geneid | 90249 |
---|---|
ensemblid | ENSG00000113763.12 |
hgncid | 12567 |
symbol | UNC5A |
name | unc-5 netrin receptor A |
refseq_nuc | NM_133369.3 |
refseq_prot | NP_588610.2 |
ensembl_nuc | ENST00000329542.9 |
ensembl_prot | ENSP00000332737.4 |
mane_status | MANE Select |
chr | chr5 |
start | 176810559 |
end | 176880898 |
strand | + |
ver | v1.2 |
region | chr5:176810559-176880898 |
region5000 | chr5:176805559-176885898 |
regionname0 | UNC5A_chr5_176810559_176880898 |
regionname5000 | UNC5A_chr5_176805559_176885898 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 842 | 249 | 81 | 52 | 72 | 8 | 34 | 45 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0002 | 0/0 | 842 | 9 | 4 | 2 | 3 | 0 | 0 | 2 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0003 | 0/0 | 842 | 7 | 5 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0004 | 0/0 | 842 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0005 | 0/0 | 842 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2529 | 242 | 76 | 51 | 72 | 8 | 33 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
c0002 | 0/0 | 2529 | 9 | 4 | 2 | 3 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
c0003 | 0/0 | 2529 | 7 | 5 | 2 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
c0004 | 0/0 | 2529 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
c0005 | 0/0 | 2529 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
c0006 | 0/0 | 2529 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
c0007 | 0/0 | 2529 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
c0008 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
c0009 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1205 | 144 | 29 | 33 | 48 | 7 | 26 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0002 | 1/0 | 1205 | 76 | 24 | 20 | 23 | 1 | 7 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0003 | 0/0 | 1205 | 20 | 20 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0004 | 0/0 | 1205 | 6 | 2 | 1 | 3 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0005 | 0/0 | 1205 | 5 | 5 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0006 | 0/0 | 1205 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0007 | 0/0 | 1205 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0008 | 0/0 | 1205 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0009 | 0/0 | 1205 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0010 | 0/0 | 1205 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0011 | 0/0 | 1205 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0012 | 0/0 | 1205 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0013 | 0/0 | 1205 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0014 | 0/0 | 1205 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0015 | 0/0 | 1205 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0016 | 0/0 | 1205 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
t0017 | 0/0 | 1205 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2529 | 242 | 76 | 51 | 72 | 8 | 33 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0004 | 0/0 | 2529 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0005 | 0/0 | 2529 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0007 | 0/0 | 2529 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0009 | 0/0 | 2529 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0002c0002 | 0/0 | 2529 | 9 | 4 | 2 | 3 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0003c0003 | 0/0 | 2529 | 7 | 5 | 2 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0004c0006 | 0/0 | 2529 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0005c0008 | 0/0 | 2529 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3733 | 136 | 25 | 30 | 48 | 7 | 25 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0002 | 1/0 | 3733 | 64 | 14 | 19 | 22 | 1 | 7 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0003 | 0/0 | 3733 | 20 | 20 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0005 | 0/0 | 3733 | 5 | 5 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0006 | 0/0 | 3733 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0007 | 0/0 | 3733 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0008 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0009 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0010 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0011 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0012 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0013 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0014 | 0/0 | 3733 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0015 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0016 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0001t0017 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0004t0002 | 0/0 | 3733 | 3 | 3 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0005t0002 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0007t0001 | 0/0 | 3733 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0001c0009t0001 | 0/0 | 3733 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0002c0002t0001 | 0/0 | 3733 | 3 | 2 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0002c0002t0004 | 0/0 | 3733 | 6 | 2 | 1 | 3 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0003c0003t0001 | 0/0 | 3733 | 3 | 2 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0003c0003t0002 | 0/0 | 3733 | 4 | 3 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0004c0006t0002 | 0/0 | 3733 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
a0005c0008t0002 | 0/0 | 3733 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | copy fasta | chr5 | 176805559 | 176885898 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0205 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0237 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0003g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0005g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0005g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0005g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0005g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0005g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0006g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0006g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0006g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0007g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0007g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0007g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0008g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0008g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0009g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0010g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0011g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0012g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0013g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0014g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0015g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0016g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0001t0017g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0004t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0004t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0004t0002g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0005t0002g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0005t0002g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0007t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0001c0009t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0002c0002t0001g0006 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0002c0002t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0002c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0002c0002t0004g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0002c0002t0004g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0002c0002t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0002c0002t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0002c0002t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0003c0003t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0003c0003t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0003c0003t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0003c0003t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0003c0003t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0003c0003t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0003c0003t0002g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0004c0006t0002g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
a0005c0008t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0209 | EUR | GBR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | CHS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | CHS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | CHS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | CHS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0089 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00639 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00642 | hp1 | a0001 | c0009 | t0001 | g0176 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0052 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00733 | hp1 | a0003 | c0003 | t0001 | g0084 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0040 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0223 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG00741 | hp2 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0218 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0062 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0085 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01109 | hp1 | a0002 | c0002 | t0004 | g0048 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0053 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0054 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0006 | AMR | PUR | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01255 | hp1 | a0001 | c0001 | t0002 | g0212 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0037 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0204 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0213 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01361 | hp1 | a0003 | c0003 | t0002 | g0107 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01496 | hp2 | a0001 | c0001 | t0017 | g0007 | AMR | CLM | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0156 | EUR | IBS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0056 | EUR | IBS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | IBS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | IBS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0001 | EUR | IBS | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01884 | hp1 | a0001 | c0001 | t0007 | g0247 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01891 | hp1 | a0003 | c0003 | t0002 | g0073 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0080 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0210 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0202 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0207 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02074 | hp2 | a0002 | c0002 | t0004 | g0144 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0108 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02132 | hp2 | a0001 | c0001 | t0002 | g0191 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0118 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02145 | hp2 | a0001 | c0001 | t0007 | g0083 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02257 | hp1 | a0003 | c0003 | t0002 | g0017 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0197 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02280 | hp2 | a0001 | c0001 | t0005 | g0256 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0063 | AMR | PEL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02451 | hp1 | a0001 | c0004 | t0002 | g0233 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02451 | hp2 | a0001 | c0001 | t0003 | g0092 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0137 | EAS | KHV | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0184 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02572 | hp2 | a0002 | c0002 | t0001 | g0112 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0162 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0250 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0252 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02630 | hp1 | a0001 | c0001 | t0014 | g0061 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0243 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02647 | hp1 | a0001 | c0001 | t0007 | g0242 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02647 | hp2 | a0001 | c0001 | t0006 | g0238 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02683 | hp2 | a0001 | c0001 | t0002 | g0214 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0171 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02717 | hp1 | a0001 | c0001 | t0003 | g0261 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0222 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02723 | hp1 | a0003 | c0003 | t0001 | g0082 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02723 | hp2 | a0001 | c0001 | t0003 | g0254 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0050 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02809 | hp2 | a0001 | c0005 | t0002 | g0235 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02818 | hp1 | a0001 | c0005 | t0002 | g0241 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0097 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0248 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02895 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0090 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0255 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0187 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02965 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0012 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0113 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02976 | hp1 | a0001 | c0001 | t0005 | g0023 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0100 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03017 | hp2 | a0001 | c0001 | t0012 | g0129 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03098 | hp1 | a0001 | c0001 | t0005 | g0008 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03098 | hp2 | a0004 | c0006 | t0002 | g0005 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0231 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03139 | hp2 | a0001 | c0001 | t0010 | g0022 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03195 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03195 | hp2 | a0001 | c0004 | t0002 | g0232 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03209 | hp1 | a0002 | c0002 | t0004 | g0066 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0074 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0244 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03453 | hp1 | a0004 | c0006 | t0002 | g0005 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0011 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0015 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03516 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | ESN | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03540 | hp1 | a0003 | c0003 | t0001 | g0188 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03540 | hp2 | a0001 | c0001 | t0005 | g0013 | AFR | GWD | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0086 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0185 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0141 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0044 | SAS | PJL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0199 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0146 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0154 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG04199 | hp2 | a0001 | c0007 | t0001 | g0135 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0033 | SAS | STU | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0065 | AFR | YRI | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18522 | hp2 | a0001 | c0001 | t0005 | g0249 | AFR | YRI | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | CHB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0035 | EAS | CHB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18906 | hp1 | a0001 | c0001 | t0003 | g0259 | AFR | YRI | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0251 | AFR | YRI | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0147 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18945 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18963 | hp1 | a0005 | c0008 | t0002 | g0125 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0148 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0150 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18975 | hp2 | a0002 | c0002 | t0004 | g0165 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18982 | hp1 | a0001 | c0001 | t0016 | g0161 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19004 | hp2 | a0001 | c0001 | t0002 | g0060 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19030 | hp1 | a0001 | c0004 | t0002 | g0078 | AFR | LWK | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0093 | AFR | LWK | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | LWK | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | LWK | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19063 | hp1 | a0001 | c0001 | t0015 | g0041 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19063 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19085 | hp2 | a0002 | c0002 | t0004 | g0166 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | YRI | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0049 | AFR | YRI | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0227 | AFR | ASW | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0246 | AFR | ASW | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0260 | SAS | GIH | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | GIH | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02109 | hp1 | a0003 | c0003 | t0002 | g0240 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02486 | hp1 | a0001 | c0001 | t0006 | g0239 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0216 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0032 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0046 | AFR | ACB | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03471 | hp1 | a0002 | c0002 | t0004 | g0021 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0253 | AFR | MSL | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0079 | AFR | USA | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
HG06807 | hp2 | a0001 | c0001 | t0003 | g0081 | AFR | USA | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | USA | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | USA | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | LWK | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
NA21309 | hp2 | a0001 | c0001 | t0013 | g0095 | AFR | LWK | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0205 | REF | REF | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0237 | REF | REF | UNC5A_chr5_176805559_176885898 | UNC5A | chr5 | 176805559 | 176885898 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:176877669
|
G | A | 1 | a0002 | 9 | HG01109.hp1 HG01243.hp2 HG02074.hp2 others(6): Show |
missense_variant | MODERATE | c.1601G>A | p.Arg534His | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 10/15 | 1793/3733 | 1601/2529 | 534/842 | chr5 | 176877669 | ||
chr5:176877954
|
A | G | 1 | a0004 | 2 | HG03098.hp2 HG03453.hp1 |
missense_variant | MODERATE | c.1696A>G | p.Ser566Gly | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 11/15 | 1888/3733 | 1696/2529 | 566/842 | chr5 | 176877954 | ||
chr5:176877966
|
G | A | 1 | a0003 | 7 | HG00733.hp1 HG01361.hp1 HG01891.hp1 others(4): Show |
missense_variant | MODERATE | c.1708G>A | p.Val570Ile | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 11/15 | 1900/3733 | 1708/2529 | 570/842 | chr5 | 176877966 | ||
chr5:176879851
|
G | T | 1 | a0005 | 1 | NA18963.hp1 | missense_variant | MODERATE | c.2494G>T | p.Ala832Ser | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 2686/3733 | 2494/2529 | 832/842 | chr5 | 176879851 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:176868176
|
C | G | 2 | a0001c0005a0004c0006 | 4 | HG02809.hp2 HG02818.hp1 HG03098.hp2 others(1): Show |
synonymous_variant | LOW | c.339C>G | p.Val113Val | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/15 | 531/3733 | 339/2529 | 113/842 | chr5 | 176868176 | ||
chr5:176868577
|
C | T | 1 | a0001c0004 | 3 | HG02451.hp1 HG03195.hp2 NA19030.hp1 |
synonymous_variant | LOW | c.453C>T | p.Phe151Phe | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 4/15 | 645/3733 | 453/2529 | 151/842 | chr5 | 176868577 | ||
chr5:176874454
|
C | T | 1 | a0001c0009 | 1 | HG00642.hp1 | synonymous_variant | LOW | c.1266C>T | p.Phe422Phe | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/15 | 1458/3733 | 1266/2529 | 422/842 | chr5 | 176874454 | ||
chr5:176878058
|
G | A | 1 | a0001c0007 | 1 | HG04199.hp2 | synonymous_variant | LOW | c.1800G>A | p.Pro600Pro | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 11/15 | 1992/3733 | 1800/2529 | 600/842 | chr5 | 176878058 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:176810575
|
G | T | 1 | a0001c0001t0017 | 1 | HG01496.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-176G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/15 | chr5 | 176810575 | ||||||
chr5:176810578
|
C | T | 1 | a0001c0001t0016 | 1 | NA18982.hp1 | 5_prime_UTR_variant | MODIFIER | c.-173C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/15 | 173 | chr5 | 176810578 | |||||
chr5:176810690
|
A | G | 1 | a0001c0001t0015 | 1 | NA19063.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-61A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/15 | chr5 | 176810690 | ||||||
chr5:176810728
|
C | G | 1 | a0001c0001t0014 | 1 | HG02630.hp1 | 5_prime_UTR_variant | MODIFIER | c.-23C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/15 | 23 | chr5 | 176810728 | |||||
chr5:176880009
|
G | A | 1 | a0002c0002t0004 | 6 | HG01109.hp1 HG02074.hp2 HG03209.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*123G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 123 | chr5 | 176880009 | |||||
chr5:176880272
|
G | T | 1 | a0001c0001t0007 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
3_prime_UTR_variant | MODIFIER | c.*386G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 386 | chr5 | 176880272 | |||||
chr5:176880454
|
C | T | 1 | a0001c0001t0013 | 1 | NA21309.hp2 | 3_prime_UTR_variant | MODIFIER | c.*568C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 568 | chr5 | 176880454 | |||||
chr5:176880457
|
C | T | 1 | a0001c0001t0005 | 5 | HG02280.hp2 HG02976.hp1 HG03098.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*571C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 571 | chr5 | 176880457 | |||||
chr5:176880463
|
C | T | 1 | a0001c0001t0008 | 2 | HG02559.hp2 HG02970.hp1 |
3_prime_UTR_variant | MODIFIER | c.*577C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 577 | chr5 | 176880463 | |||||
chr5:176880503
|
T | C | 14 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(11): Show | 163 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*617T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 617 | chr5 | 176880503 | |||||
chr5:176880705
|
C | T | 1 | a0001c0001t0012 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*819C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 819 | chr5 | 176880705 | |||||
chr5:176880725
|
G | A | 1 | a0001c0001t0009 | 1 | HG00741.hp2 | 3_prime_UTR_variant | MODIFIER | c.*839G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 839 | chr5 | 176880725 | |||||
chr5:176880744
|
C | T | 1 | a0001c0001t0011 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*858C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 858 | chr5 | 176880744 | |||||
chr5:176880756
|
T | C | 5 | a0001c0001t0003a0001c0001t0005a0001c0001t0006others(2): Show | 30 | HG01891.hp2 HG02280.hp2 HG02451.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*870T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 870 | chr5 | 176880756 | |||||
chr5:176880765
|
C | T | 1 | a0001c0001t0010 | 1 | HG03139.hp2 | 3_prime_UTR_variant | MODIFIER | c.*879C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 15/15 | 879 | chr5 | 176880765 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:176810894
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.70+74C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176810894 | ||||||
chr5:176810913
|
A | T | 1 | a0001c0001t0003g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70+93A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176810913 | ||||||
chr5:176810971
|
T | A | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+151T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176810971 | ||||||
chr5:176811002
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+182C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811002 | ||||||
chr5:176811030
|
G | A | 229 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(226): Show | 233 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(230): Show |
intron_variant | MODIFIER | c.70+210G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811030 | ||||||
chr5:176811040
|
C | G | 152 | a0001c0001t0001g0004a0001c0001t0001g0086a0001c0001t0001g0088others(149): Show | 154 | HG00099.hp1 HG00558.hp1 HG00621.hp2 others(151): Show |
intron_variant | MODIFIER | c.70+220C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811040 | ||||||
chr5:176811347
|
T | C | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+527T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811347 | ||||||
chr5:176811351
|
A | C | 1 | a0001c0001t0001g0262 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.70+531A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811351 | ||||||
chr5:176811407
|
ACAGT | A | 3 | a0001c0001t0001g0229a0001c0001t0002g0230a0001c0001t0002g0231 | 3 | HG01167.hp1 HG03130.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.70+590_70+593delGT others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176811407 | |||||
chr5:176811419
|
C | T | 11 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0224others(8): Show | 11 | HG01496.hp1 HG01891.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+599C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811419 | ||||||
chr5:176811547
|
C | T | 32 | a0001c0001t0001g0004a0001c0001t0001g0076a0001c0001t0001g0195others(29): Show | 33 | HG00099.hp1 HG00558.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.70+727C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811547 | ||||||
chr5:176811563
|
A | C | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+743A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811563 | ||||||
chr5:176811606
|
A | AG | 220 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(217): Show | 225 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(222): Show |
intron_variant | MODIFIER | c.70+790dupG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176811606 | |||||
chr5:176811611
|
C | G | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+791C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811611 | ||||||
chr5:176811612
|
T | C | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+792T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811612 | ||||||
chr5:176811613
|
T | TG | 19 | a0001c0001t0001g0072a0001c0001t0001g0192a0001c0001t0001g0227others(16): Show | 20 | HG01243.hp2 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.70+799dupG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176811613 | |||||
chr5:176811614
|
G | T | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+794G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811614 | ||||||
chr5:176811616
|
G | A | 1 | a0001c0001t0006g0243 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.70+796G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811616 | ||||||
chr5:176811619
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.70+799G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811619 | ||||||
chr5:176811712
|
A | C | 7 | a0001c0001t0001g0185a0001c0001t0001g0219a0001c0001t0001g0220others(4): Show | 7 | HG00741.hp1 HG01516.hp2 HG01943.hp2 others(4): Show |
intron_variant | MODIFIER | c.70+892A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811712 | ||||||
chr5:176811720
|
T | C | 22 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(19): Show | 22 | HG01167.hp1 HG01884.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.70+900T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811720 | ||||||
chr5:176811721
|
G | A | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+901G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811721 | ||||||
chr5:176811722
|
A | G | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+902A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811722 | ||||||
chr5:176811725
|
G | A | 1 | a0001c0001t0003g0245 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.70+905G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811725 | ||||||
chr5:176811794
|
A | G | 67 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0067others(64): Show | 70 | HG00099.hp1 HG00609.hp1 HG00609.hp2 others(67): Show |
intron_variant | MODIFIER | c.70+974A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811794 | ||||||
chr5:176811875
|
G | A | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1055G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811875 | ||||||
chr5:176811877
|
A | G | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1057A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811877 | ||||||
chr5:176811880
|
G | A | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1060G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811880 | ||||||
chr5:176811922
|
A | T | 3 | a0001c0001t0002g0096a0001c0001t0003g0065a0002c0002t0004g0066 | 3 | HG02922.hp1 HG03209.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.70+1102A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176811922 | ||||||
chr5:176812113
|
C | T | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.70+1293C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812113 | ||||||
chr5:176812212
|
CAGCTCCG others(6): Show |
C | 1 | a0001c0001t0001g0262 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.70+1396_70+1408del others(13): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176812212 | |||||
chr5:176812232
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70+1412C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812232 | ||||||
chr5:176812468
|
G | C | 35 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(32): Show | 36 | HG00099.hp2 HG00609.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.70+1648G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812468 | ||||||
chr5:176812543
|
C | T | 8 | a0001c0001t0001g0016a0001c0001t0001g0064a0001c0001t0001g0094others(5): Show | 8 | HG01106.hp1 HG01243.hp1 HG02300.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+1723C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812543 | ||||||
chr5:176812599
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70+1779G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812599 | ||||||
chr5:176812679
|
C | G | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1859C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812679 | ||||||
chr5:176812705
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+1885G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812705 | ||||||
chr5:176812720
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70+1900G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812720 | ||||||
chr5:176812745
|
T | C | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1925T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812745 | ||||||
chr5:176812746
|
G | C | 1 | a0001c0001t0001g0260 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+1926G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812746 | ||||||
chr5:176812746
|
G | T | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1926G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812746 | ||||||
chr5:176812747
|
C | G | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+1927C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812747 | ||||||
chr5:176812765
|
G | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(31): Show | 35 | HG00099.hp2 HG00609.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.70+1945G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812765 | ||||||
chr5:176812881
|
C | T | 1 | a0001c0001t0002g0184 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.70+2061C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812881 | ||||||
chr5:176812909
|
G | T | 4 | a0001c0001t0002g0096a0001c0001t0003g0065a0001c0001t0011g0015others(1): Show | 4 | HG02922.hp1 HG03209.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+2089G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812909 | ||||||
chr5:176812917
|
C | G | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.70+2097C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812917 | ||||||
chr5:176812935
|
C | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0003g0092others(2): Show | 5 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+2115C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812935 | ||||||
chr5:176812952
|
G | A | 4 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+2132G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812952 | ||||||
chr5:176812973
|
C | T | 2 | a0001c0001t0007g0242a0001c0001t0007g0247 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+2153C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176812973 | ||||||
chr5:176813184
|
C | T | 1 | a0001c0001t0007g0247 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.70+2364C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813184 | ||||||
chr5:176813464
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+2644C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813464 | ||||||
chr5:176813675
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.70+2855G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813675 | ||||||
chr5:176813738
|
T | C | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+2918T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813738 | ||||||
chr5:176813773
|
G | A | 11 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+2953G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813773 | ||||||
chr5:176813786
|
C | T | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.70+2966C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813786 | ||||||
chr5:176813797
|
C | G | 11 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+2977C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813797 | ||||||
chr5:176813836
|
C | T | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+3016C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813836 | ||||||
chr5:176813837
|
T | G | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+3017T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813837 | ||||||
chr5:176813838
|
G | C | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+3018G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813838 | ||||||
chr5:176813850
|
G | A | 1 | a0003c0003t0001g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.70+3030G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813850 | ||||||
chr5:176813929
|
T | C | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.70+3109T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813929 | ||||||
chr5:176813955
|
G | A | 1 | a0001c0001t0016g0161 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.70+3135G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813955 | ||||||
chr5:176813999
|
G | A | 5 | a0001c0001t0001g0106a0001c0001t0001g0162a0001c0001t0002g0003others(2): Show | 6 | HG01069.hp2 HG01074.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+3179G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176813999 | ||||||
chr5:176814112
|
C | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+3292C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814112 | ||||||
chr5:176814259
|
C | T | 11 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+3439C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814259 | ||||||
chr5:176814383
|
A | T | 1 | a0001c0001t0003g0254 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.70+3563A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814383 | ||||||
chr5:176814417
|
T | G | 1 | a0001c0001t0003g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.70+3597T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814417 | ||||||
chr5:176814542
|
A | G | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.70+3722A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814542 | ||||||
chr5:176814667
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.70+3847G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814667 | ||||||
chr5:176814716
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.70+3896C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814716 | ||||||
chr5:176814854
|
G | T | 1 | a0001c0001t0014g0061 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.70+4034G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814854 | ||||||
chr5:176814867
|
A | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(158): Show | 165 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.70+4047A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176814867 | ||||||
chr5:176815077
|
C | G | 9 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0001g0219others(6): Show | 9 | HG01109.hp1 HG02451.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.70+4257C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815077 | ||||||
chr5:176815110
|
A | G | 1 | a0001c0001t0001g0260 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+4290A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815110 | ||||||
chr5:176815324
|
C | T | 205 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(202): Show | 210 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(207): Show |
intron_variant | MODIFIER | c.70+4504C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815324 | ||||||
chr5:176815342
|
G | C | 1 | a0001c0001t0002g0070 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.70+4522G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815342 | ||||||
chr5:176815390
|
C | T | 1 | a0001c0001t0001g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.70+4570C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815390 | ||||||
chr5:176815466
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+4646C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815466 | ||||||
chr5:176815490
|
A | T | 11 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+4670A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815490 | ||||||
chr5:176815602
|
A | T | 1 | a0001c0001t0017g0007 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.70+4782A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815602 | ||||||
chr5:176815723
|
A | G | 1 | a0001c0001t0009g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.70+4903A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815723 | ||||||
chr5:176815894
|
A | G | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(169): Show | 176 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(173): Show |
intron_variant | MODIFIER | c.70+5074A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815894 | ||||||
chr5:176815922
|
T | C | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.70+5102T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176815922 | ||||||
chr5:176816374
|
A | C | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.70+5554A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816374 | ||||||
chr5:176816394
|
T | C | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+5574T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816394 | ||||||
chr5:176816453
|
G | T | 43 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(40): Show | 44 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.70+5633G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816453 | ||||||
chr5:176816511
|
G | C | 4 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+5691G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816511 | ||||||
chr5:176816542
|
T | A | 1 | a0001c0001t0002g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.70+5722T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816542 | ||||||
chr5:176816715
|
G | C | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+5895G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816715 | ||||||
chr5:176816750
|
T | C | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+5930T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816750 | ||||||
chr5:176816809
|
C | A | 3 | a0001c0001t0005g0008a0001c0001t0005g0023a0001c0001t0014g0061 | 3 | HG02630.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.70+5989C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816809 | ||||||
chr5:176816814
|
C | G | 2 | a0001c0001t0007g0242a0001c0001t0007g0247 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+5994C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176816814 | ||||||
chr5:176817063
|
A | G | 7 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+6243A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817063 | ||||||
chr5:176817070
|
G | T | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.70+6250G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817070 | ||||||
chr5:176817189
|
G | GGCCT | 4 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0163others(1): Show | 5 | HG01069.hp2 HG01074.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+6370_70+6373dup others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176817189 | |||||
chr5:176817281
|
G | C | 1 | a0001c0001t0001g0202 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.70+6461G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817281 | ||||||
chr5:176817305
|
A | G | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+6485A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817305 | ||||||
chr5:176817344
|
G | A | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+6524G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817344 | ||||||
chr5:176817362
|
T | C | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+6542T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817362 | ||||||
chr5:176817377
|
A | G | 1 | a0001c0001t0001g0042 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.70+6557A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817377 | ||||||
chr5:176817419
|
A | G | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+6599A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817419 | ||||||
chr5:176817522
|
G | A | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.70+6702G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817522 | ||||||
chr5:176817577
|
T | TCCCCACC others(8): Show |
4 | a0001c0001t0002g0010a0001c0001t0002g0062a0001c0001t0003g0009others(1): Show | 4 | HG01106.hp1 HG01891.hp2 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+6767_70+6768ins others(15): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176817577 | |||||
chr5:176817577
|
T | TCCCCACC others(9): Show |
2 | a0001c0001t0002g0012a0001c0001t0003g0011 | 2 | HG02965.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.70+6767_70+6768ins others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176817577 | |||||
chr5:176817577
|
T | TCCCCACC others(9): Show |
1 | a0001c0001t0002g0063 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.70+6767_70+6768ins others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176817577 | |||||
chr5:176817577
|
T | TCCCCACC others(10): Show |
2 | a0001c0001t0001g0064a0001c0001t0003g0081 | 2 | HG04184.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.70+6767_70+6768ins others(17): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176817577 | |||||
chr5:176817598
|
A | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+6778A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817598 | ||||||
chr5:176817606
|
G | T | 1 | a0001c0001t0007g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.70+6786G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817606 | ||||||
chr5:176817904
|
G | T | 165 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(162): Show | 169 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(166): Show |
intron_variant | MODIFIER | c.70+7084G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176817904 | ||||||
chr5:176818257
|
G | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+7437G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176818257 | ||||||
chr5:176818598
|
G | A | 1 | a0001c0001t0001g0002 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.70+7778G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176818598 | ||||||
chr5:176818638
|
A | G | 17 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(14): Show | 17 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.70+7818A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176818638 | ||||||
chr5:176818711
|
G | C | 1 | a0001c0001t0001g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.70+7891G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176818711 | ||||||
chr5:176818934
|
A | T | 11 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(8): Show | 11 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+8114A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176818934 | ||||||
chr5:176819017
|
G | T | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.70+8197G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819017 | ||||||
chr5:176819194
|
T | C | 17 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(14): Show | 17 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.70+8374T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819194 | ||||||
chr5:176819284
|
T | A | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+8464T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819284 | ||||||
chr5:176819289
|
C | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+8469C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819289 | ||||||
chr5:176819313
|
G | A | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+8493G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819313 | ||||||
chr5:176819373
|
AAAAGGAA others(3): Show |
A | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+8554_70+8563del others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819373 | ||||||
chr5:176819384
|
G | A | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+8564G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819384 | ||||||
chr5:176819423
|
CA | C | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+8604delA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819423 | ||||||
chr5:176819425
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.70+8605G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819425 | ||||||
chr5:176819466
|
C | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+8646C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819466 | ||||||
chr5:176819575
|
A | G | 1 | a0001c0001t0001g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.70+8755A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819575 | ||||||
chr5:176819678
|
C | T | 1 | a0001c0001t0003g0245 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.70+8858C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176819678 | ||||||
chr5:176820041
|
T | C | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+9221T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820041 | ||||||
chr5:176820115
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.70+9295G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820115 | ||||||
chr5:176820120
|
G | A | 1 | a0001c0001t0001g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.70+9300G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820120 | ||||||
chr5:176820173
|
G | A | 2 | a0001c0001t0007g0242a0001c0001t0007g0247 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+9353G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820173 | ||||||
chr5:176820179
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.70+9359C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820179 | ||||||
chr5:176820225
|
G | A | 1 | a0001c0001t0001g0024 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.70+9405G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820225 | ||||||
chr5:176820354
|
A | G | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+9534A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820354 | ||||||
chr5:176820392
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.70+9572G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820392 | ||||||
chr5:176820733
|
T | C | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+9913T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820733 | ||||||
chr5:176820851
|
C | G | 1 | a0001c0001t0001g0183 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.70+10031C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820851 | ||||||
chr5:176820989
|
C | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+10169C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176820989 | ||||||
chr5:176821035
|
G | T | 20 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(17): Show | 20 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.70+10215G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821035 | ||||||
chr5:176821080
|
A | G | 20 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(17): Show | 20 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.70+10260A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821080 | ||||||
chr5:176821191
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.70+10371G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821191 | ||||||
chr5:176821230
|
C | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+10410C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821230 | ||||||
chr5:176821377
|
A | G | 1 | a0001c0001t0001g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.70+10557A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821377 | ||||||
chr5:176821718
|
C | T | 3 | a0001c0001t0005g0008a0001c0001t0005g0023a0001c0001t0014g0061 | 3 | HG02630.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.70+10898C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821718 | ||||||
chr5:176821727
|
C | T | 62 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0045others(59): Show | 63 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(60): Show |
intron_variant | MODIFIER | c.70+10907C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821727 | ||||||
chr5:176821849
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+11029A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821849 | ||||||
chr5:176821943
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.70+11123G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176821943 | ||||||
chr5:176822108
|
C | A | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+11288C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822108 | ||||||
chr5:176822134
|
C | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+11314C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822134 | ||||||
chr5:176822253
|
C | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+11433C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822253 | ||||||
chr5:176822297
|
G | A | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+11477G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822297 | ||||||
chr5:176822311
|
G | T | 2 | a0001c0001t0001g0098a0001c0001t0001g0153 | 2 | HG02300.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.70+11491G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822311 | ||||||
chr5:176822493
|
G | C | 13 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(10): Show | 13 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.70+11673G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822493 | ||||||
chr5:176822620
|
G | A | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+11800G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822620 | ||||||
chr5:176822863
|
G | A | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+12043G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822863 | ||||||
chr5:176822870
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+12050C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822870 | ||||||
chr5:176822928
|
C | T | 2 | a0001c0001t0007g0242a0001c0001t0007g0247 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+12108C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822928 | ||||||
chr5:176822946
|
C | T | 1 | a0001c0001t0009g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.70+12126C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176822946 | ||||||
chr5:176823001
|
A | G | 235 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(232): Show | 240 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(237): Show |
intron_variant | MODIFIER | c.70+12181A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823001 | ||||||
chr5:176823029
|
G | A | 3 | a0001c0001t0001g0219a0001c0001t0003g0049a0002c0002t0004g0048 | 3 | HG01109.hp1 HG02738.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.70+12209G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823029 | ||||||
chr5:176823125
|
G | T | 3 | a0001c0001t0001g0219a0001c0001t0003g0049a0002c0002t0004g0048 | 3 | HG01109.hp1 HG02738.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.70+12305G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823125 | ||||||
chr5:176823136
|
C | T | 42 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(39): Show | 43 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(40): Show |
intron_variant | MODIFIER | c.70+12316C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823136 | ||||||
chr5:176823137
|
G | A | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+12317G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823137 | ||||||
chr5:176823148
|
G | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0170 | 3 | HG01081.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.70+12328G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823148 | ||||||
chr5:176823419
|
G | C | 2 | a0001c0001t0002g0100a0001c0001t0002g0118 | 2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.70+12599G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823419 | ||||||
chr5:176823427
|
A | G | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+12607A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823427 | ||||||
chr5:176823482
|
C | T | 1 | a0001c0001t0001g0115 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.70+12662C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823482 | ||||||
chr5:176823537
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.70+12717G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823537 | ||||||
chr5:176823835
|
G | A | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(169): Show | 176 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(173): Show |
intron_variant | MODIFIER | c.70+13015G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823835 | ||||||
chr5:176823868
|
G | C | 3 | a0001c0001t0003g0252a0001c0001t0003g0259a0001c0001t0003g0261 | 3 | HG02615.hp2 HG02717.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.70+13048G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823868 | ||||||
chr5:176823893
|
G | A | 1 | a0001c0001t0002g0189 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.70+13073G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823893 | ||||||
chr5:176823931
|
T | C | 3 | a0001c0001t0001g0119a0001c0001t0001g0172a0001c0001t0002g0171 | 3 | HG01361.hp2 HG02135.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.70+13111T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823931 | ||||||
chr5:176823985
|
T | C | 40 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(37): Show | 41 | HG00558.hp1 HG00609.hp1 HG01243.hp1 others(38): Show |
intron_variant | MODIFIER | c.70+13165T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823985 | ||||||
chr5:176823993
|
C | G | 2 | a0001c0001t0007g0242a0001c0001t0007g0247 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+13173C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176823993 | ||||||
chr5:176824046
|
C | G | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+13226C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824046 | ||||||
chr5:176824132
|
G | A | 19 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(16): Show | 19 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.70+13312G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824132 | ||||||
chr5:176824277
|
G | A | 3 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0002g0190 | 3 | HG01106.hp1 HG02083.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.70+13457G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824277 | ||||||
chr5:176824297
|
G | A | 19 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(16): Show | 19 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.70+13477G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824297 | ||||||
chr5:176824344
|
C | A | 167 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(164): Show | 171 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(168): Show |
intron_variant | MODIFIER | c.70+13524C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824344 | ||||||
chr5:176824364
|
C | G | 1 | a0002c0002t0004g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.70+13544C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824364 | ||||||
chr5:176824385
|
A | G | 19 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(16): Show | 19 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.70+13565A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824385 | ||||||
chr5:176824630
|
A | G | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.70+13810A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824630 | ||||||
chr5:176824824
|
C | G | 1 | a0001c0001t0001g0042 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.70+14004C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824824 | ||||||
chr5:176824935
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70+14115C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176824935 | ||||||
chr5:176825070
|
A | T | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.70+14250A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825070 | ||||||
chr5:176825073
|
G | A | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+14253G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825073 | ||||||
chr5:176825221
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.70+14401G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825221 | ||||||
chr5:176825302
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.70+14482G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825302 | ||||||
chr5:176825390
|
C | T | 1 | a0001c0001t0001g0182 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.70+14570C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825390 | ||||||
chr5:176825391
|
G | A | 8 | a0001c0001t0001g0014a0001c0001t0002g0186a0001c0001t0002g0187others(5): Show | 8 | HG01361.hp1 HG02055.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+14571G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825391 | ||||||
chr5:176825527
|
G | A | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(209): Show | 217 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.70+14707G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825527 | ||||||
chr5:176825573
|
G | C | 10 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0001g0219others(7): Show | 10 | HG01109.hp1 HG02451.hp1 HG02451.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+14753G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825573 | ||||||
chr5:176825599
|
G | T | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.70+14779G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825599 | ||||||
chr5:176825755
|
G | C | 1 | a0001c0001t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.70+14935G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825755 | ||||||
chr5:176825850
|
CATTT | C | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+15034_70+15037d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176825850 | |||||
chr5:176825872
|
G | A | 1 | a0001c0001t0001g0026 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.70+15052G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825872 | ||||||
chr5:176825913
|
G | A | 2 | a0001c0001t0005g0008a0001c0001t0005g0023 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.70+15093G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825913 | ||||||
chr5:176825942
|
G | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0003g0092others(2): Show | 5 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+15122G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176825942 | ||||||
chr5:176826026
|
C | T | 19 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(16): Show | 19 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(16): Show |
intron_variant | MODIFIER | c.70+15206C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826026 | ||||||
chr5:176826087
|
G | A | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+15267G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826087 | ||||||
chr5:176826165
|
G | C | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+15345G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826165 | ||||||
chr5:176826284
|
A | T | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(161): Show | 168 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.70+15464A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826284 | ||||||
chr5:176826434
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(157): Show | 164 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(161): Show |
intron_variant | MODIFIER | c.70+15614G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826434 | ||||||
chr5:176826636
|
C | CT | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0002g0075others(2): Show | 5 | HG02055.hp1 HG02559.hp2 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+15840dupT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176826636 | |||||
chr5:176826636
|
CT | C | 18 | a0001c0001t0001g0014a0001c0001t0001g0110a0001c0001t0001g0151others(15): Show | 18 | HG00733.hp1 HG01361.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.70+15840delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176826636 | |||||
chr5:176826636
|
CTT | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 197 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(194): Show |
intron_variant | MODIFIER | c.70+15839_70+15840d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176826636 | |||||
chr5:176826636
|
CTTT | C | 5 | a0001c0001t0001g0120a0001c0001t0002g0096a0001c0001t0002g0189others(2): Show | 5 | HG02615.hp2 HG02698.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+15838_70+15840d others(5): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176826636 | |||||
chr5:176826636
|
CTTTT | C | 8 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0001g0219others(5): Show | 8 | HG01109.hp1 HG02451.hp1 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.70+15837_70+15840d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176826636 | |||||
chr5:176826636
|
CTTTTT | C | 5 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063others(2): Show | 5 | HG01106.hp1 HG02300.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+15836_70+15840d others(7): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176826636 | |||||
chr5:176826697
|
G | A | 1 | a0001c0001t0001g0027 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.70+15877G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826697 | ||||||
chr5:176826782
|
A | T | 2 | a0001c0001t0002g0148a0001c0001t0002g0149 | 2 | NA18971.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.70+15962A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826782 | ||||||
chr5:176826789
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.70+15969C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826789 | ||||||
chr5:176826864
|
C | A | 1 | a0001c0001t0001g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70+16044C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826864 | ||||||
chr5:176826941
|
A | C | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.70+16121A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176826941 | ||||||
chr5:176827051
|
A | G | 14 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(11): Show | 14 | HG01106.hp1 HG01109.hp1 HG02300.hp2 others(11): Show |
intron_variant | MODIFIER | c.70+16231A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827051 | ||||||
chr5:176827179
|
C | CT | 158 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(155): Show | 162 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(159): Show |
intron_variant | MODIFIER | c.70+16380dupT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176827179 | |||||
chr5:176827179
|
C | CTT | 18 | a0001c0001t0001g0024a0001c0001t0001g0047a0001c0001t0001g0059others(15): Show | 18 | HG00735.hp1 HG01517.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.70+16379_70+16380d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176827179 | |||||
chr5:176827179
|
CT | C | 45 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0114others(42): Show | 46 | HG00558.hp1 HG00733.hp1 HG01167.hp1 others(43): Show |
intron_variant | MODIFIER | c.70+16380delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176827179 | |||||
chr5:176827207
|
G | T | 1 | a0001c0001t0007g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.70+16387G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827207 | ||||||
chr5:176827221
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.70+16401C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827221 | ||||||
chr5:176827371
|
C | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+16551C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827371 | ||||||
chr5:176827443
|
A | G | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+16623A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827443 | ||||||
chr5:176827487
|
T | C | 1 | a0001c0001t0003g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.70+16667T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827487 | ||||||
chr5:176827553
|
A | G | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+16733A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827553 | ||||||
chr5:176827571
|
C | T | 1 | a0001c0001t0001g0192 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.70+16751C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827571 | ||||||
chr5:176827628
|
G | A | 1 | a0001c0001t0001g0028 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.70+16808G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827628 | ||||||
chr5:176827684
|
G | A | 18 | a0001c0001t0001g0071a0001c0001t0001g0108a0001c0001t0001g0109others(15): Show | 18 | HG00558.hp1 HG00609.hp1 HG02027.hp1 others(15): Show |
intron_variant | MODIFIER | c.70+16864G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827684 | ||||||
chr5:176827710
|
C | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+16890C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827710 | ||||||
chr5:176827785
|
T | C | 2 | a0001c0001t0007g0242a0001c0001t0007g0247 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+16965T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827785 | ||||||
chr5:176827807
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.70+16987T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176827807 | ||||||
chr5:176828002
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(161): Show | 168 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.70+17182G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828002 | ||||||
chr5:176828045
|
T | G | 1 | a0002c0002t0004g0165 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.70+17225T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828045 | ||||||
chr5:176828111
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.70+17291C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828111 | ||||||
chr5:176828152
|
T | C | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 243 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(240): Show |
intron_variant | MODIFIER | c.70+17332T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828152 | ||||||
chr5:176828352
|
G | A | 1 | a0001c0001t0002g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.70+17532G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828352 | ||||||
chr5:176828484
|
C | T | 1 | a0003c0003t0001g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.70+17664C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828484 | ||||||
chr5:176828516
|
C | A | 5 | a0001c0001t0001g0108a0001c0001t0001g0196a0001c0001t0001g0197others(2): Show | 5 | HG02132.hp1 HG02273.hp1 NA18954.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+17696C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828516 | ||||||
chr5:176828564
|
A | G | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+17744A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828564 | ||||||
chr5:176828567
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.70+17747G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828567 | ||||||
chr5:176828609
|
G | A | 3 | a0001c0001t0002g0186a0001c0001t0002g0187a0003c0003t0001g0188 | 3 | HG02922.hp2 HG03516.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.70+17789G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828609 | ||||||
chr5:176828645
|
G | A | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(161): Show | 168 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.70+17825G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828645 | ||||||
chr5:176828656
|
T | C | 44 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(41): Show | 45 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.70+17836T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828656 | ||||||
chr5:176828747
|
T | A | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG02080.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.70+17927T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828747 | ||||||
chr5:176828814
|
T | C | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+17994T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828814 | ||||||
chr5:176828873
|
G | A | 3 | a0001c0001t0005g0008a0001c0001t0005g0023a0001c0001t0014g0061 | 3 | HG02630.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.70+18053G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828873 | ||||||
chr5:176828925
|
T | G | 2 | a0001c0001t0005g0249a0003c0003t0001g0084 | 2 | HG00733.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.70+18105T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176828925 | ||||||
chr5:176829080
|
G | A | 192 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(189): Show | 196 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(193): Show |
intron_variant | MODIFIER | c.70+18260G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829080 | ||||||
chr5:176829131
|
C | CA | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(7): Show | 10 | HG01109.hp1 HG01884.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+18328dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829131 | |||||
chr5:176829131
|
CA | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 174 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(171): Show |
intron_variant | MODIFIER | c.70+18328delA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829131 | |||||
chr5:176829145
|
A | AG | 44 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(41): Show | 45 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(42): Show |
intron_variant | MODIFIER | c.70+18325_70+18326i others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829145 | ||||||
chr5:176829156
|
AGATG | A | 25 | a0001c0001t0001g0047a0001c0001t0001g0077a0001c0001t0001g0079others(22): Show | 26 | HG01243.hp2 HG01496.hp1 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.70+18382_70+18385d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829156 | |||||
chr5:176829156
|
AGATGGAT others(1): Show |
A | 17 | a0001c0001t0001g0014a0001c0001t0001g0064a0001c0001t0001g0258others(14): Show | 17 | HG01106.hp1 HG01891.hp2 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.70+18378_70+18385d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829156 | |||||
chr5:176829156
|
AGATGGAT others(5): Show |
A | 38 | a0001c0001t0001g0016a0001c0001t0001g0071a0001c0001t0001g0108others(35): Show | 39 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(36): Show |
intron_variant | MODIFIER | c.70+18374_70+18385d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829156 | |||||
chr5:176829156
|
AGATGGAT others(9): Show |
A | 7 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(4): Show | 7 | HG01884.hp2 HG02622.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+18370_70+18385d others(18): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829156 | |||||
chr5:176829159
|
T | A | 4 | a0001c0001t0001g0045a0001c0001t0003g0009a0001c0001t0007g0242others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+18339T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829159 | ||||||
chr5:176829159
|
TGGATGGA others(18): Show |
T | 1 | a0001c0001t0002g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.70+18341_70+18365d others(27): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829159 | |||||
chr5:176829160
|
G | A | 4 | a0001c0001t0001g0045a0001c0001t0003g0009a0001c0001t0007g0242others(1): Show | 4 | HG01884.hp1 HG02647.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+18340G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829160 | ||||||
chr5:176829174
|
ATGGATGG others(25): Show |
A | 2 | a0001c0001t0002g0058a0001c0001t0002g0194 | 2 | HG01081.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.70+18366_70+18397d others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829174 | |||||
chr5:176829178
|
ATGGATGG others(21): Show |
A | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(150): Show | 156 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(153): Show |
intron_variant | MODIFIER | c.70+18370_70+18397d others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829178 | |||||
chr5:176829182
|
ATGGATGG others(17): Show |
A | 8 | a0001c0001t0001g0027a0001c0001t0001g0162a0001c0001t0001g0205others(5): Show | 9 | HG01069.hp2 HG01074.hp1 HG01928.hp2 others(6): Show |
intron_variant | MODIFIER | c.70+18374_70+18397d others(26): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829182 | |||||
chr5:176829186
|
ATGGATGG others(13): Show |
A | 2 | a0001c0001t0003g0049a0002c0002t0004g0048 | 2 | HG01109.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.70+18378_70+18397d others(22): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829186 | |||||
chr5:176829190
|
ATGGATGG others(9): Show |
A | 1 | a0001c0001t0001g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.70+18382_70+18397d others(18): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829190 | |||||
chr5:176829206
|
T | A | 1 | a0001c0001t0002g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.70+18386T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829206 | ||||||
chr5:176829231
|
A | AGATG | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+18429_70+18432d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829231 | |||||
chr5:176829269
|
C | CTGGA | 164 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(161): Show | 168 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.70+18463_70+18466d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829269 | |||||
chr5:176829305
|
GATGGATG others(1): Show |
G | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(176): Show | 183 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(180): Show |
intron_variant | MODIFIER | c.70+18493_70+18500d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829305 | |||||
chr5:176829313
|
A | T | 14 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0039others(11): Show | 14 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.70+18493A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829313 | ||||||
chr5:176829315
|
TG | T | 11 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0104others(8): Show | 11 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.70+18497delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829315 | |||||
chr5:176829316
|
GGATGTAT others(2): Show |
G | 3 | a0001c0001t0001g0039a0001c0001t0001g0145a0001c0001t0002g0116 | 3 | NA18979.hp2 NA19060.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.70+18497_70+18505d others(11): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829316 | ||||||
chr5:176829319
|
T | A | 11 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0104others(8): Show | 11 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.70+18499T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829319 | ||||||
chr5:176829320
|
G | A | 11 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0104others(8): Show | 11 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.70+18500G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829320 | ||||||
chr5:176829324
|
GAAA | G | 10 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0104others(7): Show | 10 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(7): Show |
intron_variant | MODIFIER | c.70+18505_70+18507d others(5): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829324 | ||||||
chr5:176829326
|
A | T | 1 | a0001c0001t0002g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.70+18506A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829326 | ||||||
chr5:176829327
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.70+18507A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829327 | ||||||
chr5:176829328
|
T | G | 11 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0104others(8): Show | 11 | HG01071.hp2 HG01255.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.70+18508T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829328 | ||||||
chr5:176829328
|
T | TATGG | 39 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(36): Show | 41 | HG00558.hp1 HG00609.hp1 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.70+18547_70+18550d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829328 | |||||
chr5:176829328
|
T | TATGGATG others(1): Show |
4 | a0001c0001t0001g0108a0001c0001t0003g0050a0001c0001t0003g0111others(1): Show | 4 | HG02132.hp1 HG02572.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.70+18543_70+18550d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829328 | |||||
chr5:176829328
|
TATGG | T | 29 | a0001c0001t0001g0004a0001c0001t0001g0018a0001c0001t0001g0019others(26): Show | 30 | HG00621.hp2 HG00735.hp2 HG01168.hp2 others(27): Show |
intron_variant | MODIFIER | c.70+18547_70+18550d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829328 | |||||
chr5:176829328
|
TATGGATG others(1): Show |
T | 11 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0062others(8): Show | 11 | HG01106.hp1 HG01106.hp2 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.70+18543_70+18550d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829328 | |||||
chr5:176829328
|
TATGGATG others(5): Show |
T | 1 | a0001c0001t0001g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.70+18539_70+18550d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829328 | |||||
chr5:176829416
|
A | AATGG | 14 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(11): Show | 14 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.70+18623_70+18626d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829416 | |||||
chr5:176829416
|
A | AATGGATG others(1): Show |
6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+18619_70+18626d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829416 | |||||
chr5:176829416
|
A | AATGGATG others(5): Show |
3 | a0001c0001t0001g0219a0001c0001t0003g0049a0002c0002t0004g0048 | 3 | HG01109.hp1 HG02738.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.70+18615_70+18626d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829416 | |||||
chr5:176829416
|
A | G | 1 | a0002c0002t0004g0165 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.70+18596A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829416 | ||||||
chr5:176829416
|
AATGG | A | 2 | a0001c0001t0003g0250a0001c0001t0003g0254 | 2 | HG02615.hp1 HG02723.hp2 |
intron_variant | MODIFIER | c.70+18623_70+18626d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829416 | |||||
chr5:176829485
|
GGTGGGTG others(14): Show |
G | 1 | a0001c0001t0002g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.70+18678_70+18698d others(23): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829485 | |||||
chr5:176829560
|
A | AGATG | 5 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0003g0092others(2): Show | 5 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+18760_70+18763d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829560 | |||||
chr5:176829698
|
G | C | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.70+18878G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829698 | ||||||
chr5:176829715
|
C | T | 44 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0056others(41): Show | 45 | HG00099.hp1 HG00639.hp2 HG00642.hp2 others(42): Show |
intron_variant | MODIFIER | c.70+18895C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829715 | ||||||
chr5:176829793
|
T | C | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.70+18973T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829793 | ||||||
chr5:176829830
|
G | T | 1 | a0001c0001t0001g0201 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.70+19010G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829830 | ||||||
chr5:176829881
|
C | CTTTTTTT others(4): Show |
3 | a0001c0001t0001g0219a0001c0001t0003g0049a0002c0002t0004g0048 | 3 | HG01109.hp1 HG02738.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.70+19062_70+19072d others(13): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | |||||
chr5:176829881
|
C | CTTTTTTT others(5): Show |
12 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0003g0009others(9): Show | 12 | HG01891.hp2 HG02451.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.70+19072_70+19073i others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | |||||
chr5:176829881
|
C | CTTTTTTT others(6): Show |
2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.70+19072_70+19073i others(15): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | |||||
chr5:176829881
|
C | CTTTTTTT others(7): Show |
7 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0105others(4): Show | 7 | HG00099.hp1 HG00621.hp2 HG01069.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+19072_70+19073i others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | |||||
chr5:176829881
|
C | CTTTTTTT others(8): Show |
132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(129): Show | 135 | HG00099.hp2 HG00621.hp1 HG00639.hp1 others(132): Show |
intron_variant | MODIFIER | c.70+19072_70+19073i others(17): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | |||||
chr5:176829881
|
C | CTTTTTTT others(9): Show |
31 | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0047others(28): Show | 32 | HG00558.hp2 HG00609.hp2 HG01081.hp1 others(29): Show |
intron_variant | MODIFIER | c.70+19072_70+19073i others(18): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | |||||
chr5:176829881
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0001g0104a0001c0001t0001g0251 | 2 | HG02040.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.70+19072_70+19073i others(19): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | |||||
chr5:176829881
|
C | CTTTTTTT others(13): Show |
2 | a0001c0001t0001g0018a0002c0002t0004g0021 | 2 | HG01884.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.70+19072_70+19073i others(22): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | |||||
chr5:176829881
|
C | CTTTTTTT others(17): Show |
2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.70+19072_70+19073i others(26): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176829881 | |||||
chr5:176829912
|
T | C | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+19092T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176829912 | ||||||
chr5:176830018
|
G | A | 4 | a0001c0001t0001g0094a0001c0001t0003g0092a0001c0001t0003g0093others(1): Show | 4 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+19198G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830018 | ||||||
chr5:176830074
|
C | T | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.70+19254C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830074 | ||||||
chr5:176830195
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.70+19375G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830195 | ||||||
chr5:176830273
|
C | T | 1 | a0001c0001t0002g0040 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.70+19453C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830273 | ||||||
chr5:176830366
|
ATGTGTGT others(68): Show |
A | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+19574_70+19648d others(77): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830366 | |||||
chr5:176830418
|
T | G | 5 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0003g0092others(2): Show | 5 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+19598T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830418 | ||||||
chr5:176830438
|
CAT | C | 4 | a0001c0001t0001g0094a0001c0001t0003g0092a0001c0001t0003g0093others(1): Show | 4 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+19619_70+19620d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830438 | ||||||
chr5:176830439
|
ATG | A | 175 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(172): Show | 179 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(176): Show |
intron_variant | MODIFIER | c.70+19633_70+19634d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830439 | |||||
chr5:176830459
|
C | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+19639C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830459 | ||||||
chr5:176830561
|
GGT | G | 232 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(229): Show | 237 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(234): Show |
intron_variant | MODIFIER | c.70+19759_70+19760d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830561 | |||||
chr5:176830561
|
GGTGTGTG others(3): Show |
G | 2 | a0001c0001t0001g0071a0001c0001t0001g0169 | 2 | HG00609.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.70+19751_70+19760d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830561 | |||||
chr5:176830571
|
T | TGTGTGTG others(41): Show |
3 | a0001c0001t0005g0008a0001c0001t0005g0023a0001c0001t0014g0061 | 3 | HG02630.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.70+19758_70+19759i others(50): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830571 | |||||
chr5:176830579
|
T | C | 170 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(167): Show | 174 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(171): Show |
intron_variant | MODIFIER | c.70+19759T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830579 | ||||||
chr5:176830598
|
A | G | 1 | a0002c0002t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.70+19778A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830598 | ||||||
chr5:176830633
|
TGC | T | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+19816_70+19817d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830633 | |||||
chr5:176830635
|
C | T | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(186): Show | 193 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(190): Show |
intron_variant | MODIFIER | c.70+19815C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830635 | ||||||
chr5:176830650
|
T | TTG | 5 | a0001c0001t0003g0065a0001c0001t0007g0242a0001c0001t0007g0247others(2): Show | 5 | HG01884.hp1 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+19841_70+19842d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830650 | |||||
chr5:176830651
|
T | C | 195 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(192): Show | 199 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(196): Show |
intron_variant | MODIFIER | c.70+19831T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830651 | ||||||
chr5:176830706
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.70+19886G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830706 | ||||||
chr5:176830726
|
A | G | 42 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(39): Show | 43 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.70+19906A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830726 | ||||||
chr5:176830727
|
T | TGTGTGG | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.70+19913_70+19918d others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830727 | |||||
chr5:176830739
|
C | G | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+19919C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830739 | ||||||
chr5:176830740
|
T | G | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+19920T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830740 | ||||||
chr5:176830741
|
G | T | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+19921G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830741 | ||||||
chr5:176830784
|
G | A | 1 | a0001c0001t0005g0249 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.70+19964G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176830784 | ||||||
chr5:176830897
|
CGTGT | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 182 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(179): Show |
intron_variant | MODIFIER | c.70+20082_70+20085d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830897 | |||||
chr5:176830915
|
CGTGTGTG others(3): Show |
C | 18 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0001g0219others(15): Show | 18 | HG01109.hp1 HG01891.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.70+20105_70+20114d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830915 | |||||
chr5:176830973
|
G | GGT | 21 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0001g0094others(18): Show | 21 | HG01106.hp1 HG01109.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.70+20167_70+20168d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176830973 | |||||
chr5:176831028
|
C | G | 6 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(3): Show | 6 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.70+20208C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831028 | ||||||
chr5:176831157
|
C | T | 1 | a0001c0001t0001g0202 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.70+20337C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831157 | ||||||
chr5:176831210
|
G | A | 3 | a0001c0001t0001g0101a0001c0001t0001g0104a0001c0001t0002g0102 | 3 | HG02040.hp2 NA19074.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.70+20390G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831210 | ||||||
chr5:176831361
|
C | T | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.70+20541C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831361 | ||||||
chr5:176831400
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(193): Show | 200 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(197): Show |
intron_variant | MODIFIER | c.70+20580A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831400 | ||||||
chr5:176831588
|
C | T | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.70+20768C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831588 | ||||||
chr5:176831685
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.70+20865C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831685 | ||||||
chr5:176831727
|
G | A | 42 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(39): Show | 43 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(40): Show |
intron_variant | MODIFIER | c.70+20907G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831727 | ||||||
chr5:176831767
|
C | T | 2 | a0001c0001t0001g0024a0001c0001t0001g0039 | 2 | NA18944.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.70+20947C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831767 | ||||||
chr5:176831792
|
C | T | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.70+20972C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831792 | ||||||
chr5:176831871
|
C | G | 1 | a0001c0001t0001g0260 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+21051C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831871 | ||||||
chr5:176831883
|
C | CT | 5 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(2): Show | 5 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+21064dupT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | |||||
chr5:176831883
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0003g0049 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.70+21064_70+21065i others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | |||||
chr5:176831883
|
C | CTTTTTTT others(4): Show |
1 | a0002c0002t0004g0048 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.70+21064_70+21065i others(13): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | |||||
chr5:176831883
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0001g0219 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.70+21064_70+21065i others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | |||||
chr5:176831883
|
C | T | 3 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0013g0095 | 3 | HG02451.hp2 NA19030.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.70+21063C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831883 | ||||||
chr5:176831883
|
CTCT | C | 5 | a0001c0001t0001g0045a0001c0001t0001g0064a0001c0001t0002g0062others(2): Show | 5 | HG01106.hp1 HG02300.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+21065_70+21067d others(5): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | |||||
chr5:176831883
|
CTCTTTTT others(2): Show |
C | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+21065_70+21073d others(11): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | |||||
chr5:176831883
|
CTCTTTTT others(3): Show |
C | 11 | a0001c0001t0001g0002a0001c0001t0001g0154a0001c0001t0001g0170others(8): Show | 12 | HG01081.hp1 HG01256.hp2 HG01258.hp1 others(9): Show |
intron_variant | MODIFIER | c.70+21065_70+21074d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | |||||
chr5:176831883
|
CTCTTTTT others(4): Show |
C | 146 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(143): Show | 149 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(146): Show |
intron_variant | MODIFIER | c.70+21065_70+21075d others(13): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | |||||
chr5:176831883
|
CTCTTTTT others(5): Show |
C | 8 | a0001c0001t0001g0067a0001c0001t0001g0143a0001c0001t0001g0162others(5): Show | 8 | HG02040.hp1 HG02602.hp1 HG02976.hp2 others(5): Show |
intron_variant | MODIFIER | c.70+21065_70+21076d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831883 | |||||
chr5:176831885
|
C | T | 13 | a0001c0001t0001g0094a0001c0001t0001g0219a0001c0001t0002g0010others(10): Show | 13 | HG01109.hp1 HG01891.hp2 HG02451.hp2 others(10): Show |
intron_variant | MODIFIER | c.70+21065C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176831885 | ||||||
chr5:176831885
|
CT | C | 12 | a0001c0001t0001g0077a0001c0001t0001g0079a0001c0001t0001g0224others(9): Show | 13 | HG01243.hp2 HG01496.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.70+21094delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831885 | |||||
chr5:176831885
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.70+21084_70+21094d others(13): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831885 | |||||
chr5:176831885
|
CTTTTTTT others(5): Show |
C | 40 | a0001c0001t0001g0014a0001c0001t0001g0071a0001c0001t0001g0108others(37): Show | 41 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.70+21083_70+21094d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831885 | |||||
chr5:176831885
|
CTTTTTTT others(6): Show |
C | 2 | a0001c0001t0003g0050a0001c0001t0005g0249 | 2 | HG02809.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.70+21082_70+21094d others(15): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176831885 | |||||
chr5:176832120
|
C | T | 2 | a0001c0001t0001g0119a0001c0001t0001g0172 | 2 | HG01361.hp2 HG02135.hp2 |
intron_variant | MODIFIER | c.70+21300C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832120 | ||||||
chr5:176832144
|
A | G | 238 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(235): Show | 243 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(240): Show |
intron_variant | MODIFIER | c.70+21324A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832144 | ||||||
chr5:176832181
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.70+21361G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832181 | ||||||
chr5:176832188
|
T | C | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.70+21368T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832188 | ||||||
chr5:176832243
|
C | G | 1 | a0001c0001t0002g0218 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.70+21423C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832243 | ||||||
chr5:176832309
|
A | G | 2 | a0001c0001t0007g0242a0001c0001t0007g0247 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+21489A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832309 | ||||||
chr5:176832392
|
C | T | 2 | a0001c0001t0007g0242a0001c0001t0007g0247 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+21572C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832392 | ||||||
chr5:176832406
|
T | C | 1 | a0001c0001t0003g0245 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.70+21586T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832406 | ||||||
chr5:176832644
|
G | C | 1 | a0001c0001t0001g0086 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.70+21824G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832644 | ||||||
chr5:176832813
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.70+21993G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832813 | ||||||
chr5:176832885
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.70+22065G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176832885 | ||||||
chr5:176833072
|
A | C | 38 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(35): Show | 39 | HG00609.hp1 HG01243.hp1 HG01361.hp1 others(36): Show |
intron_variant | MODIFIER | c.70+22252A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833072 | ||||||
chr5:176833103
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.70+22283C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833103 | ||||||
chr5:176833184
|
G | A | 1 | a0001c0001t0002g0040 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.70+22364G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833184 | ||||||
chr5:176833288
|
G | A | 1 | a0001c0001t0002g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.70+22468G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833288 | ||||||
chr5:176833325
|
C | T | 43 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(40): Show | 44 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.70+22505C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833325 | ||||||
chr5:176833328
|
T | TG | 43 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(40): Show | 44 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(41): Show |
intron_variant | MODIFIER | c.70+22509dupG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176833328 | |||||
chr5:176833473
|
A | T | 1 | a0001c0001t0002g0171 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.70+22653A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833473 | ||||||
chr5:176833491
|
T | G | 237 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(234): Show | 242 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(239): Show |
intron_variant | MODIFIER | c.70+22671T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833491 | ||||||
chr5:176833580
|
G | T | 2 | a0001c0001t0007g0242a0001c0001t0007g0247 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.70+22760G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833580 | ||||||
chr5:176833670
|
C | T | 3 | a0001c0001t0003g0065a0001c0001t0011g0015a0002c0002t0004g0066 | 3 | HG03209.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.70+22850C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833670 | ||||||
chr5:176833699
|
T | C | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+22879T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833699 | ||||||
chr5:176833713
|
C | CT | 28 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0018others(25): Show | 29 | HG00733.hp1 HG01109.hp1 HG01516.hp1 others(26): Show |
intron_variant | MODIFIER | c.70+22907dupT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176833713 | |||||
chr5:176833732
|
C | T | 9 | a0001c0001t0001g0025a0001c0001t0001g0027a0001c0001t0001g0028others(6): Show | 9 | HG02027.hp2 HG02080.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.70+22912C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833732 | ||||||
chr5:176833770
|
G | A | 3 | a0001c0001t0003g0050a0001c0001t0003g0111a0002c0002t0001g0112 | 3 | HG02572.hp2 HG02809.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.70+22950G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833770 | ||||||
chr5:176833858
|
A | G | 260 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(257): Show | 266 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(263): Show |
intron_variant | MODIFIER | c.70+23038A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833858 | ||||||
chr5:176833865
|
C | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0003g0092others(2): Show | 5 | HG02451.hp2 HG03130.hp2 NA19030.hp2 others(2): Show |
intron_variant | MODIFIER | c.70+23045C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833865 | ||||||
chr5:176833917
|
G | C | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(191): Show | 198 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.70+23097G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176833917 | ||||||
chr5:176834037
|
A | G | 1 | a0001c0001t0002g0035 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.70+23217A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176834037 | ||||||
chr5:176834115
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.70+23295G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176834115 | ||||||
chr5:176834210
|
G | A | 2 | a0001c0001t0001g0127a0001c0001t0002g0193 | 2 | NA18945.hp2 NA18979.hp1 |
intron_variant | MODIFIER | c.70+23390G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176834210 | ||||||
chr5:176834488
|
G | A | 1 | a0001c0001t0002g0035 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.70+23668G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176834488 | ||||||
chr5:176834665
|
T | TTC | 27 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0126others(24): Show | 29 | HG00099.hp1 HG00733.hp2 HG01168.hp1 others(26): Show |
intron_variant | MODIFIER | c.70+23883_70+23884d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834665
|
T | TTCTC | 28 | a0001c0001t0001g0071a0001c0001t0001g0076a0001c0001t0001g0106others(25): Show | 28 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.70+23881_70+23884d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834665
|
T | TTCTCTC | 55 | a0001c0001t0001g0004a0001c0001t0001g0030a0001c0001t0001g0042others(52): Show | 57 | HG00609.hp2 HG00642.hp2 HG00733.hp1 others(54): Show |
intron_variant | MODIFIER | c.70+23879_70+23884d others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834665
|
T | TTCTCTCT others(1): Show |
47 | a0001c0001t0001g0014a0001c0001t0001g0027a0001c0001t0001g0028others(44): Show | 47 | HG00621.hp2 HG00735.hp2 HG01071.hp1 others(44): Show |
intron_variant | MODIFIER | c.70+23877_70+23884d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834665
|
T | TTCTCTCT others(3): Show |
27 | a0001c0001t0001g0002a0001c0001t0001g0032a0001c0001t0001g0037others(24): Show | 28 | HG01081.hp1 HG01255.hp1 HG01255.hp2 others(25): Show |
intron_variant | MODIFIER | c.70+23875_70+23884d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834665
|
T | TTCTCTCT others(5): Show |
17 | a0001c0001t0001g0026a0001c0001t0001g0031a0001c0001t0001g0138others(14): Show | 17 | HG00099.hp2 HG00639.hp2 HG00741.hp2 others(14): Show |
intron_variant | MODIFIER | c.70+23873_70+23884d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834665
|
T | TTCTCTCT others(7): Show |
6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0094others(3): Show | 6 | HG02055.hp1 HG02451.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.70+23871_70+23884d others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834665
|
T | TTCTCTCT others(9): Show |
2 | a0001c0001t0001g0045a0001c0001t0013g0095 | 2 | NA19043.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.70+23869_70+23884d others(18): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834665
|
T | TTCTCTCT others(11): Show |
3 | a0001c0001t0002g0140a0001c0001t0002g0230a0001c0001t0003g0093 | 3 | HG01167.hp1 NA18945.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.70+23867_70+23884d others(20): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834665
|
T | TTCTCTCT others(15): Show |
1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.70+23863_70+23884d others(24): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834665
|
TTC | T | 9 | a0001c0001t0001g0142a0001c0001t0001g0251a0001c0001t0002g0090others(6): Show | 10 | HG01243.hp2 HG02145.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+23883_70+23884d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834665
|
TTCTCTC | T | 4 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(1): Show | 4 | HG02559.hp2 HG02622.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+23879_70+23884d others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834665
|
TTCTCTCT others(3): Show |
T | 2 | a0001c0001t0003g0074a0003c0003t0002g0073 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.70+23875_70+23884d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176834665 | |||||
chr5:176834711
|
C | G | 4 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(1): Show | 4 | HG01884.hp2 HG02055.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.70+23891C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176834711 | ||||||
chr5:176834751
|
T | C | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+23931T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176834751 | ||||||
chr5:176835031
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.70+24211C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835031 | ||||||
chr5:176835180
|
C | T | 1 | a0001c0001t0001g0255 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.70+24360C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835180 | ||||||
chr5:176835223
|
T | G | 2 | a0002c0002t0001g0006a0003c0003t0002g0017 | 3 | HG01243.hp2 HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.70+24403T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835223 | ||||||
chr5:176835242
|
T | C | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.70+24422T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835242 | ||||||
chr5:176835324
|
T | A | 1 | a0001c0001t0002g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.70+24504T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835324 | ||||||
chr5:176835374
|
C | G | 3 | a0001c0001t0002g0060a0001c0001t0002g0147a0001c0001t0002g0181 | 3 | NA18944.hp1 NA18977.hp1 NA19004.hp2 |
intron_variant | MODIFIER | c.70+24554C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835374 | ||||||
chr5:176835426
|
G | A | 12 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0057others(9): Show | 13 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.70+24606G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835426 | ||||||
chr5:176835512
|
C | T | 1 | a0001c0001t0001g0139 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.70+24692C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835512 | ||||||
chr5:176835520
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.70+24700G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835520 | ||||||
chr5:176835651
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.70+24831G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835651 | ||||||
chr5:176835729
|
A | ATG | 10 | a0001c0001t0001g0077a0001c0001t0001g0091a0001c0001t0001g0143others(7): Show | 10 | HG02015.hp1 HG02074.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+24941_70+24942d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | |||||
chr5:176835729
|
A | ATGTG | 132 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0024others(129): Show | 135 | HG00099.hp1 HG00099.hp2 HG00558.hp2 others(132): Show |
intron_variant | MODIFIER | c.70+24939_70+24942d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | |||||
chr5:176835729
|
A | ATGTGTG | 14 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0079others(11): Show | 15 | HG00558.hp1 HG01243.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.70+24937_70+24942d others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | |||||
chr5:176835729
|
A | ATGTGTGT others(1): Show |
5 | a0001c0001t0001g0177a0001c0001t0002g0123a0001c0001t0002g0189others(2): Show | 5 | HG02080.hp1 HG02129.hp2 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.70+24935_70+24942d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | |||||
chr5:176835729
|
A | ATGTGTGT others(3): Show |
2 | a0001c0001t0007g0242a0001c0001t0010g0022 | 2 | HG02647.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.70+24933_70+24942d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | |||||
chr5:176835729
|
A | ATGTGTGT others(5): Show |
2 | a0001c0001t0002g0035a0001c0001t0007g0247 | 2 | HG01884.hp1 NA18612.hp2 |
intron_variant | MODIFIER | c.70+24931_70+24942d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | |||||
chr5:176835729
|
ATG | A | 38 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(35): Show | 38 | HG00609.hp1 HG00733.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.70+24941_70+24942d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835729 | |||||
chr5:176835753
|
G | A | 44 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(41): Show | 45 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(42): Show |
intron_variant | MODIFIER | c.70+24933G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176835753 | ||||||
chr5:176835753
|
G | GTA | 7 | a0001c0001t0001g0219a0001c0001t0001g0255a0001c0001t0003g0011others(4): Show | 7 | HG01109.hp1 HG02451.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.70+24934_70+24935i others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835753 | |||||
chr5:176835753
|
G | GTGTA | 10 | a0001c0001t0001g0047a0001c0001t0001g0094a0001c0001t0002g0010others(7): Show | 10 | HG01891.hp2 HG02451.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+24936_70+24937i others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835753 | |||||
chr5:176835753
|
G | GTGTGTA | 10 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(7): Show | 10 | HG01106.hp1 HG01884.hp2 HG02300.hp2 others(7): Show |
intron_variant | MODIFIER | c.70+24938_70+24939i others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176835753 | |||||
chr5:176836145
|
A | T | 1 | a0001c0001t0001g0260 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.70+25325A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176836145 | ||||||
chr5:176836148
|
C | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(185): Show | 192 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(189): Show |
intron_variant | MODIFIER | c.70+25328C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176836148 | ||||||
chr5:176836496
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.70+25676C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176836496 | ||||||
chr5:176836549
|
A | G | 41 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0071others(38): Show | 41 | HG00609.hp1 HG00733.hp1 HG01167.hp1 others(38): Show |
intron_variant | MODIFIER | c.70+25729A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176836549 | ||||||
chr5:176836566
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.70+25746G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176836566 | ||||||
chr5:176836660
|
AG | A | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.70+25843delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176836660 | |||||
chr5:176836985
|
C | T | 1 | a0001c0001t0001g0057 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.71-25639C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176836985 | ||||||
chr5:176837014
|
A | T | 1 | a0002c0002t0004g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71-25610A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837014 | ||||||
chr5:176837049
|
G | A | 3 | a0001c0001t0001g0219a0001c0001t0003g0049a0002c0002t0004g0048 | 3 | HG01109.hp1 HG02738.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.71-25575G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837049 | ||||||
chr5:176837596
|
G | C | 1 | a0001c0001t0002g0085 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.71-25028G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837596 | ||||||
chr5:176837799
|
T | G | 6 | a0001c0001t0001g0224a0001c0001t0001g0226a0001c0001t0003g0074others(3): Show | 6 | HG01496.hp1 HG01891.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-24825T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837799 | ||||||
chr5:176837821
|
G | T | 1 | a0001c0001t0002g0058 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.71-24803G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837821 | ||||||
chr5:176837828
|
G | T | 1 | a0001c0001t0012g0129 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.71-24796G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837828 | ||||||
chr5:176837983
|
A | G | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.71-24641A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837983 | ||||||
chr5:176837998
|
C | T | 1 | a0001c0001t0002g0187 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.71-24626C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176837998 | ||||||
chr5:176838181
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.71-24443C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838181 | ||||||
chr5:176838224
|
T | C | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.71-24400T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838224 | ||||||
chr5:176838281
|
C | T | 2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.71-24343C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838281 | ||||||
chr5:176838282
|
T | G | 2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.71-24342T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838282 | ||||||
chr5:176838296
|
T | C | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.71-24328T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838296 | ||||||
chr5:176838543
|
A | G | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-24081A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838543 | ||||||
chr5:176838710
|
A | T | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-23914A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838710 | ||||||
chr5:176838830
|
A | G | 13 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0002g0010others(10): Show | 13 | HG01891.hp2 HG02451.hp2 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-23794A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838830 | ||||||
chr5:176838900
|
A | G | 5 | a0001c0001t0001g0047a0001c0001t0001g0099a0001c0001t0001g0229others(2): Show | 5 | HG02559.hp2 HG02622.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-23724A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838900 | ||||||
chr5:176838981
|
T | C | 212 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(209): Show | 217 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(214): Show |
intron_variant | MODIFIER | c.71-23643T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176838981 | ||||||
chr5:176839083
|
T | A | 2 | a0001c0001t0005g0008a0001c0001t0005g0023 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71-23541T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839083 | ||||||
chr5:176839368
|
C | G | 2 | a0002c0002t0001g0006a0003c0003t0002g0017 | 3 | HG01243.hp2 HG02257.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.71-23256C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839368 | ||||||
chr5:176839462
|
G | C | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-23162G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839462 | ||||||
chr5:176839472
|
T | A | 29 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(26): Show | 30 | HG01243.hp1 HG01884.hp2 HG01891.hp2 others(27): Show |
intron_variant | MODIFIER | c.71-23152T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839472 | ||||||
chr5:176839481
|
T | C | 3 | a0001c0001t0005g0008a0001c0001t0005g0023a0001c0001t0014g0061 | 3 | HG02630.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71-23143T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839481 | ||||||
chr5:176839590
|
T | G | 3 | a0001c0001t0001g0064a0001c0001t0002g0062a0001c0001t0002g0063 | 3 | HG01106.hp1 HG02300.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.71-23034T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839590 | ||||||
chr5:176839601
|
G | T | 2 | a0001c0001t0003g0080a0001c0001t0003g0081 | 2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.71-23023G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839601 | ||||||
chr5:176839673
|
G | A | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71-22951G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839673 | ||||||
chr5:176839717
|
C | A | 23 | a0001c0001t0001g0033a0001c0001t0001g0071a0001c0001t0001g0108others(20): Show | 23 | HG00558.hp1 HG00609.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.71-22907C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839717 | ||||||
chr5:176839721
|
G | A | 23 | a0001c0001t0001g0033a0001c0001t0001g0071a0001c0001t0001g0108others(20): Show | 23 | HG00558.hp1 HG00609.hp1 HG01109.hp1 others(20): Show |
intron_variant | MODIFIER | c.71-22903G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839721 | ||||||
chr5:176839740
|
A | G | 11 | a0001c0001t0001g0045a0001c0001t0002g0035a0001c0001t0002g0097others(8): Show | 11 | HG01109.hp1 HG02486.hp1 HG02818.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-22884A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839740 | ||||||
chr5:176839797
|
C | T | 5 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0007g0242others(2): Show | 5 | HG01109.hp1 HG02647.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-22827C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839797 | ||||||
chr5:176839807
|
C | CT | 16 | a0001c0001t0001g0031a0001c0001t0001g0072a0001c0001t0001g0110others(13): Show | 16 | HG00621.hp1 HG00735.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-22791dupT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176839807 | |||||
chr5:176839807
|
CT | C | 23 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(20): Show | 23 | HG01081.hp1 HG01168.hp1 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.71-22791delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176839807 | |||||
chr5:176839833
|
T | C | 8 | a0001c0001t0001g0094a0001c0001t0001g0255a0001c0001t0003g0092others(5): Show | 8 | HG02451.hp2 HG02647.hp2 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-22791T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839833 | ||||||
chr5:176839873
|
G | C | 2 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | HG02257.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.71-22751G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839873 | ||||||
chr5:176839911
|
G | T | 2 | a0001c0001t0003g0080a0001c0001t0003g0081 | 2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.71-22713G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839911 | ||||||
chr5:176839947
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.71-22677G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839947 | ||||||
chr5:176839972
|
A | G | 12 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(9): Show | 12 | HG01884.hp2 HG02055.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.71-22652A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839972 | ||||||
chr5:176839980
|
G | A | 8 | a0001c0001t0001g0219a0001c0001t0002g0186a0001c0001t0002g0187others(5): Show | 8 | HG01361.hp1 HG02572.hp2 HG02738.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-22644G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176839980 | ||||||
chr5:176840147
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.71-22477G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840147 | ||||||
chr5:176840286
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.71-22338A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840286 | ||||||
chr5:176840331
|
C | T | 1 | a0001c0001t0001g0177 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.71-22293C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840331 | ||||||
chr5:176840368
|
G | A | 4 | a0001c0001t0001g0033a0001c0001t0001g0064a0001c0001t0002g0062others(1): Show | 4 | HG01106.hp1 HG02300.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-22256G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840368 | ||||||
chr5:176840414
|
G | A | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.71-22210G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840414 | ||||||
chr5:176840465
|
T | C | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71-22159T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840465 | ||||||
chr5:176840508
|
A | T | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-22116A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840508 | ||||||
chr5:176840574
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-22050G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840574 | ||||||
chr5:176840629
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.71-21995G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840629 | ||||||
chr5:176840685
|
C | A | 2 | a0001c0001t0002g0097a0001c0001t0003g0261 | 2 | HG02717.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.71-21939C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840685 | ||||||
chr5:176840827
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.71-21797C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840827 | ||||||
chr5:176840828
|
G | A | 4 | a0001c0001t0001g0236a0001c0001t0005g0008a0001c0001t0005g0023others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-21796G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840828 | ||||||
chr5:176840845
|
G | A | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0167 | 3 | NA19000.hp1 NA19002.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.71-21779G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840845 | ||||||
chr5:176840924
|
G | A | 4 | a0001c0001t0001g0236a0001c0001t0005g0008a0001c0001t0005g0023others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-21700G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176840924 | ||||||
chr5:176841016
|
G | A | 6 | a0001c0001t0003g0250a0001c0001t0003g0254a0001c0005t0002g0235others(3): Show | 7 | HG02109.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-21608G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841016 | ||||||
chr5:176841039
|
G | A | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71-21585G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841039 | ||||||
chr5:176841040
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0229 | 2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.71-21584C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841040 | ||||||
chr5:176841134
|
G | A | 6 | a0001c0001t0003g0250a0001c0001t0003g0254a0001c0005t0002g0235others(3): Show | 7 | HG02109.hp1 HG02615.hp1 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-21490G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841134 | ||||||
chr5:176841201
|
C | G | 8 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-21423C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841201 | ||||||
chr5:176841367
|
C | G | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-21257C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841367 | ||||||
chr5:176841442
|
G | A | 9 | a0001c0001t0001g0016a0001c0001t0003g0250a0001c0001t0003g0254others(6): Show | 10 | HG01243.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-21182G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841442 | ||||||
chr5:176841499
|
T | C | 41 | a0001c0001t0001g0033a0001c0001t0001g0064a0001c0001t0001g0236others(38): Show | 41 | HG00733.hp1 HG01106.hp1 HG01109.hp1 others(38): Show |
intron_variant | MODIFIER | c.71-21125T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841499 | ||||||
chr5:176841822
|
G | T | 32 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0064others(29): Show | 34 | HG01106.hp1 HG01243.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.71-20802G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841822 | ||||||
chr5:176841868
|
T | C | 8 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0011g0015others(5): Show | 8 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-20756T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841868 | ||||||
chr5:176841922
|
G | T | 1 | a0002c0002t0004g0165 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.71-20702G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841922 | ||||||
chr5:176841925
|
C | T | 8 | a0001c0001t0003g0250a0001c0001t0003g0254a0001c0004t0002g0232others(5): Show | 9 | HG02109.hp1 HG02451.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.71-20699C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841925 | ||||||
chr5:176841939
|
G | T | 35 | a0001c0001t0001g0016a0001c0001t0001g0219a0001c0001t0001g0236others(32): Show | 37 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.71-20685G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176841939 | ||||||
chr5:176842013
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.71-20611T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842013 | ||||||
chr5:176842014
|
G | A | 1 | a0001c0001t0001g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.71-20610G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842014 | ||||||
chr5:176842070
|
G | A | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71-20554G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842070 | ||||||
chr5:176842192
|
G | A | 3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-20432G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842192 | ||||||
chr5:176842443
|
G | A | 35 | a0001c0001t0001g0016a0001c0001t0001g0219a0001c0001t0001g0236others(32): Show | 37 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.71-20181G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842443 | ||||||
chr5:176842446
|
G | A | 8 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-20178G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842446 | ||||||
chr5:176842492
|
G | GAT | 5 | a0001c0001t0001g0033a0001c0001t0001g0064a0001c0001t0001g0091others(2): Show | 5 | HG01106.hp1 HG02300.hp2 HG03017.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-20115_71-20114d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | |||||
chr5:176842492
|
G | GATATATA others(3): Show |
5 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0011others(2): Show | 5 | HG02280.hp2 HG02965.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-20123_71-20114d others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | |||||
chr5:176842492
|
G | GATATATA others(5): Show |
3 | a0001c0001t0003g0009a0001c0001t0003g0080a0001c0001t0003g0081 | 3 | HG01891.hp2 HG03041.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.71-20125_71-20114d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | |||||
chr5:176842492
|
G | GATATATA others(7): Show |
2 | a0001c0001t0005g0013a0003c0003t0001g0084 | 2 | HG00733.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.71-20127_71-20114d others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | |||||
chr5:176842492
|
G | GATATATA others(11): Show |
1 | a0001c0001t0003g0261 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.71-20131_71-20114d others(20): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | |||||
chr5:176842492
|
G | GATATATA others(13): Show |
4 | a0001c0001t0002g0097a0001c0001t0002g0100a0001c0001t0002g0118others(1): Show | 4 | HG02145.hp1 HG02615.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-20114_71-20113i others(22): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | |||||
chr5:176842492
|
G | GATATATA others(15): Show |
1 | a0001c0001t0002g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.71-20114_71-20113i others(24): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | |||||
chr5:176842492
|
G | GATATATA others(17): Show |
3 | a0001c0001t0001g0251a0001c0001t0002g0090a0001c0001t0003g0259 | 3 | HG02896.hp1 NA18906.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.71-20114_71-20113i others(26): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | |||||
chr5:176842492
|
G | GATATATA others(19): Show |
1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71-20114_71-20113i others(28): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | |||||
chr5:176842492
|
G | GATATATA others(21): Show |
2 | a0001c0001t0002g0184a0001c0001t0002g0231 | 2 | HG02572.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-20114_71-20113i others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | |||||
chr5:176842492
|
G | GATATATA others(23): Show |
1 | a0001c0001t0002g0230 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.71-20114_71-20113i others(32): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | |||||
chr5:176842492
|
GAT | G | 35 | a0001c0001t0001g0016a0001c0001t0001g0219a0001c0001t0001g0236others(32): Show | 37 | HG01109.hp1 HG01243.hp1 HG01243.hp2 others(34): Show |
intron_variant | MODIFIER | c.71-20115_71-20114d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176842492 | |||||
chr5:176842834
|
C | T | 8 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(5): Show | 8 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.71-19790C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176842834 | ||||||
chr5:176843068
|
G | A | 1 | a0003c0003t0001g0084 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.71-19556G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843068 | ||||||
chr5:176843172
|
AAAAG | A | 15 | a0001c0001t0001g0016a0001c0001t0001g0101a0001c0001t0001g0236others(12): Show | 16 | HG00733.hp1 HG01167.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-19432_71-19429d others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176843172 | |||||
chr5:176843173
|
AAAG | A | 27 | a0001c0001t0001g0219a0001c0001t0001g0224a0001c0001t0001g0226others(24): Show | 28 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.71-19448_71-19446d others(5): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176843173 | |||||
chr5:176843209
|
A | G | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-19415A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843209 | ||||||
chr5:176843242
|
G | A | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.71-19382G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843242 | ||||||
chr5:176843295
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-19329C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843295 | ||||||
chr5:176843355
|
C | T | 18 | a0001c0001t0001g0016a0001c0001t0001g0219a0001c0001t0002g0186others(15): Show | 20 | HG01243.hp1 HG01243.hp2 HG01361.hp1 others(17): Show |
intron_variant | MODIFIER | c.71-19269C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843355 | ||||||
chr5:176843359
|
A | T | 15 | a0001c0001t0001g0236a0001c0001t0003g0049a0001c0001t0003g0065others(12): Show | 15 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-19265A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843359 | ||||||
chr5:176843392
|
C | T | 11 | a0001c0001t0001g0219a0001c0001t0002g0186a0001c0001t0002g0187others(8): Show | 12 | HG01243.hp2 HG01361.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-19232C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843392 | ||||||
chr5:176843461
|
G | T | 4 | a0001c0001t0001g0236a0001c0001t0005g0008a0001c0001t0005g0023others(1): Show | 4 | HG02630.hp1 HG02976.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-19163G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843461 | ||||||
chr5:176843643
|
G | A | 2 | a0001c0001t0002g0121a0001c0001t0002g0140 | 2 | NA18945.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.71-18981G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843643 | ||||||
chr5:176843687
|
A | G | 1 | a0001c0001t0001g0251 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.71-18937A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843687 | ||||||
chr5:176843803
|
C | T | 1 | a0001c0001t0001g0183 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.71-18821C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843803 | ||||||
chr5:176843804
|
G | A | 1 | a0001c0001t0001g0205 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.71-18820G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843804 | ||||||
chr5:176843844
|
C | T | 5 | a0001c0001t0001g0236a0001c0001t0005g0008a0001c0001t0005g0023others(2): Show | 5 | HG02630.hp1 HG02976.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-18780C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843844 | ||||||
chr5:176843864
|
G | A | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.71-18760G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843864 | ||||||
chr5:176843887
|
G | A | 11 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0007g0083others(8): Show | 11 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-18737G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843887 | ||||||
chr5:176843888
|
G | A | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.71-18736G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176843888 | ||||||
chr5:176844075
|
C | G | 63 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0064others(60): Show | 65 | HG00733.hp1 HG01106.hp1 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.71-18549C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844075 | ||||||
chr5:176844270
|
G | A | 1 | a0001c0001t0001g0167 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.71-18354G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844270 | ||||||
chr5:176844529
|
T | C | 53 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0064others(50): Show | 54 | HG00733.hp1 HG01106.hp1 HG01109.hp1 others(51): Show |
intron_variant | MODIFIER | c.71-18095T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844529 | ||||||
chr5:176844730
|
C | T | 4 | a0001c0001t0001g0033a0001c0001t0001g0064a0001c0001t0002g0062others(1): Show | 4 | HG01106.hp1 HG02300.hp2 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-17894C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844730 | ||||||
chr5:176844790
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-17834G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844790 | ||||||
chr5:176844796
|
C | T | 1 | a0002c0002t0001g0112 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.71-17828C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844796 | ||||||
chr5:176844817
|
C | T | 20 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0090others(17): Show | 20 | HG00733.hp1 HG01167.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.71-17807C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844817 | ||||||
chr5:176844944
|
G | A | 11 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0007g0083others(8): Show | 11 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-17680G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176844944 | ||||||
chr5:176845167
|
C | T | 1 | a0001c0001t0002g0063 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.71-17457C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845167 | ||||||
chr5:176845180
|
T | C | 35 | a0001c0001t0001g0094a0001c0001t0001g0251a0001c0001t0002g0010others(32): Show | 35 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(32): Show |
intron_variant | MODIFIER | c.71-17444T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845180 | ||||||
chr5:176845216
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0229a0001c0001t0002g0257 | 3 | HG02622.hp1 HG03195.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.71-17408G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845216 | ||||||
chr5:176845287
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71-17337C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845287 | ||||||
chr5:176845310
|
C | T | 2 | a0001c0001t0002g0100a0001c0001t0002g0118 | 2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.71-17314C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845310 | ||||||
chr5:176845314
|
C | G | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-17310C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845314 | ||||||
chr5:176845392
|
C | T | 1 | a0003c0003t0001g0084 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.71-17232C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845392 | ||||||
chr5:176845459
|
G | A | 1 | a0001c0001t0011g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.71-17165G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845459 | ||||||
chr5:176845641
|
A | G | 2 | a0001c0001t0001g0094a0001c0001t0001g0234 | 2 | HG03130.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.71-16983A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845641 | ||||||
chr5:176845696
|
C | A | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71-16928C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845696 | ||||||
chr5:176845853
|
C | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0153 | 2 | HG02300.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.71-16771C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845853 | ||||||
chr5:176845924
|
C | T | 11 | a0001c0001t0003g0049a0001c0001t0003g0065a0001c0001t0007g0083others(8): Show | 11 | HG01109.hp1 HG01884.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-16700C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845924 | ||||||
chr5:176845948
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-16676T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845948 | ||||||
chr5:176845950
|
C | G | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-16674C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845950 | ||||||
chr5:176845952
|
G | T | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-16672G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845952 | ||||||
chr5:176845954
|
A | C | 1 | a0001c0001t0001g0016 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.71-16670A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176845954 | ||||||
chr5:176846007
|
G | A | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71-16617G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846007 | ||||||
chr5:176846069
|
G | A | 7 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(4): Show | 7 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-16555G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846069 | ||||||
chr5:176846369
|
G | A | 189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(186): Show | 194 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(191): Show |
intron_variant | MODIFIER | c.71-16255G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846369 | ||||||
chr5:176846384
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.71-16240G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846384 | ||||||
chr5:176846460
|
T | C | 40 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(37): Show | 40 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(37): Show |
intron_variant | MODIFIER | c.71-16164T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846460 | ||||||
chr5:176846641
|
C | T | 1 | a0001c0001t0001g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.71-15983C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846641 | ||||||
chr5:176846807
|
C | T | 3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-15817C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846807 | ||||||
chr5:176846808
|
G | A | 2 | a0001c0001t0002g0147a0001c0001t0002g0181 | 2 | NA18944.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.71-15816G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846808 | ||||||
chr5:176846828
|
G | A | 5 | a0001c0001t0001g0162a0001c0001t0002g0003a0001c0001t0002g0070others(2): Show | 6 | HG01069.hp2 HG01074.hp1 HG02602.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-15796G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846828 | ||||||
chr5:176846829
|
G | A | 25 | a0001c0001t0001g0219a0001c0001t0001g0236a0001c0001t0002g0186others(22): Show | 26 | HG01109.hp1 HG01243.hp2 HG01361.hp1 others(23): Show |
intron_variant | MODIFIER | c.71-15795G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846829 | ||||||
chr5:176846898
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.71-15726G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846898 | ||||||
chr5:176846919
|
T | A | 1 | a0001c0001t0001g0175 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.71-15705T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846919 | ||||||
chr5:176846951
|
A | G | 25 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0174others(22): Show | 25 | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(22): Show |
intron_variant | MODIFIER | c.71-15673A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176846951 | ||||||
chr5:176847004
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.71-15620G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847004 | ||||||
chr5:176847044
|
C | T | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-15580C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847044 | ||||||
chr5:176847138
|
G | A | 5 | a0001c0001t0002g0051a0001c0001t0002g0134a0001c0001t0002g0137others(2): Show | 5 | HG00621.hp1 HG02523.hp2 NA18943.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-15486G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847138 | ||||||
chr5:176847729
|
G | T | 5 | a0001c0001t0001g0064a0001c0001t0002g0058a0001c0001t0002g0062others(2): Show | 5 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-14895G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847729 | ||||||
chr5:176847730
|
AT | A | 6 | a0001c0001t0011g0015a0002c0002t0004g0021a0002c0002t0004g0048others(3): Show | 6 | HG01109.hp1 HG03209.hp1 HG03471.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-14891delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176847730 | |||||
chr5:176847746
|
A | C | 3 | a0001c0001t0001g0106a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | HG03704.hp1 HG03834.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.71-14878A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847746 | ||||||
chr5:176847752
|
T | A | 2 | a0001c0001t0002g0090a0001c0001t0002g0184 | 2 | HG02572.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.71-14872T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847752 | ||||||
chr5:176847901
|
G | C | 11 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0007g0083others(8): Show | 11 | HG01109.hp1 HG01167.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-14723G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176847901 | ||||||
chr5:176848086
|
A | ACTGACCA others(1): Show |
16 | a0001c0001t0001g0174a0001c0001t0002g0090a0001c0001t0002g0097others(13): Show | 16 | HG00099.hp1 HG00639.hp2 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-14528_71-14521d others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176848086 | |||||
chr5:176848139
|
C | G | 5 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0002g0075others(2): Show | 5 | HG01243.hp1 HG01884.hp2 HG02055.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-14485C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848139 | ||||||
chr5:176848188
|
G | A | 6 | a0001c0001t0001g0033a0001c0001t0001g0224a0001c0001t0001g0226others(3): Show | 6 | HG01496.hp1 HG01891.hp1 HG01943.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-14436G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848188 | ||||||
chr5:176848276
|
A | T | 1 | a0001c0001t0002g0194 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.71-14348A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848276 | ||||||
chr5:176848283
|
A | G | 6 | a0001c0001t0002g0248a0001c0001t0003g0250a0001c0001t0003g0254others(3): Show | 7 | HG02615.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-14341A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848283 | ||||||
chr5:176848529
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-14095C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848529 | ||||||
chr5:176848716
|
G | A | 22 | a0001c0001t0001g0219a0001c0001t0002g0186a0001c0001t0002g0187others(19): Show | 23 | HG01109.hp1 HG01167.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-13908G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848716 | ||||||
chr5:176848803
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.71-13821G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848803 | ||||||
chr5:176848817
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.71-13807G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848817 | ||||||
chr5:176848921
|
C | T | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.71-13703C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848921 | ||||||
chr5:176848936
|
G | A | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-13688G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176848936 | ||||||
chr5:176849184
|
C | T | 1 | a0001c0001t0001g0170 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.71-13440C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849184 | ||||||
chr5:176849445
|
T | C | 44 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0064others(41): Show | 45 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(42): Show |
intron_variant | MODIFIER | c.71-13179T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849445 | ||||||
chr5:176849451
|
G | A | 1 | a0001c0001t0001g0122 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.71-13173G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849451 | ||||||
chr5:176849510
|
G | T | 1 | a0001c0001t0002g0040 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.71-13114G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849510 | ||||||
chr5:176849541
|
C | T | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-13083C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849541 | ||||||
chr5:176849570
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-13054G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849570 | ||||||
chr5:176849583
|
A | T | 1 | a0001c0001t0002g0200 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.71-13041A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849583 | ||||||
chr5:176849744
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0156 | 2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.71-12880C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849744 | ||||||
chr5:176849986
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG02080.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.71-12638C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176849986 | ||||||
chr5:176850103
|
G | A | 6 | a0001c0001t0002g0248a0001c0001t0003g0250a0001c0001t0003g0254others(3): Show | 7 | HG02615.hp1 HG02723.hp2 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.71-12521G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850103 | ||||||
chr5:176850116
|
T | C | 53 | a0001c0001t0001g0064a0001c0001t0001g0141a0001c0001t0001g0219others(50): Show | 55 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(52): Show |
intron_variant | MODIFIER | c.71-12508T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850116 | ||||||
chr5:176850186
|
T | G | 1 | a0001c0001t0002g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.71-12438T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850186 | ||||||
chr5:176850206
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-12418G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850206 | ||||||
chr5:176850281
|
C | G | 3 | a0001c0001t0005g0008a0001c0001t0005g0023a0001c0001t0014g0061 | 3 | HG02630.hp1 HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71-12343C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850281 | ||||||
chr5:176850327
|
G | T | 11 | a0001c0001t0001g0219a0001c0001t0001g0234a0001c0001t0002g0186others(8): Show | 12 | HG01243.hp2 HG01361.hp1 HG02109.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-12297G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850327 | ||||||
chr5:176850434
|
G | A | 3 | a0001c0001t0010g0022a0001c0004t0002g0232a0001c0004t0002g0233 | 3 | HG02451.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.71-12190G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850434 | ||||||
chr5:176850453
|
G | A | 1 | a0001c0001t0002g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.71-12171G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850453 | ||||||
chr5:176850494
|
T | G | 2 | a0001c0001t0001g0077a0001c0004t0002g0078 | 2 | HG03453.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.71-12130T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850494 | ||||||
chr5:176850503
|
T | C | 1 | a0001c0001t0001g0124 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.71-12121T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850503 | ||||||
chr5:176850574
|
G | A | 3 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0045 | 3 | HG01243.hp1 HG01884.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.71-12050G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850574 | ||||||
chr5:176850599
|
G | A | 1 | a0001c0001t0001g0142 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.71-12025G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850599 | ||||||
chr5:176850628
|
G | A | 4 | a0001c0001t0010g0022a0002c0002t0004g0021a0002c0002t0004g0048others(1): Show | 4 | HG01109.hp1 HG03139.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-11996G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850628 | ||||||
chr5:176850932
|
C | T | 10 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0003g0244others(7): Show | 10 | HG01167.hp1 HG01884.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-11692C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176850932 | ||||||
chr5:176850950
|
TCCAGTGC others(12): Show |
T | 2 | a0001c0001t0002g0096a0001c0001t0008g0113 | 2 | HG02922.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.71-11648_71-11630d others(21): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176850950 | |||||
chr5:176851060
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-11564G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851060 | ||||||
chr5:176851096
|
C | G | 1 | a0001c0001t0002g0116 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.71-11528C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851096 | ||||||
chr5:176851189
|
T | G | 2 | a0001c0001t0001g0192a0001c0001t0002g0191 | 2 | HG02132.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.71-11435T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851189 | ||||||
chr5:176851453
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.71-11171A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851453 | ||||||
chr5:176851524
|
A | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0037others(25): Show | 29 | HG00558.hp1 HG00609.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.71-11100A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851524 | ||||||
chr5:176851565
|
G | A | 7 | a0001c0001t0011g0015a0002c0002t0001g0006a0002c0002t0004g0021others(4): Show | 8 | HG01109.hp1 HG01243.hp2 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-11059G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851565 | ||||||
chr5:176851657
|
C | T | 6 | a0001c0001t0002g0051a0001c0001t0002g0134a0001c0001t0002g0137others(3): Show | 6 | HG00621.hp1 HG02135.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-10967C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851657 | ||||||
chr5:176851695
|
G | A | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-10929G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851695 | ||||||
chr5:176851824
|
C | T | 5 | a0001c0001t0001g0064a0001c0001t0002g0058a0001c0001t0002g0062others(2): Show | 5 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-10800C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851824 | ||||||
chr5:176851853
|
A | G | 102 | a0001c0001t0001g0064a0001c0001t0001g0094a0001c0001t0001g0127others(99): Show | 105 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(102): Show |
intron_variant | MODIFIER | c.71-10771A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851853 | ||||||
chr5:176851857
|
C | T | 12 | a0001c0001t0003g0244a0001c0001t0005g0013a0001c0001t0007g0083others(9): Show | 13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-10767C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851857 | ||||||
chr5:176851858
|
G | A | 19 | a0001c0001t0001g0094a0001c0001t0001g0219a0001c0001t0001g0234others(16): Show | 19 | HG01361.hp1 HG01891.hp2 HG02257.hp1 others(16): Show |
intron_variant | MODIFIER | c.71-10766G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851858 | ||||||
chr5:176851997
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.71-10627C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176851997 | ||||||
chr5:176852213
|
C | T | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-10411C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852213 | ||||||
chr5:176852325
|
TCACACAC others(5): Show |
T | 1 | a0001c0001t0002g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.71-10282_71-10271d others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176852325 | |||||
chr5:176852374
|
G | GCA | 11 | a0001c0001t0003g0244a0001c0001t0007g0083a0001c0001t0007g0242others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-10234_71-10233d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176852374 | |||||
chr5:176852441
|
C | T | 36 | a0001c0001t0001g0127a0001c0001t0001g0136a0001c0001t0001g0145others(33): Show | 37 | HG00621.hp1 HG01069.hp2 HG01074.hp1 others(34): Show |
intron_variant | MODIFIER | c.71-10183C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852441 | ||||||
chr5:176852465
|
G | A | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-10159G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852465 | ||||||
chr5:176852649
|
G | A | 3 | a0001c0001t0010g0022a0001c0004t0002g0232a0001c0004t0002g0233 | 3 | HG02451.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.71-9975G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852649 | ||||||
chr5:176852696
|
G | A | 1 | a0003c0003t0002g0240 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.71-9928G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852696 | ||||||
chr5:176852703
|
C | T | 4 | a0001c0001t0002g0090a0001c0001t0002g0100a0001c0001t0002g0118others(1): Show | 4 | HG02145.hp1 HG02572.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-9921C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852703 | ||||||
chr5:176852720
|
C | T | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.71-9904C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852720 | ||||||
chr5:176852743
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.71-9881C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852743 | ||||||
chr5:176852762
|
G | C | 1 | a0001c0001t0002g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.71-9862G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852762 | ||||||
chr5:176852764
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0120 | 2 | HG02698.hp2 NA18943.hp1 |
intron_variant | MODIFIER | c.71-9860G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852764 | ||||||
chr5:176852786
|
G | A | 1 | a0001c0001t0002g0035 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.71-9838G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852786 | ||||||
chr5:176852877
|
C | T | 2 | a0001c0001t0016g0161a0002c0002t0004g0144 | 2 | HG02074.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.71-9747C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852877 | ||||||
chr5:176852878
|
G | A | 1 | a0003c0003t0002g0107 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.71-9746G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176852878 | ||||||
chr5:176853052
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.71-9572G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853052 | ||||||
chr5:176853071
|
G | A | 9 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247others(6): Show | 10 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.71-9553G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853071 | ||||||
chr5:176853260
|
C | T | 1 | a0001c0001t0003g0050 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.71-9364C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853260 | ||||||
chr5:176853310
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0059 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.71-9314G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853310 | ||||||
chr5:176853318
|
C | T | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-9306C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853318 | ||||||
chr5:176853348
|
C | T | 1 | a0001c0001t0002g0140 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.71-9276C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853348 | ||||||
chr5:176853480
|
G | C | 1 | a0001c0001t0002g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.71-9144G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853480 | ||||||
chr5:176853584
|
T | C | 29 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0094others(26): Show | 30 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.71-9040T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853584 | ||||||
chr5:176853598
|
T | C | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-9026T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853598 | ||||||
chr5:176853602
|
G | A | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.71-9022G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853602 | ||||||
chr5:176853628
|
C | T | 2 | a0001c0001t0001g0228a0001c0001t0002g0055 | 2 | HG01257.hp1 HG02257.hp2 |
intron_variant | MODIFIER | c.71-8996C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853628 | ||||||
chr5:176853801
|
G | C | 27 | a0001c0001t0001g0174a0001c0001t0002g0040a0001c0001t0002g0090others(24): Show | 28 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(25): Show |
intron_variant | MODIFIER | c.71-8823G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853801 | ||||||
chr5:176853898
|
A | G | 8 | a0001c0001t0001g0094a0001c0001t0011g0015a0002c0002t0001g0006others(5): Show | 9 | HG01109.hp1 HG01243.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.71-8726A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853898 | ||||||
chr5:176853922
|
G | A | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-8702G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853922 | ||||||
chr5:176853924
|
A | G | 33 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0037others(30): Show | 34 | HG00558.hp1 HG00609.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.71-8700A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176853924 | ||||||
chr5:176854047
|
A | G | 1 | a0002c0002t0004g0144 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.71-8577A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854047 | ||||||
chr5:176854086
|
C | T | 1 | a0001c0001t0002g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.71-8538C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854086 | ||||||
chr5:176854144
|
C | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0203a0001c0001t0001g0215 | 3 | HG01069.hp1 HG01071.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.71-8480C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854144 | ||||||
chr5:176854168
|
C | G | 30 | a0001c0001t0001g0174a0001c0001t0002g0040a0001c0001t0002g0090others(27): Show | 31 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.71-8456C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854168 | ||||||
chr5:176854286
|
GTCTCTGT others(3): Show |
G | 20 | a0001c0001t0002g0040a0001c0001t0003g0111a0001c0001t0003g0244others(17): Show | 21 | HG00735.hp1 HG01109.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-8324_71-8315del others(10): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176854286 | |||||
chr5:176854319
|
T | C | 35 | a0001c0001t0001g0127a0001c0001t0001g0136a0001c0001t0001g0145others(32): Show | 36 | HG00621.hp1 HG01069.hp2 HG01074.hp1 others(33): Show |
intron_variant | MODIFIER | c.71-8305T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854319 | ||||||
chr5:176854322
|
G | A | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-8302G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854322 | ||||||
chr5:176854327
|
G | A | 1 | a0001c0001t0001g0033 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.71-8297G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854327 | ||||||
chr5:176854529
|
C | T | 1 | a0001c0001t0003g0254 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.71-8095C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854529 | ||||||
chr5:176854670
|
C | G | 4 | a0001c0001t0002g0090a0001c0001t0002g0184a0001c0001t0002g0186others(1): Show | 4 | HG02572.hp1 HG02896.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-7954C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854670 | ||||||
chr5:176854850
|
A | G | 21 | a0001c0001t0001g0094a0001c0001t0001g0234a0001c0001t0002g0058others(18): Show | 21 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-7774A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176854850 | ||||||
chr5:176855064
|
A | G | 2 | a0001c0001t0005g0008a0001c0001t0005g0023 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71-7560A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855064 | ||||||
chr5:176855086
|
G | A | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-7538G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855086 | ||||||
chr5:176855149
|
C | T | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-7475C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855149 | ||||||
chr5:176855356
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0068 | 2 | HG02015.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.71-7268G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855356 | ||||||
chr5:176855362
|
C | T | 5 | a0001c0001t0003g0111a0003c0003t0001g0188a0003c0003t0002g0017others(2): Show | 5 | HG01361.hp1 HG02109.hp1 HG02257.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-7262C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855362 | ||||||
chr5:176855379
|
G | A | 12 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247others(9): Show | 13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-7245G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855379 | ||||||
chr5:176855425
|
G | A | 8 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(5): Show | 8 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-7199G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855425 | ||||||
chr5:176855615
|
G | A | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71-7009G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855615 | ||||||
chr5:176855731
|
C | T | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-6893C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855731 | ||||||
chr5:176855750
|
T | C | 42 | a0001c0001t0001g0064a0001c0001t0001g0127a0001c0001t0001g0136others(39): Show | 43 | HG00621.hp1 HG01069.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.71-6874T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855750 | ||||||
chr5:176855812
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0145 | 2 | NA19060.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.71-6812G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855812 | ||||||
chr5:176855980
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.71-6644C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855980 | ||||||
chr5:176855995
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-6629C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176855995 | ||||||
chr5:176856018
|
C | T | 4 | a0001c0001t0003g0244a0001c0001t0010g0022a0001c0004t0002g0232others(1): Show | 4 | HG02451.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-6606C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856018 | ||||||
chr5:176856019
|
G | A | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-6605G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856019 | ||||||
chr5:176856052
|
C | G | 13 | a0001c0001t0001g0094a0001c0001t0003g0092a0001c0001t0003g0093others(10): Show | 13 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-6572C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856052 | ||||||
chr5:176856235
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-6389G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856235 | ||||||
chr5:176856323
|
G | A | 10 | a0001c0001t0002g0035a0001c0001t0002g0051a0001c0001t0002g0123others(7): Show | 10 | HG00621.hp1 HG02080.hp1 HG02132.hp2 others(7): Show |
intron_variant | MODIFIER | c.71-6301G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856323 | ||||||
chr5:176856353
|
C | T | 42 | a0001c0001t0001g0064a0001c0001t0001g0127a0001c0001t0001g0136others(39): Show | 43 | HG00621.hp1 HG01069.hp2 HG01074.hp1 others(40): Show |
intron_variant | MODIFIER | c.71-6271C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856353 | ||||||
chr5:176856465
|
C | T | 22 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0248others(19): Show | 23 | HG01891.hp1 HG01891.hp2 HG02280.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-6159C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856465 | ||||||
chr5:176856484
|
G | A | 4 | a0001c0001t0001g0057a0001c0001t0001g0205a0001c0001t0001g0206others(1): Show | 4 | HG01928.hp2 HG02486.hp2 NA21309.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-6140G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856484 | ||||||
chr5:176856645
|
C | T | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-5979C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856645 | ||||||
chr5:176856716
|
A | G | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-5908A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856716 | ||||||
chr5:176856770
|
C | T | 3 | a0001c0001t0001g0109a0001c0001t0001g0110a0001c0001t0001g0167 | 3 | NA19000.hp1 NA19002.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.71-5854C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856770 | ||||||
chr5:176856789
|
C | T | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-5835C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176856789 | ||||||
chr5:176857036
|
T | C | 261 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(258): Show | 267 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(264): Show |
intron_variant | MODIFIER | c.71-5588T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857036 | ||||||
chr5:176857045
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.71-5579C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857045 | ||||||
chr5:176857187
|
C | G | 1 | a0001c0001t0002g0123 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.71-5437C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857187 | ||||||
chr5:176857239
|
G | A | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-5385G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857239 | ||||||
chr5:176857314
|
T | G | 43 | a0001c0001t0001g0064a0001c0001t0001g0127a0001c0001t0001g0136others(40): Show | 44 | HG00621.hp1 HG01069.hp2 HG01074.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-5310T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857314 | ||||||
chr5:176857534
|
C | T | 1 | a0002c0002t0004g0021 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.71-5090C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857534 | ||||||
chr5:176857548
|
C | T | 2 | a0001c0001t0002g0058a0001c0001t0002g0087 | 2 | HG01081.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.71-5076C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857548 | ||||||
chr5:176857655
|
G | C | 1 | a0001c0001t0001g0167 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.71-4969G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857655 | ||||||
chr5:176857712
|
C | T | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 223 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(220): Show |
intron_variant | MODIFIER | c.71-4912C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857712 | ||||||
chr5:176857797
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.71-4827C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857797 | ||||||
chr5:176857798
|
G | A | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-4826G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857798 | ||||||
chr5:176857847
|
C | T | 3 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020 | 3 | HG01884.hp2 HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.71-4777C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857847 | ||||||
chr5:176857895
|
A | G | 1 | a0001c0001t0002g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.71-4729A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857895 | ||||||
chr5:176857900
|
A | G | 218 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(215): Show | 223 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(220): Show |
intron_variant | MODIFIER | c.71-4724A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176857900 | ||||||
chr5:176858046
|
G | A | 6 | a0001c0001t0003g0111a0003c0003t0001g0188a0003c0003t0002g0017others(3): Show | 6 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-4578G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858046 | ||||||
chr5:176858053
|
C | T | 4 | a0001c0001t0002g0248a0001c0005t0002g0235a0001c0005t0002g0241others(1): Show | 5 | HG02809.hp2 HG02818.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-4571C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858053 | ||||||
chr5:176858060
|
G | C | 23 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0230others(20): Show | 24 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.71-4564G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858060 | ||||||
chr5:176858117
|
G | A | 17 | a0001c0001t0001g0094a0001c0001t0001g0234a0001c0001t0003g0092others(14): Show | 17 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.71-4507G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858117 | ||||||
chr5:176858223
|
C | T | 23 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0230others(20): Show | 24 | HG01167.hp1 HG01891.hp2 HG02280.hp2 others(21): Show |
intron_variant | MODIFIER | c.71-4401C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858223 | ||||||
chr5:176858597
|
C | T | 143 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(140): Show | 146 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(143): Show |
intron_variant | MODIFIER | c.71-4027C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858597 | ||||||
chr5:176858609
|
C | T | 8 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(5): Show | 8 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-4015C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858609 | ||||||
chr5:176858700
|
C | T | 17 | a0001c0001t0001g0094a0001c0001t0003g0092a0001c0001t0003g0093others(14): Show | 17 | HG01884.hp1 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.71-3924C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858700 | ||||||
chr5:176858711
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(138): Show | 144 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(141): Show |
intron_variant | MODIFIER | c.71-3913A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858711 | ||||||
chr5:176858714
|
A | C | 2 | a0001c0001t0001g0098a0001c0001t0001g0153 | 2 | HG02300.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.71-3910A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858714 | ||||||
chr5:176858720
|
A | AAGGAAGG others(7): Show |
1 | a0001c0001t0001g0146 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.71-3904_71-3903ins others(14): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858720 | ||||||
chr5:176858721
|
G | A | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(136): Show | 142 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.71-3903G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858721 | ||||||
chr5:176858722
|
A | AAG | 11 | a0001c0001t0001g0146a0001c0001t0002g0257a0001c0001t0003g0093others(8): Show | 11 | HG02647.hp2 HG02895.hp2 HG02976.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-3902_71-3901ins others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858722 | ||||||
chr5:176858722
|
A | AAGGAAG | 5 | a0001c0001t0001g0094a0001c0001t0003g0092a0001c0001t0003g0246others(2): Show | 5 | HG02451.hp2 HG02615.hp1 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-3902_71-3901ins others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858722 | ||||||
chr5:176858722
|
A | AGAAG | 4 | a0001c0001t0002g0055a0001c0001t0002g0075a0001c0001t0002g0190others(1): Show | 4 | HG01257.hp1 HG02055.hp1 HG02083.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3852_71-3849dup others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | |||||
chr5:176858722
|
A | AGAAGGAA others(1): Show |
13 | a0001c0001t0002g0003a0001c0001t0002g0060a0001c0001t0002g0134others(10): Show | 14 | HG01069.hp2 HG01074.hp1 HG01256.hp1 others(11): Show |
intron_variant | MODIFIER | c.71-3856_71-3849dup others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | |||||
chr5:176858722
|
A | AGAAGGAA others(5): Show |
12 | a0001c0001t0001g0136a0001c0001t0001g0145a0001c0001t0002g0012others(9): Show | 12 | HG01891.hp1 HG01891.hp2 HG01934.hp1 others(9): Show |
intron_variant | MODIFIER | c.71-3860_71-3849dup others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | |||||
chr5:176858722
|
A | AGAAGGAA others(9): Show |
11 | a0001c0001t0002g0010a0001c0001t0002g0085a0001c0001t0002g0123others(8): Show | 11 | HG01106.hp2 HG01361.hp1 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-3864_71-3849dup others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | |||||
chr5:176858722
|
A | AGAAGGAA others(13): Show |
6 | a0001c0001t0001g0127a0001c0001t0002g0070a0001c0001t0002g0102others(3): Show | 6 | HG02970.hp1 HG04228.hp1 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-3868_71-3849dup others(20): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | |||||
chr5:176858722
|
A | AGAAGGAA others(17): Show |
3 | a0001c0001t0001g0234a0001c0001t0002g0096a0003c0003t0002g0017 | 3 | HG02257.hp1 HG02922.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.71-3872_71-3849dup others(24): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | |||||
chr5:176858722
|
A | AGAAGGAA others(37): Show |
1 | a0001c0001t0002g0035 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.71-3892_71-3849dup others(44): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858722 | |||||
chr5:176858722
|
A | G | 139 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(136): Show | 142 | HG00099.hp2 HG00558.hp1 HG00609.hp1 others(139): Show |
intron_variant | MODIFIER | c.71-3902A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858722 | ||||||
chr5:176858764
|
A | C | 5 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0253others(2): Show | 5 | HG02451.hp2 HG03471.hp2 NA18522.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-3860A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858764 | ||||||
chr5:176858768
|
A | AAGGCAGG others(1): Show |
2 | a0001c0001t0005g0008a0001c0001t0005g0023 | 2 | HG02976.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.71-3853_71-3852ins others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858768 | |||||
chr5:176858768
|
A | C | 11 | a0001c0001t0001g0094a0001c0001t0003g0092a0001c0001t0003g0093others(8): Show | 11 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-3856A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858768 | ||||||
chr5:176858772
|
A | AAGGAAGG others(21): Show |
1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(28): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858772 | |||||
chr5:176858772
|
A | AAGGCAGG others(1): Show |
2 | a0001c0001t0003g0245a0001c0001t0003g0246 | 2 | HG02895.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.71-3847_71-3846ins others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858772 | |||||
chr5:176858772
|
A | C | 13 | a0001c0001t0001g0094a0001c0001t0003g0092a0001c0001t0003g0093others(10): Show | 13 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.71-3852A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858772 | ||||||
chr5:176858774
|
G | A | 6 | a0001c0001t0001g0076a0001c0001t0001g0180a0001c0001t0001g0202others(3): Show | 6 | HG00558.hp2 HG01433.hp2 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-3850G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858774 | ||||||
chr5:176858774
|
G | GGAAA | 10 | a0001c0001t0001g0002a0001c0001t0001g0069a0001c0001t0001g0138others(7): Show | 11 | HG00609.hp2 HG01081.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(1): Show |
26 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0056others(23): Show | 26 | HG00733.hp1 HG00733.hp2 HG00741.hp1 others(23): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(4): Show |
1 | a0001c0001t0009g0043 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(11): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(5): Show |
50 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0025others(47): Show | 51 | HG00609.hp1 HG01069.hp1 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(9): Show |
33 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0018others(30): Show | 34 | HG00558.hp1 HG00621.hp2 HG00639.hp1 others(31): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(12): Show |
1 | a0001c0001t0001g0133 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(19): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(13): Show |
28 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0026others(25): Show | 29 | HG00099.hp1 HG00099.hp2 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(20): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(17): Show |
11 | a0001c0001t0001g0020a0001c0001t0001g0110a0001c0001t0001g0130others(8): Show | 11 | HG00639.hp2 HG01109.hp2 HG01255.hp1 others(8): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(24): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(21): Show |
8 | a0001c0001t0001g0086a0001c0001t0002g0118a0001c0001t0002g0204others(5): Show | 8 | HG01257.hp2 HG01258.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(28): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(25): Show |
2 | a0001c0001t0001g0174a0001c0001t0002g0097 | 2 | HG02818.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(32): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(29): Show |
1 | a0001c0001t0002g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(36): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(21): Show |
2 | a0002c0002t0004g0021a0002c0002t0004g0166 | 2 | HG03471.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(28): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(13): Show |
2 | a0001c0001t0007g0242a0001c0001t0007g0247 | 2 | HG01884.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(20): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(9): Show |
1 | a0001c0001t0007g0083 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(13): Show |
3 | a0002c0002t0001g0006a0002c0002t0001g0112a0002c0002t0004g0066 | 4 | HG01243.hp2 HG02572.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(20): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(21): Show |
1 | a0001c0001t0011g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(28): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGAA others(9): Show |
1 | a0002c0002t0004g0048 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.71-3849_71-3848ins others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858774
|
G | GGAAGGCA others(5): Show |
2 | a0002c0002t0004g0144a0002c0002t0004g0165 | 2 | HG02074.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.71-3849_71-3848ins others(12): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858774 | |||||
chr5:176858776
|
C | A | 8 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(5): Show | 8 | HG01891.hp2 HG02965.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-3848C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858776 | ||||||
chr5:176858778
|
A | G | 21 | a0001c0001t0001g0094a0001c0001t0001g0234a0001c0001t0002g0058others(18): Show | 21 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(18): Show |
intron_variant | MODIFIER | c.71-3846A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858778 | ||||||
chr5:176858782
|
A | AGCAG | 3 | a0001c0001t0001g0141a0001c0001t0001g0146a0001c0001t0002g0257 | 3 | HG03195.hp1 HG03688.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.71-3836_71-3833dup others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176858782 | |||||
chr5:176858782
|
A | G | 206 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(203): Show | 211 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(208): Show |
intron_variant | MODIFIER | c.71-3842A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858782 | ||||||
chr5:176858806
|
A | G | 6 | a0001c0001t0003g0111a0003c0003t0001g0188a0003c0003t0002g0017others(3): Show | 6 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-3818A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858806 | ||||||
chr5:176858918
|
G | C | 1 | a0001c0001t0002g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.71-3706G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858918 | ||||||
chr5:176858920
|
G | C | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-3704G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858920 | ||||||
chr5:176858920
|
G | T | 42 | a0001c0001t0001g0174a0001c0001t0002g0010a0001c0001t0002g0012others(39): Show | 43 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.71-3704G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176858920 | ||||||
chr5:176859070
|
C | CATGCCCT others(83): Show |
1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.71-3504_71-3503ins others(90): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859070 | |||||
chr5:176859074
|
C | CCCTTGCT others(23): Show |
6 | a0001c0001t0002g0075a0001c0001t0002g0134a0001c0001t0002g0137others(3): Show | 6 | HG02055.hp1 HG02135.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-3533_71-3504dup others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859074 | |||||
chr5:176859083
|
G | A | 9 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0097others(6): Show | 9 | HG01891.hp2 HG02818.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-3541G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859083 | ||||||
chr5:176859091
|
AGCTGCTA others(23): Show |
A | 5 | a0001c0001t0002g0010a0001c0001t0003g0009a0001c0001t0003g0011others(2): Show | 5 | HG01891.hp2 HG03041.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3520_71-3491del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859091 | |||||
chr5:176859091
|
AGCTGCTA others(83): Show |
A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.71-3520_71-3431del others(90): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859091 | |||||
chr5:176859099
|
G | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0255 | 2 | HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.71-3525G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859099 | ||||||
chr5:176859099
|
GAATGTCC others(53): Show |
G | 104 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(101): Show | 107 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(104): Show |
intron_variant | MODIFIER | c.71-3465_71-3406del others(60): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859099 | |||||
chr5:176859104
|
T | C | 53 | a0001c0001t0001g0094a0001c0001t0001g0174a0001c0001t0002g0040others(50): Show | 54 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.71-3520T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859104 | ||||||
chr5:176859104
|
TCCTTGCT others(23): Show |
T | 22 | a0001c0001t0001g0014a0001c0001t0001g0026a0001c0001t0001g0036others(19): Show | 22 | HG00099.hp2 HG01109.hp2 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.71-3503_71-3474del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859104 | |||||
chr5:176859104
|
TCCTTGCT others(83): Show |
T | 5 | a0001c0001t0001g0045a0001c0001t0003g0244a0001c0001t0010g0022others(2): Show | 5 | HG02451.hp1 HG03139.hp2 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.71-3503_71-3414del others(90): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859104 | |||||
chr5:176859121
|
G | A | 78 | a0001c0001t0001g0016a0001c0001t0001g0033a0001c0001t0001g0056others(75): Show | 80 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(77): Show |
intron_variant | MODIFIER | c.71-3503G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859121 | ||||||
chr5:176859121
|
G | GGCTGCTA others(113): Show |
1 | a0003c0003t0002g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.71-3496_71-3495ins others(120): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859121 | |||||
chr5:176859121
|
GGCTGCTA others(23): Show |
G | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.71-3495_71-3466del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859121 | |||||
chr5:176859129
|
G | C | 16 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0033others(13): Show | 16 | HG01069.hp1 HG01243.hp1 HG01496.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-3495G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859129 | ||||||
chr5:176859129
|
GAATGCCC others(23): Show |
G | 2 | a0001c0001t0001g0032a0001c0001t0001g0255 | 2 | HG02559.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.71-3490_71-3461del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859129 | |||||
chr5:176859133
|
GCCCTTGC others(50): Show |
G | 1 | a0004c0006t0002g0005 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.71-3490_71-3434del others(57): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859133 | ||||||
chr5:176859133
|
GCCCTTGC others(80): Show |
G | 3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-3490_71-3404del others(87): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859133 | ||||||
chr5:176859133
|
GCCCTTGC others(230): Show |
G | 16 | a0001c0001t0001g0094a0001c0001t0003g0092a0001c0001t0003g0093others(13): Show | 16 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-3490_71-3254del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859133 | ||||||
chr5:176859134
|
C | CCCTTGCT others(113): Show |
4 | a0001c0001t0003g0111a0003c0003t0002g0073a0003c0003t0002g0107others(1): Show | 4 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3371_71-3370ins others(120): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859134 | |||||
chr5:176859134
|
C | CCCTTGCT others(53): Show |
1 | a0003c0003t0001g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.71-3466_71-3465ins others(60): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859134 | |||||
chr5:176859134
|
C | CCCTTGCT others(23): Show |
1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-3474_71-3473ins others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859134 | |||||
chr5:176859134
|
C | T | 30 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0033others(27): Show | 31 | HG01069.hp1 HG01081.hp2 HG01106.hp1 others(28): Show |
intron_variant | MODIFIER | c.71-3490C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859134 | ||||||
chr5:176859151
|
A | G | 14 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0033others(11): Show | 14 | HG01069.hp1 HG01243.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.71-3473A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859151 | ||||||
chr5:176859159
|
C | G | 33 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0033others(30): Show | 34 | HG01069.hp1 HG01109.hp1 HG01167.hp1 others(31): Show |
intron_variant | MODIFIER | c.71-3465C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859159 | ||||||
chr5:176859160
|
A | AATGATGT others(704): Show |
1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-3461_71-3460ins others(711): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859160 | |||||
chr5:176859163
|
GTCCTTGC others(80): Show |
G | 2 | a0001c0005t0002g0235a0001c0005t0002g0241 | 2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.71-3460_71-3374del others(87): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859163 | ||||||
chr5:176859164
|
T | C | 5 | a0001c0001t0002g0012a0001c0001t0002g0230a0001c0001t0002g0231others(2): Show | 5 | HG01167.hp1 HG02965.hp2 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3460T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859164 | ||||||
chr5:176859164
|
TCCTTGCT others(173): Show |
T | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-3370_71-3191del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859164 | |||||
chr5:176859181
|
G | A | 121 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(118): Show | 125 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.71-3443G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859181 | ||||||
chr5:176859181
|
GGCTGCTA others(143): Show |
G | 2 | a0001c0001t0001g0138a0001c0001t0001g0139 | 2 | NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.71-3413_71-3264del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859181 | |||||
chr5:176859189
|
G | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 104 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.71-3435G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859189 | ||||||
chr5:176859190
|
A | AATG | 11 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0011g0015others(8): Show | 12 | HG01109.hp1 HG01167.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.71-3433_71-3431dup others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859190 | |||||
chr5:176859194
|
C | T | 160 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(157): Show | 165 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(162): Show |
intron_variant | MODIFIER | c.71-3430C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859194 | ||||||
chr5:176859211
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(138): Show | 144 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(141): Show |
intron_variant | MODIFIER | c.71-3413A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859211 | ||||||
chr5:176859219
|
G | C | 23 | a0001c0001t0001g0174a0001c0001t0002g0040a0001c0001t0002g0090others(20): Show | 23 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.71-3405G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859219 | ||||||
chr5:176859219
|
GAATGTCC others(53): Show |
G | 5 | a0001c0001t0001g0018a0001c0001t0001g0056a0001c0001t0001g0059others(2): Show | 5 | HG01069.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3383_71-3324del others(60): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859219 | |||||
chr5:176859224
|
T | C | 24 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0020others(21): Show | 24 | HG00099.hp2 HG01109.hp2 HG02055.hp2 others(21): Show |
intron_variant | MODIFIER | c.71-3400T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859224 | ||||||
chr5:176859224
|
TCCTTGCT others(83): Show |
T | 15 | a0001c0001t0001g0016a0001c0001t0001g0032a0001c0001t0001g0033others(12): Show | 15 | HG01243.hp1 HG01496.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.71-3353_71-3264del others(90): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859224 | |||||
chr5:176859226
|
C | A | 1 | a0004c0006t0002g0005 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.71-3398C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859226 | ||||||
chr5:176859241
|
A | G | 128 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(125): Show | 131 | HG00099.hp1 HG00558.hp1 HG00558.hp2 others(128): Show |
intron_variant | MODIFIER | c.71-3383A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859241 | ||||||
chr5:176859249
|
G | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.71-3375G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859249 | ||||||
chr5:176859250
|
AATGCCCT others(176): Show |
A | 1 | a0001c0001t0014g0061 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.71-3370_71-3188del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859250 | |||||
chr5:176859253
|
GCCCTTGC others(50): Show |
G | 1 | a0001c0001t0002g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.71-3370_71-3314del others(57): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859253 | ||||||
chr5:176859254
|
C | CCCTTGCT others(23): Show |
4 | a0001c0001t0011g0015a0002c0002t0004g0144a0002c0002t0004g0165others(1): Show | 4 | HG02074.hp2 HG03516.hp1 NA18975.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-3346_71-3345ins others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859254 | |||||
chr5:176859254
|
C | CCCTTGCT others(23): Show |
5 | a0002c0002t0001g0006a0002c0002t0001g0112a0002c0002t0004g0021others(2): Show | 6 | HG01109.hp1 HG01243.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.71-3346_71-3345ins others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859254 | |||||
chr5:176859254
|
C | T | 38 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0020others(35): Show | 38 | HG00099.hp2 HG01109.hp2 HG01167.hp2 others(35): Show |
intron_variant | MODIFIER | c.71-3370C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859254 | ||||||
chr5:176859271
|
A | G | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0002g0164others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3353A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859271 | ||||||
chr5:176859271
|
AGCTGCTA others(23): Show |
A | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 104 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(101): Show |
intron_variant | MODIFIER | c.71-3345_71-3316del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859271 | |||||
chr5:176859279
|
C | G | 50 | a0001c0001t0001g0045a0001c0001t0001g0053a0001c0001t0001g0054others(47): Show | 52 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.71-3345C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859279 | ||||||
chr5:176859284
|
T | C | 3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-3340T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859284 | ||||||
chr5:176859284
|
T | TCCTTGCT others(113): Show |
5 | a0001c0001t0001g0234a0001c0001t0003g0111a0003c0003t0002g0073others(2): Show | 5 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3324_71-3323ins others(120): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859284 | |||||
chr5:176859284
|
TCCTTGCT others(23): Show |
T | 5 | a0001c0001t0001g0018a0001c0001t0001g0056a0001c0001t0001g0059others(2): Show | 5 | HG01069.hp1 HG01515.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3323_71-3294del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859284 | |||||
chr5:176859284
|
TCCTTGCT others(53): Show |
T | 23 | a0001c0001t0001g0014a0001c0001t0001g0019a0001c0001t0001g0020others(20): Show | 23 | HG00099.hp2 HG01109.hp2 HG02055.hp2 others(20): Show |
intron_variant | MODIFIER | c.71-3280_71-3221del others(60): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859284 | |||||
chr5:176859286
|
C | A | 3 | a0001c0001t0005g0256a0001c0005t0002g0235a0001c0005t0002g0241 | 3 | HG02280.hp2 HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.71-3338C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859286 | ||||||
chr5:176859301
|
G | A | 38 | a0001c0001t0001g0045a0001c0001t0001g0174a0001c0001t0001g0234others(35): Show | 39 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.71-3323G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859301 | ||||||
chr5:176859301
|
G | GGCTGCTA others(233): Show |
1 | a0003c0003t0002g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.71-3281_71-3280ins others(240): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859301 | |||||
chr5:176859301
|
G | GGCTGCTA others(353): Show |
1 | a0003c0003t0001g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.71-3281_71-3280ins others(360): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859301 | |||||
chr5:176859309
|
G | C | 2 | a0001c0001t0001g0045a0001c0001t0008g0113 | 2 | HG02970.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.71-3315G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859309 | ||||||
chr5:176859313
|
GCCCTTGC others(50): Show |
G | 23 | a0001c0001t0001g0174a0001c0001t0002g0040a0001c0001t0002g0090others(20): Show | 23 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.71-3310_71-3254del others(57): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859313 | ||||||
chr5:176859314
|
C | T | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(116): Show | 124 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.71-3310C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859314 | ||||||
chr5:176859331
|
A | G | 14 | a0001c0001t0001g0045a0001c0001t0002g0230a0001c0001t0002g0231others(11): Show | 16 | HG01109.hp1 HG01167.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-3293A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859331 | ||||||
chr5:176859339
|
G | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(130): Show | 137 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(134): Show |
intron_variant | MODIFIER | c.71-3285G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859339 | ||||||
chr5:176859340
|
AATGCCCT others(86): Show |
A | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.71-3280_71-3188del others(93): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859340 | |||||
chr5:176859344
|
C | T | 147 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(144): Show | 152 | HG00558.hp1 HG00558.hp2 HG00609.hp1 others(149): Show |
intron_variant | MODIFIER | c.71-3280C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859344 | ||||||
chr5:176859346
|
C | A | 1 | a0001c0001t0002g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.71-3278C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859346 | ||||||
chr5:176859361
|
G | A | 8 | a0001c0001t0002g0248a0001c0001t0003g0244a0001c0001t0008g0113others(5): Show | 8 | HG02451.hp1 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.71-3263G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859361 | ||||||
chr5:176859369
|
G | C | 1 | a0004c0006t0002g0005 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.71-3255G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859369 | ||||||
chr5:176859370
|
A | AATG | 4 | a0001c0001t0003g0244a0001c0001t0010g0022a0001c0004t0002g0232others(1): Show | 4 | HG02451.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-3253_71-3251dup others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859370 | |||||
chr5:176859374
|
C | T | 50 | a0001c0001t0001g0094a0001c0001t0001g0174a0001c0001t0002g0040others(47): Show | 51 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.71-3250C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859374 | ||||||
chr5:176859391
|
A | G | 6 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247others(3): Show | 7 | HG01884.hp1 HG02145.hp2 HG02647.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-3233A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859391 | ||||||
chr5:176859399
|
G | C | 3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-3225G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859399 | ||||||
chr5:176859406
|
C | A | 4 | a0001c0001t0003g0074a0001c0001t0003g0252a0001c0001t0003g0259others(1): Show | 4 | HG02615.hp2 HG02717.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3218C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859406 | ||||||
chr5:176859421
|
A | G | 5 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3203A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859421 | ||||||
chr5:176859429
|
G | C | 5 | a0001c0001t0001g0045a0001c0001t0001g0138a0001c0001t0001g0139others(2): Show | 5 | HG02809.hp2 HG02818.hp1 NA19002.hp1 others(2): Show |
intron_variant | MODIFIER | c.71-3195G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859429 | ||||||
chr5:176859430
|
AATG | A | 53 | a0001c0001t0001g0045a0001c0001t0001g0094a0001c0001t0001g0138others(50): Show | 54 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(51): Show |
intron_variant | MODIFIER | c.71-3190_71-3188del others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859430 | |||||
chr5:176859437
|
T | C | 30 | a0001c0001t0001g0174a0001c0001t0002g0040a0001c0001t0002g0090others(27): Show | 30 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(27): Show |
intron_variant | MODIFIER | c.71-3187T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859437 | ||||||
chr5:176859454
|
A | G | 6 | a0001c0001t0001g0045a0001c0001t0001g0138a0001c0001t0001g0139others(3): Show | 6 | HG02809.hp2 HG02818.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.71-3170A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859454 | ||||||
chr5:176859462
|
G | C | 3 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0014g0061 | 3 | HG01167.hp2 HG01169.hp2 HG02630.hp1 |
intron_variant | MODIFIER | c.71-3162G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859462 | ||||||
chr5:176859466
|
GTCCTTGC others(80): Show |
G | 1 | a0004c0006t0002g0005 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.71-3157_71-3071del others(87): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859466 | ||||||
chr5:176859467
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | NA19002.hp1 NA19043.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.71-3157T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859467 | ||||||
chr5:176859469
|
C | A | 9 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0009others(6): Show | 9 | HG01891.hp2 HG02280.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.71-3155C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859469 | ||||||
chr5:176859484
|
A | G | 4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0002g0248others(1): Show | 4 | HG01167.hp2 HG01169.hp2 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3140A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859484 | ||||||
chr5:176859484
|
AGCTGCTA others(143): Show |
A | 16 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0018others(13): Show | 16 | HG01243.hp1 HG01884.hp2 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.71-3050_71-2901del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859484 | |||||
chr5:176859492
|
G | C | 1 | a0001c0001t0002g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.71-3132G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859492 | ||||||
chr5:176859496
|
GCCCTTGC others(140): Show |
G | 3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-3127_71-2981del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859496 | ||||||
chr5:176859496
|
GCCCTTGC others(170): Show |
G | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-3127_71-2951del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859496 | ||||||
chr5:176859497
|
C | T | 33 | a0001c0001t0001g0045a0001c0001t0001g0138a0001c0001t0001g0139others(30): Show | 33 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.71-3127C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859497 | ||||||
chr5:176859497
|
CCCTTGCT others(23): Show |
C | 16 | a0001c0001t0001g0094a0001c0001t0003g0092a0001c0001t0003g0093others(13): Show | 16 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-3080_71-3051del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859497 | |||||
chr5:176859514
|
A | G | 153 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(150): Show | 156 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(153): Show |
intron_variant | MODIFIER | c.71-3110A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859514 | ||||||
chr5:176859526
|
GTCCTTGC others(50): Show |
G | 4 | a0001c0001t0001g0045a0001c0001t0001g0138a0001c0001t0001g0139others(1): Show | 4 | HG02630.hp1 NA19002.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.71-3097_71-3041del others(57): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859526 | ||||||
chr5:176859526
|
GTCCTTGC others(110): Show |
G | 2 | a0001c0005t0002g0235a0001c0005t0002g0241 | 2 | HG02809.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.71-3097_71-2981del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859526 | ||||||
chr5:176859544
|
A | G | 35 | a0001c0001t0001g0174a0001c0001t0002g0010a0001c0001t0002g0012others(32): Show | 35 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.71-3080A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859544 | ||||||
chr5:176859552
|
G | C | 38 | a0001c0001t0001g0033a0001c0001t0001g0174a0001c0001t0001g0224others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.71-3072G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859552 | ||||||
chr5:176859556
|
GTCCTTGC others(20): Show |
G | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01167.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.71-3067_71-3041del others(27): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859556 | ||||||
chr5:176859557
|
TCCTTGCT others(83): Show |
T | 1 | a0004c0006t0002g0005 | 2 | HG03098.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.71-3050_71-2961del others(90): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859557 | |||||
chr5:176859574
|
G | A | 118 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(115): Show | 121 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(118): Show |
intron_variant | MODIFIER | c.71-3050G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859574 | ||||||
chr5:176859582
|
G | C | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-3042G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859582 | ||||||
chr5:176859586
|
GTCCTTGC others(50): Show |
G | 1 | a0001c0001t0002g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.71-3037_71-2981del others(57): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859586 | ||||||
chr5:176859586
|
GTCCTTGC others(203): Show |
G | 117 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(114): Show | 120 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(117): Show |
intron_variant | MODIFIER | c.71-3037_71-2828del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859586 | ||||||
chr5:176859587
|
T | C | 22 | a0001c0001t0001g0033a0001c0001t0001g0174a0001c0001t0001g0224others(19): Show | 22 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(19): Show |
intron_variant | MODIFIER | c.71-3037T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859587 | ||||||
chr5:176859604
|
G | A | 36 | a0001c0001t0001g0033a0001c0001t0001g0045a0001c0001t0001g0053others(33): Show | 36 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.71-3020G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859604 | ||||||
chr5:176859612
|
C | G | 44 | a0001c0001t0001g0033a0001c0001t0001g0045a0001c0001t0001g0053others(41): Show | 44 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-3012C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859612 | ||||||
chr5:176859634
|
G | A | 44 | a0001c0001t0001g0033a0001c0001t0001g0045a0001c0001t0001g0053others(41): Show | 44 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(41): Show |
intron_variant | MODIFIER | c.71-2990G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859634 | ||||||
chr5:176859643
|
A | AATG | 38 | a0001c0001t0001g0033a0001c0001t0001g0174a0001c0001t0001g0224others(35): Show | 38 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.71-2980_71-2978dup others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859643 | |||||
chr5:176859647
|
C | CCCTTGCT others(56): Show |
12 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0008g0113others(9): Show | 13 | HG01109.hp1 HG01167.hp1 HG01243.hp2 others(10): Show |
intron_variant | MODIFIER | c.71-2918_71-2917ins others(63): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859647 | |||||
chr5:176859647
|
C | T | 45 | a0001c0001t0001g0033a0001c0001t0001g0174a0001c0001t0001g0224others(42): Show | 45 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.71-2977C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859647 | ||||||
chr5:176859647
|
CCCTTGCT others(23): Show |
C | 16 | a0001c0001t0001g0094a0001c0001t0003g0092a0001c0001t0003g0093others(13): Show | 16 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-2917_71-2888del others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859647 | |||||
chr5:176859664
|
A | G | 22 | a0001c0001t0001g0014a0001c0001t0001g0016a0001c0001t0001g0018others(19): Show | 22 | HG01167.hp2 HG01169.hp2 HG01243.hp1 others(19): Show |
intron_variant | MODIFIER | c.71-2960A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859664 | ||||||
chr5:176859707
|
T | C | 3 | a0001c0001t0001g0033a0001c0001t0001g0224a0001c0001t0001g0226 | 3 | HG01496.hp1 HG01943.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.71-2917T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859707 | ||||||
chr5:176859724
|
A | G | 3 | a0001c0001t0001g0033a0001c0001t0001g0224a0001c0001t0001g0226 | 3 | HG01496.hp1 HG01943.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.71-2900A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859724 | ||||||
chr5:176859733
|
AATG | A | 3 | a0001c0001t0001g0033a0001c0001t0001g0224a0001c0001t0001g0226 | 3 | HG01496.hp1 HG01943.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.71-2887_71-2885del others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859733 | |||||
chr5:176859736
|
G | GTCCTTGC others(20): Show |
1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.71-2888_71-2887ins others(27): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859736 | ||||||
chr5:176859753
|
GCATAGCT others(53): Show |
G | 3 | a0001c0001t0001g0138a0001c0001t0001g0139a0001c0001t0014g0061 | 3 | HG02630.hp1 NA19002.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.71-2831_71-2772del others(60): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859753 | |||||
chr5:176859796
|
A | AATG | 3 | a0001c0001t0001g0033a0001c0001t0001g0224a0001c0001t0001g0226 | 3 | HG01496.hp1 HG01943.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.71-2827_71-2825dup others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr5 | 176859796 | |||||
chr5:176859800
|
T | C | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-2824T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859800 | ||||||
chr5:176859813
|
T | G | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(122): Show | 128 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(125): Show |
intron_variant | MODIFIER | c.71-2811T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176859813 | ||||||
chr5:176860025
|
C | T | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-2599C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860025 | ||||||
chr5:176860028
|
A | G | 217 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(214): Show | 222 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(219): Show |
intron_variant | MODIFIER | c.71-2596A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860028 | ||||||
chr5:176860127
|
C | T | 28 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0037others(25): Show | 29 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.71-2497C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860127 | ||||||
chr5:176860145
|
A | G | 1 | a0002c0002t0004g0165 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.71-2479A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860145 | ||||||
chr5:176860194
|
G | C | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(226): Show |
intron_variant | MODIFIER | c.71-2430G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860194 | ||||||
chr5:176860195
|
G | A | 1 | a0001c0001t0002g0140 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.71-2429G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860195 | ||||||
chr5:176860197
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.71-2427A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860197 | ||||||
chr5:176860208
|
G | T | 1 | a0001c0001t0001g0203 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.71-2416G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860208 | ||||||
chr5:176860210
|
G | T | 17 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0248others(14): Show | 18 | HG01891.hp2 HG02280.hp2 HG02451.hp1 others(15): Show |
intron_variant | MODIFIER | c.71-2414G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860210 | ||||||
chr5:176860346
|
G | A | 7 | a0001c0001t0001g0234a0001c0001t0003g0111a0003c0003t0001g0188others(4): Show | 7 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(4): Show |
intron_variant | MODIFIER | c.71-2278G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860346 | ||||||
chr5:176860517
|
C | T | 1 | a0001c0001t0003g0009 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.71-2107C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860517 | ||||||
chr5:176860591
|
C | T | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.71-2033C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860591 | ||||||
chr5:176860629
|
G | A | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-1995G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860629 | ||||||
chr5:176860638
|
GT | G | 4 | a0001c0001t0003g0244a0001c0001t0010g0022a0001c0004t0002g0232others(1): Show | 4 | HG02451.hp1 HG03139.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-1985delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860638 | ||||||
chr5:176860652
|
C | A | 1 | a0001c0001t0001g0203 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.71-1972C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860652 | ||||||
chr5:176860821
|
G | A | 2 | a0003c0003t0001g0188a0003c0003t0002g0017 | 2 | HG02257.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.71-1803G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860821 | ||||||
chr5:176860949
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0229a0001c0001t0002g0096 | 3 | HG02622.hp1 HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.71-1675G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860949 | ||||||
chr5:176860965
|
C | T | 1 | a0001c0001t0002g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.71-1659C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860965 | ||||||
chr5:176860966
|
G | A | 3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.71-1658G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176860966 | ||||||
chr5:176861163
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(138): Show | 144 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.71-1461G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861163 | ||||||
chr5:176861330
|
C | G | 1 | a0001c0001t0001g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.71-1294C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861330 | ||||||
chr5:176861424
|
G | A | 19 | a0001c0001t0001g0174a0001c0001t0002g0040a0001c0001t0002g0090others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.71-1200G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861424 | ||||||
chr5:176861442
|
G | A | 1 | a0001c0001t0003g0065 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.71-1182G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861442 | ||||||
chr5:176861450
|
A | G | 166 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(163): Show | 169 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(166): Show |
intron_variant | MODIFIER | c.71-1174A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861450 | ||||||
chr5:176861541
|
C | T | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.71-1083C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861541 | ||||||
chr5:176861550
|
T | A | 16 | a0001c0001t0001g0094a0001c0001t0003g0092a0001c0001t0003g0093others(13): Show | 16 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-1074T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861550 | ||||||
chr5:176861581
|
C | T | 1 | a0001c0001t0001g0124 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.71-1043C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861581 | ||||||
chr5:176861728
|
A | G | 3 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0001t0008g0113 | 3 | HG01167.hp1 HG02970.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.71-896A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861728 | ||||||
chr5:176861824
|
G | GGAGGCCA others(3): Show |
224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(226): Show |
intron_variant | MODIFIER | c.71-800_71-799insGA others(8): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861824 | ||||||
chr5:176861825
|
A | T | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(221): Show | 229 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(226): Show |
intron_variant | MODIFIER | c.71-799A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861825 | ||||||
chr5:176861848
|
C | T | 3 | a0001c0001t0001g0033a0001c0001t0001g0224a0001c0001t0001g0226 | 3 | HG01496.hp1 HG01943.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.71-776C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861848 | ||||||
chr5:176861849
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(139): Show | 145 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(142): Show |
intron_variant | MODIFIER | c.71-775A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861849 | ||||||
chr5:176861854
|
G | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(116): Show | 122 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(119): Show |
intron_variant | MODIFIER | c.71-770G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861854 | ||||||
chr5:176861860
|
G | A | 2 | a0001c0001t0002g0123a0001c0001t0002g0191 | 2 | HG02080.hp1 HG02132.hp2 |
intron_variant | MODIFIER | c.71-764G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861860 | ||||||
chr5:176861891
|
T | A | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-733T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861891 | ||||||
chr5:176861892
|
C | T | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.71-732C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176861892 | ||||||
chr5:176862254
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.71-370G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176862254 | ||||||
chr5:176862459
|
T | G | 16 | a0001c0001t0001g0094a0001c0001t0003g0092a0001c0001t0003g0093others(13): Show | 16 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.71-165T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 1/14 | chr5 | 176862459 | ||||||
chr5:176862860
|
G | T | 1 | a0001c0001t0002g0096 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.292+15G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176862860 | ||||||
chr5:176862865
|
A | G | 3 | a0001c0001t0002g0210a0001c0001t0002g0211a0001c0001t0002g0217 | 3 | HG01256.hp1 HG01934.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.292+20A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176862865 | ||||||
chr5:176862866
|
G | C | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.292+21G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176862866 | ||||||
chr5:176862896
|
G | A | 1 | a0001c0001t0002g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.292+51G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176862896 | ||||||
chr5:176862903
|
C | G | 1 | a0001c0001t0001g0172 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.292+58C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176862903 | ||||||
chr5:176863060
|
C | A | 1 | a0001c0007t0001g0135 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.292+215C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863060 | ||||||
chr5:176863218
|
G | A | 1 | a0001c0001t0002g0200 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.292+373G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863218 | ||||||
chr5:176863279
|
A | C | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.292+434A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863279 | ||||||
chr5:176863420
|
T | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.292+575T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863420 | ||||||
chr5:176863497
|
G | C | 3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.292+652G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863497 | ||||||
chr5:176863626
|
C | T | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.292+781C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863626 | ||||||
chr5:176863629
|
G | A | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.292+784G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863629 | ||||||
chr5:176863674
|
C | A | 3 | a0002c0002t0004g0144a0002c0002t0004g0165a0002c0002t0004g0166 | 3 | HG02074.hp2 NA18975.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.292+829C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863674 | ||||||
chr5:176863734
|
T | TC | 6 | a0001c0001t0001g0053a0001c0001t0001g0110a0001c0001t0001g0145others(3): Show | 6 | HG00735.hp1 HG01167.hp2 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.292+894dupC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863734 | |||||
chr5:176863746
|
TCCTCCTC others(54): Show |
T | 3 | a0001c0001t0010g0022a0001c0004t0002g0232a0001c0004t0002g0233 | 3 | HG02451.hp1 HG03139.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.292+911_292+971del others(61): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863746 | |||||
chr5:176863805
|
T | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(138): Show | 144 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(141): Show |
intron_variant | MODIFIER | c.292+960T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863805 | ||||||
chr5:176863807
|
C | CCCTCCT | 127 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0014others(124): Show | 129 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.292+965_292+970dup others(6): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863807 | |||||
chr5:176863807
|
C | CCCTCCTC others(8): Show |
82 | a0001c0001t0001g0064a0001c0001t0001g0136a0001c0001t0001g0145others(79): Show | 84 | HG00099.hp1 HG00621.hp1 HG00639.hp2 others(81): Show |
intron_variant | MODIFIER | c.292+983_292+997dup others(15): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863807 | |||||
chr5:176863807
|
C | CCCTCCTC others(23): Show |
1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.292+968_292+997dup others(30): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863807 | |||||
chr5:176863807
|
C | CCCTCCTC others(14): Show |
1 | a0001c0001t0002g0257 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.292+970_292+971ins others(21): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863807 | |||||
chr5:176863808
|
C | CCTCCTCC others(8): Show |
3 | a0001c0001t0005g0008a0001c0001t0005g0013a0001c0001t0005g0023 | 3 | HG02976.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.292+977_292+978ins others(15): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863808 | |||||
chr5:176863811
|
C | T | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.292+966C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863811 | ||||||
chr5:176863813
|
T | TCCCCCTC others(9): Show |
1 | a0001c0001t0002g0186 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.292+973_292+988dup others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863813 | |||||
chr5:176863816
|
C | T | 11 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0057others(8): Show | 12 | HG00642.hp2 HG00735.hp2 HG00741.hp1 others(9): Show |
intron_variant | MODIFIER | c.292+971C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863816 | ||||||
chr5:176863819
|
T | TCCC | 10 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0057others(7): Show | 11 | HG00642.hp2 HG00735.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.292+976_292+977ins others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863819 | |||||
chr5:176863822
|
T | C | 1 | a0001c0001t0001g0223 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.292+977T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863822 | ||||||
chr5:176863828
|
T | TCCCCCTC others(9): Show |
1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.292+997_292+998ins others(16): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176863828 | |||||
chr5:176863898
|
T | C | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.292+1053T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176863898 | ||||||
chr5:176864129
|
C | T | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.292+1284C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864129 | ||||||
chr5:176864196
|
G | A | 1 | a0001c0001t0003g0050 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.292+1351G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864196 | ||||||
chr5:176864289
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.292+1444G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864289 | ||||||
chr5:176864330
|
C | A | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.292+1485C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864330 | ||||||
chr5:176864386
|
T | C | 16 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(13): Show | 17 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.292+1541T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864386 | ||||||
chr5:176864449
|
G | A | 3 | a0001c0001t0001g0158a0001c0001t0001g0159a0001c0001t0001g0202 | 3 | HG01934.hp2 HG01943.hp1 HG01978.hp1 |
intron_variant | MODIFIER | c.292+1604G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864449 | ||||||
chr5:176864510
|
A | G | 1 | a0001c0001t0002g0121 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.292+1665A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864510 | ||||||
chr5:176864540
|
C | T | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.292+1695C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864540 | ||||||
chr5:176864727
|
G | A | 12 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247others(9): Show | 13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.292+1882G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176864727 | ||||||
chr5:176865055
|
G | C | 1 | a0001c0001t0001g0104 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.292+2210G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865055 | ||||||
chr5:176865098
|
C | T | 4 | a0001c0001t0003g0111a0003c0003t0002g0073a0003c0003t0002g0107others(1): Show | 4 | HG01361.hp1 HG01891.hp1 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.292+2253C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865098 | ||||||
chr5:176865155
|
A | G | 12 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247others(9): Show | 13 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.292+2310A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865155 | ||||||
chr5:176865263
|
T | A | 16 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(13): Show | 17 | HG01081.hp2 HG01106.hp1 HG01109.hp1 others(14): Show |
intron_variant | MODIFIER | c.292+2418T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865263 | ||||||
chr5:176865392
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.292+2547G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865392 | ||||||
chr5:176865409
|
G | A | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.292+2564G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865409 | ||||||
chr5:176865569
|
G | A | 1 | a0001c0001t0001g0192 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.293-2561G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865569 | ||||||
chr5:176865606
|
C | T | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.293-2524C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865606 | ||||||
chr5:176865664
|
G | A | 1 | a0003c0003t0002g0240 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.293-2466G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865664 | ||||||
chr5:176865845
|
C | G | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.293-2285C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865845 | ||||||
chr5:176865975
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.293-2155A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176865975 | ||||||
chr5:176866016
|
C | T | 2 | a0001c0001t0003g0080a0001c0001t0003g0081 | 2 | HG01891.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.293-2114C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866016 | ||||||
chr5:176866071
|
C | G | 3 | a0001c0001t0005g0008a0001c0001t0005g0013a0001c0001t0005g0023 | 3 | HG02976.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.293-2059C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866071 | ||||||
chr5:176866073
|
G | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.293-2057G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866073 | ||||||
chr5:176866099
|
C | A | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.293-2031C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866099 | ||||||
chr5:176866106
|
G | T | 2 | a0001c0001t0002g0062a0001c0001t0002g0063 | 2 | HG01106.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.293-2024G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866106 | ||||||
chr5:176866266
|
G | A | 2 | a0001c0001t0001g0224a0001c0001t0001g0226 | 2 | HG01496.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.293-1864G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866266 | ||||||
chr5:176866339
|
C | T | 1 | a0001c0001t0001g0195 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.293-1791C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866339 | ||||||
chr5:176866692
|
C | T | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.293-1438C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866692 | ||||||
chr5:176866702
|
C | T | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(208): Show | 216 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(213): Show |
intron_variant | MODIFIER | c.293-1428C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866702 | ||||||
chr5:176866812
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.293-1318G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866812 | ||||||
chr5:176866938
|
A | C | 29 | a0001c0001t0001g0001a0001c0001t0001g0025a0001c0001t0001g0037others(26): Show | 30 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(27): Show |
intron_variant | MODIFIER | c.293-1192A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176866938 | ||||||
chr5:176867064
|
G | A | 1 | a0002c0002t0004g0166 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.293-1066G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867064 | ||||||
chr5:176867172
|
A | C | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.293-958A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867172 | ||||||
chr5:176867250
|
G | A | 1 | a0001c0001t0011g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.293-880G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867250 | ||||||
chr5:176867296
|
T | C | 2 | a0001c0001t0003g0111a0003c0003t0002g0073 | 2 | HG01891.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.293-834T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867296 | ||||||
chr5:176867483
|
G | A | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.293-647G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867483 | ||||||
chr5:176867599
|
C | T | 3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.293-531C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867599 | ||||||
chr5:176867686
|
G | A | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.293-444G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867686 | ||||||
chr5:176867894
|
G | T | 21 | a0001c0001t0001g0174a0001c0001t0002g0010a0001c0001t0002g0012others(18): Show | 21 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.293-236G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867894 | ||||||
chr5:176867911
|
A | C | 3 | a0001c0004t0002g0078a0001c0004t0002g0232a0001c0004t0002g0233 | 3 | HG02451.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.293-219A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867911 | ||||||
chr5:176867964
|
A | G | 1 | a0001c0001t0002g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.293-166A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176867964 | ||||||
chr5:176868003
|
T | A | 7 | a0001c0001t0001g0183a0001c0001t0003g0009a0001c0001t0003g0011others(4): Show | 7 | HG01891.hp2 HG02015.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.293-127T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176868003 | ||||||
chr5:176868003
|
T | TA | 17 | a0001c0001t0001g0094a0001c0001t0001g0236a0001c0001t0002g0123others(14): Show | 18 | HG02080.hp1 HG02135.hp1 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.293-114dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr5 | 176868003 | |||||
chr5:176868004
|
A | T | 5 | a0001c0001t0001g0056a0001c0001t0001g0059a0001c0001t0001g0120others(2): Show | 5 | HG01515.hp2 HG01517.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.293-126A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 2/14 | chr5 | 176868004 | ||||||
chr5:176868305
|
G | A | 1 | a0001c0001t0010g0022 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.436+32G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/14 | chr5 | 176868305 | ||||||
chr5:176868311
|
C | T | 21 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0049others(18): Show | 21 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.436+38C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/14 | chr5 | 176868311 | ||||||
chr5:176868328
|
G | A | 2 | a0001c0001t0001g0056a0001c0001t0001g0059 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.436+55G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/14 | chr5 | 176868328 | ||||||
chr5:176868363
|
C | A | 3 | a0001c0001t0001g0130a0001c0001t0001g0203a0001c0001t0001g0215 | 3 | HG01069.hp1 HG01071.hp1 HG01109.hp2 |
intron_variant | MODIFIER | c.436+90C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/14 | chr5 | 176868363 | ||||||
chr5:176868363
|
C | T | 1 | a0001c0001t0011g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.436+90C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/14 | chr5 | 176868363 | ||||||
chr5:176868492
|
G | A | 1 | a0003c0003t0001g0084 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.437-69G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 3/14 | chr5 | 176868492 | ||||||
chr5:176868720
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.540+56G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 4/14 | chr5 | 176868720 | ||||||
chr5:176868977
|
A | G | 67 | a0001c0001t0001g0174a0001c0001t0002g0010a0001c0001t0002g0012others(64): Show | 69 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.721+13A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176868977 | ||||||
chr5:176868981
|
C | T | 1 | a0001c0001t0002g0190 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.721+17C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176868981 | ||||||
chr5:176869138
|
T | C | 3 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0160 | 3 | HG02027.hp2 HG02523.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.721+174T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176869138 | ||||||
chr5:176869203
|
G | T | 15 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(12): Show | 15 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.721+239G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176869203 | ||||||
chr5:176869358
|
G | T | 1 | a0001c0001t0001g0155 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.721+394G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176869358 | ||||||
chr5:176869396
|
G | A | 3 | a0001c0001t0006g0238a0001c0001t0006g0239a0001c0001t0006g0243 | 3 | HG02486.hp1 HG02630.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.721+432G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176869396 | ||||||
chr5:176869925
|
G | A | 3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.722-445G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176869925 | ||||||
chr5:176870225
|
C | T | 1 | a0001c0001t0001g0001 | 2 | HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.722-145C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176870225 | ||||||
chr5:176870367
|
T | C | 1 | a0001c0001t0005g0249 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.722-3T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 5/14 | chr5 | 176870367 | ||||||
chr5:176870544
|
C | T | 1 | a0001c0001t0002g0200 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.886+10C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870544 | ||||||
chr5:176870603
|
G | C | 22 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0049others(19): Show | 22 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.886+69G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870603 | ||||||
chr5:176870628
|
C | A | 22 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0049others(19): Show | 22 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.886+94C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870628 | ||||||
chr5:176870673
|
C | T | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+139C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870673 | ||||||
chr5:176870691
|
G | A | 3 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015 | 3 | HG02970.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.886+157G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870691 | ||||||
chr5:176870737
|
C | T | 21 | a0001c0001t0001g0174a0001c0001t0002g0010a0001c0001t0002g0012others(18): Show | 21 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(18): Show |
intron_variant | MODIFIER | c.886+203C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870737 | ||||||
chr5:176870840
|
C | T | 1 | a0001c0001t0005g0256 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.886+306C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870840 | ||||||
chr5:176870842
|
G | T | 7 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0250others(4): Show | 7 | HG02486.hp1 HG02615.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.886+308G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870842 | ||||||
chr5:176870888
|
CCCACACC others(14): Show |
C | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+355_886+375del others(21): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870888 | ||||||
chr5:176870920
|
ACCCCACA others(197): Show |
A | 19 | a0001c0001t0001g0174a0001c0001t0002g0040a0001c0001t0002g0090others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.886+416_886+619del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176870920 | |||||
chr5:176870950
|
A | G | 14 | a0001c0001t0001g0077a0001c0001t0001g0227a0001c0001t0003g0050others(11): Show | 15 | HG01109.hp1 HG01243.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.886+416A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870950 | ||||||
chr5:176870954
|
G | A | 4 | a0001c0001t0001g0077a0001c0001t0003g0244a0001c0001t0008g0113others(1): Show | 4 | HG02970.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+420G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870954 | ||||||
chr5:176870958
|
A | AACACCAC others(61): Show |
1 | a0001c0001t0002g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.886+450_886+517dup others(68): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176870958 | |||||
chr5:176870958
|
A | C | 4 | a0001c0001t0001g0077a0001c0001t0003g0244a0001c0001t0008g0113others(1): Show | 4 | HG02970.hp1 HG03225.hp2 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+424A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870958 | ||||||
chr5:176870984
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.886+450G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870984 | ||||||
chr5:176870984
|
G | GCTCGCCC others(27): Show |
1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+586_886+619dup others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176870984 | |||||
chr5:176870984
|
GCTCGCCC others(27): Show |
G | 163 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(160): Show | 168 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(165): Show |
intron_variant | MODIFIER | c.886+586_886+619del others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176870984 | |||||
chr5:176870988
|
G | A | 5 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0003g0244others(2): Show | 5 | HG02970.hp1 HG03225.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.886+454G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870988 | ||||||
chr5:176870990
|
CCCACACC others(25): Show |
C | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+459_886+490del others(32): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176870990 | |||||
chr5:176870992
|
C | A | 1 | a0001c0001t0001g0077 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.886+458C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176870992 | ||||||
chr5:176871018
|
A | G | 15 | a0001c0001t0001g0077a0001c0001t0001g0132a0001c0001t0001g0133others(12): Show | 15 | HG01081.hp2 HG01106.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.886+484A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871018 | ||||||
chr5:176871022
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+488G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871022 | ||||||
chr5:176871026
|
C | A | 3 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015 | 3 | HG02970.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.886+492C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871026 | ||||||
chr5:176871026
|
CACACCAC others(264): Show |
C | 2 | a0001c0004t0002g0078a0001c0004t0002g0233 | 2 | HG02451.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.886+620_886+890del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871026 | |||||
chr5:176871052
|
A | G | 36 | a0001c0001t0001g0024a0001c0001t0001g0034a0001c0001t0001g0039others(33): Show | 38 | HG01109.hp1 HG01243.hp2 HG01928.hp1 others(35): Show |
intron_variant | MODIFIER | c.886+518A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871052 | ||||||
chr5:176871056
|
G | A | 1 | a0001c0001t0001g0045 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.886+522G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871056 | ||||||
chr5:176871056
|
GCCCCACA others(230): Show |
G | 1 | a0001c0001t0001g0132 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.886+526_886+762del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871056 | |||||
chr5:176871060
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.886+526C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871060 | ||||||
chr5:176871060
|
C | CACACCAC others(196): Show |
18 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+585_886+586ins others(203): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871060 | |||||
chr5:176871086
|
A | G | 4 | a0001c0001t0001g0133a0001c0001t0003g0244a0001c0001t0008g0113others(1): Show | 4 | HG02970.hp1 HG03225.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.886+552A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871086 | ||||||
chr5:176871094
|
C | CACACCAC others(26): Show |
1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+585_886+586ins others(33): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871094 | |||||
chr5:176871098
|
C | A | 2 | a0001c0001t0002g0003a0001c0001t0002g0163 | 3 | HG01069.hp2 HG01074.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.886+564C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871098 | ||||||
chr5:176871120
|
A | G | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.886+586A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871120 | ||||||
chr5:176871128
|
CACACCAC others(26): Show |
C | 3 | a0001c0001t0003g0244a0001c0001t0011g0015a0002c0002t0004g0144 | 3 | HG02074.hp2 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.886+620_886+652del others(33): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871128 | |||||
chr5:176871128
|
CACACCAC others(162): Show |
C | 1 | a0001c0001t0001g0133 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.886+620_886+788del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871128 | |||||
chr5:176871154
|
G | A | 18 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+620G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871154 | ||||||
chr5:176871154
|
GCTCACCA others(26): Show |
G | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.886+624_886+656del others(33): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871154 | |||||
chr5:176871158
|
A | ACCAACAC others(61): Show |
1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+640_886+641ins others(68): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871158 | |||||
chr5:176871158
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+624A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871158 | ||||||
chr5:176871175
|
C | A | 18 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+641C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871175 | ||||||
chr5:176871189
|
T | C | 18 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+655T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871189 | ||||||
chr5:176871190
|
C | T | 18 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+656C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871190 | ||||||
chr5:176871195
|
CA | C | 5 | a0001c0001t0001g0157a0001c0001t0003g0244a0001c0001t0008g0113others(2): Show | 5 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.886+663delA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871195 | |||||
chr5:176871222
|
G | A | 19 | a0001c0001t0001g0157a0001c0001t0003g0092a0001c0001t0003g0093others(16): Show | 19 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.886+688G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871222 | ||||||
chr5:176871222
|
GCTCACCA others(776): Show |
G | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+709_886+1491de others(1): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871222 | |||||
chr5:176871225
|
C | CG | 19 | a0001c0001t0001g0157a0001c0001t0003g0092a0001c0001t0003g0093others(16): Show | 19 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.886+691_886+692ins others(1): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871225 | ||||||
chr5:176871226
|
A | C | 19 | a0001c0001t0001g0157a0001c0001t0003g0092a0001c0001t0003g0093others(16): Show | 19 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(16): Show |
intron_variant | MODIFIER | c.886+692A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871226 | ||||||
chr5:176871229
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+695A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871229 | ||||||
chr5:176871243
|
A | C | 17 | a0001c0001t0001g0157a0001c0001t0003g0092a0001c0001t0003g0093others(14): Show | 17 | HG02074.hp2 HG02451.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.886+709A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871243 | ||||||
chr5:176871256
|
CTCACCAA others(128): Show |
C | 7 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0049others(4): Show | 7 | HG01891.hp2 HG03041.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.886+723_886+857del | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871256 | ||||||
chr5:176871257
|
T | TCG | 4 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015others(1): Show | 4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+724_886+725ins others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871257 | |||||
chr5:176871259
|
A | C | 4 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015others(1): Show | 4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+725A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871259 | ||||||
chr5:176871276
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+742C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871276 | ||||||
chr5:176871288
|
A | G | 4 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015others(1): Show | 4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+754A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871288 | ||||||
chr5:176871289
|
CCT | C | 4 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015others(1): Show | 4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+756_886+757del others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871289 | ||||||
chr5:176871290
|
C | T | 18 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+756C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871290 | ||||||
chr5:176871291
|
T | C | 18 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+757T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871291 | ||||||
chr5:176871292
|
G | T | 4 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015others(1): Show | 4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+758G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871292 | ||||||
chr5:176871294
|
C | A | 4 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015others(1): Show | 4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+760C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871294 | ||||||
chr5:176871297
|
AACACCAC others(27): Show |
A | 1 | a0001c0001t0001g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.886+891_886+924del others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871297 | |||||
chr5:176871297
|
AACACCAC others(61): Show |
A | 7 | a0001c0001t0001g0174a0001c0001t0002g0040a0001c0001t0002g0118others(4): Show | 7 | HG00099.hp1 HG00735.hp1 HG01257.hp2 others(4): Show |
intron_variant | MODIFIER | c.886+857_886+924del others(68): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871297 | |||||
chr5:176871311
|
C | A | 4 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015others(1): Show | 4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+777C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871311 | ||||||
chr5:176871323
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.886+789A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871323 | ||||||
chr5:176871326
|
CG | C | 4 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015others(1): Show | 4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+793delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871326 | ||||||
chr5:176871328
|
C | A | 4 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015others(1): Show | 4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+794C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871328 | ||||||
chr5:176871331
|
C | A | 23 | a0001c0001t0001g0157a0001c0001t0003g0092a0001c0001t0003g0093others(20): Show | 23 | HG01884.hp1 HG02074.hp2 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.886+797C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871331 | ||||||
chr5:176871345
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+811C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871345 | ||||||
chr5:176871359
|
T | C | 4 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015others(1): Show | 4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+825T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871359 | ||||||
chr5:176871360
|
C | T | 4 | a0001c0001t0003g0244a0001c0001t0008g0113a0001c0001t0011g0015others(1): Show | 4 | HG02074.hp2 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+826C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871360 | ||||||
chr5:176871360
|
CG | C | 3 | a0001c0001t0001g0099a0001c0001t0001g0157a0001c0001t0001g0229 | 3 | HG02622.hp1 NA19005.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+827delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871360 | ||||||
chr5:176871362
|
C | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0157a0001c0001t0001g0229 | 3 | HG02622.hp1 NA19005.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+828C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871362 | ||||||
chr5:176871365
|
C | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0157a0001c0001t0001g0229 | 3 | HG02622.hp1 NA19005.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+831C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871365 | ||||||
chr5:176871365
|
C | CA | 19 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0244others(16): Show | 19 | HG02074.hp2 HG02451.hp2 HG02486.hp1 others(16): Show |
intron_variant | MODIFIER | c.886+832dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871365 | |||||
chr5:176871365
|
C | CAACACCA others(29): Show |
3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.886+832_886+833ins others(36): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871365 | |||||
chr5:176871379
|
C | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0229 | 2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+845C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871379 | ||||||
chr5:176871379
|
CCATCTGC others(162): Show |
C | 134 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(131): Show | 137 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.886+861_886+1029de others(1): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871379 | |||||
chr5:176871391
|
ACTCGCCC others(61): Show |
A | 31 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0090others(28): Show | 33 | HG00639.hp2 HG01074.hp2 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.886+861_886+928del others(68): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871391 | |||||
chr5:176871393
|
T | C | 2 | a0001c0001t0001g0099a0001c0001t0001g0229 | 2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+859T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871393 | ||||||
chr5:176871394
|
C | CACCAACA others(26): Show |
1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+860_886+861ins others(33): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871394 | ||||||
chr5:176871394
|
C | G | 7 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0049others(4): Show | 7 | HG01891.hp2 HG03041.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.886+860C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871394 | ||||||
chr5:176871394
|
C | T | 2 | a0001c0001t0001g0099a0001c0001t0001g0229 | 2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+860C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871394 | ||||||
chr5:176871395
|
G | C | 7 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0049others(4): Show | 7 | HG01891.hp2 HG03041.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.886+861G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871395 | ||||||
chr5:176871396
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.886+862C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871396 | ||||||
chr5:176871399
|
C | A | 8 | a0001c0001t0001g0120a0001c0001t0003g0009a0001c0001t0003g0011others(5): Show | 8 | HG01891.hp2 HG02698.hp2 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.886+865C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871399 | ||||||
chr5:176871399
|
C | CA | 22 | a0001c0001t0001g0099a0001c0001t0001g0157a0001c0001t0001g0229others(19): Show | 22 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(19): Show |
intron_variant | MODIFIER | c.886+866dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871399 | |||||
chr5:176871399
|
C | CACACCAC others(196): Show |
2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.886+925_886+1127du others(204): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871399 | |||||
chr5:176871413
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.886+879C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871413 | ||||||
chr5:176871417
|
C | T | 1 | a0001c0001t0001g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.886+883C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871417 | ||||||
chr5:176871427
|
T | C | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.886+893T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871427 | ||||||
chr5:176871428
|
C | T | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.886+894C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871428 | ||||||
chr5:176871433
|
C | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0229a0001c0004t0002g0232 | 3 | HG02622.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.886+899C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871433 | ||||||
chr5:176871433
|
C | CA | 20 | a0001c0001t0001g0120a0001c0001t0001g0157a0001c0001t0003g0092others(17): Show | 20 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(17): Show |
intron_variant | MODIFIER | c.886+900dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871433 | |||||
chr5:176871447
|
C | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0229a0001c0004t0002g0232 | 3 | HG02622.hp1 HG03195.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.886+913C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871447 | ||||||
chr5:176871459
|
G | A | 42 | a0001c0001t0001g0037a0001c0001t0001g0099a0001c0001t0001g0120others(39): Show | 42 | HG00099.hp1 HG00735.hp1 HG01255.hp2 others(39): Show |
intron_variant | MODIFIER | c.886+925G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871459 | ||||||
chr5:176871459
|
G | GCTCACCA others(196): Show |
1 | a0001c0001t0002g0051 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.886+992_886+993ins others(203): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871459 | |||||
chr5:176871463
|
A | C | 2 | a0001c0001t0001g0120a0001c0001t0001g0157 | 2 | HG02698.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.886+929A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871463 | ||||||
chr5:176871463
|
A | G | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+929A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871463 | ||||||
chr5:176871464
|
CCAACACC others(60): Show |
C | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+932_886+998del others(67): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871464 | |||||
chr5:176871470
|
C | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+936C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871470 | ||||||
chr5:176871480
|
C | A | 48 | a0001c0001t0001g0120a0001c0001t0001g0174a0001c0001t0002g0040others(45): Show | 50 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.886+946C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871480 | ||||||
chr5:176871494
|
T | C | 49 | a0001c0001t0001g0174a0001c0001t0002g0010a0001c0001t0002g0012others(46): Show | 51 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.886+960T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871494 | ||||||
chr5:176871495
|
C | T | 49 | a0001c0001t0001g0174a0001c0001t0002g0010a0001c0001t0002g0012others(46): Show | 51 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.886+961C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871495 | ||||||
chr5:176871498
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.886+964C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871498 | ||||||
chr5:176871498
|
CCCAACAC others(297): Show |
C | 2 | a0001c0001t0001g0099a0001c0001t0001g0229 | 2 | HG02622.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.886+993_886+1296de others(1): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871498 | |||||
chr5:176871522
|
C | T | 20 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(17): Show | 20 | HG01884.hp1 HG02109.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.886+988C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871522 | ||||||
chr5:176871527
|
G | A | 50 | a0001c0001t0001g0120a0001c0001t0001g0157a0001c0001t0001g0174others(47): Show | 52 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.886+993G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871527 | ||||||
chr5:176871530
|
C | CG | 48 | a0001c0001t0001g0174a0001c0001t0002g0040a0001c0001t0002g0090others(45): Show | 50 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.886+996_886+997ins others(1): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871530 | ||||||
chr5:176871531
|
A | C | 49 | a0001c0001t0001g0120a0001c0001t0001g0174a0001c0001t0002g0040others(46): Show | 51 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(48): Show |
intron_variant | MODIFIER | c.886+997A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871531 | ||||||
chr5:176871548
|
A | C | 23 | a0001c0001t0001g0037a0001c0001t0001g0120a0001c0001t0001g0157others(20): Show | 23 | HG01255.hp2 HG01884.hp1 HG02145.hp2 others(20): Show |
intron_variant | MODIFIER | c.886+1014A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871548 | ||||||
chr5:176871562
|
T | TCG | 3 | a0001c0001t0001g0120a0001c0001t0001g0157a0001c0004t0002g0232 | 3 | HG02698.hp2 HG03195.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.886+1029_886+1030i others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871562 | |||||
chr5:176871564
|
A | C | 3 | a0001c0001t0001g0120a0001c0001t0001g0157a0001c0004t0002g0232 | 3 | HG02698.hp2 HG03195.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.886+1030A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871564 | ||||||
chr5:176871567
|
A | AACACCAC others(27): Show |
1 | a0001c0001t0006g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.886+1046_886+1047i others(36): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871567 | |||||
chr5:176871581
|
C | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(148): Show | 154 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.886+1047C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871581 | ||||||
chr5:176871581
|
CCATCTGC others(129): Show |
C | 1 | a0001c0001t0002g0116 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.886+1102_886+1237d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871581 | |||||
chr5:176871588
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1054C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871588 | ||||||
chr5:176871593
|
A | G | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1059A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871593 | ||||||
chr5:176871594
|
C | CTCACCCC others(26): Show |
17 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(14): Show | 17 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(14): Show |
intron_variant | MODIFIER | c.886+1060_886+1061i others(35): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871594 | ||||||
chr5:176871595
|
C | T | 50 | a0001c0001t0001g0037a0001c0001t0001g0120a0001c0001t0001g0174others(47): Show | 52 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.886+1061C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871595 | ||||||
chr5:176871596
|
T | C | 50 | a0001c0001t0001g0037a0001c0001t0001g0120a0001c0001t0001g0174others(47): Show | 52 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.886+1062T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871596 | ||||||
chr5:176871597
|
G | C | 18 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+1063G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871597 | ||||||
chr5:176871597
|
G | T | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1063G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871597 | ||||||
chr5:176871598
|
C | A | 18 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+1064C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871598 | ||||||
chr5:176871599
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1065C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871599 | ||||||
chr5:176871602
|
A | C | 18 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+1068A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871602 | ||||||
chr5:176871613
|
T | C | 18 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+1079T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871613 | ||||||
chr5:176871616
|
C | A | 18 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(15): Show | 18 | HG01884.hp1 HG02145.hp2 HG02451.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+1082C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871616 | ||||||
chr5:176871633
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1099C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871633 | ||||||
chr5:176871636
|
C | A | 183 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(180): Show | 188 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(185): Show |
intron_variant | MODIFIER | c.886+1102C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871636 | ||||||
chr5:176871638
|
C | T | 13 | a0001c0001t0002g0248a0001c0001t0003g0074a0001c0001t0003g0244others(10): Show | 14 | HG02280.hp2 HG02615.hp2 HG02717.hp1 others(11): Show |
intron_variant | MODIFIER | c.886+1104C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871638 | ||||||
chr5:176871650
|
C | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 138 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.886+1116C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871650 | ||||||
chr5:176871657
|
C | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1123C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871657 | ||||||
chr5:176871665
|
CG | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 138 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.886+1132delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871665 | ||||||
chr5:176871665
|
CGCCCCAC others(60): Show |
C | 3 | a0001c0001t0005g0256a0001c0001t0008g0113a0001c0001t0010g0022 | 3 | HG02280.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.886+1138_886+1204d others(69): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871665 | |||||
chr5:176871666
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1132G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871666 | ||||||
chr5:176871667
|
C | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 138 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.886+1133C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871667 | ||||||
chr5:176871668
|
CCCACACC others(127): Show |
C | 34 | a0001c0001t0001g0037a0001c0001t0002g0040a0001c0001t0002g0090others(31): Show | 36 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(33): Show |
intron_variant | MODIFIER | c.886+1138_886+1271d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871668 | |||||
chr5:176871670
|
C | A | 135 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(132): Show | 138 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(135): Show |
intron_variant | MODIFIER | c.886+1136C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871670 | ||||||
chr5:176871670
|
C | CA | 11 | a0001c0001t0001g0174a0001c0001t0003g0009a0001c0001t0003g0011others(8): Show | 11 | HG01891.hp2 HG02717.hp1 HG03041.hp1 others(8): Show |
intron_variant | MODIFIER | c.886+1137dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871670 | |||||
chr5:176871691
|
C | G | 2 | a0001c0001t0001g0131a0001c0001t0001g0156 | 2 | HG00733.hp2 HG01515.hp1 |
intron_variant | MODIFIER | c.886+1157C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871691 | ||||||
chr5:176871700
|
A | C | 1 | a0001c0001t0003g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.886+1166A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871700 | ||||||
chr5:176871700
|
A | G | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(141): Show | 147 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.886+1166A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871700 | ||||||
chr5:176871702
|
CAACACCA others(93): Show |
C | 144 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(141): Show | 147 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(144): Show |
intron_variant | MODIFIER | c.886+1169_886+1268d others(102): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871702 | ||||||
chr5:176871703
|
A | C | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1169A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871703 | ||||||
chr5:176871714
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1180T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871714 | ||||||
chr5:176871717
|
A | C | 1 | a0001c0001t0003g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.886+1183A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871717 | ||||||
chr5:176871722
|
T | C | 1 | a0001c0001t0002g0121 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.886+1188T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871722 | ||||||
chr5:176871731
|
C | T | 2 | a0001c0001t0001g0157a0001c0001t0003g0259 | 2 | NA18906.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.886+1197C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871731 | ||||||
chr5:176871732
|
T | C | 2 | a0001c0001t0001g0157a0001c0001t0003g0259 | 2 | NA18906.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.886+1198T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871732 | ||||||
chr5:176871733
|
G | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1199G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871733 | ||||||
chr5:176871734
|
C | A | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1200C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871734 | ||||||
chr5:176871735
|
C | CCCAACAC others(60): Show |
3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.886+1238_886+1304d others(69): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871735 | |||||
chr5:176871738
|
A | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1204A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871738 | ||||||
chr5:176871768
|
G | A | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1234G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871768 | ||||||
chr5:176871768
|
G | GC | 4 | a0001c0001t0003g0259a0001c0001t0005g0256a0001c0001t0008g0113others(1): Show | 4 | HG02280.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+1237dupC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871768 | |||||
chr5:176871772
|
A | C | 2 | a0001c0001t0001g0157a0001c0004t0002g0232 | 2 | HG03195.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.886+1238A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871772 | ||||||
chr5:176871783
|
T | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1249T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871783 | ||||||
chr5:176871786
|
A | C | 5 | a0001c0001t0001g0157a0001c0001t0003g0259a0001c0001t0005g0256others(2): Show | 5 | HG02280.hp2 HG02970.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.886+1252A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871786 | ||||||
chr5:176871800
|
T | TCG | 3 | a0001c0001t0005g0256a0001c0001t0008g0113a0001c0001t0010g0022 | 3 | HG02280.hp2 HG02970.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.886+1267_886+1268i others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871800 | |||||
chr5:176871802
|
A | C | 4 | a0001c0001t0005g0256a0001c0001t0008g0113a0001c0001t0010g0022others(1): Show | 4 | HG02280.hp2 HG02970.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+1268A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871802 | ||||||
chr5:176871805
|
A | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1271A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871805 | ||||||
chr5:176871809
|
C | T | 4 | a0001c0001t0002g0230a0001c0001t0002g0231a0001c0004t0002g0078others(1): Show | 4 | HG01167.hp1 HG02451.hp1 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.886+1275C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871809 | ||||||
chr5:176871819
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1285C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871819 | ||||||
chr5:176871819
|
C | CCATCTGC others(60): Show |
1 | a0001c0001t0006g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.886+1304_886+1305i others(69): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871819 | |||||
chr5:176871833
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1299T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871833 | ||||||
chr5:176871834
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1300C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871834 | ||||||
chr5:176871835
|
GC | G | 15 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(12): Show | 15 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.886+1305delC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871835 | |||||
chr5:176871836
|
CCCCAACA others(27): Show |
C | 4 | a0001c0001t0001g0120a0001c0001t0001g0174a0001c0001t0003g0244others(1): Show | 4 | HG02698.hp2 HG02717.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.886+1340_886+1373d others(36): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871836 | |||||
chr5:176871842
|
C | T | 1 | a0001c0001t0003g0259 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.886+1308C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871842 | ||||||
chr5:176871854
|
C | A | 14 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(11): Show | 14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1320C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871854 | ||||||
chr5:176871868
|
TCGCCCAA others(64): Show |
T | 10 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0049others(7): Show | 10 | HG01891.hp2 HG02280.hp2 HG02970.hp1 others(7): Show |
intron_variant | MODIFIER | c.886+1336_886+1406d others(73): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871868 | |||||
chr5:176871869
|
CG | C | 16 | a0001c0001t0001g0037a0001c0001t0003g0092a0001c0001t0003g0093others(13): Show | 16 | HG01255.hp2 HG02451.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.886+1336delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871869 | ||||||
chr5:176871870
|
G | GC | 172 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(169): Show | 177 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(174): Show |
intron_variant | MODIFIER | c.886+1339dupC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871870 | |||||
chr5:176871871
|
C | A | 16 | a0001c0001t0001g0037a0001c0001t0003g0092a0001c0001t0003g0093others(13): Show | 16 | HG01255.hp2 HG02451.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.886+1337C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871871 | ||||||
chr5:176871888
|
C | A | 2 | a0001c0001t0001g0157a0001c0004t0002g0232 | 2 | HG03195.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.886+1354C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871888 | ||||||
chr5:176871899
|
C | T | 14 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(11): Show | 14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1365C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871899 | ||||||
chr5:176871902
|
T | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1368T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871902 | ||||||
chr5:176871903
|
C | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1369C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871903 | ||||||
chr5:176871906
|
C | A | 1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1372C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871906 | ||||||
chr5:176871937
|
TCG | T | 188 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(185): Show | 193 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(190): Show |
intron_variant | MODIFIER | c.886+1405_886+1406d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871937 | |||||
chr5:176871938
|
C | CACCAACA others(26): Show |
1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886+1404_886+1405i others(35): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871938 | ||||||
chr5:176871940
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+1406C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871940 | ||||||
chr5:176871941
|
C | A | 198 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(195): Show | 203 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(200): Show |
intron_variant | MODIFIER | c.886+1407C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871941 | ||||||
chr5:176871941
|
C | CCAACACC others(25): Show |
1 | a0001c0001t0001g0157 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.886+1408_886+1409i others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871941 | |||||
chr5:176871941
|
C | CCCAACAC others(26): Show |
1 | a0001c0001t0001g0105 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.886+1439_886+1440i others(35): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871941 | |||||
chr5:176871941
|
C | CCCAACAC others(61): Show |
1 | a0001c0001t0006g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.886+1445_886+1446i others(70): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871941 | |||||
chr5:176871958
|
C | A | 14 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(11): Show | 14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1424C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871958 | ||||||
chr5:176871971
|
CTCGCCCC others(60): Show |
C | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.886+1438_886+1504d others(69): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871971 | ||||||
chr5:176871972
|
T | C | 13 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(10): Show | 13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.886+1438T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871972 | ||||||
chr5:176871972
|
TCG | T | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0004t0002g0232 | 3 | HG03195.hp2 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1440_886+1441d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176871972 | |||||
chr5:176871973
|
C | T | 13 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(10): Show | 13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.886+1439C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871973 | ||||||
chr5:176871976
|
C | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0004t0002g0232 | 3 | HG03195.hp2 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1442C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871976 | ||||||
chr5:176871980
|
G | A | 209 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(206): Show | 214 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(211): Show |
intron_variant | MODIFIER | c.886+1446G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871980 | ||||||
chr5:176871993
|
C | A | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886+1459C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176871993 | ||||||
chr5:176872000
|
T | C | 18 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0002g0010others(15): Show | 18 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(15): Show |
intron_variant | MODIFIER | c.886+1466T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872000 | ||||||
chr5:176872005
|
A | G | 193 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(190): Show | 198 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(195): Show |
intron_variant | MODIFIER | c.886+1471A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872005 | ||||||
chr5:176872007
|
T | TCG | 4 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0002g0010others(1): Show | 4 | HG02965.hp2 HG03704.hp1 HG03834.hp1 others(1): Show |
intron_variant | MODIFIER | c.886+1474_886+1475i others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872007 | |||||
chr5:176872008
|
C | CG | 13 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(10): Show | 13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.886+1474_886+1475i others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872008 | ||||||
chr5:176872009
|
A | C | 17 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0002g0010others(14): Show | 17 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.886+1475A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872009 | ||||||
chr5:176872020
|
A | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.886+1486A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872020 | ||||||
chr5:176872026
|
C | A | 14 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(11): Show | 14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1492C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872026 | ||||||
chr5:176872033
|
C | T | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1499C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872033 | ||||||
chr5:176872038
|
A | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1504A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872038 | ||||||
chr5:176872040
|
T | G | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886+1506T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872040 | ||||||
chr5:176872042
|
A | C | 1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.886+1508A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872042 | ||||||
chr5:176872059
|
A | C | 19 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0002g0010others(16): Show | 19 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(16): Show |
intron_variant | MODIFIER | c.886+1525A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872059 | ||||||
chr5:176872075
|
A | G | 17 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0092others(14): Show | 17 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.886+1541A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872075 | ||||||
chr5:176872075
|
ACCCCACA others(61): Show |
A | 19 | a0001c0001t0001g0174a0001c0001t0002g0040a0001c0001t0002g0090others(16): Show | 19 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(16): Show |
intron_variant | MODIFIER | c.886+1575_886+1642d others(70): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872075 | |||||
chr5:176872079
|
C | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0005g0013 | 3 | HG03540.hp2 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1545C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872079 | ||||||
chr5:176872079
|
C | CA | 16 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0092others(13): Show | 16 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(13): Show |
intron_variant | MODIFIER | c.886+1546dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872079 | |||||
chr5:176872093
|
C | A | 3 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0005g0013 | 3 | HG03540.hp2 HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1559C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872093 | ||||||
chr5:176872100
|
C | T | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1566C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872100 | ||||||
chr5:176872101
|
C | A | 1 | a0003c0003t0002g0017 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.886+1567C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872101 | ||||||
chr5:176872105
|
A | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1571A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872105 | ||||||
chr5:176872109
|
A | G | 14 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(11): Show | 14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1575A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872109 | ||||||
chr5:176872109
|
ACCCCACA others(62): Show |
A | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1579_886+1647d others(71): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872109 | |||||
chr5:176872113
|
C | A | 15 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(12): Show | 15 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.886+1579C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872113 | ||||||
chr5:176872120
|
C | T | 1 | a0003c0003t0001g0188 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.886+1586C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872120 | ||||||
chr5:176872124
|
C | T | 17 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0003g0092others(14): Show | 17 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.886+1590C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872124 | ||||||
chr5:176872127
|
A | C | 17 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0003g0092others(14): Show | 17 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.886+1593A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872127 | ||||||
chr5:176872143
|
G | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1609G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872143 | ||||||
chr5:176872147
|
C | A | 2 | a0001c0001t0001g0037a0001c0004t0002g0232 | 2 | HG01255.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.886+1613C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872147 | ||||||
chr5:176872147
|
C | CA | 14 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(11): Show | 14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1614dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872147 | |||||
chr5:176872149
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.886+1615C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872149 | ||||||
chr5:176872158
|
T | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1624T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872158 | ||||||
chr5:176872161
|
C | A | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1627C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872161 | ||||||
chr5:176872181
|
C | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0005g0013 | 3 | HG02965.hp2 HG03540.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1647C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872181 | ||||||
chr5:176872181
|
C | CA | 14 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(11): Show | 14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1648dupA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872181 | |||||
chr5:176872209
|
T | TCG | 14 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(11): Show | 14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.886+1676_886+1677i others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872209 | |||||
chr5:176872211
|
A | C | 15 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(12): Show | 15 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.886+1677A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872211 | ||||||
chr5:176872211
|
A | G | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1677A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872211 | ||||||
chr5:176872212
|
CCAACACC others(127): Show |
C | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.886+1680_887-1621d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872212 | |||||
chr5:176872228
|
A | C | 15 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(12): Show | 15 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(12): Show |
intron_variant | MODIFIER | c.886+1694A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872228 | ||||||
chr5:176872241
|
CCT | C | 13 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(10): Show | 13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.886+1708_886+1709d others(4): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872241 | ||||||
chr5:176872242
|
C | T | 2 | a0001c0001t0005g0013a0001c0004t0002g0232 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.886+1708C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872242 | ||||||
chr5:176872243
|
T | C | 2 | a0001c0001t0005g0013a0001c0004t0002g0232 | 2 | HG03195.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.886+1709T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872243 | ||||||
chr5:176872243
|
TGCCCCAA others(161): Show |
T | 78 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0026others(75): Show | 80 | HG00099.hp2 HG00558.hp2 HG00609.hp2 others(77): Show |
intron_variant | MODIFIER | c.887-1671_887-1504d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872243 | |||||
chr5:176872244
|
G | C | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1710G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872244 | ||||||
chr5:176872244
|
G | T | 13 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(10): Show | 13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.886+1710G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872244 | ||||||
chr5:176872245
|
C | A | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1711C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872245 | ||||||
chr5:176872246
|
C | A | 13 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(10): Show | 13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.886+1712C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872246 | ||||||
chr5:176872249
|
A | C | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.886+1715A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872249 | ||||||
chr5:176872263
|
C | A | 12 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 12 | HG01928.hp1 HG02027.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.887-1705C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872263 | ||||||
chr5:176872270
|
C | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1698C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872270 | ||||||
chr5:176872275
|
A | G | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1693A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872275 | ||||||
chr5:176872276
|
CTCGCCCA others(125): Show |
C | 12 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 12 | HG01928.hp1 HG02027.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.887-1691_887-1560d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872276 | ||||||
chr5:176872279
|
G | GC | 14 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(11): Show | 14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.887-1686dupC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872279 | |||||
chr5:176872280
|
C | A | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1688C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872280 | ||||||
chr5:176872283
|
A | C | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887-1685A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872283 | ||||||
chr5:176872287
|
C | A | 1 | a0001c0001t0002g0103 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.887-1681C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872287 | ||||||
chr5:176872297
|
A | C | 17 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0003g0092others(14): Show | 17 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(14): Show |
intron_variant | MODIFIER | c.887-1671A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872297 | ||||||
chr5:176872304
|
C | T | 13 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(10): Show | 13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1664C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872304 | ||||||
chr5:176872309
|
A | G | 13 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(10): Show | 13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1659A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872309 | ||||||
chr5:176872313
|
A | ACCAACAC others(28): Show |
1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.887-1632_887-1631i others(37): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872313 | |||||
chr5:176872313
|
ACCAACAC others(94): Show |
A | 13 | a0001c0001t0002g0040a0001c0001t0002g0118a0001c0001t0002g0184others(10): Show | 13 | HG00099.hp1 HG00735.hp1 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1631_887-1531d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872313 | |||||
chr5:176872321
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-1647C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872321 | ||||||
chr5:176872322
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-1646A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872322 | ||||||
chr5:176872323
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-1645C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872323 | ||||||
chr5:176872330
|
C | A | 3 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0004t0002g0232 | 3 | HG02965.hp2 HG03195.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887-1638C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872330 | ||||||
chr5:176872337
|
T | C | 104 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(101): Show | 107 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.887-1631T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872337 | ||||||
chr5:176872342
|
G | A | 104 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(101): Show | 107 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(104): Show |
intron_variant | MODIFIER | c.887-1626G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872342 | ||||||
chr5:176872344
|
T | G | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887-1624T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872344 | ||||||
chr5:176872345
|
C | CG | 87 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(84): Show | 90 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(87): Show |
intron_variant | MODIFIER | c.887-1623_887-1622i others(3): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872345 | ||||||
chr5:176872345
|
C | CGCCCAAC others(164): Show |
1 | a0001c0001t0006g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.887-1623_887-1622i others(173): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872345 | ||||||
chr5:176872346
|
A | ACCCCACA others(131): Show |
1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1620_887-1619i others(140): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872346 | |||||
chr5:176872346
|
A | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0014a0001c0001t0001g0016others(87): Show | 93 | HG00558.hp1 HG00609.hp1 HG00621.hp2 others(90): Show |
intron_variant | MODIFIER | c.887-1622A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872346 | ||||||
chr5:176872349
|
A | C | 2 | a0001c0001t0001g0132a0001c0001t0001g0133 | 2 | HG03704.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.887-1619A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872349 | ||||||
chr5:176872357
|
A | T | 1 | a0001c0004t0002g0233 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.887-1611A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872357 | ||||||
chr5:176872363
|
A | C | 7 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0001g0251others(4): Show | 7 | HG02965.hp2 HG03195.hp2 HG03540.hp2 others(4): Show |
intron_variant | MODIFIER | c.887-1605A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872363 | ||||||
chr5:176872363
|
ACATCTGC others(26): Show |
A | 1 | a0001c0001t0001g0064 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.887-1589_887-1557d others(35): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872363 | |||||
chr5:176872378
|
C | T | 2 | a0001c0001t0001g0071a0001c0001t0001g0169 | 2 | HG00609.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.887-1590C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872378 | ||||||
chr5:176872379
|
A | AC | 13 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(10): Show | 13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1587dupC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872379 | |||||
chr5:176872379
|
A | C | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887-1589A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872379 | ||||||
chr5:176872379
|
ACCAACAC others(96): Show |
A | 13 | a0001c0001t0001g0174a0001c0001t0002g0090a0001c0001t0002g0097others(10): Show | 13 | HG00639.hp2 HG01074.hp2 HG01255.hp1 others(10): Show |
intron_variant | MODIFIER | c.887-1483_887-1381d others(2): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872379 | |||||
chr5:176872382
|
A | C | 13 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(10): Show | 13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1586A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872382 | ||||||
chr5:176872396
|
C | A | 5 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0002g0010others(2): Show | 5 | HG02965.hp2 HG03540.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.887-1572C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872396 | ||||||
chr5:176872410
|
T | C | 5 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0002g0010others(2): Show | 5 | HG02965.hp2 HG03195.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.887-1558T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872410 | ||||||
chr5:176872410
|
TC | T | 12 | a0001c0001t0001g0024a0001c0001t0001g0027a0001c0001t0001g0028others(9): Show | 12 | HG01928.hp1 HG02027.hp2 HG02080.hp2 others(9): Show |
intron_variant | MODIFIER | c.887-1557delC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872410 | ||||||
chr5:176872411
|
C | T | 5 | a0001c0001t0001g0132a0001c0001t0001g0133a0001c0001t0002g0010others(2): Show | 5 | HG02965.hp2 HG03195.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.887-1557C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872411 | ||||||
chr5:176872412
|
G | A | 14 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(11): Show | 14 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(11): Show |
intron_variant | MODIFIER | c.887-1556G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872412 | ||||||
chr5:176872413
|
CCCCAACA others(27): Show |
C | 24 | a0001c0001t0002g0248a0001c0001t0003g0074a0001c0001t0003g0244others(21): Show | 26 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.887-1483_887-1450d others(36): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872413 | |||||
chr5:176872414
|
C | CCCACACC others(195): Show |
13 | a0001c0001t0003g0092a0001c0001t0003g0093a0001c0001t0003g0245others(10): Show | 13 | HG02451.hp2 HG02615.hp1 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.887-1551_887-1550i others(204): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872414 | |||||
chr5:176872414
|
C | CCCACACC others(229): Show |
1 | a0001c0001t0005g0013 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.887-1551_887-1550i others(238): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872414 | |||||
chr5:176872447
|
G | A | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1521G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872447 | ||||||
chr5:176872465
|
C | A | 16 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0040others(13): Show | 16 | HG00099.hp1 HG00735.hp1 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.887-1503C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872465 | ||||||
chr5:176872480
|
CG | C | 29 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0040others(26): Show | 29 | HG00099.hp1 HG00735.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.887-1487delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872480 | ||||||
chr5:176872481
|
G | A | 2 | a0001c0001t0001g0183a0001c0004t0002g0232 | 2 | HG02015.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.887-1487G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872481 | ||||||
chr5:176872482
|
C | A | 29 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0040others(26): Show | 29 | HG00099.hp1 HG00735.hp1 HG01257.hp2 others(26): Show |
intron_variant | MODIFIER | c.887-1486C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872482 | ||||||
chr5:176872482
|
C | CCCCAACA others(536): Show |
1 | a0001c0001t0006g0239 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.887-1484_887-1483i others(545): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872482 | |||||
chr5:176872497
|
T | G | 1 | a0001c0001t0001g0223 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.887-1471T>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872497 | ||||||
chr5:176872513
|
T | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1455T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872513 | ||||||
chr5:176872514
|
C | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1454C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872514 | ||||||
chr5:176872530
|
C | T | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1438C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872530 | ||||||
chr5:176872549
|
CG | C | 24 | a0001c0001t0002g0248a0001c0001t0003g0074a0001c0001t0003g0244others(21): Show | 26 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.887-1418delG | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872549 | ||||||
chr5:176872550
|
G | A | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1418G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872550 | ||||||
chr5:176872550
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-1418G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872550 | ||||||
chr5:176872551
|
C | A | 24 | a0001c0001t0002g0248a0001c0001t0003g0074a0001c0001t0003g0244others(21): Show | 26 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.887-1417C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872551 | ||||||
chr5:176872551
|
C | G | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-1417C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872551 | ||||||
chr5:176872584
|
G | A | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1384G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872584 | ||||||
chr5:176872585
|
C | CCAACACC others(25): Show |
1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1382_887-1381i others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872585 | |||||
chr5:176872586
|
CCCAACAC others(59): Show |
C | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887-1365_887-1300d others(68): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872586 | |||||
chr5:176872589
|
A | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1379A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872589 | ||||||
chr5:176872610
|
T | C | 1 | a0001c0004t0002g0232 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.887-1358T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872610 | ||||||
chr5:176872615
|
G | A | 2 | a0001c0001t0002g0257a0001c0004t0002g0232 | 2 | HG03195.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.887-1353G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872615 | ||||||
chr5:176872648
|
A | G | 2 | a0001c0001t0001g0255a0001c0001t0008g0046 | 2 | HG02559.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.887-1320A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872648 | ||||||
chr5:176872669
|
A | C | 2 | a0001c0001t0002g0103a0001c0004t0002g0232 | 2 | HG01433.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.887-1299A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872669 | ||||||
chr5:176872681
|
A | G | 1 | a0001c0001t0002g0103 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.887-1287A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872681 | ||||||
chr5:176872698
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.887-1270G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872698 | ||||||
chr5:176872803
|
T | C | 1 | a0001c0001t0003g0050 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.887-1165T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872803 | ||||||
chr5:176872855
|
CACCAACA others(26): Show |
C | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.887-1112_887-1080d others(35): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872855 | ||||||
chr5:176872873
|
C | A | 3 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247 | 3 | HG01884.hp1 HG02145.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.887-1095C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872873 | ||||||
chr5:176872893
|
CAACACCA others(28): Show |
C | 1 | a0001c0001t0003g0244 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.887-1073_887-1039d others(37): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872893 | |||||
chr5:176872903
|
G | A | 5 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0049others(2): Show | 5 | HG03041.hp1 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.887-1065G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872903 | ||||||
chr5:176872988
|
AC | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 182 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(179): Show |
intron_variant | MODIFIER | c.887-978delC | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176872988 | |||||
chr5:176872992
|
G | C | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 182 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(179): Show |
intron_variant | MODIFIER | c.887-976G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872992 | ||||||
chr5:176872992
|
G | T | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-976G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872992 | ||||||
chr5:176872993
|
C | A | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(175): Show | 182 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(179): Show |
intron_variant | MODIFIER | c.887-975C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872993 | ||||||
chr5:176872994
|
C | A | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-974C>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872994 | ||||||
chr5:176872997
|
A | C | 1 | a0001c0001t0001g0037 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.887-971A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176872997 | ||||||
chr5:176873007
|
T | C | 214 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(211): Show | 219 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(216): Show |
intron_variant | MODIFIER | c.887-961T>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873007 | ||||||
chr5:176873027
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.887-941A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873027 | ||||||
chr5:176873051
|
G | T | 5 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0049others(2): Show | 5 | HG03041.hp1 HG03139.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.887-917G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873051 | ||||||
chr5:176873129
|
C | CCCAACAC others(26): Show |
2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.887-806_887-774dup others(33): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176873129 | |||||
chr5:176873164
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.887-804C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873164 | ||||||
chr5:176873186
|
C | T | 15 | a0001c0001t0002g0051a0001c0001t0002g0116a0001c0001t0002g0134others(12): Show | 16 | HG00621.hp1 HG01109.hp1 HG01243.hp2 others(13): Show |
intron_variant | MODIFIER | c.887-782C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873186 | ||||||
chr5:176873199
|
A | AACACCAC others(27): Show |
1 | a0001c0001t0001g0143 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.887-747_887-746ins others(34): Show |
UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176873199 | |||||
chr5:176873319
|
AT | A | 7 | a0001c0001t0001g0037a0001c0001t0002g0248a0001c0001t0003g0093others(4): Show | 8 | HG01255.hp2 HG02809.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.887-638delT | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr5 | 176873319 | |||||
chr5:176873522
|
A | G | 2 | a0001c0004t0002g0232a0001c0004t0002g0233 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.887-446A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873522 | ||||||
chr5:176873611
|
C | G | 1 | a0001c0001t0002g0097 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.887-357C>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873611 | ||||||
chr5:176873746
|
C | T | 2 | a0003c0003t0002g0107a0003c0003t0002g0240 | 2 | HG01361.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.887-222C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873746 | ||||||
chr5:176873838
|
A | G | 1 | a0001c0001t0001g0192 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.887-130A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 6/14 | chr5 | 176873838 | ||||||
chr5:176874587
|
C | T | 11 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1378+21C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176874587 | ||||||
chr5:176874721
|
G | A | 1 | a0001c0004t0002g0078 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1378+155G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176874721 | ||||||
chr5:176874849
|
A | C | 22 | a0001c0001t0003g0009a0001c0001t0003g0011a0001c0001t0003g0049others(19): Show | 22 | HG01891.hp2 HG02451.hp2 HG02486.hp1 others(19): Show |
intron_variant | MODIFIER | c.1378+283A>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176874849 | ||||||
chr5:176874870
|
G | A | 1 | a0001c0001t0002g0189 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1378+304G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176874870 | ||||||
chr5:176874912
|
G | A | 1 | a0001c0001t0011g0015 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1378+346G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176874912 | ||||||
chr5:176874932
|
C | T | 11 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1378+366C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176874932 | ||||||
chr5:176875092
|
G | C | 11 | a0001c0001t0007g0083a0001c0001t0007g0242a0001c0001t0007g0247others(8): Show | 12 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1378+526G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875092 | ||||||
chr5:176875409
|
G | A | 4 | a0001c0001t0002g0058a0001c0001t0002g0062a0001c0001t0002g0063others(1): Show | 4 | HG01081.hp2 HG01106.hp1 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.1378+843G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875409 | ||||||
chr5:176875555
|
C | T | 1 | a0001c0001t0002g0248 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1378+989C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875555 | ||||||
chr5:176875634
|
G | A | 1 | a0001c0001t0001g0038 | 1 | HG01071.hp2 | intron_variant | MODIFIER | c.1378+1068G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875634 | ||||||
chr5:176875767
|
C | T | 1 | a0003c0003t0001g0082 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1378+1201C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875767 | ||||||
chr5:176875826
|
C | T | 2 | a0001c0001t0001g0174a0001c0001t0010g0022 | 2 | HG03139.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.1378+1260C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875826 | ||||||
chr5:176875832
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02622.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.1378+1266C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875832 | ||||||
chr5:176875895
|
G | T | 2 | a0001c0001t0002g0010a0001c0001t0002g0012 | 2 | HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1379-1297G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176875895 | ||||||
chr5:176876029
|
G | A | 1 | a0001c0001t0001g0106 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1379-1163G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876029 | ||||||
chr5:176876345
|
C | T | 1 | a0001c0001t0008g0113 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1379-847C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876345 | ||||||
chr5:176876455
|
G | C | 1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1379-737G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876455 | ||||||
chr5:176876523
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1379-669A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876523 | ||||||
chr5:176876580
|
C | T | 2 | a0001c0001t0001g0029a0001c0001t0001g0030 | 2 | HG02080.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1379-612C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876580 | ||||||
chr5:176876670
|
A | G | 37 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0040others(34): Show | 38 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(35): Show |
intron_variant | MODIFIER | c.1379-522A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876670 | ||||||
chr5:176876809
|
G | A | 1 | a0001c0009t0001g0176 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1379-383G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 8/14 | chr5 | 176876809 | ||||||
chr5:176877302
|
C | T | 1 | a0001c0001t0002g0168 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1466+23C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 9/14 | chr5 | 176877302 | ||||||
chr5:176877398
|
A | G | 226 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(223): Show | 231 | HG00099.hp1 HG00099.hp2 HG00558.hp1 others(228): Show |
intron_variant | MODIFIER | c.1466+119A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 9/14 | chr5 | 176877398 | ||||||
chr5:176877755
|
G | A | 18 | a0001c0001t0002g0040a0001c0001t0002g0090a0001c0001t0002g0097others(15): Show | 18 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.1635+52G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 10/14 | chr5 | 176877755 | ||||||
chr5:176877792
|
C | T | 2 | a0001c0001t0001g0201a0002c0002t0004g0166 | 2 | NA18971.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1635+89C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 10/14 | chr5 | 176877792 | ||||||
chr5:176877817
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1636-77C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 10/14 | chr5 | 176877817 | ||||||
chr5:176878136
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1869+9C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 11/14 | chr5 | 176878136 | ||||||
chr5:176878137
|
G | A | 1 | a0001c0001t0002g0181 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1869+10G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 11/14 | chr5 | 176878137 | ||||||
chr5:176878164
|
C | T | 13 | a0001c0001t0003g0050a0001c0001t0003g0092a0001c0001t0003g0093others(10): Show | 13 | HG02451.hp2 HG02486.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.1869+37C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 11/14 | chr5 | 176878164 | ||||||
chr5:176878465
|
T | A | 140 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(137): Show | 143 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.2020-10T>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 12/14 | chr5 | 176878465 | ||||||
chr5:176878677
|
C | T | 41 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0026others(38): Show | 42 | HG00099.hp2 HG00642.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.2184+38C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878677 | ||||||
chr5:176878694
|
A | T | 1 | a0001c0001t0001g0044 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2184+55A>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878694 | ||||||
chr5:176878862
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0009g0043 | 2 | HG00741.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.2184+223G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878862 | ||||||
chr5:176878867
|
A | G | 3 | a0001c0001t0001g0018a0001c0001t0002g0010a0001c0001t0002g0012 | 3 | HG01884.hp2 HG02965.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.2184+228A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878867 | ||||||
chr5:176878889
|
G | A | 7 | a0003c0003t0001g0082a0003c0003t0001g0084a0003c0003t0001g0188others(4): Show | 7 | HG00733.hp1 HG01361.hp1 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.2184+250G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878889 | ||||||
chr5:176878918
|
G | A | 2 | a0001c0001t0002g0230a0001c0001t0002g0231 | 2 | HG01167.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2184+279G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878918 | ||||||
chr5:176878952
|
A | G | 35 | a0001c0001t0001g0018a0001c0001t0002g0010a0001c0001t0002g0012others(32): Show | 35 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(32): Show |
intron_variant | MODIFIER | c.2184+313A>G | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878952 | ||||||
chr5:176878973
|
G | A | 42 | a0001c0001t0002g0010a0001c0001t0002g0012a0001c0001t0002g0040others(39): Show | 42 | HG00099.hp1 HG00639.hp2 HG00735.hp1 others(39): Show |
intron_variant | MODIFIER | c.2184+334G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176878973 | ||||||
chr5:176879019
|
G | C | 1 | a0001c0001t0002g0150 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.2185-291G>C | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176879019 | ||||||
chr5:176879107
|
C | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0160 | 3 | HG02027.hp2 HG02523.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2185-203C>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176879107 | ||||||
chr5:176879129
|
G | T | 3 | a0001c0001t0001g0036a0001c0001t0001g0042a0001c0001t0001g0160 | 3 | HG02027.hp2 HG02523.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.2185-181G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176879129 | ||||||
chr5:176879250
|
G | T | 1 | a0001c0001t0003g0074 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2185-60G>T | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 13/14 | chr5 | 176879250 | ||||||
chr5:176879655
|
CA | C | 3 | a0002c0002t0004g0021a0002c0002t0004g0048a0002c0002t0004g0066 | 3 | HG01109.hp1 HG03209.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2364-65delA | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 14/14 | chr5 | 176879655 | ||||||
chr5:176879658
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030 | 3 | HG02080.hp2 HG03834.hp2 NA18999.hp1 |
intron_variant | MODIFIER | c.2364-63G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 14/14 | chr5 | 176879658 | ||||||
chr5:176879675
|
G | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(122): Show | 129 | HG00099.hp2 HG00558.hp1 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.2364-46G>A | UNC5A | ENSG00000113763.12 | transcript | ENST00000329542.9 | protein_coding | 14/14 | chr5 | 176879675 |