0039 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19056 | hp1 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19065 | hp1 | a0002 | c0002 | t0002 | g0035 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19068 | hp2 | a0002 | c0002 | t0002 | g0007 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19075 | hp1 | a0002 | c0002 | t0001 | g0127 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19075 | hp2 | a0001 | c0004 | t0001 | g0029 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0059 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19087 | hp2 | a0002 | c0002 | t0002 | g0081 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19090 | hp1 | a0002 | c0002 | t0002 | g0028 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0068 | AFR | ASW | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA20129 | hp2 | a0002 | c0002 | t0001 | g0168 | AFR | ASW | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0046 | EUR | TSI | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA20752 | hp2 | a0003 | c0007 | t0002 | g0037 | EUR | TSI | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0061 | EUR | TSI | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA20805 | hp2 | a0001 | c0001 | t0003 | g0004 | EUR | TSI | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02109 | hp1 | a0002 | c0002 | t0001 | g0010 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0178 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0215 | AFR | ACB | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG06807 | hp1 | a0002 | c0002 | t0001 | g0187 | AFR | USA | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0119 | AFR | USA | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | JPT | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | LWK | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0154 | REF | REF | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0034 | REF | REF | BRINP2_chr1_177165958_177287422 | BRINP2 | chr1 | 177165958 | 177287422 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:177257367
|
G | A | 1 | a0006 | 1 | HG03041.hp1 | missense_variant | MODERATE | c.652G>A | p.Ala218Thr | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/8 | 1503/4097 | 652/2352 | 218/783 | chr1 | 177257367 | ||
chr1:177276417
|
G | A | 1 | a0003 | 1 | NA20752.hp2 | missense_variant | MODERATE | c.995G>A | p.Arg332Gln | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/8 | 1846/4097 | 995/2352 | 332/783 | chr1 | 177276417 | ||
chr1:177278718
|
C | G | 3 | a0002a0003a0005 | 76 | HG00099.hp2 HG00438.hp2 HG00558.hp1 others(73): Show |
missense_variant | MODERATE | c.1168C>G | p.Leu390Val | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 7/8 | 2019/4097 | 1168/2352 | 390/783 | chr1 | 177278718 | ||
chr1:177280944
|
G | A | 1 | a0005 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1768G>A | p.Val590Ile | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 8/8 | 2619/4097 | 1768/2352 | 590/783 | chr1 | 177280944 | ||
chr1:177281394
|
C | A | 1 | a0004 | 1 | NA18942.hp2 | missense_variant | MODERATE | c.2218C>A | p.Leu740Ile | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 8/8 | 3069/4097 | 2218/2352 | 740/783 | chr1 | 177281394 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:177230056
|
A | G | 1 | a0001c0012 | 1 | HG02132.hp2 | synonymous_variant | LOW | c.180A>G | p.Thr60Thr | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/8 | 1031/4097 | 180/2352 | 60/783 | chr1 | 177230056 | ||
chr1:177273493
|
C | T | 2 | a0001c0004a0002c0003 | 7 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(4): Show |
synonymous_variant | LOW | c.675C>T | p.Thr225Thr | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/8 | 1526/4097 | 675/2352 | 225/783 | chr1 | 177273493 | ||
chr1:177276259
|
C | T | 1 | a0001c0005 | 2 | HG01358.hp1 HG01993.hp2 |
synonymous_variant | LOW | c.837C>T | p.Tyr279Tyr | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/8 | 1688/4097 | 837/2352 | 279/783 | chr1 | 177276259 | ||
chr1:177276286
|
C | T | 1 | a0002c0011 | 1 | HG03098.hp2 | synonymous_variant | LOW | c.864C>T | p.Leu288Leu | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/8 | 1715/4097 | 864/2352 | 288/783 | chr1 | 177276286 | ||
chr1:177278771
|
C | T | 1 | a0001c0009 | 1 | NA18972.hp1 | synonymous_variant | LOW | c.1221C>T | p.Arg407Arg | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 7/8 | 2072/4097 | 1221/2352 | 407/783 | chr1 | 177278771 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:177171092
|
G | A | 2 | a0002c0002t0009a0002c0002t0010 | 2 | HG01192.hp1 HG02886.hp1 |
5_prime_UTR_variant | MODIFIER | c.-717G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/8 | 58785 | chr1 | 177171092 | |||||
chr1:177171292
|
C | G | 1 | a0001c0001t0005 | 8 | HG00741.hp1 HG01071.hp1 HG01243.hp2 others(5): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-517C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/8 | chr1 | 177171292 | ||||||
chr1:177171312
|
C | A | 1 | a0002c0002t0011 | 1 | HG02809.hp1 | 5_prime_UTR_variant | MODIFIER | c.-497C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/8 | 58565 | chr1 | 177171312 | |||||
chr1:177171425
|
C | A | 2 | a0001c0001t0012a0002c0002t0013 | 2 | HG01884.hp2 NA19030.hp2 |
5_prime_UTR_variant | MODIFIER | c.-384C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/8 | 58452 | chr1 | 177171425 | |||||
chr1:177171531
|
G | C | 1 | a0002c0002t0014 | 1 | HG02055.hp1 | 5_prime_UTR_variant | MODIFIER | c.-278G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/8 | 58346 | chr1 | 177171531 | |||||
chr1:177229829
|
C | T | 1 | a0002c0002t0018 | 1 | HG02970.hp1 | 5_prime_UTR_variant | MODIFIER | c.-48C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/8 | 48 | chr1 | 177229829 | |||||
chr1:177229862
|
T | C | 9 | a0001c0001t0003a0001c0001t0004a0001c0001t0012others(6): Show | 38 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-15T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/8 | 15 | chr1 | 177229862 | |||||
chr1:177281534
|
G | A | 2 | a0001c0001t0003a0001c0001t0006 | 22 | HG00280.hp1 HG00639.hp1 HG00738.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*6G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 8/8 | 6 | chr1 | 177281534 | |||||
chr1:177281552
|
G | A | 1 | a0001c0001t0016 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*24G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 8/8 | 24 | chr1 | 177281552 | |||||
chr1:177281719
|
T | TAC | 10 | a0001c0001t0002a0002c0002t0002a0002c0002t0009others(7): Show | 47 | HG00438.hp2 HG00558.hp1 HG01099.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*210_*211dupAC | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 8/8 | 212 | INFO_REALIGN_3_PRIME | chr1 | 177281719 | ||||
chr1:177282129
|
C | G | 1 | a0001c0001t0007 | 2 | HG02738.hp2 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*601C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 8/8 | 601 | chr1 | 177282129 | |||||
chr1:177282129
|
C | T | 1 | a0001c0001t0008 | 2 | HG00438.hp1 NA18989.hp2 |
3_prime_UTR_variant | MODIFIER | c.*601C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 8/8 | 601 | chr1 | 177282129 | |||||
chr1:177282130
|
T | G | 1 | a0001c0001t0007 | 2 | HG02738.hp2 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*602T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 8/8 | 602 | chr1 | 177282130 | |||||
chr1:177282312
|
T | A | 1 | a0001c0001t0017 | 1 | NA19005.hp1 | 3_prime_UTR_variant | MODIFIER | c.*784T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 8/8 | 784 | chr1 | 177282312 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:177171913
|
T | A | 1 | a0001c0001t0001g0011 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-77+181T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177171913 | ||||||
chr1:177172095
|
T | C | 7 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0003g0015others(4): Show | 7 | HG00280.hp1 HG01175.hp1 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.-77+363T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177172095 | ||||||
chr1:177172247
|
C | T | 1 | a0002c0002t0004g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-77+515C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177172247 | ||||||
chr1:177172408
|
T | C | 1 | a0001c0001t0007g0019 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-77+676T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177172408 | ||||||
chr1:177172553
|
T | A | 1 | a0002c0002t0014g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-77+821T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177172553 | ||||||
chr1:177172867
|
T | C | 1 | a0002c0002t0014g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-77+1135T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177172867 | ||||||
chr1:177172970
|
C | T | 61 | a0001c0001t0001g0011a0001c0001t0001g0183a0001c0001t0001g0184others(58): Show | 62 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.-77+1238C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177172970 | ||||||
chr1:177172975
|
A | G | 2 | a0002c0002t0009g0180a0002c0002t0010g0181 | 2 | HG01192.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-77+1243A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177172975 | ||||||
chr1:177173000
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-77+1268T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177173000 | ||||||
chr1:177173647
|
C | G | 65 | a0001c0001t0001g0011a0001c0001t0001g0177a0001c0001t0001g0178others(62): Show | 66 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-77+1915C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177173647 | ||||||
chr1:177174059
|
C | T | 10 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0175others(7): Show | 10 | HG00280.hp1 HG01175.hp1 HG01255.hp1 others(7): Show |
intron_variant | MODIFIER | c.-77+2327C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177174059 | ||||||
chr1:177174454
|
G | A | 62 | a0001c0001t0001g0011a0001c0001t0001g0183a0001c0001t0001g0184others(59): Show | 63 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-77+2722G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177174454 | ||||||
chr1:177174616
|
T | C | 1 | a0001c0001t0016g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-77+2884T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177174616 | ||||||
chr1:177174671
|
C | T | 9 | a0001c0001t0001g0166a0001c0001t0001g0171a0001c0001t0001g0172others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77+2939C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177174671 | ||||||
chr1:177174676
|
C | T | 2 | a0002c0002t0001g0162a0002c0002t0002g0163 | 2 | HG01192.hp2 HG01978.hp2 |
intron_variant | MODIFIER | c.-77+2944C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177174676 | ||||||
chr1:177174977
|
G | T | 4 | a0001c0001t0001g0160a0001c0001t0003g0159a0001c0001t0003g0161others(1): Show | 4 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77+3245G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177174977 | ||||||
chr1:177175020
|
A | C | 56 | a0001c0001t0001g0009a0001c0001t0001g0108a0001c0001t0001g0109others(53): Show | 59 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(56): Show |
intron_variant | MODIFIER | c.-77+3288A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177175020 | ||||||
chr1:177175037
|
A | C | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-77+3305A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177175037 | ||||||
chr1:177175038
|
A | G | 1 | a0001c0001t0001g0240 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-77+3306A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177175038 | ||||||
chr1:177175075
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-77+3343A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177175075 | ||||||
chr1:177175290
|
T | TG | 67 | a0001c0001t0001g0104a0001c0001t0001g0105a0001c0001t0001g0177others(64): Show | 68 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.-77+3566dupG | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177175290 | |||||
chr1:177175291
|
G | A | 2 | a0002c0002t0009g0180a0002c0002t0010g0181 | 2 | HG01192.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-77+3559G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177175291 | ||||||
chr1:177175310
|
G | A | 1 | a0001c0001t0001g0022 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-77+3578G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177175310 | ||||||
chr1:177175577
|
C | T | 1 | a0001c0001t0001g0239 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-77+3845C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177175577 | ||||||
chr1:177175686
|
C | T | 1 | a0001c0001t0003g0238 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-77+3954C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177175686 | ||||||
chr1:177175906
|
T | C | 93 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(90): Show | 94 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(91): Show |
intron_variant | MODIFIER | c.-77+4174T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177175906 | ||||||
chr1:177176004
|
T | C | 65 | a0001c0001t0001g0011a0001c0001t0001g0177a0001c0001t0001g0178others(62): Show | 66 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-77+4272T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177176004 | ||||||
chr1:177176142
|
T | A | 2 | a0002c0002t0009g0180a0002c0002t0010g0181 | 2 | HG01192.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.-77+4410T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177176142 | ||||||
chr1:177176280
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-77+4548C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177176280 | ||||||
chr1:177176303
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-77+4571G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177176303 | ||||||
chr1:177176347
|
G | T | 2 | a0001c0001t0001g0235a0001c0001t0001g0236 | 2 | HG02965.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.-77+4615G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177176347 | ||||||
chr1:177176405
|
T | A | 1 | a0002c0002t0004g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-77+4673T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177176405 | ||||||
chr1:177176407
|
C | T | 1 | a0002c0002t0004g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-77+4675C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177176407 | ||||||
chr1:177176512
|
C | CATT | 22 | a0001c0001t0001g0012a0001c0001t0001g0022a0001c0001t0001g0025others(19): Show | 22 | HG00558.hp2 HG01257.hp2 HG01884.hp1 others(19): Show |
intron_variant | MODIFIER | c.-77+4820_-77+4822d others(5): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177176512 | |||||
chr1:177176512
|
CATT | C | 35 | a0001c0001t0001g0005a0001c0001t0001g0013a0001c0001t0001g0021others(32): Show | 37 | HG00099.hp1 HG00280.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.-77+4820_-77+4822d others(5): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177176512 | |||||
chr1:177176512
|
CATTATT | C | 11 | a0001c0001t0001g0160a0001c0001t0001g0175a0001c0001t0001g0177others(8): Show | 11 | HG00408.hp2 HG01099.hp1 HG01106.hp2 others(8): Show |
intron_variant | MODIFIER | c.-77+4817_-77+4822d others(8): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177176512 | |||||
chr1:177176512
|
CATTATTA others(2): Show |
C | 14 | a0001c0001t0001g0103a0001c0001t0001g0166a0001c0001t0001g0171others(11): Show | 14 | HG01243.hp1 HG01358.hp1 HG01993.hp2 others(11): Show |
intron_variant | MODIFIER | c.-77+4814_-77+4822d others(11): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177176512 | |||||
chr1:177176512
|
CATTATTA others(5): Show |
C | 58 | a0001c0001t0001g0011a0001c0001t0001g0183a0001c0001t0001g0186others(55): Show | 59 | HG00544.hp1 HG00544.hp2 HG00609.hp1 others(56): Show |
intron_variant | MODIFIER | c.-77+4811_-77+4822d others(14): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177176512 | |||||
chr1:177176512
|
CATTATTA others(8): Show |
C | 1 | a0006c0006t0001g0234 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-77+4808_-77+4822d others(17): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177176512 | |||||
chr1:177176639
|
T | C | 65 | a0001c0001t0001g0011a0001c0001t0001g0177a0001c0001t0001g0178others(62): Show | 66 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-77+4907T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177176639 | ||||||
chr1:177176644
|
T | C | 1 | a0001c0001t0001g0185 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-77+4912T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177176644 | ||||||
chr1:177176669
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-77+4937G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177176669 | ||||||
chr1:177176732
|
G | A | 8 | a0001c0001t0001g0166a0001c0001t0001g0171a0002c0002t0001g0164others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77+5000G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177176732 | ||||||
chr1:177176766
|
G | GA | 62 | a0001c0001t0001g0011a0001c0001t0001g0183a0001c0001t0001g0184others(59): Show | 63 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-77+5036dupA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177176766 | |||||
chr1:177176821
|
A | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.-77+5089A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177176821 | ||||||
chr1:177177134
|
A | C | 1 | a0001c0001t0001g0150 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.-77+5402A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177177134 | ||||||
chr1:177177281
|
AAAAC | A | 13 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0077others(10): Show | 13 | HG00408.hp1 HG00438.hp2 HG00621.hp2 others(10): Show |
intron_variant | MODIFIER | c.-77+5564_-77+5567d others(6): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177177281 | |||||
chr1:177177294
|
AAAC | A | 3 | a0002c0002t0001g0006a0002c0002t0001g0120a0002c0002t0001g0151 | 4 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+5589_-77+5591d others(5): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177177294 | |||||
chr1:177177294
|
AAACAACA others(5): Show |
A | 1 | a0002c0003t0004g0018 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.-77+5580_-77+5591d others(14): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177177294 | |||||
chr1:177177327
|
T | A | 1 | a0002c0002t0002g0035 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.-77+5595T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177177327 | ||||||
chr1:177177374
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.-77+5642A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177177374 | ||||||
chr1:177177650
|
A | ACTACT | 65 | a0001c0001t0001g0011a0001c0001t0001g0177a0001c0001t0001g0178others(62): Show | 66 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-77+5924_-77+5928d others(7): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177177650 | |||||
chr1:177177730
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-77+5998T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177177730 | ||||||
chr1:177177736
|
T | C | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-77+6004T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177177736 | ||||||
chr1:177177772
|
G | T | 81 | a0001c0001t0001g0011a0001c0001t0001g0160a0001c0001t0001g0166others(78): Show | 82 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.-77+6040G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177177772 | ||||||
chr1:177177797
|
A | G | 65 | a0001c0001t0001g0011a0001c0001t0001g0177a0001c0001t0001g0178others(62): Show | 66 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-77+6065A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177177797 | ||||||
chr1:177177821
|
G | A | 1 | a0003c0007t0002g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-77+6089G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177177821 | ||||||
chr1:177177823
|
C | T | 62 | a0001c0001t0001g0011a0001c0001t0001g0183a0001c0001t0001g0184others(59): Show | 63 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-77+6091C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177177823 | ||||||
chr1:177177826
|
A | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0018g0179 | 3 | HG02486.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-77+6094A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177177826 | ||||||
chr1:177178025
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0149 | 2 | HG02735.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.-77+6293C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177178025 | ||||||
chr1:177178034
|
T | C | 1 | a0002c0002t0004g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-77+6302T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177178034 | ||||||
chr1:177178385
|
C | T | 4 | a0001c0001t0001g0071a0001c0001t0003g0072a0001c0001t0004g0069others(1): Show | 4 | HG02451.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77+6653C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177178385 | ||||||
chr1:177178532
|
T | C | 65 | a0001c0001t0001g0011a0001c0001t0001g0177a0001c0001t0001g0178others(62): Show | 66 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(63): Show |
intron_variant | MODIFIER | c.-77+6800T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177178532 | ||||||
chr1:177178642
|
C | A | 1 | a0001c0012t0001g0084 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-77+6910C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177178642 | ||||||
chr1:177178829
|
G | T | 9 | a0001c0001t0001g0166a0001c0001t0001g0171a0001c0001t0001g0172others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77+7097G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177178829 | ||||||
chr1:177178863
|
G | A | 62 | a0001c0001t0001g0011a0001c0001t0001g0183a0001c0001t0001g0184others(59): Show | 63 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-77+7131G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177178863 | ||||||
chr1:177178931
|
T | C | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-77+7199T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177178931 | ||||||
chr1:177179023
|
C | A | 91 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(88): Show | 92 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.-77+7291C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177179023 | ||||||
chr1:177179126
|
CT | C | 14 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110others(11): Show | 14 | HG00558.hp1 HG02071.hp1 HG02080.hp1 others(11): Show |
intron_variant | MODIFIER | c.-77+7397delT | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177179126 | |||||
chr1:177179229
|
TG | T | 62 | a0001c0001t0001g0011a0001c0001t0001g0183a0001c0001t0001g0184others(59): Show | 63 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-77+7498delG | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177179229 | ||||||
chr1:177179237
|
C | T | 2 | a0001c0001t0012g0024a0002c0002t0013g0023 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-77+7505C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177179237 | ||||||
chr1:177179293
|
A | G | 7 | a0001c0001t0001g0229a0001c0004t0004g0228a0001c0004t0004g0230others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.-77+7561A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177179293 | ||||||
chr1:177179567
|
G | GCACACAC others(13): Show |
4 | a0001c0001t0001g0160a0001c0001t0003g0159a0001c0001t0003g0161others(1): Show | 4 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77+7867_-77+7886d others(22): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177179567 | |||||
chr1:177179609
|
A | T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-77+7877A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177179609 | ||||||
chr1:177179755
|
A | G | 3 | a0001c0001t0001g0226a0002c0002t0001g0224a0002c0002t0001g0225 | 3 | NA18952.hp1 NA18988.hp2 NA19011.hp2 |
intron_variant | MODIFIER | c.-77+8023A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177179755 | ||||||
chr1:177179772
|
G | T | 1 | a0001c0001t0016g0182 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-77+8040G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177179772 | ||||||
chr1:177179823
|
G | A | 62 | a0001c0001t0001g0011a0001c0001t0001g0183a0001c0001t0001g0184others(59): Show | 63 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(60): Show |
intron_variant | MODIFIER | c.-77+8091G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177179823 | ||||||
chr1:177179828
|
G | A | 1 | a0002c0002t0002g0074 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-77+8096G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177179828 | ||||||
chr1:177180417
|
C | G | 3 | a0001c0001t0001g0030a0001c0001t0001g0067a0001c0001t0001g0102 | 3 | HG01074.hp1 HG01884.hp1 HG02109.hp2 |
intron_variant | MODIFIER | c.-77+8685C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177180417 | ||||||
chr1:177180470
|
A | G | 1 | a0001c0001t0001g0032 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.-77+8738A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177180470 | ||||||
chr1:177180503
|
T | G | 1 | a0002c0002t0004g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-77+8771T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177180503 | ||||||
chr1:177180508
|
C | T | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0003g0015others(3): Show | 6 | HG00280.hp1 HG01175.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-77+8776C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177180508 | ||||||
chr1:177180740
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-77+9008C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177180740 | ||||||
chr1:177180812
|
A | G | 3 | a0001c0001t0001g0221a0001c0001t0001g0223a0002c0002t0002g0222 | 3 | HG00544.hp2 NA18946.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-77+9080A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177180812 | ||||||
chr1:177180895
|
G | C | 2 | a0001c0001t0001g0013a0001c0001t0006g0014 | 2 | HG00280.hp1 HG01175.hp1 |
intron_variant | MODIFIER | c.-77+9163G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177180895 | ||||||
chr1:177181066
|
C | A | 4 | a0001c0001t0001g0160a0001c0001t0003g0159a0001c0001t0003g0161others(1): Show | 4 | HG01099.hp1 HG01106.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77+9334C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177181066 | ||||||
chr1:177181289
|
A | AT | 21 | a0001c0001t0001g0001a0001c0001t0001g0022a0001c0001t0001g0033others(18): Show | 22 | HG01099.hp2 HG01192.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.-77+9565dupT | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177181289 | |||||
chr1:177181301
|
C | T | 8 | a0001c0001t0001g0166a0001c0001t0001g0171a0002c0002t0001g0164others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77+9569C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177181301 | ||||||
chr1:177181608
|
G | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0018g0179 | 3 | HG02486.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-77+9876G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177181608 | ||||||
chr1:177181611
|
G | A | 3 | a0001c0001t0001g0186a0002c0002t0001g0187a0006c0006t0001g0234 | 3 | HG02451.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-77+9879G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177181611 | ||||||
chr1:177181657
|
G | A | 4 | a0001c0001t0004g0173a0001c0001t0004g0174a0002c0002t0018g0179others(1): Show | 4 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+9925G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177181657 | ||||||
chr1:177181674
|
C | T | 9 | a0001c0001t0001g0166a0001c0001t0001g0171a0001c0001t0001g0220others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77+9942C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177181674 | ||||||
chr1:177181713
|
G | C | 1 | a0001c0001t0001g0235 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-77+9981G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177181713 | ||||||
chr1:177181733
|
G | A | 41 | a0001c0001t0001g0011a0001c0001t0001g0132a0001c0001t0001g0184others(38): Show | 41 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.-77+10001G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177181733 | ||||||
chr1:177181735
|
G | C | 4 | a0001c0001t0001g0175a0001c0001t0004g0173a0001c0001t0004g0174others(1): Show | 4 | HG02630.hp2 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+10003G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177181735 | ||||||
chr1:177181778
|
C | T | 1 | a0002c0002t0002g0060 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-77+10046C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177181778 | ||||||
chr1:177181958
|
C | T | 2 | a0001c0001t0012g0024a0002c0002t0013g0023 | 2 | HG01884.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.-77+10226C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177181958 | ||||||
chr1:177182090
|
A | G | 57 | a0001c0001t0001g0011a0001c0001t0001g0129a0001c0001t0001g0130others(54): Show | 57 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.-77+10358A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177182090 | ||||||
chr1:177182111
|
C | CCCTCCCT others(16): Show |
1 | a0001c0001t0001g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-77+10410_-77+1043 others(27): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177182111 | |||||
chr1:177182427
|
G | A | 1 | a0001c0001t0001g0189 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-77+10695G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177182427 | ||||||
chr1:177182585
|
C | A | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0018g0179 | 3 | HG02486.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-77+10853C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177182585 | ||||||
chr1:177183137
|
C | CT | 14 | a0001c0001t0001g0032a0001c0001t0001g0104a0001c0001t0001g0157others(11): Show | 14 | HG01934.hp1 HG02055.hp2 HG02257.hp2 others(11): Show |
intron_variant | MODIFIER | c.-77+11430dupT | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177183137 | |||||
chr1:177183137
|
C | CTT | 10 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0160others(7): Show | 10 | HG00280.hp1 HG01099.hp1 HG01192.hp1 others(7): Show |
intron_variant | MODIFIER | c.-77+11429_-77+1143 others(6): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177183137 | |||||
chr1:177183137
|
CT | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0038a0001c0001t0001g0119others(14): Show | 18 | HG00558.hp1 HG01070.hp2 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.-77+11430delT | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177183137 | |||||
chr1:177183145
|
T | C | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0018g0179 | 3 | HG02486.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-77+11413T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177183145 | ||||||
chr1:177183155
|
T | C | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0018g0179 | 3 | HG02486.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-77+11423T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177183155 | ||||||
chr1:177183224
|
A | G | 35 | a0001c0001t0001g0011a0001c0001t0001g0129a0001c0001t0001g0130others(32): Show | 35 | HG00408.hp2 HG00544.hp1 HG02055.hp2 others(32): Show |
intron_variant | MODIFIER | c.-77+11492A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177183224 | ||||||
chr1:177183712
|
G | A | 1 | a0002c0002t0002g0075 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-77+11980G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177183712 | ||||||
chr1:177183733
|
T | C | 1 | a0002c0002t0010g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-77+12001T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177183733 | ||||||
chr1:177183828
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-77+12096C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177183828 | ||||||
chr1:177183883
|
C | T | 3 | a0001c0001t0001g0118a0001c0001t0001g0157a0002c0002t0002g0146 | 3 | HG00558.hp2 HG02135.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.-77+12151C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177183883 | ||||||
chr1:177183900
|
G | T | 4 | a0001c0001t0001g0189a0001c0001t0001g0207a0001c0001t0001g0208others(1): Show | 4 | HG02165.hp1 HG04228.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+12168G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177183900 | ||||||
chr1:177183969
|
A | G | 1 | a0002c0002t0002g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-77+12237A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177183969 | ||||||
chr1:177183982
|
G | A | 70 | a0001c0001t0001g0011a0001c0001t0001g0129a0001c0001t0001g0130others(67): Show | 70 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.-77+12250G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177183982 | ||||||
chr1:177184344
|
C | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0003g0015others(5): Show | 8 | HG00280.hp1 HG01175.hp1 HG01255.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77+12612C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177184344 | ||||||
chr1:177184570
|
G | A | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-77+12838G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177184570 | ||||||
chr1:177184572
|
G | A | 1 | a0002c0002t0014g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-77+12840G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177184572 | ||||||
chr1:177184608
|
T | C | 1 | a0001c0001t0005g0135 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-77+12876T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177184608 | ||||||
chr1:177184641
|
G | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0003g0015others(3): Show | 6 | HG00280.hp1 HG01175.hp1 HG01255.hp1 others(3): Show |
intron_variant | MODIFIER | c.-77+12909G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177184641 | ||||||
chr1:177184645
|
CTT | C | 61 | a0001c0001t0001g0011a0001c0001t0001g0129a0001c0001t0001g0130others(58): Show | 61 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.-77+12924_-77+1292 others(6): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177184645 | |||||
chr1:177184725
|
T | TAAAAATA others(311): Show |
1 | a0001c0001t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-77+13008_-77+1300 others(322): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177184725 | |||||
chr1:177184821
|
T | C | 8 | a0001c0001t0001g0166a0001c0001t0001g0171a0002c0002t0001g0164others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77+13089T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177184821 | ||||||
chr1:177184895
|
G | A | 57 | a0001c0001t0001g0011a0001c0001t0001g0129a0001c0001t0001g0130others(54): Show | 57 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(54): Show |
intron_variant | MODIFIER | c.-77+13163G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177184895 | ||||||
chr1:177184995
|
G | A | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-77+13263G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177184995 | ||||||
chr1:177185037
|
C | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0018g0179 | 3 | HG02486.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-77+13305C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177185037 | ||||||
chr1:177185038
|
G | A | 16 | a0001c0001t0001g0012a0001c0001t0001g0013a0001c0001t0001g0166others(13): Show | 16 | HG00280.hp1 HG01175.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.-77+13306G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177185038 | ||||||
chr1:177185111
|
G | A | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-77+13379G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177185111 | ||||||
chr1:177185246
|
G | T | 2 | a0001c0001t0001g0206a0002c0002t0002g0205 | 2 | NA19056.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.-77+13514G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177185246 | ||||||
chr1:177185502
|
A | G | 8 | a0001c0001t0001g0056a0001c0001t0001g0057a0001c0001t0001g0058others(5): Show | 8 | NA18940.hp2 NA18946.hp2 NA18957.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77+13770A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177185502 | ||||||
chr1:177185918
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0003g0159a0001c0001t0003g0161 | 3 | HG01099.hp1 HG01106.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-77+14186G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177185918 | ||||||
chr1:177186401
|
C | T | 82 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0105others(79): Show | 82 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.-77+14669C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177186401 | ||||||
chr1:177186608
|
G | C | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-77+14876G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177186608 | ||||||
chr1:177186781
|
G | A | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-77+15049G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177186781 | ||||||
chr1:177186975
|
A | C | 1 | a0001c0001t0001g0055 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-77+15243A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177186975 | ||||||
chr1:177186992
|
A | T | 1 | a0001c0001t0001g0193 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-77+15260A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177186992 | ||||||
chr1:177187160
|
C | T | 4 | a0001c0001t0003g0215a0001c0001t0003g0216a0001c0001t0003g0217others(1): Show | 4 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.-77+15428C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177187160 | ||||||
chr1:177187202
|
A | G | 7 | a0001c0001t0001g0160a0001c0001t0003g0159a0001c0001t0003g0161others(4): Show | 7 | HG01099.hp1 HG01106.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.-77+15470A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177187202 | ||||||
chr1:177187206
|
G | C | 1 | a0001c0001t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-77+15474G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177187206 | ||||||
chr1:177187218
|
A | G | 11 | a0001c0001t0001g0160a0001c0001t0001g0172a0001c0001t0001g0177others(8): Show | 11 | HG01099.hp1 HG01106.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.-77+15486A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177187218 | ||||||
chr1:177187221
|
A | G | 89 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0030others(86): Show | 89 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.-77+15489A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177187221 | ||||||
chr1:177187228
|
GC | G | 85 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0030others(82): Show | 85 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.-77+15502delC | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177187228 | |||||
chr1:177187234
|
C | T | 60 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0030others(57): Show | 60 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.-77+15502C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177187234 | ||||||
chr1:177187253
|
A | C | 9 | a0001c0001t0001g0172a0001c0001t0001g0177a0001c0001t0001g0178others(6): Show | 9 | HG01358.hp1 HG01884.hp2 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77+15521A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177187253 | ||||||
chr1:177187279
|
T | C | 1 | a0002c0002t0004g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-77+15547T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177187279 | ||||||
chr1:177187391
|
C | T | 58 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0067others(55): Show | 58 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.-77+15659C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177187391 | ||||||
chr1:177187422
|
A | T | 8 | a0001c0001t0001g0166a0001c0001t0001g0171a0002c0002t0001g0164others(5): Show | 8 | HG02257.hp1 HG02258.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-77+15690A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177187422 | ||||||
chr1:177187679
|
G | A | 22 | a0001c0001t0001g0160a0001c0001t0003g0004a0001c0001t0003g0015others(19): Show | 24 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.-77+15947G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177187679 | ||||||
chr1:177187866
|
G | A | 1 | a0002c0002t0014g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-77+16134G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177187866 | ||||||
chr1:177188039
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-77+16307G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177188039 | ||||||
chr1:177188124
|
GTTA | G | 49 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0067others(46): Show | 49 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.-77+16398_-77+1640 others(7): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177188124 | |||||
chr1:177188380
|
A | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(100): Show | 106 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-77+16648A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177188380 | ||||||
chr1:177188389
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-77+16657A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177188389 | ||||||
chr1:177188826
|
A | AT | 182 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(179): Show | 185 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(182): Show |
intron_variant | MODIFIER | c.-77+17094_-77+1709 others(5): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177188826 | ||||||
chr1:177188955
|
T | C | 1 | a0001c0001t0004g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-77+17223T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177188955 | ||||||
chr1:177188983
|
G | C | 1 | a0002c0002t0001g0124 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-77+17251G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177188983 | ||||||
chr1:177189008
|
G | A | 1 | a0001c0001t0012g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-77+17276G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177189008 | ||||||
chr1:177189310
|
G | A | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-77+17578G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177189310 | ||||||
chr1:177189401
|
T | TG | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.-77+17670dupG | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177189401 | |||||
chr1:177189409
|
C | G | 1 | a0001c0001t0001g0036 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-77+17677C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177189409 | ||||||
chr1:177189417
|
A | C | 103 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(100): Show | 106 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-77+17685A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177189417 | ||||||
chr1:177189460
|
G | A | 108 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(105): Show | 111 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-77+17728G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177189460 | ||||||
chr1:177189495
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(105): Show | 111 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.-77+17763C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177189495 | ||||||
chr1:177189603
|
G | C | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-77+17871G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177189603 | ||||||
chr1:177189747
|
G | A | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-77+18015G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177189747 | ||||||
chr1:177189985
|
C | T | 1 | a0001c0001t0001g0204 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-77+18253C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177189985 | ||||||
chr1:177190036
|
C | G | 2 | a0001c0001t0001g0022a0002c0002t0001g0053 | 2 | NA18960.hp2 NA18991.hp2 |
intron_variant | MODIFIER | c.-77+18304C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177190036 | ||||||
chr1:177190096
|
C | T | 4 | a0001c0001t0001g0172a0001c0001t0004g0173a0001c0001t0004g0174others(1): Show | 4 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+18364C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177190096 | ||||||
chr1:177190122
|
T | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0195 | 2 | HG02523.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.-77+18390T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177190122 | ||||||
chr1:177190144
|
G | A | 123 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(120): Show | 126 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.-77+18412G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177190144 | ||||||
chr1:177190218
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(100): Show | 106 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-77+18486G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177190218 | ||||||
chr1:177190567
|
G | C | 1 | a0001c0001t0003g0015 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.-77+18835G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177190567 | ||||||
chr1:177190720
|
G | C | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-77+18988G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177190720 | ||||||
chr1:177190752
|
C | T | 1 | a0002c0002t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-77+19020C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177190752 | ||||||
chr1:177190767
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-77+19035G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177190767 | ||||||
chr1:177190985
|
C | A | 1 | a0001c0001t0012g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-77+19253C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177190985 | ||||||
chr1:177191029
|
A | C | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-77+19297A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177191029 | ||||||
chr1:177191133
|
C | A | 4 | a0001c0001t0001g0172a0001c0001t0004g0173a0001c0001t0004g0174others(1): Show | 4 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+19401C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177191133 | ||||||
chr1:177191250
|
G | C | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-77+19518G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177191250 | ||||||
chr1:177191485
|
A | C | 185 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(182): Show | 188 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(185): Show |
intron_variant | MODIFIER | c.-77+19753A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177191485 | ||||||
chr1:177191505
|
A | G | 1 | a0001c0004t0001g0029 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-77+19773A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177191505 | ||||||
chr1:177191705
|
C | T | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-77+19973C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177191705 | ||||||
chr1:177191745
|
C | T | 1 | a0002c0002t0010g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-77+20013C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177191745 | ||||||
chr1:177191796
|
C | G | 3 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0001g0153 | 3 | HG00738.hp2 HG02300.hp1 HG03490.hp2 |
intron_variant | MODIFIER | c.-77+20064C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177191796 | ||||||
chr1:177191937
|
C | G | 1 | a0002c0002t0001g0124 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-77+20205C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177191937 | ||||||
chr1:177191946
|
C | T | 3 | a0001c0001t0001g0229a0001c0004t0004g0228a0001c0004t0004g0230 | 3 | HG01070.hp2 HG01071.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.-77+20214C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177191946 | ||||||
chr1:177191971
|
T | C | 1 | a0002c0002t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-77+20239T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177191971 | ||||||
chr1:177192102
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-77+20370A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177192102 | ||||||
chr1:177192340
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-77+20608G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177192340 | ||||||
chr1:177192559
|
T | C | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-77+20827T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177192559 | ||||||
chr1:177192588
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.-77+20856G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177192588 | ||||||
chr1:177193268
|
A | G | 1 | a0002c0002t0010g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-77+21536A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177193268 | ||||||
chr1:177193673
|
C | T | 53 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0040others(50): Show | 53 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-77+21941C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177193673 | ||||||
chr1:177193776
|
G | A | 15 | a0001c0001t0001g0012a0001c0001t0001g0121a0001c0001t0001g0175others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-77+22044G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177193776 | ||||||
chr1:177193927
|
A | G | 1 | a0002c0002t0001g0096 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-77+22195A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177193927 | ||||||
chr1:177194062
|
C | T | 1 | a0001c0001t0012g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-77+22330C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177194062 | ||||||
chr1:177194082
|
C | A | 6 | a0001c0001t0001g0160a0001c0001t0003g0159a0001c0001t0003g0161others(3): Show | 6 | HG01099.hp1 HG01106.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.-77+22350C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177194082 | ||||||
chr1:177194660
|
G | T | 1 | a0001c0001t0001g0223 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-77+22928G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177194660 | ||||||
chr1:177194764
|
T | TG | 69 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0030others(66): Show | 69 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.-77+23033dupG | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177194764 | |||||
chr1:177194775
|
A | ATG | 5 | a0001c0001t0001g0160a0001c0001t0003g0159a0001c0001t0003g0161others(2): Show | 5 | HG01099.hp1 HG01106.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77+23058_-77+2305 others(6): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177194775 | |||||
chr1:177194856
|
C | T | 5 | a0001c0001t0001g0160a0001c0001t0003g0159a0001c0001t0003g0161others(2): Show | 5 | HG01099.hp1 HG01106.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77+23124C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177194856 | ||||||
chr1:177195403
|
C | T | 190 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(187): Show | 194 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(191): Show |
intron_variant | MODIFIER | c.-77+23671C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177195403 | ||||||
chr1:177195932
|
C | T | 4 | a0001c0001t0001g0172a0001c0001t0004g0173a0001c0001t0004g0174others(1): Show | 4 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+24200C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177195932 | ||||||
chr1:177196010
|
C | T | 69 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0030others(66): Show | 69 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.-77+24278C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177196010 | ||||||
chr1:177196023
|
A | C | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-77+24291A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177196023 | ||||||
chr1:177196165
|
G | A | 184 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(181): Show | 187 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(184): Show |
intron_variant | MODIFIER | c.-77+24433G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177196165 | ||||||
chr1:177196308
|
C | T | 1 | a0002c0002t0002g0116 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-77+24576C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177196308 | ||||||
chr1:177196635
|
GA | G | 5 | a0001c0001t0001g0172a0001c0001t0004g0173a0001c0001t0004g0174others(2): Show | 5 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77+24908delA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177196635 | |||||
chr1:177196910
|
T | A | 1 | a0001c0001t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-77+25178T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177196910 | ||||||
chr1:177196911
|
C | T | 1 | a0001c0001t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-77+25179C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177196911 | ||||||
chr1:177196950
|
C | A | 5 | a0001c0001t0001g0172a0001c0001t0004g0173a0001c0001t0004g0174others(2): Show | 5 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.-77+25218C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177196950 | ||||||
chr1:177196975
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-77+25243C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177196975 | ||||||
chr1:177197047
|
C | T | 54 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0040others(51): Show | 54 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-77+25315C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177197047 | ||||||
chr1:177197166
|
C | T | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-77+25434C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177197166 | ||||||
chr1:177197238
|
A | G | 6 | a0001c0001t0001g0172a0001c0001t0004g0173a0001c0001t0004g0174others(3): Show | 6 | HG01192.hp1 HG02723.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-77+25506A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177197238 | ||||||
chr1:177197302
|
C | A | 54 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0040others(51): Show | 54 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-77+25570C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177197302 | ||||||
chr1:177197417
|
G | A | 24 | a0001c0001t0001g0022a0001c0001t0001g0031a0001c0001t0001g0108others(21): Show | 24 | HG00558.hp1 HG01192.hp2 HG01257.hp2 others(21): Show |
intron_variant | MODIFIER | c.-77+25685G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177197417 | ||||||
chr1:177197443
|
G | A | 5 | a0001c0001t0003g0215a0001c0001t0003g0216a0001c0001t0003g0217others(2): Show | 6 | HG01346.hp2 HG02109.hp1 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.-77+25711G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177197443 | ||||||
chr1:177197562
|
A | G | 1 | a0002c0002t0001g0010 | 2 | HG01346.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-77+25830A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177197562 | ||||||
chr1:177197693
|
C | T | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-77+25961C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177197693 | ||||||
chr1:177197832
|
G | T | 1 | a0001c0001t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-77+26100G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177197832 | ||||||
chr1:177197939
|
G | A | 15 | a0001c0001t0001g0012a0001c0001t0001g0121a0001c0001t0001g0175others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-77+26207G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177197939 | ||||||
chr1:177198176
|
T | C | 1 | a0002c0002t0010g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-77+26444T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177198176 | ||||||
chr1:177198521
|
T | C | 1 | a0001c0001t0001g0207 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-77+26789T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177198521 | ||||||
chr1:177198601
|
A | G | 4 | a0001c0001t0005g0114a0002c0002t0001g0162a0002c0002t0002g0126others(1): Show | 4 | HG01192.hp2 HG01978.hp2 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+26869A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177198601 | ||||||
chr1:177198715
|
A | G | 1 | a0002c0002t0001g0154 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.-77+26983A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177198715 | ||||||
chr1:177198747
|
C | G | 59 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0040others(56): Show | 59 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(56): Show |
intron_variant | MODIFIER | c.-77+27015C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177198747 | ||||||
chr1:177199053
|
A | G | 1 | a0002c0002t0014g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-77+27321A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177199053 | ||||||
chr1:177199058
|
G | T | 1 | a0001c0001t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-77+27326G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177199058 | ||||||
chr1:177199267
|
G | A | 1 | a0002c0002t0002g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-77+27535G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177199267 | ||||||
chr1:177199371
|
T | A | 53 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0040others(50): Show | 53 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-77+27639T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177199371 | ||||||
chr1:177199783
|
A | T | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-77+28051A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177199783 | ||||||
chr1:177200024
|
G | C | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-77+28292G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200024 | ||||||
chr1:177200116
|
A | G | 1 | a0002c0002t0001g0010 | 2 | HG01346.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.-77+28384A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200116 | ||||||
chr1:177200144
|
G | A | 103 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(100): Show | 106 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.-77+28412G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200144 | ||||||
chr1:177200232
|
C | CAGTAAGC others(1): Show |
68 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0030others(65): Show | 68 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(65): Show |
intron_variant | MODIFIER | c.-77+28503_-77+2850 others(12): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200232 | |||||
chr1:177200236
|
G | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-77+28504G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200236 | ||||||
chr1:177200280
|
G | A | 3 | a0001c0001t0001g0160a0001c0001t0003g0159a0001c0001t0003g0161 | 3 | HG01099.hp1 HG01106.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-77+28548G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200280 | ||||||
chr1:177200293
|
C | CA | 10 | a0001c0001t0001g0057a0001c0001t0003g0088a0001c0001t0003g0089others(7): Show | 10 | HG00438.hp1 HG00733.hp2 HG00738.hp1 others(7): Show |
intron_variant | MODIFIER | c.-77+28590dupA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200293
|
C | CAA | 10 | a0001c0001t0001g0013a0001c0001t0001g0056a0001c0001t0001g0107others(7): Show | 11 | HG01175.hp1 HG01175.hp2 HG03490.hp1 others(8): Show |
intron_variant | MODIFIER | c.-77+28589_-77+2859 others(6): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200293
|
C | CAAAAAAA others(3): Show |
54 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(51): Show | 56 | HG00099.hp2 HG00280.hp1 HG00558.hp1 others(53): Show |
intron_variant | MODIFIER | c.-77+28581_-77+2859 others(14): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200293
|
C | CAAAAAAA others(4): Show |
39 | a0001c0001t0001g0031a0001c0001t0001g0032a0001c0001t0001g0033others(36): Show | 40 | HG00438.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.-77+28580_-77+2859 others(15): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200293
|
C | CAAAAAAA others(5): Show |
3 | a0001c0001t0003g0072a0002c0002t0002g0148a0002c0002t0002g0156 | 3 | HG03516.hp2 HG03831.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-77+28579_-77+2859 others(16): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200293
|
C | CAAAAAAA others(7): Show |
1 | a0002c0002t0002g0155 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-77+28577_-77+2859 others(18): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200293
|
C | CAAAAAAA others(10): Show |
1 | a0002c0002t0002g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-77+28574_-77+2859 others(21): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200293
|
C | CAAAAAAA others(15): Show |
1 | a0001c0001t0003g0161 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.-77+28569_-77+2859 others(26): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200293
|
C | CAAAAAAA others(16): Show |
2 | a0001c0001t0001g0160a0001c0001t0003g0159 | 2 | HG01106.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.-77+28568_-77+2859 others(27): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200293
|
CAA | C | 9 | a0001c0001t0001g0040a0001c0001t0001g0109a0001c0001t0001g0129others(6): Show | 9 | HG00544.hp2 HG02080.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.-77+28589_-77+2859 others(6): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200293
|
CAAA | C | 49 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0067others(46): Show | 49 | HG00408.hp2 HG00544.hp1 HG01074.hp1 others(46): Show |
intron_variant | MODIFIER | c.-77+28588_-77+2859 others(7): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200293
|
CAAAA | C | 12 | a0001c0001t0001g0030a0001c0001t0001g0192a0001c0001t0001g0229others(9): Show | 12 | HG00609.hp1 HG01070.hp2 HG01071.hp2 others(9): Show |
intron_variant | MODIFIER | c.-77+28587_-77+2859 others(8): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200293
|
CAAAAAAA others(5): Show |
C | 4 | a0001c0001t0001g0172a0001c0001t0004g0173a0001c0001t0004g0174others(1): Show | 4 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+28579_-77+2859 others(16): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177200293 | |||||
chr1:177200380
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-77+28648C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200380 | ||||||
chr1:177200380
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0004c0008t0001g0131 | 3 | NA18942.hp2 NA18973.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.-77+28648C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200380 | ||||||
chr1:177200525
|
C | A | 1 | a0001c0001t0012g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-77+28793C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200525 | ||||||
chr1:177200603
|
G | A | 1 | a0001c0001t0001g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.-77+28871G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200603 | ||||||
chr1:177200687
|
G | A | 4 | a0001c0001t0001g0172a0001c0001t0004g0173a0001c0001t0004g0174others(1): Show | 4 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-77+28955G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200687 | ||||||
chr1:177200726
|
A | C | 1 | a0001c0001t0001g0186 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-77+28994A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200726 | ||||||
chr1:177200733
|
C | T | 1 | a0001c0001t0006g0014 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-77+29001C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200733 | ||||||
chr1:177200999
|
C | A | 54 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0040others(51): Show | 54 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-76-28802C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177200999 | ||||||
chr1:177201304
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-76-28497A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177201304 | ||||||
chr1:177201334
|
C | T | 1 | a0002c0002t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-76-28467C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177201334 | ||||||
chr1:177201454
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(180): Show | 186 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(183): Show |
intron_variant | MODIFIER | c.-76-28347C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177201454 | ||||||
chr1:177201466
|
G | C | 1 | a0001c0001t0001g0240 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-76-28335G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177201466 | ||||||
chr1:177201556
|
A | T | 1 | a0001c0001t0001g0157 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.-76-28245A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177201556 | ||||||
chr1:177201584
|
C | G | 92 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(89): Show | 95 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.-76-28217C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177201584 | ||||||
chr1:177201660
|
G | C | 177 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(174): Show | 180 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(177): Show |
intron_variant | MODIFIER | c.-76-28141G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177201660 | ||||||
chr1:177201712
|
C | T | 1 | a0002c0002t0010g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-76-28089C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177201712 | ||||||
chr1:177201861
|
A | G | 1 | a0002c0002t0002g0075 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-76-27940A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177201861 | ||||||
chr1:177201966
|
A | C | 4 | a0001c0001t0001g0172a0001c0001t0004g0173a0001c0001t0004g0174others(1): Show | 4 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-76-27835A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177201966 | ||||||
chr1:177202015
|
T | A | 53 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0040others(50): Show | 53 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-76-27786T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202015 | ||||||
chr1:177202102
|
A | G | 1 | a0001c0001t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-76-27699A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202102 | ||||||
chr1:177202117
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-76-27684G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202117 | ||||||
chr1:177202295
|
C | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0013g0023 | 3 | HG01884.hp2 HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-76-27506C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202295 | ||||||
chr1:177202295
|
C | T | 1 | a0001c0001t0003g0237 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-76-27506C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202295 | ||||||
chr1:177202382
|
A | G | 1 | a0001c0001t0001g0166 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-76-27419A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202382 | ||||||
chr1:177202596
|
T | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0121a0001c0001t0002g0218others(3): Show | 6 | HG01167.hp2 HG01358.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.-76-27205T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202596 | ||||||
chr1:177202652
|
G | A | 3 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045 | 3 | HG01070.hp1 HG03492.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.-76-27149G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202652 | ||||||
chr1:177202705
|
G | A | 1 | a0001c0001t0003g0092 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-76-27096G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202705 | ||||||
chr1:177202767
|
C | T | 53 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0040others(50): Show | 53 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.-76-27034C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202767 | ||||||
chr1:177202791
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-76-27010C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202791 | ||||||
chr1:177202796
|
A | C | 1 | a0001c0012t0001g0084 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.-76-27005A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202796 | ||||||
chr1:177202804
|
G | A | 54 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0040others(51): Show | 54 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.-76-26997G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202804 | ||||||
chr1:177202880
|
G | A | 1 | a0002c0003t0004g0231 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-76-26921G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177202880 | ||||||
chr1:177203028
|
G | A | 3 | a0001c0001t0004g0173a0001c0001t0004g0174a0002c0003t0015g0176 | 3 | HG02723.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-76-26773G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177203028 | ||||||
chr1:177203042
|
G | T | 1 | a0001c0001t0001g0143 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-76-26759G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177203042 | ||||||
chr1:177203165
|
A | G | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-76-26636A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177203165 | ||||||
chr1:177203173
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-76-26628T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177203173 | ||||||
chr1:177203228
|
CA | C | 58 | a0001c0001t0001g0011a0001c0001t0001g0030a0001c0001t0001g0040others(55): Show | 58 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(55): Show |
intron_variant | MODIFIER | c.-76-26566delA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177203228 | |||||
chr1:177203572
|
T | A | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-76-26229T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177203572 | ||||||
chr1:177203573
|
A | T | 1 | a0001c0004t0001g0029 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-76-26228A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177203573 | ||||||
chr1:177203613
|
T | C | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-76-26188T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177203613 | ||||||
chr1:177203643
|
C | A | 8 | a0001c0001t0001g0105a0001c0001t0001g0109a0001c0001t0001g0110others(5): Show | 8 | HG00544.hp1 HG02055.hp2 HG02071.hp1 others(5): Show |
intron_variant | MODIFIER | c.-76-26158C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177203643 | ||||||
chr1:177203848
|
G | A | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-76-25953G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177203848 | ||||||
chr1:177204017
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-76-25784G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177204017 | ||||||
chr1:177204105
|
G | C | 8 | a0001c0001t0001g0160a0001c0001t0003g0159a0001c0001t0003g0161others(5): Show | 8 | HG01099.hp1 HG01106.hp2 HG01192.hp1 others(5): Show |
intron_variant | MODIFIER | c.-76-25696G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177204105 | ||||||
chr1:177204227
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(101): Show | 107 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.-76-25574G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177204227 | ||||||
chr1:177204329
|
C | G | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-76-25472C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177204329 | ||||||
chr1:177204348
|
A | G | 1 | a0002c0003t0015g0176 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-76-25453A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177204348 | ||||||
chr1:177204730
|
A | G | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-76-25071A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177204730 | ||||||
chr1:177204748
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0022others(102): Show | 108 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(105): Show |
intron_variant | MODIFIER | c.-76-25053A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177204748 | ||||||
chr1:177204790
|
T | C | 1 | a0002c0002t0010g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-76-25011T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177204790 | ||||||
chr1:177204938
|
G | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(164): Show | 170 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(167): Show |
intron_variant | MODIFIER | c.-76-24863G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177204938 | ||||||
chr1:177205220
|
A | C | 15 | a0001c0001t0001g0012a0001c0001t0001g0121a0001c0001t0001g0175others(12): Show | 15 | HG01070.hp2 HG01071.hp2 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.-76-24581A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177205220 | ||||||
chr1:177205230
|
T | A | 1 | a0006c0006t0001g0234 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-76-24571T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177205230 | ||||||
chr1:177205269
|
G | A | 1 | a0002c0002t0010g0181 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.-76-24532G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177205269 | ||||||
chr1:177205313
|
G | T | 1 | a0001c0001t0001g0240 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-76-24488G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177205313 | ||||||
chr1:177205431
|
A | C | 1 | a0001c0001t0007g0142 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-76-24370A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177205431 | ||||||
chr1:177205593
|
C | T | 1 | a0002c0002t0002g0205 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.-76-24208C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177205593 | ||||||
chr1:177205600
|
G | C | 163 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0011others(160): Show | 166 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(163): Show |
intron_variant | MODIFIER | c.-76-24201G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177205600 | ||||||
chr1:177205900
|
C | T | 1 | a0002c0002t0002g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-76-23901C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177205900 | ||||||
chr1:177206077
|
A | G | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-76-23724A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177206077 | ||||||
chr1:177206203
|
GA | G | 4 | a0001c0001t0001g0172a0001c0001t0004g0173a0001c0001t0004g0174others(1): Show | 4 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.-76-23597delA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177206203 | ||||||
chr1:177206387
|
T | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0013g0023 | 3 | HG01884.hp2 HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-76-23414T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177206387 | ||||||
chr1:177206519
|
G | A | 1 | a0002c0002t0014g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-76-23282G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177206519 | ||||||
chr1:177206556
|
C | T | 6 | a0002c0002t0001g0053a0002c0002t0002g0027a0002c0002t0002g0062others(3): Show | 6 | HG02886.hp1 NA18960.hp2 NA18969.hp2 others(3): Show |
intron_variant | MODIFIER | c.-76-23245C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177206556 | ||||||
chr1:177206561
|
A | G | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-76-23240A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177206561 | ||||||
chr1:177206975
|
A | G | 2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG00408.hp1 HG00621.hp2 |
intron_variant | MODIFIER | c.-76-22826A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177206975 | ||||||
chr1:177207076
|
C | T | 38 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0022others(35): Show | 38 | HG00544.hp2 HG00609.hp1 HG01192.hp1 others(35): Show |
intron_variant | MODIFIER | c.-76-22725C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177207076 | ||||||
chr1:177207077
|
A | G | 129 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0011others(126): Show | 134 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(131): Show |
intron_variant | MODIFIER | c.-76-22724A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177207077 | ||||||
chr1:177207314
|
C | A | 1 | a0001c0001t0001g0229 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-76-22487C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177207314 | ||||||
chr1:177207566
|
C | G | 1 | a0001c0001t0001g0013 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-76-22235C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177207566 | ||||||
chr1:177207731
|
G | T | 1 | a0001c0004t0001g0029 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-76-22070G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177207731 | ||||||
chr1:177207733
|
T | A | 1 | a0001c0004t0001g0029 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-76-22068T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177207733 | ||||||
chr1:177207734
|
A | C | 1 | a0001c0004t0001g0029 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-76-22067A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177207734 | ||||||
chr1:177207952
|
C | T | 1 | a0001c0001t0004g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-76-21849C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177207952 | ||||||
chr1:177208207
|
G | A | 1 | a0001c0001t0003g0211 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.-76-21594G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177208207 | ||||||
chr1:177208317
|
C | A | 1 | a0002c0002t0002g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-76-21484C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177208317 | ||||||
chr1:177208392
|
A | G | 5 | a0001c0001t0001g0229a0001c0004t0004g0228a0001c0004t0004g0230others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-76-21409A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177208392 | ||||||
chr1:177208415
|
G | C | 3 | a0001c0001t0003g0072a0001c0001t0004g0069a0001c0001t0004g0070 | 3 | HG02451.hp2 HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-76-21386G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177208415 | ||||||
chr1:177208520
|
T | C | 2 | a0001c0001t0003g0215a0001c0001t0003g0216 | 2 | HG02486.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-76-21281T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177208520 | ||||||
chr1:177208559
|
T | C | 1 | a0001c0001t0003g0092 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-76-21242T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177208559 | ||||||
chr1:177208613
|
A | G | 1 | a0001c0001t0001g0239 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.-76-21188A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177208613 | ||||||
chr1:177209044
|
T | C | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-76-20757T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177209044 | ||||||
chr1:177209082
|
G | A | 76 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(73): Show | 77 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-76-20719G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177209082 | ||||||
chr1:177209108
|
T | A | 3 | a0001c0001t0003g0072a0001c0001t0004g0069a0001c0001t0004g0070 | 3 | HG02451.hp2 HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-76-20693T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177209108 | ||||||
chr1:177209222
|
A | C | 1 | a0001c0001t0012g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-76-20579A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177209222 | ||||||
chr1:177209572
|
T | C | 24 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(21): Show | 25 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(22): Show |
intron_variant | MODIFIER | c.-76-20229T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177209572 | ||||||
chr1:177209613
|
G | A | 1 | a0002c0002t0001g0124 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.-76-20188G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177209613 | ||||||
chr1:177209666
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-76-20135A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177209666 | ||||||
chr1:177209928
|
C | A | 3 | a0002c0002t0001g0006a0002c0002t0001g0120a0002c0002t0001g0154 | 4 | HG00099.hp2 HG00733.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-76-19873C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177209928 | ||||||
chr1:177210108
|
T | C | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-76-19693T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177210108 | ||||||
chr1:177210254
|
CTTTCTAT others(1): Show |
C | 4 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-76-19543_-76-1953 others(12): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177210254 | |||||
chr1:177210296
|
A | G | 3 | a0001c0001t0001g0119a0001c0001t0001g0149a0001c0001t0001g0214 | 3 | HG02735.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-76-19505A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177210296 | ||||||
chr1:177210350
|
C | T | 2 | a0002c0002t0002g0147a0002c0002t0002g0156 | 2 | HG02257.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.-76-19451C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177210350 | ||||||
chr1:177210481
|
A | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(75): Show | 79 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.-76-19320A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177210481 | ||||||
chr1:177210638
|
TA | T | 3 | a0002c0002t0002g0155a0002c0002t0002g0213a0002c0002t0011g0054 | 3 | HG02809.hp1 HG02922.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.-76-19162delA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177210638 | ||||||
chr1:177210997
|
TG | T | 31 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(28): Show | 32 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-76-18803delG | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177210997 | ||||||
chr1:177211039
|
A | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-76-18762A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177211039 | ||||||
chr1:177211440
|
G | A | 1 | a0001c0001t0001g0046 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.-76-18361G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177211440 | ||||||
chr1:177211450
|
T | C | 1 | a0002c0002t0013g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-76-18351T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177211450 | ||||||
chr1:177211693
|
C | T | 1 | a0001c0001t0005g0135 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-76-18108C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177211693 | ||||||
chr1:177211712
|
ATTACT | A | 4 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-76-18088_-76-1808 others(9): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177211712 | ||||||
chr1:177211720
|
T | A | 4 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-76-18081T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177211720 | ||||||
chr1:177211721
|
G | C | 4 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-76-18080G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177211721 | ||||||
chr1:177212066
|
C | CAGAT | 15 | a0001c0001t0001g0097a0001c0001t0001g0121a0001c0001t0001g0132others(12): Show | 15 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(12): Show |
intron_variant | MODIFIER | c.-76-17694_-76-1769 others(8): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177212066 | |||||
chr1:177212066
|
CAGAT | C | 122 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(119): Show | 128 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(125): Show |
intron_variant | MODIFIER | c.-76-17694_-76-1769 others(8): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177212066 | |||||
chr1:177212066
|
CAGATAGA others(1): Show |
C | 31 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0036others(28): Show | 33 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(30): Show |
intron_variant | MODIFIER | c.-76-17698_-76-1769 others(12): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177212066 | |||||
chr1:177212066
|
CAGATAGA others(5): Show |
C | 2 | a0001c0001t0001g0171a0002c0002t0018g0179 | 2 | HG02615.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.-76-17702_-76-1769 others(16): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177212066 | |||||
chr1:177212066
|
CAGATAGA others(9): Show |
C | 1 | a0001c0001t0004g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-76-17706_-76-1769 others(20): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177212066 | |||||
chr1:177212066
|
CAGATAGA others(13): Show |
C | 3 | a0001c0001t0003g0215a0001c0001t0003g0216a0001c0001t0003g0217 | 3 | HG02486.hp2 HG02818.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-76-17710_-76-1769 others(24): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177212066 | |||||
chr1:177212183
|
G | A | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-76-17618G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177212183 | ||||||
chr1:177212211
|
C | A | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(75): Show | 79 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.-76-17590C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177212211 | ||||||
chr1:177212419
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-76-17382C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177212419 | ||||||
chr1:177212519
|
T | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(75): Show | 79 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.-76-17282T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177212519 | ||||||
chr1:177212806
|
T | C | 4 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-76-16995T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177212806 | ||||||
chr1:177212900
|
G | T | 1 | a0001c0001t0004g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-76-16901G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177212900 | ||||||
chr1:177212906
|
G | A | 31 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(28): Show | 32 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-76-16895G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177212906 | ||||||
chr1:177212924
|
G | C | 1 | a0002c0002t0001g0151 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-76-16877G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177212924 | ||||||
chr1:177212996
|
G | A | 31 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(28): Show | 32 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-76-16805G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177212996 | ||||||
chr1:177213091
|
T | C | 1 | a0002c0002t0002g0152 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-76-16710T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177213091 | ||||||
chr1:177214044
|
G | T | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-76-15757G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177214044 | ||||||
chr1:177214089
|
T | G | 31 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(28): Show | 32 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-76-15712T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177214089 | ||||||
chr1:177214105
|
G | C | 4 | a0002c0002t0001g0008a0002c0002t0001g0124a0002c0002t0001g0127others(1): Show | 5 | NA18950.hp2 NA18961.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.-76-15696G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177214105 | ||||||
chr1:177214198
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0071a0001c0001t0001g0220others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-76-15603G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177214198 | ||||||
chr1:177214310
|
G | C | 1 | a0002c0002t0002g0060 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-76-15491G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177214310 | ||||||
chr1:177214364
|
C | T | 15 | a0001c0001t0001g0160a0001c0001t0001g0226a0001c0001t0003g0159others(12): Show | 17 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-76-15437C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177214364 | ||||||
chr1:177214382
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-76-15419G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177214382 | ||||||
chr1:177214584
|
T | C | 1 | a0001c0001t0003g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-76-15217T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177214584 | ||||||
chr1:177214602
|
G | GT | 9 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0184others(6): Show | 9 | HG00408.hp2 NA18942.hp2 NA18955.hp2 others(6): Show |
intron_variant | MODIFIER | c.-76-15198dupT | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177214602 | |||||
chr1:177214614
|
G | A | 1 | a0001c0001t0004g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-76-15187G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177214614 | ||||||
chr1:177215041
|
G | T | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-76-14760G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177215041 | ||||||
chr1:177215138
|
A | G | 3 | a0001c0001t0001g0192a0001c0001t0001g0221a0001c0001t0001g0223 | 3 | HG00544.hp2 HG00609.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-76-14663A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177215138 | ||||||
chr1:177215220
|
A | G | 31 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(28): Show | 32 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(29): Show |
intron_variant | MODIFIER | c.-76-14581A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177215220 | ||||||
chr1:177215241
|
C | T | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-76-14560C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177215241 | ||||||
chr1:177215464
|
G | T | 1 | a0002c0003t0015g0176 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-76-14337G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177215464 | ||||||
chr1:177215587
|
T | C | 78 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(75): Show | 79 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.-76-14214T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177215587 | ||||||
chr1:177215738
|
A | T | 2 | a0001c0001t0012g0024a0002c0003t0015g0176 | 2 | HG02723.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-76-14063A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177215738 | ||||||
chr1:177215740
|
C | G | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-76-14061C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177215740 | ||||||
chr1:177215770
|
C | T | 1 | a0001c0001t0004g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-76-14031C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177215770 | ||||||
chr1:177215922
|
T | C | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-76-13879T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177215922 | ||||||
chr1:177216044
|
G | T | 3 | a0001c0001t0001g0191a0001c0001t0001g0210a0001c0001t0001g0239 | 3 | NA18974.hp2 NA18991.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.-76-13757G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177216044 | ||||||
chr1:177216163
|
T | C | 1 | a0001c0001t0001g0021 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-76-13638T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177216163 | ||||||
chr1:177216230
|
G | A | 2 | a0001c0001t0001g0095a0001c0001t0004g0065 | 2 | HG01261.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-76-13571G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177216230 | ||||||
chr1:177216563
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.-76-13238C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177216563 | ||||||
chr1:177216590
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-76-13211T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177216590 | ||||||
chr1:177216643
|
A | G | 1 | a0002c0003t0015g0176 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.-76-13158A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177216643 | ||||||
chr1:177216668
|
A | AG | 242 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(239): Show | 251 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.-76-13132dupG | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177216668 | |||||
chr1:177216718
|
T | G | 3 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099 | 3 | HG00639.hp2 HG03669.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.-76-13083T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177216718 | ||||||
chr1:177216779
|
G | GT | 39 | a0001c0001t0001g0052a0001c0001t0001g0055a0001c0001t0001g0056others(36): Show | 41 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(38): Show |
intron_variant | MODIFIER | c.-76-13005dupT | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177216779 | |||||
chr1:177216836
|
G | A | 1 | a0001c0001t0012g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-76-12965G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177216836 | ||||||
chr1:177216841
|
C | T | 30 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(27): Show | 31 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.-76-12960C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177216841 | ||||||
chr1:177217189
|
C | A | 1 | a0001c0001t0001g0132 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.-76-12612C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177217189 | ||||||
chr1:177217272
|
G | A | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-76-12529G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177217272 | ||||||
chr1:177217338
|
A | G | 1 | a0002c0002t0013g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-76-12463A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177217338 | ||||||
chr1:177217394
|
T | C | 30 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(27): Show | 31 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.-76-12407T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177217394 | ||||||
chr1:177217695
|
G | T | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-76-12106G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177217695 | ||||||
chr1:177217816
|
A | G | 1 | a0001c0001t0001g0140 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-76-11985A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177217816 | ||||||
chr1:177217874
|
A | C | 15 | a0001c0001t0001g0160a0001c0001t0001g0226a0001c0001t0003g0159others(12): Show | 17 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-76-11927A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177217874 | ||||||
chr1:177217895
|
G | A | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-76-11906G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177217895 | ||||||
chr1:177217925
|
T | A | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-76-11876T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177217925 | ||||||
chr1:177217986
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-76-11815A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177217986 | ||||||
chr1:177218002
|
G | A | 1 | a0001c0001t0001g0144 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-76-11799G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177218002 | ||||||
chr1:177218039
|
C | A | 3 | a0001c0001t0003g0072a0001c0001t0004g0069a0001c0001t0004g0070 | 3 | HG02451.hp2 HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-76-11762C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177218039 | ||||||
chr1:177218666
|
C | T | 1 | a0001c0001t0004g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-76-11135C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177218666 | ||||||
chr1:177218875
|
C | G | 30 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(27): Show | 31 | HG00280.hp1 HG00639.hp1 HG00733.hp2 others(28): Show |
intron_variant | MODIFIER | c.-76-10926C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177218875 | ||||||
chr1:177218898
|
C | A | 40 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0050others(37): Show | 40 | HG00408.hp2 HG00544.hp2 HG00558.hp2 others(37): Show |
intron_variant | MODIFIER | c.-76-10903C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177218898 | ||||||
chr1:177219044
|
G | A | 15 | a0001c0001t0001g0058a0001c0001t0001g0194a0001c0001t0001g0203others(12): Show | 15 | HG00438.hp2 HG02071.hp2 HG02165.hp1 others(12): Show |
intron_variant | MODIFIER | c.-76-10757G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177219044 | ||||||
chr1:177219115
|
G | A | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(232): Show | 243 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.-76-10686G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177219115 | ||||||
chr1:177219272
|
C | T | 109 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(106): Show | 111 | HG00280.hp1 HG00408.hp2 HG00544.hp1 others(108): Show |
intron_variant | MODIFIER | c.-76-10529C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177219272 | ||||||
chr1:177219330
|
A | G | 4 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(1): Show | 4 | HG01070.hp2 HG01071.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.-76-10471A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177219330 | ||||||
chr1:177219496
|
T | C | 3 | a0001c0001t0001g0192a0001c0001t0001g0221a0001c0001t0001g0223 | 3 | HG00544.hp2 HG00609.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.-76-10305T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177219496 | ||||||
chr1:177219846
|
C | G | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-76-9955C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177219846 | ||||||
chr1:177219872
|
A | T | 3 | a0002c0002t0002g0007a0002c0002t0002g0111a0002c0002t0002g0112 | 4 | NA18940.hp1 NA18995.hp2 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.-76-9929A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177219872 | ||||||
chr1:177219925
|
C | A | 8 | a0001c0001t0001g0226a0002c0002t0001g0008a0002c0002t0001g0059others(5): Show | 9 | NA18950.hp2 NA18952.hp1 NA18961.hp1 others(6): Show |
intron_variant | MODIFIER | c.-76-9876C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177219925 | ||||||
chr1:177220051
|
C | A | 1 | a0002c0002t0002g0222 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-76-9750C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177220051 | ||||||
chr1:177220403
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-76-9398C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177220403 | ||||||
chr1:177220484
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-76-9317G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177220484 | ||||||
chr1:177220762
|
G | T | 45 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(42): Show | 48 | HG00099.hp2 HG00280.hp1 HG00639.hp1 others(45): Show |
intron_variant | MODIFIER | c.-76-9039G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177220762 | ||||||
chr1:177220796
|
T | C | 134 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(131): Show | 138 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-76-9005T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177220796 | ||||||
chr1:177220850
|
G | A | 134 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(131): Show | 138 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-76-8951G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177220850 | ||||||
chr1:177220896
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-76-8905G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177220896 | ||||||
chr1:177221000
|
T | G | 3 | a0001c0001t0003g0072a0001c0001t0004g0069a0001c0001t0004g0070 | 3 | HG02451.hp2 HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-76-8801T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177221000 | ||||||
chr1:177221091
|
C | G | 1 | a0001c0001t0001g0185 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.-76-8710C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177221091 | ||||||
chr1:177221558
|
G | A | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-76-8243G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177221558 | ||||||
chr1:177221595
|
A | C | 134 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(131): Show | 138 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.-76-8206A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177221595 | ||||||
chr1:177221612
|
C | A | 1 | a0002c0002t0001g0059 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-76-8189C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177221612 | ||||||
chr1:177221708
|
T | C | 1 | a0001c0001t0001g0022 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.-76-8093T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177221708 | ||||||
chr1:177221797
|
C | T | 3 | a0001c0001t0003g0211a0001c0001t0003g0237a0001c0001t0003g0238 | 3 | HG01167.hp2 HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.-76-8004C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177221797 | ||||||
chr1:177222087
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-76-7714C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177222087 | ||||||
chr1:177222184
|
C | T | 1 | a0003c0007t0002g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-76-7617C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177222184 | ||||||
chr1:177222245
|
CCT | C | 15 | a0001c0001t0001g0160a0001c0001t0001g0226a0001c0001t0003g0159others(12): Show | 17 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-76-7555_-76-7554d others(4): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177222245 | ||||||
chr1:177222355
|
A | G | 1 | a0001c0001t0001g0012 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-76-7446A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177222355 | ||||||
chr1:177222433
|
T | C | 1 | a0002c0002t0002g0227 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-76-7368T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177222433 | ||||||
chr1:177222457
|
A | G | 123 | a0001c0001t0001g0009a0001c0001t0001g0011a0001c0001t0001g0012others(120): Show | 127 | HG00099.hp2 HG00280.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.-76-7344A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177222457 | ||||||
chr1:177223045
|
T | C | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(161): Show | 172 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(169): Show |
intron_variant | MODIFIER | c.-76-6756T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177223045 | ||||||
chr1:177223072
|
C | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(114): Show | 122 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.-76-6729C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177223072 | ||||||
chr1:177223121
|
G | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 113 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-76-6680G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177223121 | ||||||
chr1:177223269
|
T | C | 15 | a0001c0001t0001g0160a0001c0001t0001g0226a0001c0001t0003g0159others(12): Show | 17 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.-76-6532T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177223269 | ||||||
chr1:177223476
|
G | C | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-76-6325G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177223476 | ||||||
chr1:177223807
|
C | G | 14 | a0001c0001t0001g0160a0001c0001t0001g0226a0002c0002t0001g0006others(11): Show | 16 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-76-5994C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177223807 | ||||||
chr1:177223903
|
C | T | 14 | a0001c0001t0001g0160a0001c0001t0001g0226a0002c0002t0001g0006others(11): Show | 16 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-76-5898C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177223903 | ||||||
chr1:177223965
|
T | C | 3 | a0002c0002t0001g0006a0002c0002t0001g0120a0002c0002t0001g0154 | 4 | HG00099.hp2 HG00733.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.-76-5836T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177223965 | ||||||
chr1:177224216
|
A | G | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(131): Show | 139 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.-76-5585A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177224216 | ||||||
chr1:177224272
|
G | A | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(130): Show | 138 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.-76-5529G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177224272 | ||||||
chr1:177224421
|
T | C | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-76-5380T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177224421 | ||||||
chr1:177224439
|
A | T | 14 | a0001c0001t0001g0160a0001c0001t0001g0226a0002c0002t0001g0006others(11): Show | 16 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(13): Show |
intron_variant | MODIFIER | c.-76-5362A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177224439 | ||||||
chr1:177224486
|
G | A | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-76-5315G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177224486 | ||||||
chr1:177224519
|
G | A | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-76-5282G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177224519 | ||||||
chr1:177224520
|
A | T | 6 | a0001c0001t0012g0024a0001c0004t0004g0228a0001c0004t0004g0230others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-76-5281A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177224520 | ||||||
chr1:177224561
|
G | T | 132 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(129): Show | 139 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.-76-5240G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177224561 | ||||||
chr1:177224814
|
G | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(43): Show | 49 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(46): Show |
intron_variant | MODIFIER | c.-76-4987G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177224814 | ||||||
chr1:177225291
|
C | T | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-76-4510C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177225291 | ||||||
chr1:177225314
|
G | A | 1 | a0001c0001t0003g0158 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-76-4487G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177225314 | ||||||
chr1:177225365
|
T | G | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-76-4436T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177225365 | ||||||
chr1:177225433
|
C | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(127): Show | 137 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(134): Show |
intron_variant | MODIFIER | c.-76-4368C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177225433 | ||||||
chr1:177225681
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-76-4120C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177225681 | ||||||
chr1:177225855
|
A | G | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-76-3946A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177225855 | ||||||
chr1:177225914
|
G | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(160): Show | 171 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(168): Show |
intron_variant | MODIFIER | c.-76-3887G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177225914 | ||||||
chr1:177226419
|
C | T | 108 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(105): Show | 113 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.-76-3382C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177226419 | ||||||
chr1:177226462
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-76-3339A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177226462 | ||||||
chr1:177226595
|
AC | A | 29 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(26): Show | 30 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.-76-3205delC | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177226595 | ||||||
chr1:177226821
|
G | A | 1 | a0002c0002t0002g0148 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-76-2980G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177226821 | ||||||
chr1:177226860
|
GTGGCCCC others(18): Show |
G | 6 | a0001c0001t0012g0024a0001c0004t0004g0228a0001c0004t0004g0230others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.-76-2936_-76-2912d others(27): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177226860 | |||||
chr1:177226923
|
C | T | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-76-2878C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177226923 | ||||||
chr1:177226932
|
G | T | 149 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(146): Show | 155 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(152): Show |
intron_variant | MODIFIER | c.-76-2869G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177226932 | ||||||
chr1:177227101
|
C | T | 1 | a0002c0002t0004g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-76-2700C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177227101 | ||||||
chr1:177227249
|
A | G | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-76-2552A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177227249 | ||||||
chr1:177227610
|
G | GT | 16 | a0001c0001t0001g0160a0001c0001t0001g0226a0001c0001t0004g0173others(13): Show | 18 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(15): Show |
intron_variant | MODIFIER | c.-76-2179dupT | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr1 | 177227610 | |||||
chr1:177227836
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-76-1965G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177227836 | ||||||
chr1:177228067
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-76-1734C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177228067 | ||||||
chr1:177228312
|
G | A | 25 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(22): Show | 26 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-76-1489G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177228312 | ||||||
chr1:177228366
|
A | T | 1 | a0001c0001t0001g0013 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-76-1435A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177228366 | ||||||
chr1:177228526
|
T | C | 1 | a0001c0001t0001g0221 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.-76-1275T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177228526 | ||||||
chr1:177228668
|
C | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(95): Show | 102 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.-76-1133C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177228668 | ||||||
chr1:177228672
|
C | G | 25 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(22): Show | 26 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-76-1129C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177228672 | ||||||
chr1:177228720
|
T | C | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-76-1081T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177228720 | ||||||
chr1:177229029
|
C | G | 1 | a0002c0002t0002g0146 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-76-772C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177229029 | ||||||
chr1:177229464
|
T | G | 1 | a0003c0007t0002g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-76-337T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177229464 | ||||||
chr1:177229647
|
G | T | 1 | a0001c0001t0001g0021 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.-76-154G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177229647 | ||||||
chr1:177229682
|
G | T | 25 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(22): Show | 26 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.-76-119G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 1/7 | chr1 | 177229682 | ||||||
chr1:177230181
|
T | C | 5 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.269+36T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177230181 | ||||||
chr1:177230187
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(96): Show | 103 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.269+42C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177230187 | ||||||
chr1:177230238
|
T | C | 4 | a0001c0001t0001g0009a0001c0001t0005g0009a0001c0001t0005g0115others(1): Show | 4 | HG01071.hp1 HG01257.hp1 HG01358.hp2 others(1): Show |
intron_variant | MODIFIER | c.269+93T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177230238 | ||||||
chr1:177230290
|
G | A | 26 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(23): Show | 27 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(24): Show |
intron_variant | MODIFIER | c.269+145G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177230290 | ||||||
chr1:177230424
|
A | G | 37 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(34): Show | 38 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.269+279A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177230424 | ||||||
chr1:177230468
|
G | C | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.269+323G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177230468 | ||||||
chr1:177230543
|
A | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.269+398A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177230543 | ||||||
chr1:177230913
|
T | C | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.269+768T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177230913 | ||||||
chr1:177231160
|
G | T | 1 | a0001c0001t0005g0141 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.269+1015G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177231160 | ||||||
chr1:177231171
|
A | G | 1 | a0001c0001t0001g0186 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.269+1026A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177231171 | ||||||
chr1:177231387
|
T | G | 1 | a0001c0001t0003g0238 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.269+1242T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177231387 | ||||||
chr1:177231692
|
T | C | 3 | a0002c0003t0004g0169a0002c0003t0004g0231a0002c0003t0015g0176 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.269+1547T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177231692 | ||||||
chr1:177231693
|
G | A | 3 | a0002c0003t0004g0169a0002c0003t0004g0231a0002c0003t0015g0176 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.269+1548G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177231693 | ||||||
chr1:177232509
|
G | C | 25 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(22): Show | 26 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(23): Show |
intron_variant | MODIFIER | c.269+2364G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177232509 | ||||||
chr1:177232783
|
GA | G | 28 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(25): Show | 29 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.269+2649delA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177232783 | |||||
chr1:177233389
|
T | C | 1 | a0001c0001t0004g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.269+3244T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177233389 | ||||||
chr1:177233552
|
G | T | 3 | a0002c0003t0004g0169a0002c0003t0004g0231a0002c0003t0015g0176 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.269+3407G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177233552 | ||||||
chr1:177233617
|
C | T | 1 | a0001c0001t0003g0158 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.269+3472C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177233617 | ||||||
chr1:177233852
|
C | G | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.269+3707C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177233852 | ||||||
chr1:177233877
|
A | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(96): Show | 103 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.269+3732A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177233877 | ||||||
chr1:177233918
|
C | T | 1 | a0001c0001t0003g0068 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.269+3773C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177233918 | ||||||
chr1:177234211
|
C | A | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.269+4066C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177234211 | ||||||
chr1:177234384
|
C | T | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.269+4239C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177234384 | ||||||
chr1:177234501
|
T | G | 1 | a0001c0001t0001g0094 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.269+4356T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177234501 | ||||||
chr1:177234649
|
G | A | 1 | a0002c0002t0002g0062 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.269+4504G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177234649 | ||||||
chr1:177234692
|
T | C | 1 | a0001c0001t0001g0118 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.269+4547T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177234692 | ||||||
chr1:177234717
|
C | T | 37 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(34): Show | 38 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.269+4572C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177234717 | ||||||
chr1:177234813
|
A | T | 8 | a0001c0001t0004g0173a0001c0001t0004g0174a0001c0004t0004g0228others(5): Show | 8 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.269+4668A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177234813 | ||||||
chr1:177235001
|
C | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 141 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.269+4856C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177235001 | ||||||
chr1:177235114
|
C | A | 104 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(101): Show | 108 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.269+4969C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177235114 | ||||||
chr1:177235363
|
G | T | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.269+5218G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177235363 | ||||||
chr1:177235660
|
C | T | 1 | a0003c0007t0002g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.269+5515C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177235660 | ||||||
chr1:177235717
|
A | G | 34 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(31): Show | 35 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.269+5572A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177235717 | ||||||
chr1:177235718
|
G | A | 4 | a0001c0001t0001g0067a0001c0001t0001g0183a0001c0001t0001g0219others(1): Show | 4 | HG01074.hp1 HG02886.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.269+5573G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177235718 | ||||||
chr1:177235766
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(133): Show | 141 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(138): Show |
intron_variant | MODIFIER | c.269+5621A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177235766 | ||||||
chr1:177235775
|
A | G | 1 | a0002c0002t0004g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.269+5630A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177235775 | ||||||
chr1:177235833
|
G | A | 2 | a0001c0001t0004g0065a0001c0001t0012g0024 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.269+5688G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177235833 | ||||||
chr1:177235837
|
A | G | 24 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(21): Show | 25 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.269+5692A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177235837 | ||||||
chr1:177235886
|
G | A | 3 | a0001c0001t0004g0173a0001c0001t0004g0174a0002c0002t0009g0180 | 3 | HG02886.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.269+5741G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177235886 | ||||||
chr1:177235971
|
C | T | 1 | a0001c0001t0001g0123 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.269+5826C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177235971 | ||||||
chr1:177236169
|
A | T | 1 | a0001c0001t0001g0133 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.269+6024A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177236169 | ||||||
chr1:177236233
|
C | T | 1 | a0001c0001t0001g0003 | 2 | NA18943.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.269+6088C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177236233 | ||||||
chr1:177236360
|
A | C | 11 | a0001c0001t0004g0065a0001c0001t0004g0173a0001c0001t0004g0174others(8): Show | 11 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.269+6215A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177236360 | ||||||
chr1:177236423
|
A | G | 2 | a0001c0001t0004g0065a0001c0001t0012g0024 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.269+6278A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177236423 | ||||||
chr1:177236510
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.269+6365C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177236510 | ||||||
chr1:177236526
|
A | G | 1 | a0002c0002t0011g0054 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.269+6381A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177236526 | ||||||
chr1:177236727
|
C | T | 5 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.269+6582C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177236727 | ||||||
chr1:177236747
|
T | A | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.269+6602T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177236747 | ||||||
chr1:177236862
|
G | T | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.269+6717G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177236862 | ||||||
chr1:177236918
|
T | TA | 5 | a0001c0001t0001g0032a0001c0001t0001g0052a0001c0001t0004g0086others(2): Show | 5 | HG02258.hp2 NA18949.hp1 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.269+6789dupA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177236918 | |||||
chr1:177236918
|
TA | T | 5 | a0001c0001t0001g0226a0001c0001t0004g0065a0001c0001t0012g0024others(2): Show | 5 | HG02922.hp2 NA18522.hp2 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.269+6789delA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177236918 | |||||
chr1:177237273
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.269+7128C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177237273 | ||||||
chr1:177237329
|
G | C | 1 | a0001c0001t0012g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.269+7184G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177237329 | ||||||
chr1:177237407
|
CA | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(96): Show | 103 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.269+7263delA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177237407 | ||||||
chr1:177237616
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0206 | 2 | HG00558.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.269+7471A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177237616 | ||||||
chr1:177237710
|
A | T | 5 | a0002c0002t0001g0053a0002c0002t0002g0027a0002c0002t0002g0062others(2): Show | 5 | NA18960.hp2 NA18969.hp2 NA18970.hp1 others(2): Show |
intron_variant | MODIFIER | c.269+7565A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177237710 | ||||||
chr1:177237952
|
T | C | 2 | a0001c0001t0004g0065a0001c0001t0012g0024 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.269+7807T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177237952 | ||||||
chr1:177238132
|
G | A | 4 | a0001c0001t0003g0215a0001c0001t0003g0216a0001c0001t0003g0217others(1): Show | 4 | HG02486.hp2 HG02818.hp1 HG02895.hp1 others(1): Show |
intron_variant | MODIFIER | c.269+7987G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177238132 | ||||||
chr1:177238381
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.269+8236G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177238381 | ||||||
chr1:177238554
|
C | T | 1 | a0001c0001t0001g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.269+8409C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177238554 | ||||||
chr1:177238604
|
G | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(96): Show | 103 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.269+8459G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177238604 | ||||||
chr1:177238664
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(96): Show | 103 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.269+8519G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177238664 | ||||||
chr1:177238815
|
A | T | 1 | a0002c0002t0001g0164 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.269+8670A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177238815 | ||||||
chr1:177238861
|
T | A | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.269+8716T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177238861 | ||||||
chr1:177238945
|
A | C | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.269+8800A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177238945 | ||||||
chr1:177239225
|
G | A | 3 | a0002c0002t0002g0035a0002c0002t0002g0039a0002c0002t0009g0180 | 3 | HG02886.hp1 NA19055.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.269+9080G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177239225 | ||||||
chr1:177239368
|
T | A | 1 | a0001c0001t0001g0044 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.269+9223T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177239368 | ||||||
chr1:177239375
|
G | A | 5 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.269+9230G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177239375 | ||||||
chr1:177239614
|
T | A | 1 | a0002c0002t0001g0124 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.269+9469T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177239614 | ||||||
chr1:177239704
|
C | T | 1 | a0001c0001t0001g0121 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.269+9559C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177239704 | ||||||
chr1:177239804
|
C | A | 1 | a0001c0001t0017g0196 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.269+9659C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177239804 | ||||||
chr1:177239818
|
G | T | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.269+9673G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177239818 | ||||||
chr1:177239844
|
G | T | 100 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(97): Show | 104 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.269+9699G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177239844 | ||||||
chr1:177239915
|
C | A | 1 | a0002c0002t0002g0062 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.269+9770C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177239915 | ||||||
chr1:177240167
|
A | G | 1 | a0001c0001t0001g0139 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.269+10022A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177240167 | ||||||
chr1:177240537
|
G | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(96): Show | 103 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.269+10392G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177240537 | ||||||
chr1:177240611
|
C | T | 3 | a0002c0003t0004g0169a0002c0003t0004g0231a0002c0003t0015g0176 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.269+10466C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177240611 | ||||||
chr1:177240784
|
T | C | 1 | a0001c0001t0005g0136 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.269+10639T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177240784 | ||||||
chr1:177240899
|
C | G | 3 | a0002c0003t0004g0169a0002c0003t0004g0231a0002c0003t0015g0176 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.269+10754C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177240899 | ||||||
chr1:177240962
|
C | A | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.269+10817C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177240962 | ||||||
chr1:177240978
|
T | A | 3 | a0001c0001t0004g0173a0001c0001t0004g0174a0002c0002t0009g0180 | 3 | HG02886.hp1 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.269+10833T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177240978 | ||||||
chr1:177241032
|
T | C | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.269+10887T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177241032 | ||||||
chr1:177241064
|
C | T | 24 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(21): Show | 25 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.269+10919C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177241064 | ||||||
chr1:177241132
|
C | T | 1 | a0001c0001t0001g0208 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.269+10987C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177241132 | ||||||
chr1:177241133
|
G | A | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.269+10988G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177241133 | ||||||
chr1:177241263
|
G | T | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.269+11118G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177241263 | ||||||
chr1:177241324
|
A | T | 8 | a0001c0001t0004g0065a0001c0001t0004g0173a0001c0001t0004g0174others(5): Show | 8 | HG02723.hp1 HG02886.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.269+11179A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177241324 | ||||||
chr1:177241431
|
G | C | 1 | a0001c0001t0017g0196 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.269+11286G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177241431 | ||||||
chr1:177241744
|
A | G | 1 | a0002c0002t0002g0027 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.269+11599A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177241744 | ||||||
chr1:177241794
|
G | A | 4 | a0001c0001t0001g0226a0002c0002t0001g0059a0002c0002t0001g0224others(1): Show | 4 | NA18952.hp1 NA18988.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.269+11649G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177241794 | ||||||
chr1:177241803
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.269+11658C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177241803 | ||||||
chr1:177241993
|
T | G | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(132): Show | 140 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.269+11848T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177241993 | ||||||
chr1:177242115
|
C | A | 1 | a0001c0001t0001g0144 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.269+11970C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242115 | ||||||
chr1:177242157
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.269+12012C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242157 | ||||||
chr1:177242278
|
C | G | 7 | a0002c0002t0001g0162a0002c0002t0001g0164a0002c0002t0001g0165others(4): Show | 7 | HG01192.hp2 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.269+12133C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242278 | ||||||
chr1:177242279
|
A | C | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(96): Show | 103 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.269+12134A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242279 | ||||||
chr1:177242591
|
C | T | 1 | a0002c0002t0013g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.269+12446C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242591 | ||||||
chr1:177242596
|
G | T | 2 | a0001c0001t0004g0065a0001c0001t0012g0024 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.269+12451G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242596 | ||||||
chr1:177242599
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.269+12454G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242599 | ||||||
chr1:177242654
|
T | G | 1 | a0001c0005t0001g0016 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.269+12509T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242654 | ||||||
chr1:177242726
|
C | T | 2 | a0001c0001t0001g0121a0001c0001t0002g0218 | 2 | HG02723.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.269+12581C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242726 | ||||||
chr1:177242773
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(96): Show | 103 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.269+12628C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242773 | ||||||
chr1:177242789
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.269+12644G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242789 | ||||||
chr1:177242845
|
G | A | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.269+12700G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242845 | ||||||
chr1:177242909
|
T | C | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.269+12764T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177242909 | ||||||
chr1:177243111
|
G | A | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.270-12808G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177243111 | ||||||
chr1:177243390
|
C | T | 3 | a0002c0003t0004g0169a0002c0003t0004g0231a0002c0003t0015g0176 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.270-12529C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177243390 | ||||||
chr1:177243495
|
T | C | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270-12424T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177243495 | ||||||
chr1:177243686
|
C | T | 4 | a0001c0001t0001g0226a0002c0002t0001g0059a0002c0002t0001g0224others(1): Show | 4 | NA18952.hp1 NA18988.hp2 NA19011.hp2 others(1): Show |
intron_variant | MODIFIER | c.270-12233C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177243686 | ||||||
chr1:177243740
|
C | T | 99 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(96): Show | 103 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.270-12179C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177243740 | ||||||
chr1:177244084
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.270-11835G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177244084 | ||||||
chr1:177244289
|
T | C | 4 | a0002c0002t0001g0006a0002c0002t0001g0120a0002c0002t0001g0151others(1): Show | 5 | HG00099.hp2 HG00733.hp1 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.270-11630T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177244289 | ||||||
chr1:177244510
|
G | A | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270-11409G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177244510 | ||||||
chr1:177244974
|
T | C | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(131): Show | 139 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(136): Show |
intron_variant | MODIFIER | c.270-10945T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177244974 | ||||||
chr1:177245134
|
TAATAACT others(2): Show |
T | 2 | a0002c0003t0004g0169a0002c0003t0004g0231 | 2 | HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.270-10782_270-1077 others(13): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177245134 | |||||
chr1:177245318
|
G | A | 16 | a0001c0001t0007g0019a0002c0002t0002g0007a0002c0002t0002g0028others(13): Show | 17 | HG00438.hp2 HG02071.hp2 HG02135.hp2 others(14): Show |
intron_variant | MODIFIER | c.270-10601G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177245318 | ||||||
chr1:177246320
|
G | A | 1 | a0001c0001t0001g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.270-9599G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177246320 | ||||||
chr1:177246436
|
A | G | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270-9483A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177246436 | ||||||
chr1:177246464
|
C | T | 3 | a0002c0003t0004g0169a0002c0003t0004g0231a0002c0003t0015g0176 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.270-9455C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177246464 | ||||||
chr1:177246548
|
C | G | 1 | a0001c0001t0001g0223 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.270-9371C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177246548 | ||||||
chr1:177246577
|
G | C | 5 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.270-9342G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177246577 | ||||||
chr1:177246580
|
C | T | 1 | a0002c0002t0013g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.270-9339C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177246580 | ||||||
chr1:177246667
|
A | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.270-9252A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177246667 | ||||||
chr1:177246669
|
C | G | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270-9250C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177246669 | ||||||
chr1:177246729
|
T | G | 7 | a0002c0002t0001g0162a0002c0002t0001g0164a0002c0002t0001g0165others(4): Show | 7 | HG01192.hp2 HG02258.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.270-9190T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177246729 | ||||||
chr1:177247128
|
G | A | 1 | a0001c0001t0001g0032 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.270-8791G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177247128 | ||||||
chr1:177247194
|
G | A | 1 | a0002c0002t0014g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.270-8725G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177247194 | ||||||
chr1:177247199
|
A | C | 1 | a0001c0009t0001g0026 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.270-8720A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177247199 | ||||||
chr1:177247229
|
T | G | 4 | a0002c0002t0002g0028a0002c0002t0002g0035a0002c0002t0002g0039others(1): Show | 4 | NA18946.hp1 NA19055.hp2 NA19065.hp1 others(1): Show |
intron_variant | MODIFIER | c.270-8690T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177247229 | ||||||
chr1:177247298
|
G | T | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.270-8621G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177247298 | ||||||
chr1:177247715
|
C | T | 1 | a0002c0002t0002g0156 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.270-8204C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177247715 | ||||||
chr1:177247789
|
C | T | 1 | a0001c0001t0001g0003 | 2 | NA18943.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.270-8130C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177247789 | ||||||
chr1:177248133
|
A | G | 1 | a0001c0001t0003g0093 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.270-7786A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177248133 | ||||||
chr1:177248360
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270-7559C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177248360 | ||||||
chr1:177248435
|
TTG | T | 3 | a0001c0001t0004g0173a0001c0001t0004g0174a0002c0002t0001g0187 | 3 | HG02895.hp2 HG02897.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.270-7465_270-7464d others(4): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177248435 | |||||
chr1:177248452
|
T | C | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.270-7467T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177248452 | ||||||
chr1:177248461
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.270-7458G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177248461 | ||||||
chr1:177248470
|
T | C | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.270-7449T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177248470 | ||||||
chr1:177248472
|
C | CGT | 3 | a0001c0001t0004g0173a0001c0001t0004g0174a0006c0006t0001g0234 | 3 | HG02895.hp2 HG02897.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.270-7431_270-7430d others(4): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177248472 | |||||
chr1:177248472
|
C | T | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.270-7447C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177248472 | ||||||
chr1:177248688
|
G | A | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.270-7231G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177248688 | ||||||
chr1:177248709
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.270-7210G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177248709 | ||||||
chr1:177248806
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.270-7113G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177248806 | ||||||
chr1:177248968
|
T | C | 221 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(218): Show | 230 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(227): Show |
intron_variant | MODIFIER | c.270-6951T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177248968 | ||||||
chr1:177249164
|
A | G | 1 | a0002c0002t0001g0187 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.270-6755A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177249164 | ||||||
chr1:177249630
|
G | A | 5 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.270-6289G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177249630 | ||||||
chr1:177249896
|
G | A | 1 | a0001c0001t0004g0070 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.270-6023G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177249896 | ||||||
chr1:177249966
|
C | T | 6 | a0001c0001t0004g0065a0001c0001t0004g0173a0001c0001t0004g0174others(3): Show | 6 | HG02886.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.270-5953C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177249966 | ||||||
chr1:177250108
|
G | A | 4 | a0001c0001t0004g0065a0001c0001t0004g0173a0001c0001t0004g0174others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.270-5811G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177250108 | ||||||
chr1:177250119
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(132): Show | 140 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.270-5800T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177250119 | ||||||
chr1:177250200
|
C | T | 4 | a0001c0001t0001g0030a0001c0001t0001g0071a0001c0001t0001g0220others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.270-5719C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177250200 | ||||||
chr1:177250227
|
T | C | 4 | a0001c0001t0004g0065a0001c0001t0004g0173a0001c0001t0004g0174others(1): Show | 4 | HG02895.hp2 HG02897.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.270-5692T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177250227 | ||||||
chr1:177250317
|
C | CTTTG | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(115): Show | 123 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(120): Show |
intron_variant | MODIFIER | c.270-5577_270-5574d others(6): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177250317 | |||||
chr1:177250409
|
C | T | 23 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(20): Show | 24 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.270-5510C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177250409 | ||||||
chr1:177250567
|
C | T | 3 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0132 | 3 | NA18942.hp1 NA18973.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.270-5352C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177250567 | ||||||
chr1:177250613
|
C | T | 1 | a0001c0001t0004g0065 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.270-5306C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177250613 | ||||||
chr1:177250621
|
G | A | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270-5298G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177250621 | ||||||
chr1:177250626
|
C | A | 3 | a0002c0003t0004g0169a0002c0003t0004g0231a0002c0003t0015g0176 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.270-5293C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177250626 | ||||||
chr1:177250920
|
T | G | 3 | a0002c0002t0002g0213a0002c0002t0011g0054a0005c0010t0002g0212 | 3 | HG02809.hp1 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.270-4999T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177250920 | ||||||
chr1:177250945
|
A | G | 3 | a0002c0002t0002g0213a0002c0002t0011g0054a0005c0010t0002g0212 | 3 | HG02809.hp1 HG02922.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.270-4974A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177250945 | ||||||
chr1:177251078
|
A | G | 9 | a0001c0001t0001g0031a0001c0001t0001g0080a0001c0001t0001g0139others(6): Show | 9 | HG00621.hp1 HG02074.hp2 HG02165.hp2 others(6): Show |
intron_variant | MODIFIER | c.270-4841A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177251078 | ||||||
chr1:177251371
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.270-4548G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177251371 | ||||||
chr1:177251658
|
T | C | 1 | a0002c0002t0013g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.270-4261T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177251658 | ||||||
chr1:177251836
|
G | A | 4 | a0002c0002t0002g0155a0002c0002t0002g0213a0002c0002t0011g0054others(1): Show | 4 | HG02809.hp1 HG02922.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.270-4083G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177251836 | ||||||
chr1:177252678
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270-3241C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177252678 | ||||||
chr1:177253017
|
A | T | 1 | a0001c0001t0008g0041 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.270-2902A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177253017 | ||||||
chr1:177253021
|
A | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.270-2898A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177253021 | ||||||
chr1:177253149
|
T | G | 1 | a0001c0001t0001g0064 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.270-2770T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177253149 | ||||||
chr1:177253288
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.270-2631C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177253288 | ||||||
chr1:177253477
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.270-2442C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177253477 | ||||||
chr1:177253558
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.270-2361A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177253558 | ||||||
chr1:177253675
|
T | C | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(132): Show | 140 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(137): Show |
intron_variant | MODIFIER | c.270-2244T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177253675 | ||||||
chr1:177253935
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.270-1984T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177253935 | ||||||
chr1:177253944
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.270-1975G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177253944 | ||||||
chr1:177254378
|
G | GCA | 11 | a0001c0001t0001g0050a0001c0001t0001g0201a0001c0001t0001g0240others(8): Show | 12 | HG02071.hp2 HG02257.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.270-1511_270-1510d others(4): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177254378 | |||||
chr1:177254378
|
G | GCACA | 4 | a0001c0001t0001g0208a0001c0001t0012g0024a0002c0002t0001g0127others(1): Show | 4 | HG02970.hp1 HG04228.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.270-1513_270-1510d others(6): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177254378 | |||||
chr1:177254378
|
G | GCACACAC others(3): Show |
5 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.270-1519_270-1510d others(12): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177254378 | |||||
chr1:177254378
|
GCA | G | 26 | a0001c0001t0001g0097a0001c0001t0001g0105a0001c0001t0001g0166others(23): Show | 26 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(23): Show |
intron_variant | MODIFIER | c.270-1511_270-1510d others(4): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177254378 | |||||
chr1:177254378
|
GCACA | G | 9 | a0001c0001t0001g0117a0001c0001t0001g0144a0001c0001t0001g0153others(6): Show | 9 | HG00738.hp2 HG02055.hp2 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.270-1513_270-1510d others(6): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177254378 | |||||
chr1:177254378
|
GCACACA | G | 11 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(8): Show | 12 | HG00639.hp1 HG01099.hp1 HG01106.hp2 others(9): Show |
intron_variant | MODIFIER | c.270-1515_270-1510d others(8): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177254378 | |||||
chr1:177254529
|
A | G | 2 | a0001c0001t0004g0065a0001c0001t0012g0024 | 2 | HG02922.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.270-1390A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177254529 | ||||||
chr1:177254537
|
G | A | 23 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(20): Show | 24 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.270-1382G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177254537 | ||||||
chr1:177254573
|
C | A | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.270-1346C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177254573 | ||||||
chr1:177254679
|
G | A | 2 | a0001c0001t0003g0237a0001c0001t0003g0238 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.270-1240G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177254679 | ||||||
chr1:177254691
|
C | CA | 9 | a0001c0001t0001g0102a0001c0001t0001g0166a0001c0001t0001g0171others(6): Show | 9 | HG02109.hp2 HG02257.hp1 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.270-1216dupA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177254691 | |||||
chr1:177254691
|
CA | C | 63 | a0001c0001t0001g0050a0001c0001t0001g0052a0001c0001t0001g0056others(60): Show | 66 | HG00099.hp2 HG00609.hp2 HG00639.hp1 others(63): Show |
intron_variant | MODIFIER | c.270-1216delA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177254691 | |||||
chr1:177255608
|
T | C | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.270-311T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177255608 | ||||||
chr1:177255611
|
A | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.270-308A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177255611 | ||||||
chr1:177255621
|
A | C | 5 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.270-298A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177255621 | ||||||
chr1:177255690
|
G | C | 1 | a0002c0002t0013g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.270-229G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177255690 | ||||||
chr1:177255732
|
G | GTGAA | 5 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.270-183_270-180dup others(4): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr1 | 177255732 | |||||
chr1:177255886
|
C | G | 1 | a0003c0007t0002g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.270-33C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 2/7 | chr1 | 177255886 | ||||||
chr1:177256229
|
T | C | 2 | a0001c0001t0001g0031a0001c0001t0001g0193 | 2 | HG02074.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.460+120T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 3/7 | chr1 | 177256229 | ||||||
chr1:177256264
|
G | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.460+155G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 3/7 | chr1 | 177256264 | ||||||
chr1:177256326
|
A | G | 1 | a0002c0002t0013g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.460+217A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 3/7 | chr1 | 177256326 | ||||||
chr1:177256398
|
G | T | 2 | a0002c0002t0002g0081a0002c0002t0002g0083 | 2 | NA18973.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.460+289G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 3/7 | chr1 | 177256398 | ||||||
chr1:177257420
|
G | A | 4 | a0001c0001t0001g0030a0001c0001t0001g0071a0001c0001t0001g0220others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.669+36G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177257420 | ||||||
chr1:177257479
|
G | A | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.669+95G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177257479 | ||||||
chr1:177257707
|
C | T | 1 | a0003c0007t0002g0037 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.669+323C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177257707 | ||||||
chr1:177257717
|
G | A | 1 | a0002c0002t0013g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.669+333G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177257717 | ||||||
chr1:177257851
|
A | G | 5 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+467A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177257851 | ||||||
chr1:177258092
|
A | G | 1 | a0002c0002t0002g0051 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.669+708A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258092 | ||||||
chr1:177258367
|
A | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0214 | 2 | HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.669+983A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258367 | ||||||
chr1:177258382
|
G | A | 3 | a0001c0001t0004g0173a0001c0001t0004g0174a0001c0001t0012g0024 | 3 | HG02895.hp2 HG02897.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.669+998G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258382 | ||||||
chr1:177258486
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+1102G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258486 | ||||||
chr1:177258487
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+1103A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258487 | ||||||
chr1:177258601
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+1217T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258601 | ||||||
chr1:177258602
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+1218A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258602 | ||||||
chr1:177258603
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+1219T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258603 | ||||||
chr1:177258685
|
A | G | 1 | a0001c0001t0001g0109 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.669+1301A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258685 | ||||||
chr1:177258737
|
G | T | 3 | a0002c0003t0004g0169a0002c0003t0004g0231a0002c0003t0015g0176 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.669+1353G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258737 | ||||||
chr1:177258878
|
T | C | 1 | a0002c0002t0001g0010 | 2 | HG01346.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.669+1494T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258878 | ||||||
chr1:177258890
|
G | T | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+1506G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258890 | ||||||
chr1:177258933
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.669+1549A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177258933 | ||||||
chr1:177259034
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+1650G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259034 | ||||||
chr1:177259099
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+1715A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259099 | ||||||
chr1:177259225
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+1841A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259225 | ||||||
chr1:177259265
|
A | T | 1 | a0001c0001t0012g0024 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.669+1881A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259265 | ||||||
chr1:177259330
|
T | C | 1 | a0002c0002t0004g0241 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.669+1946T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259330 | ||||||
chr1:177259375
|
C | G | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+1991C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259375 | ||||||
chr1:177259376
|
G | A | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(87): Show | 94 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.669+1992G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259376 | ||||||
chr1:177259376
|
G | C | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+1992G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259376 | ||||||
chr1:177259452
|
G | T | 122 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(119): Show | 127 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.669+2068G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259452 | ||||||
chr1:177259553
|
A | G | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+2169A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259553 | ||||||
chr1:177259554
|
G | A | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+2170G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259554 | ||||||
chr1:177259569
|
G | C | 14 | a0001c0001t0001g0098a0001c0001t0001g0226a0002c0002t0001g0006others(11): Show | 16 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.669+2185G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259569 | ||||||
chr1:177259645
|
C | G | 2 | a0001c0001t0003g0072a0001c0001t0004g0069 | 2 | HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.669+2261C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259645 | ||||||
chr1:177259651
|
C | T | 3 | a0001c0001t0001g0119a0001c0001t0001g0149a0001c0001t0001g0214 | 3 | HG02735.hp1 HG02809.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.669+2267C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259651 | ||||||
chr1:177259720
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+2336A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259720 | ||||||
chr1:177259723
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+2339T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259723 | ||||||
chr1:177259724
|
G | T | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+2340G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259724 | ||||||
chr1:177259742
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+2358T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259742 | ||||||
chr1:177259781
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.669+2397T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259781 | ||||||
chr1:177259939
|
C | T | 4 | a0002c0002t0018g0179a0002c0003t0004g0169a0002c0003t0004g0231others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+2555C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259939 | ||||||
chr1:177259952
|
A | T | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+2568A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177259952 | ||||||
chr1:177260093
|
A | G | 1 | a0001c0009t0001g0026 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.669+2709A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177260093 | ||||||
chr1:177260253
|
T | A | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+2869T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177260253 | ||||||
chr1:177260529
|
C | G | 1 | a0001c0001t0006g0190 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.669+3145C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177260529 | ||||||
chr1:177260541
|
G | C | 40 | a0001c0001t0001g0009a0001c0001t0001g0031a0001c0001t0001g0038others(37): Show | 40 | HG00408.hp2 HG00558.hp2 HG00621.hp1 others(37): Show |
intron_variant | MODIFIER | c.669+3157G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177260541 | ||||||
chr1:177260708
|
A | T | 2 | a0001c0001t0004g0086a0002c0002t0013g0023 | 2 | HG01884.hp2 HG02258.hp2 |
intron_variant | MODIFIER | c.669+3324A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177260708 | ||||||
chr1:177260931
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.669+3547A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177260931 | ||||||
chr1:177261046
|
C | T | 1 | a0002c0002t0014g0020 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.669+3662C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177261046 | ||||||
chr1:177261125
|
C | T | 1 | a0002c0002t0013g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.669+3741C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177261125 | ||||||
chr1:177261550
|
G | A | 1 | a0001c0001t0005g0137 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.669+4166G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177261550 | ||||||
chr1:177261646
|
C | T | 23 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(20): Show | 24 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.669+4262C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177261646 | ||||||
chr1:177261734
|
C | A | 1 | a0001c0001t0001g0107 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.669+4350C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177261734 | ||||||
chr1:177261981
|
A | G | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.669+4597A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177261981 | ||||||
chr1:177262004
|
G | A | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.669+4620G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177262004 | ||||||
chr1:177262176
|
T | C | 23 | a0001c0001t0003g0004a0001c0001t0003g0015a0001c0001t0003g0068others(20): Show | 24 | HG00639.hp1 HG00733.hp2 HG00738.hp1 others(21): Show |
intron_variant | MODIFIER | c.669+4792T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177262176 | ||||||
chr1:177262511
|
G | GA | 127 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(124): Show | 131 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.669+5140dupA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 177262511 | |||||
chr1:177262607
|
A | G | 201 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(198): Show | 208 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(205): Show |
intron_variant | MODIFIER | c.669+5223A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177262607 | ||||||
chr1:177262635
|
C | G | 4 | a0001c0001t0001g0108a0002c0002t0002g0122a0002c0002t0002g0138others(1): Show | 4 | HG00558.hp1 HG02080.hp1 NA18941.hp1 others(1): Show |
intron_variant | MODIFIER | c.669+5251C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177262635 | ||||||
chr1:177262692
|
A | G | 1 | a0001c0001t0001g0145 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.669+5308A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177262692 | ||||||
chr1:177262729
|
G | C | 1 | a0001c0001t0001g0145 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.669+5345G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177262729 | ||||||
chr1:177262928
|
C | T | 131 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(128): Show | 136 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.669+5544C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177262928 | ||||||
chr1:177263024
|
G | A | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.669+5640G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177263024 | ||||||
chr1:177263344
|
A | G | 5 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+5960A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177263344 | ||||||
chr1:177263414
|
C | G | 1 | a0001c0001t0003g0091 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.669+6030C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177263414 | ||||||
chr1:177263651
|
A | G | 1 | a0001c0001t0002g0218 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.669+6267A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177263651 | ||||||
chr1:177263789
|
T | C | 5 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.669+6405T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177263789 | ||||||
chr1:177263818
|
A | AT | 13 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(10): Show | 13 | HG00408.hp2 NA18940.hp2 NA18942.hp1 others(10): Show |
intron_variant | MODIFIER | c.669+6441dupT | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 177263818 | |||||
chr1:177263933
|
T | G | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.669+6549T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177263933 | ||||||
chr1:177264302
|
C | T | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.669+6918C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177264302 | ||||||
chr1:177264965
|
A | C | 1 | a0001c0001t0004g0086 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.669+7581A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177264965 | ||||||
chr1:177265000
|
A | G | 1 | a0001c0001t0001g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.669+7616A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177265000 | ||||||
chr1:177265393
|
C | A | 4 | a0002c0002t0001g0008a0002c0002t0001g0124a0002c0002t0001g0127others(1): Show | 5 | NA18950.hp2 NA18961.hp1 NA18999.hp2 others(2): Show |
intron_variant | MODIFIER | c.669+8009C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177265393 | ||||||
chr1:177265535
|
T | C | 6 | a0001c0001t0004g0173a0001c0001t0004g0174a0002c0002t0018g0179others(3): Show | 6 | HG02723.hp1 HG02895.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.670-7953T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177265535 | ||||||
chr1:177265678
|
T | C | 3 | a0002c0003t0004g0169a0002c0003t0004g0231a0002c0003t0015g0176 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.670-7810T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177265678 | ||||||
chr1:177265785
|
A | C | 1 | a0001c0001t0001g0125 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.670-7703A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177265785 | ||||||
chr1:177265835
|
T | G | 2 | a0002c0002t0002g0233a0002c0011t0002g0232 | 2 | HG02630.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.670-7653T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177265835 | ||||||
chr1:177265853
|
G | T | 2 | a0002c0002t0002g0075a0002c0002t0002g0082 | 2 | HG02071.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.670-7635G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177265853 | ||||||
chr1:177265981
|
G | A | 69 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(66): Show | 73 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(70): Show |
intron_variant | MODIFIER | c.670-7507G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177265981 | ||||||
chr1:177266051
|
T | C | 4 | a0002c0002t0018g0179a0002c0003t0004g0169a0002c0003t0004g0231others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-7437T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177266051 | ||||||
chr1:177266121
|
A | AAAT | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(68): Show | 76 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(73): Show |
intron_variant | MODIFIER | c.670-7344_670-7342d others(5): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 177266121 | |||||
chr1:177266121
|
A | AAATAAT | 3 | a0001c0001t0001g0047a0001c0001t0001g0104a0001c0001t0003g0089 | 3 | HG00280.hp2 HG00738.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.670-7347_670-7342d others(8): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 177266121 | |||||
chr1:177266124
|
T | A | 4 | a0002c0002t0018g0179a0002c0003t0004g0169a0002c0003t0004g0231others(1): Show | 4 | HG02723.hp1 HG02970.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-7364T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177266124 | ||||||
chr1:177266325
|
C | T | 1 | a0001c0001t0004g0069 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.670-7163C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177266325 | ||||||
chr1:177266604
|
C | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.670-6884C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177266604 | ||||||
chr1:177266616
|
C | T | 1 | a0001c0001t0001g0067 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.670-6872C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177266616 | ||||||
chr1:177266629
|
G | A | 1 | a0002c0002t0002g0146 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.670-6859G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177266629 | ||||||
chr1:177266716
|
C | T | 2 | a0001c0001t0001g0067a0006c0006t0001g0234 | 2 | HG01074.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.670-6772C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177266716 | ||||||
chr1:177266751
|
C | G | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.670-6737C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177266751 | ||||||
chr1:177266758
|
T | TA | 15 | a0001c0001t0001g0011a0001c0001t0001g0031a0001c0001t0001g0078others(12): Show | 15 | HG00621.hp2 HG02055.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.670-6708dupA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 177266758 | |||||
chr1:177266758
|
TA | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0188a0001c0001t0001g0191others(2): Show | 5 | HG01884.hp2 HG02735.hp2 HG03927.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-6708delA | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 177266758 | |||||
chr1:177266777
|
A | G | 7 | a0001c0001t0001g0052a0001c0001t0001g0056a0001c0001t0001g0057others(4): Show | 7 | HG01884.hp2 NA18940.hp2 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.670-6711A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177266777 | ||||||
chr1:177266935
|
G | A | 6 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0002t0018g0179others(3): Show | 6 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(3): Show |
intron_variant | MODIFIER | c.670-6553G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177266935 | ||||||
chr1:177267034
|
G | T | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.670-6454G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177267034 | ||||||
chr1:177267252
|
C | CG | 138 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(135): Show | 143 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(140): Show |
intron_variant | MODIFIER | c.670-6235dupG | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 177267252 | |||||
chr1:177267312
|
G | A | 1 | a0002c0002t0002g0233 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.670-6176G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177267312 | ||||||
chr1:177267409
|
C | G | 5 | a0001c0001t0003g0088a0001c0001t0003g0089a0001c0001t0003g0091others(2): Show | 5 | HG00733.hp2 HG00738.hp1 HG01074.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-6079C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177267409 | ||||||
chr1:177268258
|
C | T | 135 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(132): Show | 140 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(137): Show |
intron_variant | MODIFIER | c.670-5230C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177268258 | ||||||
chr1:177268397
|
G | A | 43 | a0002c0002t0001g0053a0002c0002t0002g0007a0002c0002t0002g0027others(40): Show | 44 | HG00438.hp2 HG00558.hp1 HG01099.hp2 others(41): Show |
intron_variant | MODIFIER | c.670-5091G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177268397 | ||||||
chr1:177268496
|
T | G | 1 | a0002c0002t0018g0179 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.670-4992T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177268496 | ||||||
chr1:177268831
|
C | G | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.670-4657C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177268831 | ||||||
chr1:177269027
|
T | A | 4 | a0002c0002t0002g0007a0002c0002t0002g0074a0002c0002t0002g0111others(1): Show | 5 | HG00438.hp2 NA18940.hp1 NA18995.hp2 others(2): Show |
intron_variant | MODIFIER | c.670-4461T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177269027 | ||||||
chr1:177269345
|
T | A | 5 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0003t0004g0169others(2): Show | 5 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-4143T>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177269345 | ||||||
chr1:177269515
|
C | T | 1 | a0002c0002t0013g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.670-3973C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177269515 | ||||||
chr1:177269571
|
T | G | 1 | a0001c0001t0001g0071 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.670-3917T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177269571 | ||||||
chr1:177269742
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.670-3746G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177269742 | ||||||
chr1:177269949
|
C | A | 11 | a0001c0001t0001g0098a0002c0002t0001g0008a0002c0002t0001g0059others(8): Show | 12 | HG00609.hp2 HG03669.hp2 HG06807.hp1 others(9): Show |
intron_variant | MODIFIER | c.670-3539C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177269949 | ||||||
chr1:177270082
|
T | TG | 16 | a0001c0001t0001g0067a0001c0001t0001g0100a0001c0001t0001g0123others(13): Show | 16 | HG00544.hp2 HG00609.hp2 HG01071.hp2 others(13): Show |
intron_variant | MODIFIER | c.670-3398dupG | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 177270082 | |||||
chr1:177270082
|
T | TGG | 79 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(76): Show | 84 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(81): Show |
intron_variant | MODIFIER | c.670-3399_670-3398d others(4): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 177270082 | |||||
chr1:177270082
|
T | TGGG | 39 | a0001c0001t0001g0022a0001c0001t0001g0045a0001c0001t0001g0073others(36): Show | 39 | HG00408.hp1 HG00438.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.670-3400_670-3398d others(5): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 177270082 | |||||
chr1:177270085
|
G | T | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG02486.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.670-3403G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177270085 | ||||||
chr1:177270090
|
GT | G | 3 | a0001c0001t0001g0177a0001c0001t0001g0178a0002c0002t0018g0179 | 3 | HG02486.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.670-3397delT | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177270090 | ||||||
chr1:177270091
|
T | C | 119 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(116): Show | 124 | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.670-3397T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177270091 | ||||||
chr1:177270091
|
T | G | 28 | a0001c0001t0001g0067a0001c0001t0001g0098a0001c0001t0004g0065others(25): Show | 29 | HG00609.hp2 HG00741.hp2 HG01070.hp2 others(26): Show |
intron_variant | MODIFIER | c.670-3397T>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177270091 | ||||||
chr1:177270549
|
G | A | 7 | a0001c0001t0001g0235a0001c0004t0004g0228a0001c0004t0004g0230others(4): Show | 7 | HG01070.hp2 HG01071.hp2 HG02723.hp1 others(4): Show |
intron_variant | MODIFIER | c.670-2939G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177270549 | ||||||
chr1:177270554
|
G | A | 3 | a0001c0001t0004g0086a0001c0001t0004g0173a0001c0001t0004g0174 | 3 | HG02258.hp2 HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.670-2934G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177270554 | ||||||
chr1:177270620
|
C | T | 2 | a0001c0001t0004g0173a0001c0001t0004g0174 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.670-2868C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177270620 | ||||||
chr1:177271031
|
T | C | 3 | a0002c0002t0002g0122a0002c0002t0002g0138a0002c0002t0002g0152 | 3 | HG00558.hp1 NA18941.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.670-2457T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177271031 | ||||||
chr1:177271487
|
G | A | 1 | a0001c0001t0017g0196 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.670-2001G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177271487 | ||||||
chr1:177271579
|
G | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0132 | 2 | NA18942.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.670-1909G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177271579 | ||||||
chr1:177271622
|
A | T | 1 | a0001c0001t0001g0188 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.670-1866A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177271622 | ||||||
chr1:177272333
|
T | C | 1 | a0002c0002t0002g0156 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.670-1155T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177272333 | ||||||
chr1:177272458
|
C | T | 1 | a0002c0002t0002g0082 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.670-1030C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177272458 | ||||||
chr1:177272612
|
G | A | 4 | a0001c0001t0001g0067a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG01074.hp1 HG02486.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.670-876G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177272612 | ||||||
chr1:177272724
|
ATTGT | A | 4 | a0001c0001t0001g0001a0001c0001t0002g0001a0001c0001t0005g0137others(1): Show | 5 | HG01243.hp2 HG02818.hp2 HG03139.hp1 others(2): Show |
intron_variant | MODIFIER | c.670-762_670-759del others(4): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr1 | 177272724 | |||||
chr1:177272830
|
A | G | 2 | a0001c0005t0001g0016a0001c0005t0001g0017 | 2 | HG01358.hp1 HG01993.hp2 |
intron_variant | MODIFIER | c.670-658A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177272830 | ||||||
chr1:177273074
|
C | T | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.670-414C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 4/7 | chr1 | 177273074 | ||||||
chr1:177273906
|
GC | G | 45 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0005others(42): Show | 48 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(45): Show |
intron_variant | MODIFIER | c.775+315delC | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr1 | 177273906 | |||||
chr1:177273907
|
C | A | 1 | a0002c0002t0002g0066 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.775+314C>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177273907 | ||||||
chr1:177273907
|
C | G | 1 | a0001c0001t0001g0210 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.775+314C>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177273907 | ||||||
chr1:177274027
|
A | G | 23 | a0001c0001t0004g0086a0001c0001t0004g0173a0001c0001t0004g0174others(20): Show | 25 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.775+434A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177274027 | ||||||
chr1:177274247
|
C | T | 1 | a0001c0001t0008g0076 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.775+654C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177274247 | ||||||
chr1:177274446
|
G | A | 48 | a0001c0004t0004g0228a0001c0004t0004g0230a0002c0002t0001g0053others(45): Show | 49 | HG00438.hp2 HG00558.hp1 HG01070.hp2 others(46): Show |
intron_variant | MODIFIER | c.775+853G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177274446 | ||||||
chr1:177274501
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.775+908G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177274501 | ||||||
chr1:177275013
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.776-1185G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177275013 | ||||||
chr1:177275019
|
G | A | 2 | a0001c0001t0003g0237a0001c0001t0003g0238 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.776-1179G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177275019 | ||||||
chr1:177275343
|
G | T | 1 | a0001c0001t0001g0226 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.776-855G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177275343 | ||||||
chr1:177275585
|
A | C | 14 | a0002c0002t0001g0006a0002c0002t0001g0008a0002c0002t0001g0059others(11): Show | 16 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.776-613A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177275585 | ||||||
chr1:177275678
|
C | T | 1 | a0001c0001t0003g0217 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.776-520C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177275678 | ||||||
chr1:177275928
|
G | A | 1 | a0002c0002t0002g0061 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.776-270G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177275928 | ||||||
chr1:177276067
|
G | A | 2 | a0001c0001t0001g0022a0001c0004t0001g0029 | 2 | NA18991.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.776-131G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 5/7 | chr1 | 177276067 | ||||||
chr1:177276530
|
A | T | 4 | a0002c0003t0004g0018a0002c0003t0004g0169a0002c0003t0004g0231others(1): Show | 4 | HG02723.hp1 HG02895.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1012+96A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/7 | chr1 | 177276530 | ||||||
chr1:177276673
|
A | G | 2 | a0002c0003t0004g0169a0002c0003t0004g0231 | 2 | HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1012+239A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/7 | chr1 | 177276673 | ||||||
chr1:177276942
|
C | T | 1 | a0001c0001t0001g0201 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.1012+508C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/7 | chr1 | 177276942 | ||||||
chr1:177277157
|
T | TTA | 3 | a0002c0003t0004g0169a0002c0003t0004g0231a0002c0003t0015g0176 | 3 | HG02723.hp1 HG03225.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1012+733_1012+734d others(4): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 177277157 | |||||
chr1:177277545
|
G | A | 1 | a0001c0001t0001g0203 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1013-1018G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/7 | chr1 | 177277545 | ||||||
chr1:177277569
|
A | G | 12 | a0002c0002t0001g0006a0002c0002t0001g0008a0002c0002t0001g0059others(9): Show | 14 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(11): Show |
intron_variant | MODIFIER | c.1013-994A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/7 | chr1 | 177277569 | ||||||
chr1:177277630
|
G | T | 14 | a0002c0002t0001g0006a0002c0002t0001g0008a0002c0002t0001g0059others(11): Show | 16 | HG00099.hp2 HG00609.hp2 HG00733.hp1 others(13): Show |
intron_variant | MODIFIER | c.1013-933G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/7 | chr1 | 177277630 | ||||||
chr1:177278122
|
T | C | 8 | a0001c0001t0001g0001a0001c0001t0001g0064a0001c0001t0001g0101others(5): Show | 9 | HG01070.hp2 HG01071.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.1013-441T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/7 | chr1 | 177278122 | ||||||
chr1:177278362
|
C | T | 1 | a0001c0001t0003g0091 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1013-201C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/7 | chr1 | 177278362 | ||||||
chr1:177278392
|
T | TTCTCAAT others(141): Show |
4 | a0001c0001t0001g0067a0001c0001t0001g0177a0001c0001t0001g0178others(1): Show | 4 | HG01074.hp1 HG02486.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1013-161_1013-160i others(150): Show |
BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr1 | 177278392 | |||||
chr1:177278435
|
A | G | 2 | a0001c0001t0001g0012a0001c0001t0001g0210 | 2 | NA18991.hp1 NA19065.hp2 |
intron_variant | MODIFIER | c.1013-128A>G | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/7 | chr1 | 177278435 | ||||||
chr1:177278557
|
C | T | 1 | a0001c0001t0001g0125 | 1 | NA18952.hp2 | splice_region_variant&intron_variant | LOW | c.1013-6C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 6/7 | chr1 | 177278557 | ||||||
chr1:177278822
|
A | T | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1235+37A>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 7/7 | chr1 | 177278822 | ||||||
chr1:177278830
|
T | C | 1 | a0002c0002t0009g0180 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1235+45T>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 7/7 | chr1 | 177278830 | ||||||
chr1:177278871
|
G | T | 1 | a0001c0001t0001g0175 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1235+86G>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 7/7 | chr1 | 177278871 | ||||||
chr1:177278953
|
G | A | 1 | a0002c0002t0002g0062 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1235+168G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 7/7 | chr1 | 177278953 | ||||||
chr1:177278960
|
G | A | 1 | a0002c0003t0004g0018 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1235+175G>A | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 7/7 | chr1 | 177278960 | ||||||
chr1:177279070
|
A | C | 1 | a0002c0002t0013g0023 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1235+285A>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 7/7 | chr1 | 177279070 | ||||||
chr1:177279878
|
C | T | 1 | a0002c0003t0004g0018 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1236-534C>T | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 7/7 | chr1 | 177279878 | ||||||
chr1:177280034
|
G | C | 2 | a0001c0001t0003g0237a0001c0001t0003g0238 | 2 | HG02055.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1236-378G>C | BRINP2 | ENSG00000198797.7 | transcript | ENST00000361539.5 | protein_coding | 7/7 | chr1 | 177280034 |