geneid | 324 |
---|---|
ensemblid | ENSG00000134982.18 |
hgncid | 583 |
symbol | APC |
name | APC regulator of WNT signaling pathway |
refseq_nuc | NM_000038.6 |
refseq_prot | NP_000029.2 |
ensembl_nuc | ENST00000257430.9 |
ensembl_prot | ENSP00000257430.4 |
mane_status | MANE Select |
chr | chr5 |
start | 112737885 |
end | 112846239 |
strand | + |
ver | v1.2 |
region | chr5:112737885-112846239 |
region5000 | chr5:112732885-112851239 |
regionname0 | APC_chr5_112737885_112846239 |
regionname5000 | APC_chr5_112732885_112851239 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 2843 | 234 | 75 | 43 | 88 | 4 | 23 | 67 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0002 | 1/0 | 2843 | 42 | 3 | 11 | 18 | 2 | 7 | 17 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0003 | 0/0 | 2843 | 3 | 1 | 1 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0004 | 0/0 | 2842 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0005 | 0/0 | 2843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0006 | 0/0 | 2843 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0007 | 0/0 | 2843 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0008 | 0/0 | 2843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0009 | 0/0 | 2843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0010 | 0/0 | 2843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0011 | 0/0 | 2843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0012 | 0/0 | 2843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0013 | 0/0 | 2843 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0014 | 0/0 | 2843 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 8532 | 96 | 5 | 26 | 47 | 2 | 15 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0002 | 0/0 | 8532 | 67 | 30 | 6 | 26 | 1 | 4 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0003 | 0/0 | 8532 | 44 | 20 | 8 | 13 | 1 | 2 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0004 | 1/0 | 8532 | 40 | 2 | 11 | 17 | 2 | 7 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0005 | 0/0 | 8532 | 8 | 8 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0006 | 0/0 | 8532 | 3 | 1 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0007 | 0/0 | 8532 | 3 | 1 | 2 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0008 | 0/0 | 8532 | 3 | 3 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0009 | 0/0 | 8529 | 3 | 2 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0010 | 0/0 | 8532 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0011 | 0/0 | 8532 | 2 | 0 | 0 | 0 | 0 | 2 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0012 | 0/0 | 8532 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0013 | 0/0 | 8532 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0014 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0015 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0016 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0017 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0018 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0019 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0020 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0021 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0022 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0023 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0024 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0025 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0026 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0027 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0028 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0029 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0030 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0031 | 0/0 | 8532 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
c0032 | 0/0 | 8532 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 2174 | 99 | 5 | 24 | 54 | 2 | 13 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0002 | 1/0 | 2173 | 94 | 28 | 20 | 30 | 3 | 12 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0003 | 0/0 | 2174 | 40 | 10 | 2 | 24 | 0 | 4 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0004 | 0/0 | 2174 | 28 | 17 | 8 | 0 | 0 | 3 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0005 | 0/0 | 2174 | 11 | 11 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0006 | 0/0 | 2173 | 9 | 8 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0007 | 0/0 | 2174 | 3 | 3 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0008 | 0/0 | 2174 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0009 | 0/0 | 2174 | 2 | 1 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0010 | 0/0 | 2173 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0011 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0012 | 0/0 | 2174 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0013 | 0/0 | 2174 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0014 | 0/0 | 2173 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
t0015 | 0/0 | 2174 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0233 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 8532 | 96 | 5 | 26 | 47 | 2 | 15 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0002 | 0/0 | 8532 | 67 | 30 | 6 | 26 | 1 | 4 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0003 | 0/0 | 8532 | 44 | 20 | 8 | 13 | 1 | 2 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0005 | 0/0 | 8532 | 8 | 8 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0007 | 0/0 | 8532 | 3 | 1 | 2 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0008 | 0/0 | 8532 | 3 | 3 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0010 | 0/0 | 8532 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0011 | 0/0 | 8532 | 2 | 0 | 0 | 0 | 0 | 2 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0014 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0015 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0016 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0019 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0026 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0027 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0029 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0030 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0031 | 0/0 | 8532 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0002c0004 | 1/0 | 8532 | 40 | 2 | 11 | 17 | 2 | 7 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0002c0020 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0002c0025 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0003c0006 | 0/0 | 8532 | 3 | 1 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0004c0009 | 0/0 | 8529 | 3 | 2 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0005c0013 | 0/0 | 8532 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0006c0012 | 0/0 | 8532 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0007c0032 | 0/0 | 8532 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0008c0022 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0009c0017 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0010c0018 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0011c0023 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0012c0028 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0013c0024 | 0/0 | 8532 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0014c0021 | 0/0 | 8532 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 10705 | 89 | 4 | 23 | 47 | 2 | 12 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0001t0004 | 0/0 | 10705 | 7 | 1 | 3 | 0 | 0 | 3 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0002t0001 | 0/0 | 10705 | 4 | 0 | 0 | 4 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0002t0003 | 0/0 | 10705 | 37 | 9 | 2 | 22 | 0 | 4 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0002t0004 | 0/0 | 10705 | 16 | 13 | 3 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0002t0005 | 0/0 | 10705 | 4 | 4 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0002t0008 | 0/0 | 10705 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0002t0009 | 0/0 | 10705 | 2 | 1 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0002t0013 | 0/0 | 10705 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0002t0015 | 0/0 | 10705 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0003t0002 | 0/0 | 10704 | 34 | 12 | 7 | 12 | 1 | 2 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0003t0006 | 0/0 | 10704 | 8 | 7 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0003t0010 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0003t0014 | 0/0 | 10704 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0005t0005 | 0/0 | 10705 | 7 | 7 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0005t0011 | 0/0 | 10705 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0007t0004 | 0/0 | 10705 | 3 | 1 | 2 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0008t0002 | 0/0 | 10704 | 3 | 3 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0010t0007 | 0/0 | 10705 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0011t0002 | 0/0 | 10704 | 2 | 0 | 0 | 0 | 0 | 2 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0014t0007 | 0/0 | 10705 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0015t0002 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0016t0001 | 0/0 | 10705 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0019t0002 | 0/0 | 10704 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0026t0006 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0027t0004 | 0/0 | 10705 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0029t0002 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0030t0002 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0001c0031t0002 | 0/0 | 10704 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0002c0004t0002 | 1/0 | 10704 | 40 | 2 | 11 | 17 | 2 | 7 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0002c0020t0012 | 0/0 | 10705 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0002c0025t0002 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0003c0006t0001 | 0/0 | 10705 | 3 | 1 | 1 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0004c0009t0002 | 0/0 | 10701 | 3 | 2 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0005c0013t0002 | 0/0 | 10704 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0006c0012t0002 | 0/0 | 10704 | 2 | 2 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0007c0032t0002 | 0/0 | 10704 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0008c0022t0003 | 0/0 | 10705 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0009c0017t0001 | 0/0 | 10705 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0010c0018t0001 | 0/0 | 10705 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0011c0023t0004 | 0/0 | 10705 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0012c0028t0002 | 0/0 | 10704 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0013c0024t0003 | 0/0 | 10705 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
a0014c0021t0003 | 0/0 | 10705 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | copy fasta | chr5 | 112732885 | 112851239 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0233 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0004g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0001t0004g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0002 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0004g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0005g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0008g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0008g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0009g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0009g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0013g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0002t0015g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0006g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0006g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0006g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0006g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0006g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0006g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0006g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0006g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0010g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0003t0014g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0005t0005g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0005t0005g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0005t0005g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0005t0005g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0005t0005g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0005t0005g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0005t0005g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0005t0011g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0007t0004g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0007t0004g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0007t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0008t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0008t0002g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0008t0002g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0010t0007g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0010t0007g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0011t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0011t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0014t0007g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0015t0002g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0016t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0019t0002g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0026t0006g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0027t0004g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0029t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0030t0002g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0001c0031t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0102 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0004t0002g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0020t0012g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0002c0025t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0003c0006t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0003c0006t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0003c0006t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0004c0009t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0004c0009t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0004c0009t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0005c0013t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0005c0013t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0006c0012t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0006c0012t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0007c0032t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0008c0022t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0009c0017t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0010c0018t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0011c0023t0004g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0012c0028t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0013c0024t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
a0014c0021t0003g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0001 | c0002 | t0015 | g0191 | EUR | FIN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00323 | hp2 | a0002 | c0004 | t0002 | g0031 | EUR | FIN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00408 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | CHS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00408 | hp2 | a0002 | c0004 | t0002 | g0044 | EAS | CHS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00609 | hp1 | a0001 | c0002 | t0003 | g0177 | EAS | CHS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00639 | hp2 | a0002 | c0004 | t0002 | g0085 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00642 | hp1 | a0001 | c0002 | t0003 | g0174 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | CHS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0275 | EAS | CHS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0209 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00733 | hp2 | a0002 | c0004 | t0002 | g0063 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG00741 | hp2 | a0001 | c0003 | t0006 | g0140 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01070 | hp1 | a0003 | c0006 | t0001 | g0248 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01070 | hp2 | a0001 | c0002 | t0004 | g0189 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01071 | hp2 | a0001 | c0002 | t0004 | g0190 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0173 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01081 | hp1 | a0001 | c0007 | t0004 | g0118 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01081 | hp2 | a0001 | c0031 | t0002 | g0074 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01099 | hp2 | a0002 | c0004 | t0002 | g0107 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01106 | hp1 | a0001 | c0003 | t0002 | g0059 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01106 | hp2 | a0001 | c0007 | t0004 | g0119 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01109 | hp1 | a0002 | c0004 | t0002 | g0040 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0260 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01169 | hp1 | a0001 | c0003 | t0002 | g0086 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0212 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01175 | hp2 | a0002 | c0004 | t0002 | g0039 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01243 | hp1 | a0004 | c0009 | t0002 | g0099 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01243 | hp2 | a0001 | c0002 | t0009 | g0131 | AMR | PUR | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01256 | hp2 | a0002 | c0004 | t0002 | g0083 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01257 | hp1 | a0002 | c0004 | t0002 | g0037 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0205 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0194 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01258 | hp2 | a0002 | c0004 | t0002 | g0038 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01346 | hp1 | a0001 | c0003 | t0002 | g0042 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0263 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0124 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0287 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01361 | hp1 | a0001 | c0001 | t0004 | g0123 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0255 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01433 | hp1 | a0002 | c0004 | t0002 | g0071 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01496 | hp1 | a0001 | c0003 | t0002 | g0137 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01496 | hp2 | a0001 | c0003 | t0002 | g0138 | AMR | CLM | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01515 | hp1 | a0001 | c0003 | t0002 | g0056 | EUR | IBS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0257 | EUR | IBS | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01884 | hp1 | a0001 | c0003 | t0002 | g0135 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01884 | hp2 | a0001 | c0002 | t0004 | g0014 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01891 | hp1 | a0001 | c0030 | t0002 | g0129 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01891 | hp2 | a0001 | c0002 | t0003 | g0172 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01975 | hp1 | a0002 | c0004 | t0002 | g0073 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0208 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01978 | hp1 | a0001 | c0002 | t0004 | g0188 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0280 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01981 | hp2 | a0001 | c0001 | t0004 | g0116 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01993 | hp1 | a0002 | c0004 | t0002 | g0070 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0282 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02056 | hp1 | a0001 | c0019 | t0002 | g0078 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02071 | hp1 | a0001 | c0002 | t0003 | g0160 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02129 | hp1 | a0001 | c0002 | t0003 | g0167 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02129 | hp2 | a0001 | c0002 | t0003 | g0075 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02132 | hp1 | a0001 | c0003 | t0002 | g0046 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0239 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02145 | hp2 | a0001 | c0005 | t0005 | g0011 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02155 | hp1 | a0001 | c0002 | t0003 | g0155 | EAS | CDX | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02155 | hp2 | a0001 | c0003 | t0002 | g0004 | EAS | CDX | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02257 | hp1 | a0001 | c0002 | t0005 | g0128 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02258 | hp1 | a0001 | c0005 | t0011 | g0008 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02258 | hp2 | a0001 | c0002 | t0004 | g0019 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02280 | hp1 | a0001 | c0005 | t0005 | g0010 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02280 | hp2 | a0001 | c0003 | t0002 | g0151 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02293 | hp1 | a0001 | c0003 | t0002 | g0062 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0206 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0285 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02300 | hp2 | a0001 | c0003 | t0002 | g0058 | AMR | PEL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02451 | hp1 | a0001 | c0002 | t0003 | g0171 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02451 | hp2 | a0001 | c0003 | t0002 | g0035 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02523 | hp1 | a0001 | c0002 | t0003 | g0180 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02523 | hp2 | a0001 | c0016 | t0001 | g0242 | EAS | KHV | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02572 | hp1 | a0001 | c0003 | t0006 | g0142 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02572 | hp2 | a0004 | c0009 | t0002 | g0098 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02602 | hp2 | a0002 | c0004 | t0002 | g0028 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02615 | hp1 | a0001 | c0002 | t0004 | g0023 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02615 | hp2 | a0001 | c0002 | t0008 | g0184 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02622 | hp1 | a0001 | c0003 | t0006 | g0144 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02622 | hp2 | a0001 | c0010 | t0007 | g0132 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02630 | hp1 | a0001 | c0015 | t0002 | g0134 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02630 | hp2 | a0001 | c0003 | t0006 | g0145 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02647 | hp1 | a0001 | c0002 | t0003 | g0159 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02647 | hp2 | a0001 | c0002 | t0004 | g0025 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02683 | hp2 | a0001 | c0002 | t0003 | g0161 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02698 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0234 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02717 | hp1 | a0001 | c0002 | t0004 | g0013 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02717 | hp2 | a0001 | c0007 | t0004 | g0120 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02735 | hp1 | a0002 | c0004 | t0002 | g0041 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0198 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02818 | hp1 | a0001 | c0005 | t0005 | g0012 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02818 | hp2 | a0001 | c0003 | t0002 | g0101 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02886 | hp1 | a0001 | c0002 | t0004 | g0022 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02886 | hp2 | a0001 | c0003 | t0002 | g0150 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02895 | hp1 | a0005 | c0013 | t0002 | g0148 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02895 | hp2 | a0001 | c0008 | t0002 | g0095 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02896 | hp1 | a0001 | c0003 | t0010 | g0139 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02896 | hp2 | a0001 | c0002 | t0005 | g0126 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02897 | hp1 | a0005 | c0013 | t0002 | g0149 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02897 | hp2 | a0001 | c0002 | t0005 | g0127 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02922 | hp1 | a0001 | c0008 | t0002 | g0112 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02922 | hp2 | a0001 | c0003 | t0006 | g0152 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02965 | hp1 | a0001 | c0002 | t0003 | g0181 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02965 | hp2 | a0001 | c0003 | t0002 | g0136 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0210 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02970 | hp2 | a0001 | c0002 | t0004 | g0015 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02976 | hp1 | a0001 | c0002 | t0008 | g0185 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02976 | hp2 | a0001 | c0005 | t0005 | g0006 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0200 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03041 | hp2 | a0001 | c0003 | t0002 | g0103 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03098 | hp1 | a0011 | c0023 | t0004 | g0026 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03098 | hp2 | a0001 | c0003 | t0002 | g0105 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03130 | hp1 | a0001 | c0026 | t0006 | g0143 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03130 | hp2 | a0001 | c0010 | t0007 | g0027 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03139 | hp1 | a0001 | c0003 | t0002 | g0036 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03139 | hp2 | a0001 | c0002 | t0005 | g0115 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03195 | hp1 | a0001 | c0002 | t0003 | g0163 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03195 | hp2 | a0001 | c0003 | t0002 | g0104 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03225 | hp1 | a0001 | c0003 | t0006 | g0147 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03225 | hp2 | a0001 | c0014 | t0007 | g0133 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03239 | hp2 | a0002 | c0004 | t0002 | g0082 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03453 | hp1 | a0006 | c0012 | t0002 | g0097 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03453 | hp2 | a0001 | c0002 | t0004 | g0018 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03486 | hp1 | a0001 | c0002 | t0003 | g0168 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03486 | hp2 | a0001 | c0008 | t0002 | g0130 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0232 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03490 | hp2 | a0001 | c0011 | t0002 | g0055 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03491 | hp1 | a0002 | c0004 | t0002 | g0064 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03491 | hp2 | a0001 | c0001 | t0004 | g0246 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0247 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03492 | hp2 | a0001 | c0011 | t0002 | g0061 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03516 | hp1 | a0001 | c0002 | t0013 | g0003 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03516 | hp2 | a0001 | c0003 | t0006 | g0146 | AFR | ESN | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03540 | hp2 | a0001 | c0002 | t0004 | g0024 | AFR | GWD | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03579 | hp1 | a0001 | c0002 | t0004 | g0034 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03579 | hp2 | a0001 | c0003 | t0006 | g0141 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03654 | hp1 | a0002 | c0004 | t0002 | g0084 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03654 | hp2 | a0001 | c0001 | t0004 | g0121 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03669 | hp2 | a0001 | c0003 | t0002 | g0067 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0002 | SAS | STU | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03688 | hp2 | a0001 | c0003 | t0002 | g0030 | SAS | STU | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0264 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03704 | hp2 | a0001 | c0002 | t0003 | g0162 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03710 | hp2 | a0007 | c0032 | t0002 | g0032 | SAS | PJL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03927 | hp1 | a0003 | c0006 | t0001 | g0262 | SAS | BEB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0265 | SAS | BEB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | STU | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG04115 | hp2 | a0002 | c0004 | t0002 | g0029 | SAS | STU | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0238 | SAS | BEB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG04184 | hp2 | a0002 | c0004 | t0002 | g0106 | SAS | BEB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18612 | hp1 | a0001 | c0002 | t0003 | g0164 | EAS | CHB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | CHB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18747 | hp1 | a0001 | c0003 | t0014 | g0052 | EAS | CHB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | CHB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18906 | hp1 | a0001 | c0002 | t0004 | g0017 | AFR | YRI | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18906 | hp2 | a0001 | c0003 | t0002 | g0068 | AFR | YRI | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18948 | hp1 | a0001 | c0003 | t0002 | g0049 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18950 | hp2 | a0001 | c0002 | t0001 | g0291 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18952 | hp1 | a0001 | c0003 | t0002 | g0050 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18953 | hp1 | a0002 | c0020 | t0012 | g0057 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18954 | hp1 | a0001 | c0003 | t0002 | g0048 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18957 | hp1 | a0002 | c0004 | t0002 | g0094 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0289 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18963 | hp1 | a0002 | c0004 | t0002 | g0092 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18963 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18968 | hp2 | a0001 | c0003 | t0002 | g0047 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18970 | hp1 | a0002 | c0004 | t0002 | g0072 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0253 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18971 | hp2 | a0001 | c0002 | t0003 | g0165 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18973 | hp1 | a0001 | c0002 | t0003 | g0158 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0274 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18974 | hp2 | a0001 | c0002 | t0003 | g0182 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18975 | hp1 | a0010 | c0018 | t0001 | g0268 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18975 | hp2 | a0002 | c0004 | t0002 | g0091 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18980 | hp1 | a0001 | c0003 | t0002 | g0051 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18980 | hp2 | a0009 | c0017 | t0001 | g0196 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18981 | hp2 | a0001 | c0002 | t0003 | g0153 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18983 | hp1 | a0001 | c0002 | t0003 | g0001 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18985 | hp1 | a0002 | c0004 | t0002 | g0043 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18990 | hp2 | a0001 | c0002 | t0003 | g0156 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18992 | hp1 | a0001 | c0002 | t0003 | g0176 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18994 | hp1 | a0002 | c0004 | t0002 | g0077 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18998 | hp2 | a0002 | c0004 | t0002 | g0114 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19000 | hp1 | a0002 | c0004 | t0002 | g0111 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19002 | hp1 | a0001 | c0002 | t0001 | g0288 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0278 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19006 | hp1 | a0001 | c0002 | t0003 | g0215 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19009 | hp2 | a0001 | c0003 | t0002 | g0054 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19010 | hp1 | a0002 | c0004 | t0002 | g0088 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0250 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19011 | hp2 | a0001 | c0002 | t0003 | g0110 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19030 | hp1 | a0001 | c0002 | t0003 | g0154 | AFR | LWK | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19030 | hp2 | a0001 | c0005 | t0005 | g0009 | AFR | LWK | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19058 | hp2 | a0002 | c0004 | t0002 | g0093 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19060 | hp2 | a0001 | c0002 | t0003 | g0157 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19064 | hp2 | a0002 | c0004 | t0002 | g0087 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19065 | hp1 | a0014 | c0021 | t0003 | g0166 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19065 | hp2 | a0001 | c0002 | t0001 | g0290 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19066 | hp1 | a0001 | c0003 | t0002 | g0053 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19070 | hp2 | a0002 | c0004 | t0002 | g0090 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19074 | hp1 | a0001 | c0003 | t0002 | g0079 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19074 | hp2 | a0001 | c0002 | t0003 | g0186 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19077 | hp1 | a0001 | c0002 | t0003 | g0187 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19082 | hp2 | a0002 | c0004 | t0002 | g0080 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19083 | hp2 | a0001 | c0002 | t0003 | g0169 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19084 | hp1 | a0002 | c0004 | t0002 | g0076 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19085 | hp1 | a0008 | c0022 | t0003 | g0175 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19086 | hp1 | a0001 | c0003 | t0002 | g0066 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19087 | hp2 | a0001 | c0003 | t0002 | g0192 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19089 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19089 | hp2 | a0001 | c0002 | t0003 | g0170 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19091 | hp1 | a0002 | c0004 | t0002 | g0045 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19240 | hp1 | a0012 | c0028 | t0002 | g0113 | AFR | YRI | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA19240 | hp2 | a0001 | c0002 | t0004 | g0021 | AFR | YRI | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA20129 | hp1 | a0001 | c0002 | t0009 | g0125 | AFR | ASW | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA20129 | hp2 | a0001 | c0029 | t0002 | g0033 | AFR | ASW | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA20805 | hp1 | a0002 | c0004 | t0002 | g0108 | EUR | TSI | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0223 | EUR | TSI | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02109 | hp1 | a0002 | c0025 | t0002 | g0065 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02109 | hp2 | a0003 | c0006 | t0001 | g0261 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02486 | hp1 | a0001 | c0005 | t0005 | g0005 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02486 | hp2 | a0004 | c0009 | t0002 | g0100 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02559 | hp1 | a0001 | c0002 | t0004 | g0016 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG02559 | hp2 | a0001 | c0005 | t0005 | g0007 | AFR | ACB | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03471 | hp1 | a0001 | c0003 | t0002 | g0060 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG03471 | hp2 | a0001 | c0002 | t0003 | g0179 | AFR | MSL | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG06807 | hp1 | a0001 | c0002 | t0003 | g0178 | AFR | USA | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
HG06807 | hp2 | a0002 | c0004 | t0002 | g0081 | AFR | USA | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18955 | hp1 | a0002 | c0004 | t0002 | g0089 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA20300 | hp1 | a0002 | c0004 | t0002 | g0069 | AFR | USA | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA20300 | hp2 | a0001 | c0027 | t0004 | g0020 | AFR | USA | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA21309 | hp1 | a0006 | c0012 | t0002 | g0096 | AFR | LWK | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
NA21309 | hp2 | a0013 | c0024 | t0003 | g0183 | AFR | LWK | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0233 | REF | REF | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
homoSapiens_grch38 | hp1 | a0002 | c0004 | t0002 | g0102 | REF | REF | APC_chr5_112732885_112851239 | APC | chr5 | 112732885 | 112851239 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:112827167
|
A | G | 1 | a0005 | 2 | HG02895.hp1 HG02897.hp1 |
missense_variant | MODERATE | c.1468A>G | p.Asn490Asp | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 12/16 | 1527/10704 | 1468/8532 | 490/2843 | chr5 | 112827167 | ||
chr5:112838180
|
C | G | 1 | a0007 | 1 | HG03710.hp2 | missense_variant | MODERATE | c.2586C>G | p.Asn862Lys | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 2645/10704 | 2586/8532 | 862/2843 | chr5 | 112838180 | ||
chr5:112838202
|
C | T | 1 | a0006 | 2 | HG03453.hp1 NA21309.hp1 |
missense_variant | MODERATE | c.2608C>T | p.Pro870Ser | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 2667/10704 | 2608/8532 | 870/2843 | chr5 | 112838202 | ||
chr5:112838542
|
T | C | 1 | a0014 | 1 | NA19065.hp1 | missense_variant | MODERATE | c.2948T>C | p.Ile983Thr | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3007/10704 | 2948/8532 | 983/2843 | chr5 | 112838542 | ||
chr5:112839053
|
TGAA | T | 1 | a0004 | 3 | HG01243.hp1 HG02486.hp2 HG02572.hp2 |
disruptive_inframe_deletion | MODERATE | c.3468_3470delAGA | p.Glu1157del | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3527/10704 | 3468/8532 | 1156/2843 | INFO_REALIGN_3_PRIME | chr5 | 112839053 | |
chr5:112839244
|
A | C | 1 | a0013 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.3650A>C | p.Asn1217Thr | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3709/10704 | 3650/8532 | 1217/2843 | chr5 | 112839244 | ||
chr5:112839284
|
G | C | 1 | a0008 | 1 | NA19085.hp1 | missense_variant | MODERATE | c.3690G>C | p.Gln1230His | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3749/10704 | 3690/8532 | 1230/2843 | chr5 | 112839284 | ||
chr5:112840212
|
G | C | 1 | a0012 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.4618G>C | p.Glu1540Gln | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 4677/10704 | 4618/8532 | 1540/2843 | chr5 | 112840212 | ||
chr5:112840957
|
G | A | 1 | a0009 | 1 | NA18980.hp2 | missense_variant | MODERATE | c.5363G>A | p.Arg1788His | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 5422/10704 | 5363/8532 | 1788/2843 | chr5 | 112840957 | ||
chr5:112841059
|
T | A | 12 | a0001a0003a0004others(9): Show | 251 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(248): Show |
missense_variant | MODERATE | c.5465T>A | p.Val1822Asp | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 5524/10704 | 5465/8532 | 1822/2843 | chr5 | 112841059 | ||
chr5:112843098
|
G | A | 1 | a0003 | 3 | HG01070.hp1 HG02109.hp2 HG03927.hp1 |
missense_variant | MODERATE | c.7504G>A | p.Gly2502Ser | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 7563/10704 | 7504/8532 | 2502/2843 | chr5 | 112843098 | ||
chr5:112843219
|
A | G | 1 | a0011 | 1 | HG03098.hp1 | missense_variant | MODERATE | c.7625A>G | p.Asn2542Ser | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 7684/10704 | 7625/8532 | 2542/2843 | chr5 | 112843219 | ||
chr5:112843240
|
G | A | 1 | a0010 | 1 | NA18975.hp1 | missense_variant | MODERATE | c.7646G>A | p.Arg2549His | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 7705/10704 | 7646/8532 | 2549/2843 | chr5 | 112843240 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:112755010
|
G | A | 1 | a0001c0014 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.120G>A | p.Glu40Glu | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/16 | 179/10704 | 120/8532 | 40/2843 | chr5 | 112755010 | ||
chr5:112827142
|
G | A | 1 | a0001c0015 | 1 | HG02630.hp1 | synonymous_variant | LOW | c.1443G>A | p.Val481Val | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 12/16 | 1502/10704 | 1443/8532 | 481/2843 | chr5 | 112827142 | ||
chr5:112827157
|
T | C | 11 | a0001c0001a0001c0005a0001c0007others(8): Show | 118 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(115): Show |
synonymous_variant | LOW | c.1458T>C | p.Tyr486Tyr | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 12/16 | 1517/10704 | 1458/8532 | 486/2843 | chr5 | 112827157 | ||
chr5:112828864
|
G | A | 13 | a0001c0001a0001c0002a0001c0005others(10): Show | 184 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(181): Show |
synonymous_variant | LOW | c.1635G>A | p.Ala545Ala | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/16 | 1694/10704 | 1635/8532 | 545/2843 | chr5 | 112828864 | ||
chr5:112828924
|
A | G | 1 | a0001c0005 | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
synonymous_variant | LOW | c.1695A>G | p.Glu565Glu | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/16 | 1754/10704 | 1695/8532 | 565/2843 | chr5 | 112828924 | ||
chr5:112837553
|
G | A | 1 | a0002c0025 | 1 | HG02109.hp1 | splice_region_variant&synonymous_variant | LOW | c.1959G>A | p.Arg653Arg | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 2018/10704 | 1959/8532 | 653/2843 | chr5 | 112837553 | ||
chr5:112838234
|
C | T | 1 | a0001c0031 | 1 | HG01081.hp2 | synonymous_variant | LOW | c.2640C>T | p.Ile880Ile | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 2699/10704 | 2640/8532 | 880/2843 | chr5 | 112838234 | ||
chr5:112838759
|
A | T | 1 | a0001c0011 | 2 | HG03490.hp2 HG03492.hp2 |
synonymous_variant | LOW | c.3165A>T | p.Ile1055Ile | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3224/10704 | 3165/8532 | 1055/2843 | chr5 | 112838759 | ||
chr5:112838858
|
G | A | 1 | a0001c0026 | 1 | HG03130.hp1 | synonymous_variant | LOW | c.3264G>A | p.Lys1088Lys | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3323/10704 | 3264/8532 | 1088/2843 | chr5 | 112838858 | ||
chr5:112839326
|
A | G | 1 | a0001c0005 | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
synonymous_variant | LOW | c.3732A>G | p.Gln1244Gln | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 3791/10704 | 3732/8532 | 1244/2843 | chr5 | 112839326 | ||
chr5:112839959
|
T | C | 1 | a0001c0016 | 1 | HG02523.hp2 | synonymous_variant | LOW | c.4365T>C | p.Asn1455Asn | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 4424/10704 | 4365/8532 | 1455/2843 | chr5 | 112839959 | ||
chr5:112840073
|
G | A | 14 | a0001c0001a0001c0002a0001c0005others(11): Show | 185 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(182): Show |
synonymous_variant | LOW | c.4479G>A | p.Thr1493Thr | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 4538/10704 | 4479/8532 | 1493/2843 | chr5 | 112840073 | ||
chr5:112840379
|
C | G | 1 | a0002c0020 | 1 | NA18953.hp1 | synonymous_variant | LOW | c.4785C>G | p.Ala1595Ala | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 4844/10704 | 4785/8532 | 1595/2843 | chr5 | 112840379 | ||
chr5:112840628
|
G | A | 15 | a0001c0001a0001c0002a0001c0005others(12): Show | 186 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(183): Show |
synonymous_variant | LOW | c.5034G>A | p.Gly1678Gly | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 5093/10704 | 5034/8532 | 1678/2843 | chr5 | 112840628 | ||
chr5:112840844
|
C | G | 2 | a0001c0010a0001c0014 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
synonymous_variant | LOW | c.5250C>G | p.Val1750Val | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 5309/10704 | 5250/8532 | 1750/2843 | chr5 | 112840844 | ||
chr5:112840862
|
T | G | 15 | a0001c0001a0001c0002a0001c0005others(12): Show | 186 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(183): Show |
synonymous_variant | LOW | c.5268T>G | p.Ser1756Ser | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 5327/10704 | 5268/8532 | 1756/2843 | chr5 | 112840862 | ||
chr5:112841474
|
G | A | 14 | a0001c0001a0001c0002a0001c0005others(11): Show | 185 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(182): Show |
synonymous_variant | LOW | c.5880G>A | p.Pro1960Pro | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 5939/10704 | 5880/8532 | 1960/2843 | chr5 | 112841474 | ||
chr5:112842788
|
C | T | 1 | a0001c0030 | 1 | HG01891.hp1 | synonymous_variant | LOW | c.7194C>T | p.Ser2398Ser | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 7253/10704 | 7194/8532 | 2398/2843 | chr5 | 112842788 | ||
chr5:112842795
|
C | T | 1 | a0001c0007 | 3 | HG01081.hp1 HG01106.hp2 HG02717.hp2 |
synonymous_variant | LOW | c.7201C>T | p.Leu2401Leu | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 7260/10704 | 7201/8532 | 2401/2843 | chr5 | 112842795 | ||
chr5:112843298
|
A | G | 5 | a0001c0008a0001c0030a0004c0009others(2): Show | 10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
synonymous_variant | LOW | c.7704A>G | p.Gly2568Gly | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 7763/10704 | 7704/8532 | 2568/2843 | chr5 | 112843298 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:112844212
|
C | A | 7 | a0001c0002t0003a0001c0003t0006a0001c0003t0010others(4): Show | 50 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*86C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 86 | chr5 | 112844212 | |||||
chr5:112844374
|
A | G | 1 | a0001c0002t0015 | 1 | HG00323.hp1 | 3_prime_UTR_variant | MODIFIER | c.*248A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 248 | chr5 | 112844374 | |||||
chr5:112844531
|
C | CA | 25 | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(22): Show | 189 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(186): Show |
3_prime_UTR_variant | MODIFIER | c.*414dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 415 | INFO_REALIGN_3_PRIME | chr5 | 112844531 | ||||
chr5:112844560
|
C | T | 6 | a0001c0002t0003a0001c0003t0006a0001c0026t0006others(3): Show | 49 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*434C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 434 | chr5 | 112844560 | |||||
chr5:112844635
|
C | A | 1 | a0001c0003t0014 | 1 | NA18747.hp1 | 3_prime_UTR_variant | MODIFIER | c.*509C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 509 | chr5 | 112844635 | |||||
chr5:112844781
|
G | T | 1 | a0001c0002t0009 | 2 | HG01243.hp2 NA20129.hp1 |
3_prime_UTR_variant | MODIFIER | c.*655G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 655 | chr5 | 112844781 | |||||
chr5:112845176
|
T | C | 3 | a0001c0002t0005a0001c0005t0005a0001c0005t0011 | 12 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1050T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1050 | chr5 | 112845176 | |||||
chr5:112845224
|
T | C | 7 | a0001c0001t0001a0001c0002t0001a0001c0016t0001others(4): Show | 100 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(97): Show |
3_prime_UTR_variant | MODIFIER | c.*1098T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1098 | chr5 | 112845224 | |||||
chr5:112845314
|
C | G | 1 | a0001c0005t0011 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1188C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1188 | chr5 | 112845314 | |||||
chr5:112845329
|
A | C | 1 | a0001c0002t0008 | 2 | HG02615.hp2 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1203A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1203 | chr5 | 112845329 | |||||
chr5:112845430
|
G | A | 1 | a0001c0002t0013 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1304G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1304 | chr5 | 112845430 | |||||
chr5:112845586
|
C | T | 6 | a0001c0002t0003a0001c0003t0006a0001c0026t0006others(3): Show | 49 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*1460C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1460 | chr5 | 112845586 | |||||
chr5:112845682
|
C | G | 9 | a0001c0001t0001a0001c0002t0001a0001c0010t0007others(6): Show | 103 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(100): Show |
3_prime_UTR_variant | MODIFIER | c.*1556C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1556 | chr5 | 112845682 | |||||
chr5:112845879
|
G | A | 26 | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(23): Show | 197 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(194): Show |
3_prime_UTR_variant | MODIFIER | c.*1753G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 16/16 | 1753 | chr5 | 112845879 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:112737970
|
G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+45G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112737970 | ||||||
chr5:112737978
|
T | C | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+53T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112737978 | ||||||
chr5:112738420
|
T | C | 1 | a0001c0003t0002g0004 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.-19+495T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738420 | ||||||
chr5:112738564
|
G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+639G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738564 | ||||||
chr5:112738572
|
A | G | 101 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(98): Show | 101 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.-19+647A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738572 | ||||||
chr5:112738659
|
C | T | 163 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(160): Show | 165 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(162): Show |
intron_variant | MODIFIER | c.-19+734C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738659 | ||||||
chr5:112738768
|
T | A | 2 | a0001c0010t0007g0132a0001c0014t0007g0133 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-19+843T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738768 | ||||||
chr5:112738890
|
A | G | 1 | a0001c0002t0009g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-19+965A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738890 | ||||||
chr5:112738893
|
C | T | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+968C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738893 | ||||||
chr5:112738910
|
A | G | 2 | a0001c0008t0002g0130a0001c0030t0002g0129 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-19+985A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112738910 | ||||||
chr5:112739025
|
C | G | 101 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(98): Show | 101 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.-19+1100C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739025 | ||||||
chr5:112739072
|
A | G | 2 | a0001c0002t0003g0186a0001c0002t0003g0187 | 2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-19+1147A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739072 | ||||||
chr5:112739271
|
C | G | 3 | a0001c0002t0005g0126a0001c0002t0005g0127a0001c0002t0005g0128 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-19+1346C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739271 | ||||||
chr5:112739299
|
G | T | 2 | a0001c0002t0009g0125a0001c0002t0009g0131 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-19+1374G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739299 | ||||||
chr5:112739447
|
C | T | 1 | a0001c0014t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.-19+1522C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739447 | ||||||
chr5:112739492
|
C | G | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-19+1567C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739492 | ||||||
chr5:112739662
|
C | T | 1 | a0013c0024t0003g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.-19+1737C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739662 | ||||||
chr5:112739788
|
C | T | 10 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(7): Show | 10 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+1863C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739788 | ||||||
chr5:112739888
|
T | C | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-19+1963T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112739888 | ||||||
chr5:112740067
|
CAG | C | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-19+2145_-19+2146d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112740067 | |||||
chr5:112740081
|
A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+2156A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740081 | ||||||
chr5:112740159
|
A | G | 1 | a0002c0004t0002g0114 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.-19+2234A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740159 | ||||||
chr5:112740250
|
T | C | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-19+2325T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740250 | ||||||
chr5:112740503
|
T | C | 1 | a0001c0015t0002g0134 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.-19+2578T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740503 | ||||||
chr5:112740523
|
TC | T | 9 | a0001c0001t0001g0122a0001c0001t0004g0117a0001c0001t0004g0121others(6): Show | 9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+2599delC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740523 | ||||||
chr5:112740524
|
C | CT | 10 | a0001c0001t0001g0109a0001c0002t0003g0110a0001c0002t0004g0189others(7): Show | 10 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+2618dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112740524 | |||||
chr5:112740524
|
C | T | 39 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0155others(36): Show | 41 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.-19+2599C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740524 | ||||||
chr5:112740524
|
CT | C | 122 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(119): Show | 122 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(119): Show |
intron_variant | MODIFIER | c.-19+2618delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112740524 | |||||
chr5:112740525
|
T | C | 38 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0155others(35): Show | 40 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.-19+2600T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740525 | ||||||
chr5:112740526
|
T | C | 9 | a0001c0001t0001g0122a0001c0001t0004g0117a0001c0001t0004g0121others(6): Show | 9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+2601T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740526 | ||||||
chr5:112740547
|
A | G | 1 | a0002c0004t0002g0106 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.-19+2622A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740547 | ||||||
chr5:112740580
|
G | A | 2 | a0002c0004t0002g0028a0002c0004t0002g0029 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.-19+2655G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740580 | ||||||
chr5:112740594
|
G | A | 19 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(16): Show | 19 | HG00741.hp2 HG01496.hp1 HG01496.hp2 others(16): Show |
intron_variant | MODIFIER | c.-19+2669G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740594 | ||||||
chr5:112740645
|
C | T | 1 | a0001c0005t0005g0012 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.-19+2720C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740645 | ||||||
chr5:112740704
|
T | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-19+2779T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740704 | ||||||
chr5:112740752
|
G | C | 287 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(284): Show | 289 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.-19+2827G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740752 | ||||||
chr5:112740856
|
T | C | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+2931T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740856 | ||||||
chr5:112740907
|
A | C | 1 | a0001c0003t0006g0152 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-19+2982A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740907 | ||||||
chr5:112740924
|
T | C | 1 | a0001c0001t0001g0195 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-19+2999T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112740924 | ||||||
chr5:112741124
|
TATC | T | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0292 | 3 | NA18953.hp2 NA18974.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.-19+3203_-19+3205d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112741124 | |||||
chr5:112741182
|
C | T | 10 | a0001c0008t0002g0095a0001c0008t0002g0112a0001c0008t0002g0130others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+3257C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741182 | ||||||
chr5:112741560
|
T | G | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-19+3635T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741560 | ||||||
chr5:112741600
|
A | T | 1 | a0001c0003t0002g0137 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-19+3675A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741600 | ||||||
chr5:112741620
|
A | C | 5 | a0002c0004t0002g0090a0002c0004t0002g0091a0002c0004t0002g0092others(2): Show | 5 | NA18957.hp1 NA18963.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+3695A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741620 | ||||||
chr5:112741652
|
T | C | 1 | a0009c0017t0001g0196 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-19+3727T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741652 | ||||||
chr5:112741750
|
T | A | 96 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(93): Show | 96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.-19+3825T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741750 | ||||||
chr5:112741759
|
A | G | 2 | a0001c0002t0003g0186a0001c0002t0003g0187 | 2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-19+3834A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741759 | ||||||
chr5:112741983
|
T | C | 3 | a0001c0003t0002g0030a0002c0004t0002g0031a0007c0032t0002g0032 | 3 | HG00323.hp2 HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-19+4058T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741983 | ||||||
chr5:112741984
|
C | T | 58 | a0001c0002t0001g0288a0001c0002t0001g0289a0001c0002t0001g0290others(55): Show | 60 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(57): Show |
intron_variant | MODIFIER | c.-19+4059C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741984 | ||||||
chr5:112741991
|
A | G | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+4066A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112741991 | ||||||
chr5:112742073
|
A | G | 171 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(168): Show | 173 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(170): Show |
intron_variant | MODIFIER | c.-19+4148A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742073 | ||||||
chr5:112742082
|
G | A | 16 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(13): Show | 16 | HG01884.hp2 HG02258.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.-19+4157G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742082 | ||||||
chr5:112742106
|
G | T | 1 | a0001c0001t0001g0269 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-19+4181G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742106 | ||||||
chr5:112742223
|
G | C | 104 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(101): Show | 104 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.-19+4298G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742223 | ||||||
chr5:112742398
|
C | T | 1 | a0010c0018t0001g0268 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.-19+4473C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742398 | ||||||
chr5:112742896
|
G | A | 3 | a0001c0002t0003g0155a0001c0002t0003g0156a0001c0002t0003g0157 | 3 | HG02155.hp1 NA18990.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.-19+4971G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742896 | ||||||
chr5:112742955
|
C | G | 1 | a0001c0001t0001g0267 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-19+5030C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112742955 | ||||||
chr5:112743054
|
C | T | 1 | a0001c0001t0001g0266 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.-19+5129C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743054 | ||||||
chr5:112743085
|
A | G | 5 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0121others(2): Show | 5 | HG01358.hp1 HG01361.hp1 HG01981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-19+5160A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743085 | ||||||
chr5:112743129
|
CCT | C | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+5207_-19+5208d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112743129 | |||||
chr5:112743174
|
T | C | 3 | a0001c0002t0005g0126a0001c0002t0005g0127a0001c0002t0005g0128 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-19+5249T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743174 | ||||||
chr5:112743234
|
T | C | 3 | a0002c0004t0002g0037a0002c0004t0002g0038a0002c0004t0002g0039 | 3 | HG01175.hp2 HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.-19+5309T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743234 | ||||||
chr5:112743420
|
AT | A | 158 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(155): Show | 160 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(157): Show |
intron_variant | MODIFIER | c.-19+5503delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112743420 | |||||
chr5:112743470
|
T | C | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-19+5545T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743470 | ||||||
chr5:112743510
|
A | G | 15 | a0001c0003t0002g0138a0001c0003t0002g0150a0001c0003t0002g0151others(12): Show | 15 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+5585A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743510 | ||||||
chr5:112743906
|
C | T | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.-19+5981C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112743906 | ||||||
chr5:112744160
|
T | C | 10 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(7): Show | 10 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+6235T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744160 | ||||||
chr5:112744178
|
A | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-19+6253A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744178 | ||||||
chr5:112744185
|
T | G | 101 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(98): Show | 101 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.-19+6260T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744185 | ||||||
chr5:112744582
|
A | G | 9 | a0001c0002t0013g0003a0001c0005t0005g0005a0001c0005t0005g0006others(6): Show | 9 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.-19+6657A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744582 | ||||||
chr5:112744600
|
A | G | 1 | a0001c0010t0007g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-19+6675A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744600 | ||||||
chr5:112744697
|
T | C | 1 | a0001c0001t0001g0197 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-19+6772T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744697 | ||||||
chr5:112744815
|
T | G | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-19+6890T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744815 | ||||||
chr5:112744993
|
G | A | 10 | a0001c0003t0006g0140a0001c0003t0006g0141a0001c0003t0006g0142others(7): Show | 10 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-19+7068G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112744993 | ||||||
chr5:112745031
|
G | A | 71 | a0001c0001t0001g0109a0001c0002t0003g0075a0001c0002t0003g0110others(68): Show | 71 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(68): Show |
intron_variant | MODIFIER | c.-19+7106G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745031 | ||||||
chr5:112745059
|
T | C | 2 | a0001c0001t0001g0193a0001c0001t0001g0194 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.-19+7134T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745059 | ||||||
chr5:112745130
|
G | GTA | 167 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(164): Show | 169 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(166): Show |
intron_variant | MODIFIER | c.-19+7205_-19+7206i others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745130 | ||||||
chr5:112745205
|
A | G | 1 | a0002c0004t0002g0089 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.-19+7280A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745205 | ||||||
chr5:112745341
|
A | G | 15 | a0001c0003t0002g0138a0001c0003t0002g0150a0001c0003t0002g0151others(12): Show | 15 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+7416A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745341 | ||||||
chr5:112745548
|
T | TTTA | 99 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(96): Show | 99 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.-19+7650_-19+7652d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112745548 | |||||
chr5:112745548
|
T | TTTATTA | 10 | a0001c0001t0001g0198a0001c0003t0002g0150a0001c0010t0007g0027others(7): Show | 10 | HG01175.hp2 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.-19+7647_-19+7652d others(8): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112745548 | |||||
chr5:112745548
|
TTTA | T | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-19+7650_-19+7652d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112745548 | |||||
chr5:112745548
|
TTTATTA | T | 4 | a0001c0001t0001g0263a0001c0002t0008g0184a0001c0002t0008g0185others(1): Show | 4 | HG01346.hp2 HG02615.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.-19+7647_-19+7652d others(8): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112745548 | |||||
chr5:112745548
|
TTTATTAT others(2): Show |
T | 3 | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0002t0003g0181 | 3 | HG02965.hp1 HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-19+7644_-19+7652d others(11): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112745548 | |||||
chr5:112745565
|
T | C | 1 | a0002c0004t0002g0040 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19+7640T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745565 | ||||||
chr5:112745575
|
A | T | 1 | a0001c0001t0004g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.-19+7650A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745575 | ||||||
chr5:112745644
|
A | G | 13 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(10): Show | 13 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.-19+7719A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745644 | ||||||
chr5:112745670
|
CT | C | 15 | a0001c0003t0002g0138a0001c0003t0002g0150a0001c0003t0002g0151others(12): Show | 15 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.-19+7747delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112745670 | |||||
chr5:112745679
|
C | G | 2 | a0001c0003t0002g0035a0001c0003t0002g0036 | 2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-19+7754C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745679 | ||||||
chr5:112745682
|
C | A | 80 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(77): Show | 80 | HG00609.hp2 HG00642.hp2 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.-19+7757C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745682 | ||||||
chr5:112745725
|
G | A | 2 | a0001c0003t0002g0035a0001c0003t0002g0036 | 2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.-19+7800G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745725 | ||||||
chr5:112745815
|
A | C | 1 | a0001c0001t0001g0263 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-19+7890A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112745815 | ||||||
chr5:112746136
|
GGAAA | G | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.-19+8216_-19+8219d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112746136 | |||||
chr5:112746227
|
A | G | 101 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(98): Show | 101 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.-19+8302A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112746227 | ||||||
chr5:112746307
|
G | T | 1 | a0002c0004t0002g0040 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-19+8382G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112746307 | ||||||
chr5:112746449
|
T | A | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-8424T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112746449 | ||||||
chr5:112746476
|
T | C | 9 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(6): Show | 9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-8397T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112746476 | ||||||
chr5:112746951
|
TTA | T | 98 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(95): Show | 98 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.-18-7920_-18-7919d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112746951 | |||||
chr5:112747122
|
C | T | 1 | a0001c0002t0003g0180 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.-18-7751C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747122 | ||||||
chr5:112747192
|
A | G | 2 | a0003c0006t0001g0261a0003c0006t0001g0262 | 2 | HG02109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.-18-7681A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747192 | ||||||
chr5:112747241
|
A | AG | 185 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(182): Show | 187 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(184): Show |
intron_variant | MODIFIER | c.-18-7626dupG | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112747241 | |||||
chr5:112747387
|
G | A | 1 | a0001c0001t0001g0199 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-18-7486G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747387 | ||||||
chr5:112747598
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-18-7275C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747598 | ||||||
chr5:112747607
|
C | T | 2 | a0001c0002t0009g0125a0001c0002t0009g0131 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-18-7266C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747607 | ||||||
chr5:112747643
|
A | G | 1 | a0004c0009t0002g0100 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-18-7230A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747643 | ||||||
chr5:112747672
|
G | C | 1 | a0001c0001t0001g0269 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-18-7201G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747672 | ||||||
chr5:112747720
|
A | G | 15 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0278others(12): Show | 15 | HG01981.hp1 HG01993.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.-18-7153A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747720 | ||||||
chr5:112747761
|
A | G | 1 | a0001c0002t0005g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.-18-7112A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747761 | ||||||
chr5:112747844
|
A | G | 14 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(11): Show | 14 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.-18-7029A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747844 | ||||||
chr5:112747862
|
A | G | 2 | a0001c0002t0009g0125a0001c0002t0009g0131 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.-18-7011A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747862 | ||||||
chr5:112747956
|
T | C | 1 | a0001c0003t0002g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18-6917T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112747956 | ||||||
chr5:112748072
|
A | G | 1 | a0001c0002t0015g0191 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.-18-6801A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748072 | ||||||
chr5:112748109
|
G | A | 1 | a0001c0001t0001g0200 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-18-6764G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748109 | ||||||
chr5:112748148
|
C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18-6725C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748148 | ||||||
chr5:112748205
|
A | T | 1 | a0001c0003t0002g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-18-6668A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748205 | ||||||
chr5:112748259
|
A | G | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-6614A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748259 | ||||||
chr5:112748329
|
A | T | 2 | a0001c0003t0006g0146a0001c0003t0006g0147 | 2 | HG03225.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.-18-6544A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748329 | ||||||
chr5:112748343
|
G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18-6530G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748343 | ||||||
chr5:112748392
|
G | C | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-6481G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748392 | ||||||
chr5:112748599
|
C | T | 3 | a0001c0002t0003g0154a0001c0002t0003g0178a0001c0002t0003g0179 | 3 | HG03471.hp2 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.-18-6274C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748599 | ||||||
chr5:112748855
|
G | A | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-18-6018G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112748855 | ||||||
chr5:112749046
|
G | T | 1 | a0007c0032t0002g0032 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-18-5827G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749046 | ||||||
chr5:112749132
|
G | A | 1 | a0001c0003t0002g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-18-5741G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749132 | ||||||
chr5:112749138
|
C | G | 1 | a0001c0003t0002g0086 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-18-5735C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749138 | ||||||
chr5:112749194
|
C | T | 1 | a0002c0004t0002g0031 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-18-5679C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749194 | ||||||
chr5:112749311
|
A | T | 1 | a0011c0023t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-18-5562A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749311 | ||||||
chr5:112749373
|
A | G | 1 | a0002c0004t0002g0111 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-18-5500A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749373 | ||||||
chr5:112749479
|
A | AT | 111 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(108): Show | 111 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(108): Show |
intron_variant | MODIFIER | c.-18-5371dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112749479 | |||||
chr5:112749479
|
A | ATT | 31 | a0001c0001t0001g0199a0001c0001t0001g0239a0001c0001t0001g0240others(28): Show | 31 | HG00639.hp2 HG00673.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.-18-5372_-18-5371d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112749479 | |||||
chr5:112749479
|
A | ATTT | 29 | a0001c0001t0001g0286a0001c0002t0003g0001a0001c0002t0003g0002others(26): Show | 31 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(28): Show |
intron_variant | MODIFIER | c.-18-5373_-18-5371d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112749479 | |||||
chr5:112749502
|
TG | T | 13 | a0001c0003t0002g0138a0001c0003t0006g0140a0001c0003t0006g0141others(10): Show | 13 | HG00741.hp2 HG01496.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.-18-5370delG | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749502 | ||||||
chr5:112749510
|
A | G | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-5363A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749510 | ||||||
chr5:112749517
|
C | T | 4 | a0001c0002t0003g0176a0001c0002t0003g0177a0001c0002t0003g0180others(1): Show | 4 | HG00609.hp1 HG02523.hp1 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-5356C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749517 | ||||||
chr5:112749564
|
A | G | 1 | a0001c0001t0001g0275 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-18-5309A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749564 | ||||||
chr5:112749590
|
C | T | 1 | a0001c0001t0001g0238 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.-18-5283C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749590 | ||||||
chr5:112749623
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-18-5250G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749623 | ||||||
chr5:112749648
|
C | T | 1 | a0001c0001t0001g0197 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.-18-5225C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749648 | ||||||
chr5:112749662
|
A | G | 1 | a0001c0001t0001g0285 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-18-5211A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749662 | ||||||
chr5:112749676
|
C | T | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-5197C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749676 | ||||||
chr5:112749740
|
C | G | 21 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(18): Show | 21 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(18): Show |
intron_variant | MODIFIER | c.-18-5133C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749740 | ||||||
chr5:112749776
|
C | T | 1 | a0001c0002t0003g0075 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.-18-5097C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749776 | ||||||
chr5:112749803
|
A | G | 40 | a0001c0001t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(37): Show | 42 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.-18-5070A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749803 | ||||||
chr5:112749914
|
T | G | 101 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(98): Show | 101 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.-18-4959T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749914 | ||||||
chr5:112749932
|
A | G | 4 | a0001c0001t0001g0235a0001c0001t0001g0236a0001c0001t0001g0237others(1): Show | 4 | HG02071.hp2 HG02132.hp2 NA18955.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-4941A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749932 | ||||||
chr5:112749968
|
G | GT | 25 | a0001c0001t0001g0199a0001c0001t0001g0275a0001c0001t0001g0276others(22): Show | 25 | HG00642.hp1 HG00673.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.-18-4893dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112749968 | |||||
chr5:112749968
|
G | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.-18-4905G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112749968 | ||||||
chr5:112750023
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-18-4850C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750023 | ||||||
chr5:112750025
|
C | T | 2 | a0001c0002t0003g0186a0001c0002t0003g0187 | 2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-18-4848C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750025 | ||||||
chr5:112750032
|
G | A | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-4841G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750032 | ||||||
chr5:112750218
|
C | G | 1 | a0001c0001t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-18-4655C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750218 | ||||||
chr5:112750353
|
C | T | 2 | a0001c0008t0002g0130a0001c0030t0002g0129 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-18-4520C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750353 | ||||||
chr5:112750468
|
T | A | 99 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(96): Show | 99 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.-18-4405T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750468 | ||||||
chr5:112750488
|
A | ATGTT | 99 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(96): Show | 99 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.-18-4375_-18-4372d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr5 | 112750488 | |||||
chr5:112750679
|
C | A | 1 | a0002c0004t0002g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-18-4194C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750679 | ||||||
chr5:112750700
|
A | G | 1 | a0002c0004t0002g0111 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-18-4173A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112750700 | ||||||
chr5:112751005
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.-18-3868C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751005 | ||||||
chr5:112751050
|
C | T | 9 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(6): Show | 9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.-18-3823C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751050 | ||||||
chr5:112751067
|
T | C | 1 | a0001c0001t0004g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-18-3806T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751067 | ||||||
chr5:112751177
|
C | T | 54 | a0001c0002t0001g0288a0001c0002t0001g0289a0001c0002t0001g0290others(51): Show | 56 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(53): Show |
intron_variant | MODIFIER | c.-18-3696C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751177 | ||||||
chr5:112751228
|
AC | A | 3 | a0001c0002t0003g0171a0001c0002t0003g0172a0001c0002t0003g0173 | 3 | HG01074.hp2 HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.-18-3644delC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751228 | ||||||
chr5:112751249
|
A | G | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-3624A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751249 | ||||||
chr5:112751293
|
A | G | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-18-3580A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751293 | ||||||
chr5:112751343
|
A | G | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-3530A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751343 | ||||||
chr5:112751416
|
TAA | T | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.-18-3456_-18-3455d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751416 | ||||||
chr5:112751478
|
A | C | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.-18-3395A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751478 | ||||||
chr5:112751523
|
T | C | 1 | a0001c0002t0003g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.-18-3350T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751523 | ||||||
chr5:112751630
|
T | G | 172 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(169): Show | 174 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(171): Show |
intron_variant | MODIFIER | c.-18-3243T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751630 | ||||||
chr5:112751684
|
A | T | 4 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(1): Show | 4 | HG00741.hp1 HG01109.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.-18-3189A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751684 | ||||||
chr5:112751808
|
A | G | 1 | a0001c0001t0001g0234 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-18-3065A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112751808 | ||||||
chr5:112752015
|
T | C | 48 | a0001c0001t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(45): Show | 50 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(47): Show |
intron_variant | MODIFIER | c.-18-2858T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752015 | ||||||
chr5:112752803
|
C | T | 2 | a0002c0004t0002g0031a0007c0032t0002g0032 | 2 | HG00323.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.-18-2070C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752803 | ||||||
chr5:112752810
|
G | A | 287 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(284): Show | 289 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.-18-2063G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752810 | ||||||
chr5:112752907
|
T | C | 1 | a0001c0002t0004g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-18-1966T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752907 | ||||||
chr5:112752907
|
T | G | 37 | a0001c0002t0001g0288a0001c0002t0001g0289a0001c0002t0001g0290others(34): Show | 39 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.-18-1966T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752907 | ||||||
chr5:112752948
|
C | T | 1 | a0001c0029t0002g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.-18-1925C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752948 | ||||||
chr5:112752969
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-18-1904G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112752969 | ||||||
chr5:112753564
|
A | T | 1 | a0001c0005t0005g0010 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-18-1309A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753564 | ||||||
chr5:112753585
|
T | C | 97 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(94): Show | 97 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.-18-1288T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753585 | ||||||
chr5:112753667
|
G | A | 2 | a0001c0003t0002g0138a0001c0003t0002g0151 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.-18-1206G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753667 | ||||||
chr5:112753747
|
C | T | 1 | a0003c0006t0001g0248 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.-18-1126C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753747 | ||||||
chr5:112753748
|
G | A | 1 | a0001c0003t0002g0042 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.-18-1125G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753748 | ||||||
chr5:112753783
|
T | C | 203 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(200): Show | 205 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(202): Show |
intron_variant | MODIFIER | c.-18-1090T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753783 | ||||||
chr5:112753847
|
A | G | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.-18-1026A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753847 | ||||||
chr5:112753865
|
C | G | 1 | a0001c0010t0007g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-18-1008C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112753865 | ||||||
chr5:112754002
|
T | C | 2 | a0001c0002t0004g0189a0001c0002t0004g0190 | 2 | HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.-18-871T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112754002 | ||||||
chr5:112754116
|
T | C | 10 | a0001c0003t0006g0140a0001c0003t0006g0141a0001c0003t0006g0142others(7): Show | 10 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.-18-757T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112754116 | ||||||
chr5:112754239
|
A | G | 1 | a0001c0003t0002g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.-18-634A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112754239 | ||||||
chr5:112754258
|
A | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-18-615A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112754258 | ||||||
chr5:112754312
|
C | A | 2 | a0002c0004t0002g0076a0002c0004t0002g0089 | 2 | NA18955.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.-18-561C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 1/15 | chr5 | 112754312 | ||||||
chr5:112755248
|
T | G | 4 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0023others(1): Show | 4 | HG01884.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+223T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112755248 | ||||||
chr5:112755707
|
C | T | 1 | a0001c0003t0002g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.135+682C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112755707 | ||||||
chr5:112755944
|
C | CA | 21 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0240others(18): Show | 21 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(18): Show |
intron_variant | MODIFIER | c.135+934dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112755944 | |||||
chr5:112755944
|
CA | C | 8 | a0001c0001t0001g0260a0001c0002t0003g0173a0001c0002t0008g0185others(5): Show | 8 | HG01074.hp2 HG01081.hp2 HG01109.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+934delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112755944 | |||||
chr5:112756007
|
C | G | 168 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(165): Show | 170 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(167): Show |
intron_variant | MODIFIER | c.135+982C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756007 | ||||||
chr5:112756013
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.135+988T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756013 | ||||||
chr5:112756276
|
C | T | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.135+1251C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756276 | ||||||
chr5:112756358
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.135+1333A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756358 | ||||||
chr5:112756367
|
CATTTT | C | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.135+1346_135+1350d others(7): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112756367 | |||||
chr5:112756481
|
A | T | 1 | a0001c0002t0003g0075 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.135+1456A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756481 | ||||||
chr5:112756619
|
G | A | 9 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(6): Show | 9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.135+1594G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756619 | ||||||
chr5:112756672
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.135+1647A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756672 | ||||||
chr5:112756705
|
T | G | 103 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(100): Show | 103 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.135+1680T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756705 | ||||||
chr5:112756738
|
C | G | 1 | a0001c0001t0001g0233 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.135+1713C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756738 | ||||||
chr5:112756801
|
A | G | 1 | a0001c0001t0001g0266 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.135+1776A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756801 | ||||||
chr5:112756803
|
A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+1778A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756803 | ||||||
chr5:112756928
|
G | A | 1 | a0001c0001t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.135+1903G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112756928 | ||||||
chr5:112757185
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.135+2160A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757185 | ||||||
chr5:112757259
|
A | G | 1 | a0001c0002t0003g0002 | 2 | HG02698.hp1 HG03688.hp1 |
intron_variant | MODIFIER | c.135+2234A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757259 | ||||||
chr5:112757335
|
A | C | 3 | a0001c0002t0005g0126a0001c0002t0005g0127a0001c0002t0005g0128 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.135+2310A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757335 | ||||||
chr5:112757353
|
T | A | 1 | a0001c0001t0001g0275 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.135+2328T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757353 | ||||||
chr5:112757407
|
G | A | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.135+2382G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757407 | ||||||
chr5:112757411
|
C | G | 2 | a0001c0002t0003g0186a0001c0002t0003g0187 | 2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.135+2386C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757411 | ||||||
chr5:112757728
|
G | C | 1 | a0002c0004t0002g0044 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.135+2703G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757728 | ||||||
chr5:112757874
|
C | T | 1 | a0001c0010t0007g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.135+2849C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757874 | ||||||
chr5:112757876
|
C | T | 5 | a0002c0004t0002g0090a0002c0004t0002g0091a0002c0004t0002g0092others(2): Show | 5 | NA18957.hp1 NA18963.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+2851C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112757876 | ||||||
chr5:112758182
|
T | C | 1 | a0001c0001t0001g0275 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.135+3157T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758182 | ||||||
chr5:112758251
|
G | A | 3 | a0002c0004t0002g0044a0002c0004t0002g0045a0002c0004t0002g0077 | 3 | HG00408.hp2 NA18994.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.135+3226G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758251 | ||||||
chr5:112758258
|
A | G | 287 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(284): Show | 289 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.135+3233A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758258 | ||||||
chr5:112758305
|
T | TTTTG | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.135+3292_135+3295d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112758305 | |||||
chr5:112758313
|
GTTTGTTT | G | 102 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(99): Show | 102 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.135+3311_135+3317d others(9): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112758313 | |||||
chr5:112758412
|
C | T | 6 | a0002c0004t0002g0069a0002c0004t0002g0070a0002c0004t0002g0071others(3): Show | 6 | HG01433.hp1 HG01975.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.135+3387C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758412 | ||||||
chr5:112758430
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.135+3405G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758430 | ||||||
chr5:112758515
|
C | T | 4 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(1): Show | 4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+3490C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758515 | ||||||
chr5:112758638
|
T | A | 2 | a0001c0001t0004g0121a0001c0001t0004g0124 | 2 | HG01358.hp1 HG03654.hp2 |
intron_variant | MODIFIER | c.135+3613T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758638 | ||||||
chr5:112758647
|
A | G | 1 | a0001c0003t0002g0068 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.135+3622A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758647 | ||||||
chr5:112758707
|
G | A | 166 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(163): Show | 168 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(165): Show |
intron_variant | MODIFIER | c.135+3682G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758707 | ||||||
chr5:112758755
|
C | T | 1 | a0001c0005t0005g0011 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.135+3730C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758755 | ||||||
chr5:112758757
|
C | T | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+3732C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758757 | ||||||
chr5:112758919
|
A | G | 3 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG00642.hp2 HG01074.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.135+3894A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112758919 | ||||||
chr5:112759036
|
C | T | 1 | a0002c0004t0002g0084 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.135+4011C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759036 | ||||||
chr5:112759139
|
C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.135+4114C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759139 | ||||||
chr5:112759245
|
G | T | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+4220G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759245 | ||||||
chr5:112759335
|
A | G | 2 | a0001c0002t0003g0170a0001c0002t0003g0182 | 2 | NA18974.hp2 NA19089.hp2 |
intron_variant | MODIFIER | c.135+4310A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759335 | ||||||
chr5:112759356
|
C | CT | 72 | a0001c0001t0001g0229a0001c0001t0001g0234a0001c0001t0001g0240others(69): Show | 74 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.135+4351dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112759356 | |||||
chr5:112759356
|
CT | C | 8 | a0001c0001t0001g0193a0001c0001t0001g0198a0001c0001t0001g0204others(5): Show | 8 | HG01169.hp1 HG01256.hp1 HG01257.hp2 others(5): Show |
intron_variant | MODIFIER | c.135+4351delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112759356 | |||||
chr5:112759360
|
T | C | 15 | a0001c0003t0002g0004a0001c0003t0002g0035a0001c0003t0002g0046others(12): Show | 15 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(12): Show |
intron_variant | MODIFIER | c.135+4335T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759360 | ||||||
chr5:112759385
|
G | A | 1 | a0001c0003t0002g0068 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.135+4360G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759385 | ||||||
chr5:112759443
|
C | T | 97 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(94): Show | 97 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.135+4418C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759443 | ||||||
chr5:112759444
|
G | A | 1 | a0002c0004t0002g0091 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.135+4419G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759444 | ||||||
chr5:112759451
|
G | A | 15 | a0001c0003t0002g0138a0001c0003t0002g0150a0001c0003t0002g0151others(12): Show | 15 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.135+4426G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759451 | ||||||
chr5:112759502
|
C | T | 1 | a0002c0004t0002g0073 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.135+4477C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759502 | ||||||
chr5:112759566
|
C | G | 1 | a0002c0004t0002g0040 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.135+4541C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759566 | ||||||
chr5:112759635
|
G | A | 56 | a0001c0001t0001g0109a0001c0002t0003g0075a0001c0002t0003g0110others(53): Show | 56 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.135+4610G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759635 | ||||||
chr5:112759672
|
A | T | 2 | a0001c0002t0003g0161a0001c0002t0003g0162 | 2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.135+4647A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759672 | ||||||
chr5:112759796
|
T | C | 1 | a0001c0002t0003g0165 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.135+4771T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112759796 | ||||||
chr5:112760078
|
T | A | 96 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(93): Show | 96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.135+5053T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760078 | ||||||
chr5:112760171
|
A | G | 1 | a0001c0002t0003g0159 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.135+5146A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760171 | ||||||
chr5:112760255
|
G | A | 1 | a0002c0004t0002g0080 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.135+5230G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760255 | ||||||
chr5:112760570
|
C | A | 1 | a0002c0004t0002g0089 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.135+5545C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760570 | ||||||
chr5:112760679
|
G | C | 1 | a0001c0002t0003g0165 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.136-5647G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760679 | ||||||
chr5:112760812
|
AT | A | 11 | a0001c0001t0001g0109a0001c0008t0002g0095a0001c0008t0002g0112others(8): Show | 11 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.136-5500delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112760812 | |||||
chr5:112760929
|
C | T | 99 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(96): Show | 99 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-5397C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760929 | ||||||
chr5:112760968
|
C | A | 1 | a0001c0001t0001g0285 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.136-5358C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760968 | ||||||
chr5:112760973
|
C | A | 8 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(5): Show | 8 | HG02258.hp2 HG02559.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.136-5353C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112760973 | ||||||
chr5:112761014
|
T | C | 2 | a0006c0012t0002g0096a0006c0012t0002g0097 | 2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.136-5312T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761014 | ||||||
chr5:112761020
|
A | G | 1 | a0001c0001t0001g0238 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.136-5306A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761020 | ||||||
chr5:112761045
|
G | A | 1 | a0001c0003t0002g0086 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.136-5281G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761045 | ||||||
chr5:112761089
|
G | A | 1 | a0001c0002t0003g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.136-5237G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761089 | ||||||
chr5:112761108
|
G | A | 1 | a0002c0025t0002g0065 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.136-5218G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761108 | ||||||
chr5:112761507
|
C | T | 2 | a0001c0003t0002g0138a0001c0003t0002g0151 | 2 | HG01496.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.136-4819C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761507 | ||||||
chr5:112761534
|
C | G | 1 | a0001c0001t0004g0116 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.136-4792C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761534 | ||||||
chr5:112761537
|
G | A | 96 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(93): Show | 96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.136-4789G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761537 | ||||||
chr5:112761558
|
A | G | 1 | a0001c0001t0001g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.136-4768A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761558 | ||||||
chr5:112761792
|
A | G | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-4534A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761792 | ||||||
chr5:112761819
|
A | G | 1 | a0001c0002t0003g0158 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.136-4507A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761819 | ||||||
chr5:112761859
|
A | C | 3 | a0001c0002t0005g0126a0001c0002t0005g0127a0001c0002t0005g0128 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.136-4467A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761859 | ||||||
chr5:112761996
|
CAGTTCAG others(4): Show |
C | 1 | a0011c0023t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.136-4329_136-4319d others(13): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112761996 | ||||||
chr5:112762060
|
A | G | 110 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(107): Show | 110 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(107): Show |
intron_variant | MODIFIER | c.136-4266A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112762060 | ||||||
chr5:112762073
|
T | TA | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.136-4249dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112762073 | |||||
chr5:112762313
|
A | G | 1 | a0001c0003t0002g0042 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.136-4013A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112762313 | ||||||
chr5:112762398
|
A | G | 4 | a0001c0001t0001g0122a0001c0001t0004g0121a0001c0001t0004g0123others(1): Show | 4 | HG01358.hp1 HG01361.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.136-3928A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112762398 | ||||||
chr5:112762399
|
C | T | 1 | a0001c0002t0009g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.136-3927C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112762399 | ||||||
chr5:112762406
|
A | G | 1 | a0002c0004t0002g0108 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.136-3920A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112762406 | ||||||
chr5:112762630
|
C | T | 14 | a0001c0003t0002g0138a0001c0003t0002g0150a0001c0003t0002g0151others(11): Show | 14 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-3696C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112762630 | ||||||
chr5:112762943
|
T | TA | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0267 | 3 | HG00673.hp1 NA19011.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.136-3381dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112762943 | |||||
chr5:112763162
|
A | C | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.136-3164A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763162 | ||||||
chr5:112763214
|
G | A | 287 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(284): Show | 289 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.136-3112G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763214 | ||||||
chr5:112763221
|
CA | C | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-3097delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112763221 | |||||
chr5:112763241
|
T | A | 103 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(100): Show | 103 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.136-3085T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763241 | ||||||
chr5:112763252
|
A | T | 2 | a0001c0003t0002g0036a0001c0005t0005g0012 | 2 | HG02818.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.136-3074A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763252 | ||||||
chr5:112763331
|
A | G | 102 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(99): Show | 102 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.136-2995A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763331 | ||||||
chr5:112763362
|
GT | G | 204 | a0001c0001t0001g0122a0001c0001t0001g0193a0001c0001t0001g0194others(201): Show | 206 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(203): Show |
intron_variant | MODIFIER | c.136-2954delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112763362 | |||||
chr5:112763363
|
T | G | 2 | a0002c0004t0002g0028a0002c0004t0002g0029 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.136-2963T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763363 | ||||||
chr5:112763396
|
C | T | 1 | a0001c0002t0004g0021 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.136-2930C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763396 | ||||||
chr5:112763457
|
A | C | 1 | a0001c0003t0002g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.136-2869A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763457 | ||||||
chr5:112763765
|
T | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-2561T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763765 | ||||||
chr5:112763766
|
A | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.136-2560A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763766 | ||||||
chr5:112763799
|
G | A | 49 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(46): Show | 51 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.136-2527G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763799 | ||||||
chr5:112763839
|
C | T | 1 | a0001c0001t0001g0228 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.136-2487C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763839 | ||||||
chr5:112763849
|
C | T | 1 | a0002c0004t0002g0089 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.136-2477C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763849 | ||||||
chr5:112763964
|
G | A | 1 | a0003c0006t0001g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.136-2362G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763964 | ||||||
chr5:112763993
|
T | C | 14 | a0001c0003t0002g0138a0001c0003t0002g0150a0001c0003t0002g0151others(11): Show | 14 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-2333T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112763993 | ||||||
chr5:112764013
|
G | A | 1 | a0001c0001t0001g0267 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.136-2313G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764013 | ||||||
chr5:112764033
|
C | G | 1 | a0001c0014t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.136-2293C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764033 | ||||||
chr5:112764078
|
TA | T | 252 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(249): Show | 254 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(251): Show |
intron_variant | MODIFIER | c.136-2230delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112764078 | |||||
chr5:112764245
|
C | CA | 7 | a0001c0002t0005g0115a0001c0002t0009g0125a0001c0002t0009g0131others(4): Show | 7 | HG01243.hp2 HG03139.hp2 HG03688.hp2 others(4): Show |
intron_variant | MODIFIER | c.136-2063dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112764245 | |||||
chr5:112764245
|
CA | C | 169 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(166): Show | 171 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(168): Show |
intron_variant | MODIFIER | c.136-2063delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112764245 | |||||
chr5:112764311
|
G | A | 10 | a0001c0008t0002g0095a0001c0008t0002g0112a0001c0008t0002g0130others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.136-2015G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764311 | ||||||
chr5:112764330
|
G | A | 174 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(171): Show | 176 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(173): Show |
intron_variant | MODIFIER | c.136-1996G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764330 | ||||||
chr5:112764392
|
A | G | 2 | a0001c0003t0002g0035a0001c0003t0002g0036 | 2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.136-1934A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764392 | ||||||
chr5:112764423
|
G | C | 1 | a0001c0001t0001g0284 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.136-1903G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764423 | ||||||
chr5:112764598
|
A | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0244 | 2 | NA18981.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.136-1728A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764598 | ||||||
chr5:112764719
|
C | T | 14 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(11): Show | 14 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.136-1607C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764719 | ||||||
chr5:112764774
|
A | T | 1 | a0001c0010t0007g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.136-1552A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764774 | ||||||
chr5:112764830
|
A | G | 1 | a0002c0004t0002g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.136-1496A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764830 | ||||||
chr5:112764858
|
G | T | 28 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(25): Show | 28 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(25): Show |
intron_variant | MODIFIER | c.136-1468G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764858 | ||||||
chr5:112764898
|
A | C | 289 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(286): Show | 291 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.136-1428A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112764898 | ||||||
chr5:112765016
|
A | C | 2 | a0001c0008t0002g0130a0001c0030t0002g0129 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.136-1310A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765016 | ||||||
chr5:112765197
|
T | A | 1 | a0001c0001t0001g0250 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.136-1129T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765197 | ||||||
chr5:112765285
|
T | G | 5 | a0001c0002t0003g0001a0001c0002t0003g0155a0001c0002t0003g0156others(2): Show | 6 | HG00408.hp1 HG02155.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.136-1041T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765285 | ||||||
chr5:112765322
|
C | T | 3 | a0001c0001t0001g0257a0001c0001t0001g0259a0001c0001t0001g0260 | 3 | HG01109.hp2 HG01433.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.136-1004C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765322 | ||||||
chr5:112765431
|
A | G | 3 | a0002c0004t0002g0064a0002c0004t0002g0087a0002c0004t0002g0088 | 3 | HG03491.hp1 NA19010.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.136-895A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765431 | ||||||
chr5:112765677
|
CAAAGTTC others(3): Show |
C | 9 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(6): Show | 9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.136-646_136-637del others(10): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112765677 | |||||
chr5:112765760
|
G | T | 144 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(141): Show | 146 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(143): Show |
intron_variant | MODIFIER | c.136-566G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765760 | ||||||
chr5:112765799
|
G | A | 287 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(284): Show | 289 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.136-527G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765799 | ||||||
chr5:112765808
|
A | T | 1 | a0003c0006t0001g0248 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.136-518A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765808 | ||||||
chr5:112765815
|
C | G | 1 | a0001c0002t0005g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.136-511C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765815 | ||||||
chr5:112765937
|
C | CA | 4 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0023others(1): Show | 4 | HG01884.hp2 HG02615.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-388dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr5 | 112765937 | |||||
chr5:112765954
|
A | C | 1 | a0001c0001t0001g0285 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.136-372A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765954 | ||||||
chr5:112765976
|
A | G | 30 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(27): Show | 32 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(29): Show |
intron_variant | MODIFIER | c.136-350A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112765976 | ||||||
chr5:112766096
|
C | A | 217 | a0001c0001t0001g0122a0001c0001t0001g0193a0001c0001t0001g0194others(214): Show | 219 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(216): Show |
intron_variant | MODIFIER | c.136-230C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112766096 | ||||||
chr5:112766143
|
A | G | 5 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0287others(2): Show | 5 | HG00639.hp1 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.136-183A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112766143 | ||||||
chr5:112766162
|
C | T | 1 | a0002c0004t0002g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.136-164C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112766162 | ||||||
chr5:112766273
|
T | C | 50 | a0001c0001t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(47): Show | 52 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(49): Show |
intron_variant | MODIFIER | c.136-53T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 2/15 | chr5 | 112766273 | ||||||
chr5:112766534
|
C | G | 3 | a0003c0006t0001g0248a0003c0006t0001g0261a0003c0006t0001g0262 | 3 | HG01070.hp1 HG02109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.220+124C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 3/15 | chr5 | 112766534 | ||||||
chr5:112766659
|
C | T | 1 | a0002c0004t0002g0063 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.220+249C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 3/15 | chr5 | 112766659 | ||||||
chr5:112766689
|
C | T | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.220+279C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 3/15 | chr5 | 112766689 | ||||||
chr5:112767038
|
G | C | 13 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(10): Show | 13 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(10): Show |
intron_variant | MODIFIER | c.221-151G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 3/15 | chr5 | 112767038 | ||||||
chr5:112767465
|
T | C | 2 | a0001c0008t0002g0130a0001c0030t0002g0129 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.422+75T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767465 | ||||||
chr5:112767526
|
A | G | 2 | a0001c0002t0009g0125a0001c0002t0009g0131 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.422+136A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767526 | ||||||
chr5:112767619
|
T | C | 1 | a0001c0003t0002g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.422+229T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767619 | ||||||
chr5:112767632
|
T | C | 1 | a0002c0004t0002g0044 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.422+242T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767632 | ||||||
chr5:112767949
|
C | A | 1 | a0002c0004t0002g0063 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.422+559C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767949 | ||||||
chr5:112767950
|
A | T | 1 | a0002c0004t0002g0083 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.422+560A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767950 | ||||||
chr5:112767983
|
G | A | 96 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(93): Show | 96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.422+593G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112767983 | ||||||
chr5:112768043
|
CT | C | 9 | a0001c0001t0001g0207a0001c0001t0001g0208a0001c0001t0001g0254others(6): Show | 9 | HG00639.hp1 HG01070.hp1 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.422+670delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112768043 | |||||
chr5:112768230
|
A | G | 1 | a0001c0003t0002g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.422+840A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768230 | ||||||
chr5:112768266
|
C | G | 100 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(97): Show | 100 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.422+876C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768266 | ||||||
chr5:112768430
|
TATTCAGT others(20): Show |
T | 1 | a0001c0001t0004g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.422+1041_422+1067d others(29): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768430 | ||||||
chr5:112768434
|
C | G | 1 | a0002c0004t0002g0090 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.422+1044C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768434 | ||||||
chr5:112768537
|
T | A | 10 | a0001c0008t0002g0095a0001c0008t0002g0112a0001c0008t0002g0130others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.422+1147T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768537 | ||||||
chr5:112768585
|
A | G | 10 | a0001c0008t0002g0095a0001c0008t0002g0112a0001c0008t0002g0130others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.422+1195A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768585 | ||||||
chr5:112768600
|
A | G | 99 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(96): Show | 99 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.422+1210A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768600 | ||||||
chr5:112768715
|
A | G | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.422+1325A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768715 | ||||||
chr5:112768734
|
CCCTGTAC others(18): Show |
C | 51 | a0001c0001t0001g0227a0001c0001t0001g0286a0001c0002t0001g0288others(48): Show | 53 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.422+1446_422+1470d others(27): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112768734 | |||||
chr5:112768848
|
G | A | 1 | a0001c0002t0003g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.422+1458G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768848 | ||||||
chr5:112768863
|
A | G | 2 | a0001c0010t0007g0132a0001c0014t0007g0133 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.422+1473A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768863 | ||||||
chr5:112768900
|
A | G | 1 | a0001c0002t0004g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.422+1510A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768900 | ||||||
chr5:112768987
|
C | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.422+1597C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112768987 | ||||||
chr5:112769050
|
C | CT | 100 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0197others(97): Show | 100 | HG00609.hp2 HG00639.hp1 HG00673.hp1 others(97): Show |
intron_variant | MODIFIER | c.422+1680dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112769050 | |||||
chr5:112769050
|
C | CTT | 35 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0001t0001g0271others(32): Show | 35 | HG00323.hp1 HG00673.hp2 HG01070.hp2 others(32): Show |
intron_variant | MODIFIER | c.422+1679_422+1680d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112769050 | |||||
chr5:112769050
|
C | CTTT | 45 | a0001c0001t0001g0283a0001c0001t0001g0286a0001c0002t0001g0288others(42): Show | 47 | HG00408.hp1 HG00609.hp1 HG00741.hp2 others(44): Show |
intron_variant | MODIFIER | c.422+1678_422+1680d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112769050 | |||||
chr5:112769071
|
G | T | 43 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(40): Show | 43 | HG00741.hp2 HG01496.hp2 HG01884.hp2 others(40): Show |
intron_variant | MODIFIER | c.422+1681G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769071 | ||||||
chr5:112769097
|
G | GC | 15 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(12): Show | 15 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.422+1708dupC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112769097 | |||||
chr5:112769099
|
T | A | 15 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(12): Show | 15 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.422+1709T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769099 | ||||||
chr5:112769113
|
G | A | 12 | a0001c0003t0002g0138a0001c0003t0002g0151a0001c0003t0006g0140others(9): Show | 12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.422+1723G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769113 | ||||||
chr5:112769128
|
G | A | 3 | a0001c0002t0003g0171a0001c0002t0003g0172a0001c0002t0003g0173 | 3 | HG01074.hp2 HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.422+1738G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769128 | ||||||
chr5:112769176
|
G | A | 1 | a0001c0002t0005g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.422+1786G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769176 | ||||||
chr5:112769379
|
T | G | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.422+1989T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769379 | ||||||
chr5:112769458
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.422+2068A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769458 | ||||||
chr5:112769511
|
T | G | 49 | a0001c0001t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(46): Show | 51 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.422+2121T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769511 | ||||||
chr5:112769515
|
T | C | 1 | a0001c0003t0002g0046 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.422+2125T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769515 | ||||||
chr5:112769520
|
TG | T | 96 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(93): Show | 96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.422+2131delG | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769520 | ||||||
chr5:112769526
|
A | T | 96 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(93): Show | 96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.422+2136A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769526 | ||||||
chr5:112769712
|
A | G | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.422+2322A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769712 | ||||||
chr5:112769817
|
T | G | 2 | a0001c0002t0009g0125a0001c0002t0009g0131 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.422+2427T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769817 | ||||||
chr5:112769837
|
G | A | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0292 | 3 | NA18953.hp2 NA18974.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.422+2447G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769837 | ||||||
chr5:112769918
|
T | C | 1 | a0001c0001t0001g0240 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.422+2528T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769918 | ||||||
chr5:112769986
|
TTTCCCCT others(5): Show |
T | 7 | a0002c0004t0002g0081a0002c0004t0002g0082a0002c0004t0002g0083others(4): Show | 7 | HG00639.hp2 HG01099.hp2 HG01256.hp2 others(4): Show |
intron_variant | MODIFIER | c.422+2597_422+2608d others(14): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112769986 | ||||||
chr5:112770024
|
A | C | 10 | a0001c0008t0002g0095a0001c0008t0002g0112a0001c0008t0002g0130others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.422+2634A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770024 | ||||||
chr5:112770137
|
A | T | 1 | a0001c0001t0001g0195 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.422+2747A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770137 | ||||||
chr5:112770229
|
C | G | 14 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(11): Show | 14 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.422+2839C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770229 | ||||||
chr5:112770524
|
C | T | 1 | a0001c0008t0002g0095 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.422+3134C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770524 | ||||||
chr5:112770527
|
T | C | 4 | a0001c0001t0001g0122a0001c0001t0004g0121a0001c0001t0004g0123others(1): Show | 4 | HG01358.hp1 HG01361.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.422+3137T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770527 | ||||||
chr5:112770551
|
A | G | 1 | a0001c0029t0002g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.422+3161A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770551 | ||||||
chr5:112770567
|
A | G | 2 | a0001c0002t0009g0125a0001c0002t0009g0131 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.422+3177A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770567 | ||||||
chr5:112770568
|
T | A | 3 | a0001c0002t0005g0126a0001c0002t0005g0127a0001c0002t0005g0128 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.422+3178T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770568 | ||||||
chr5:112770573
|
T | G | 1 | a0001c0001t0001g0213 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.422+3183T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770573 | ||||||
chr5:112770891
|
C | A | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.422+3501C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112770891 | ||||||
chr5:112771090
|
G | A | 1 | a0001c0002t0003g0159 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.422+3700G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771090 | ||||||
chr5:112771351
|
G | T | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.422+3961G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771351 | ||||||
chr5:112771361
|
G | A | 97 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(94): Show | 97 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.422+3971G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771361 | ||||||
chr5:112771432
|
T | A | 3 | a0002c0004t0002g0044a0002c0004t0002g0045a0002c0004t0002g0077 | 3 | HG00408.hp2 NA18994.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.422+4042T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771432 | ||||||
chr5:112771439
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.422+4049T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771439 | ||||||
chr5:112771533
|
T | C | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.423-4096T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771533 | ||||||
chr5:112771819
|
A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.423-3810A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771819 | ||||||
chr5:112771907
|
T | C | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-3722T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771907 | ||||||
chr5:112771999
|
T | C | 1 | a0001c0002t0003g0181 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.423-3630T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112771999 | ||||||
chr5:112772021
|
G | A | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.423-3608G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772021 | ||||||
chr5:112772029
|
C | T | 96 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(93): Show | 96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.423-3600C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772029 | ||||||
chr5:112772384
|
C | T | 2 | a0001c0001t0001g0201a0001c0001t0001g0245 | 2 | NA18612.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.423-3245C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772384 | ||||||
chr5:112772455
|
C | G | 3 | a0001c0007t0004g0118a0001c0007t0004g0119a0001c0007t0004g0120 | 3 | HG01081.hp1 HG01106.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.423-3174C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772455 | ||||||
chr5:112772472
|
C | T | 12 | a0001c0003t0002g0138a0001c0003t0002g0151a0001c0003t0006g0140others(9): Show | 12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.423-3157C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772472 | ||||||
chr5:112772516
|
C | CT | 12 | a0001c0001t0001g0238a0001c0003t0002g0151a0001c0003t0006g0140others(9): Show | 12 | HG00741.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.423-3095dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112772516 | |||||
chr5:112772516
|
CT | C | 28 | a0001c0001t0001g0122a0001c0001t0001g0193a0001c0001t0001g0204others(25): Show | 28 | HG00639.hp2 HG00733.hp2 HG01081.hp1 others(25): Show |
intron_variant | MODIFIER | c.423-3095delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112772516 | |||||
chr5:112772539
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.423-3090C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772539 | ||||||
chr5:112772564
|
T | C | 2 | a0001c0010t0007g0132a0001c0014t0007g0133 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.423-3065T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772564 | ||||||
chr5:112772672
|
G | A | 15 | a0001c0003t0002g0138a0001c0003t0002g0150a0001c0003t0002g0151others(12): Show | 15 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.423-2957G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772672 | ||||||
chr5:112772737
|
G | A | 4 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(1): Show | 4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-2892G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772737 | ||||||
chr5:112772761
|
C | T | 1 | a0001c0010t0007g0132 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.423-2868C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772761 | ||||||
chr5:112772806
|
C | A | 1 | a0001c0003t0002g0079 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.423-2823C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772806 | ||||||
chr5:112772860
|
GAA | G | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-2767_423-2766d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112772860 | |||||
chr5:112772863
|
A | T | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.423-2766A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772863 | ||||||
chr5:112772889
|
C | G | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.423-2740C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772889 | ||||||
chr5:112772984
|
C | G | 1 | a0001c0029t0002g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.423-2645C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112772984 | ||||||
chr5:112773156
|
A | G | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.423-2473A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773156 | ||||||
chr5:112773168
|
T | C | 111 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(108): Show | 111 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(108): Show |
intron_variant | MODIFIER | c.423-2461T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773168 | ||||||
chr5:112773308
|
A | G | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.423-2321A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773308 | ||||||
chr5:112773375
|
C | G | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.423-2254C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773375 | ||||||
chr5:112773497
|
G | C | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.423-2132G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773497 | ||||||
chr5:112773504
|
A | G | 2 | a0001c0002t0009g0125a0001c0002t0009g0131 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.423-2125A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773504 | ||||||
chr5:112773619
|
T | C | 2 | a0001c0002t0004g0025a0011c0023t0004g0026 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.423-2010T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112773619 | ||||||
chr5:112774082
|
G | C | 182 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(179): Show | 184 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(181): Show |
intron_variant | MODIFIER | c.423-1547G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774082 | ||||||
chr5:112774306
|
A | G | 16 | a0001c0001t0001g0275a0001c0001t0001g0276a0001c0001t0001g0277others(13): Show | 16 | HG00673.hp2 HG01981.hp1 HG01993.hp2 others(13): Show |
intron_variant | MODIFIER | c.423-1323A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774306 | ||||||
chr5:112774371
|
A | G | 2 | a0001c0008t0002g0130a0001c0030t0002g0129 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.423-1258A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774371 | ||||||
chr5:112774375
|
A | G | 3 | a0001c0002t0005g0126a0001c0002t0005g0127a0001c0002t0005g0128 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.423-1254A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774375 | ||||||
chr5:112774464
|
A | AT | 17 | a0001c0001t0001g0209a0001c0001t0001g0279a0001c0001t0004g0116others(14): Show | 17 | HG00609.hp1 HG00733.hp1 HG01081.hp2 others(14): Show |
intron_variant | MODIFIER | c.423-1145dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112774464 | |||||
chr5:112774464
|
A | ATT | 90 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(87): Show | 90 | HG00609.hp2 HG00642.hp2 HG00673.hp1 others(87): Show |
intron_variant | MODIFIER | c.423-1146_423-1145d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112774464 | |||||
chr5:112774464
|
A | ATTT | 9 | a0001c0001t0001g0237a0001c0001t0001g0238a0001c0001t0001g0241others(6): Show | 9 | HG00639.hp1 HG01358.hp2 HG01361.hp2 others(6): Show |
intron_variant | MODIFIER | c.423-1147_423-1145d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112774464 | |||||
chr5:112774637
|
T | C | 1 | a0001c0001t0001g0109 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.423-992T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774637 | ||||||
chr5:112774677
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.423-952A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774677 | ||||||
chr5:112774736
|
C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.423-893C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774736 | ||||||
chr5:112774963
|
G | A | 31 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(28): Show | 33 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(30): Show |
intron_variant | MODIFIER | c.423-666G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774963 | ||||||
chr5:112774965
|
G | C | 1 | a0001c0001t0001g0258 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.423-664G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112774965 | ||||||
chr5:112775125
|
G | A | 1 | a0001c0002t0003g0158 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.423-504G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112775125 | ||||||
chr5:112775373
|
G | A | 286 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(283): Show | 288 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.423-256G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112775373 | ||||||
chr5:112775459
|
A | G | 2 | a0001c0008t0002g0112a0012c0028t0002g0113 | 2 | HG02922.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.423-170A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112775459 | ||||||
chr5:112775494
|
T | A | 1 | a0001c0010t0007g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.423-135T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | chr5 | 112775494 | ||||||
chr5:112775605
|
C | CT | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.423-17dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112775605 | |||||
chr5:112775612
|
TA | T | 11 | a0001c0001t0001g0204a0001c0003t0002g0056a0001c0003t0002g0062others(8): Show | 11 | HG01243.hp1 HG01515.hp1 HG02293.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.423-4delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr5 | 112775612 | |||||
chr5:112775958
|
A | G | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.531+221A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112775958 | ||||||
chr5:112776169
|
G | C | 98 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(95): Show | 98 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.531+432G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776169 | ||||||
chr5:112776178
|
C | T | 3 | a0001c0002t0009g0125a0001c0002t0009g0131a0001c0003t0002g0104 | 3 | HG01243.hp2 HG03195.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.531+441C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776178 | ||||||
chr5:112776325
|
C | T | 1 | a0001c0001t0001g0250 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.531+588C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776325 | ||||||
chr5:112776414
|
C | T | 1 | a0001c0003t0002g0150 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.531+677C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776414 | ||||||
chr5:112776416
|
A | G | 6 | a0001c0003t0002g0046a0001c0003t0002g0051a0001c0003t0002g0053others(3): Show | 6 | HG02132.hp1 NA18747.hp1 NA18980.hp1 others(3): Show |
intron_variant | MODIFIER | c.531+679A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776416 | ||||||
chr5:112776659
|
G | A | 1 | a0001c0003t0002g0105 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.531+922G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776659 | ||||||
chr5:112776829
|
A | C | 1 | a0001c0007t0004g0120 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.531+1092A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776829 | ||||||
chr5:112776862
|
T | TA | 38 | a0001c0001t0001g0109a0001c0002t0003g0001a0001c0002t0003g0002others(35): Show | 40 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.531+1136dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112776862 | |||||
chr5:112776870
|
A | T | 6 | a0002c0004t0002g0069a0002c0004t0002g0070a0002c0004t0002g0071others(3): Show | 6 | HG01433.hp1 HG01975.hp1 HG01993.hp1 others(3): Show |
intron_variant | MODIFIER | c.531+1133A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776870 | ||||||
chr5:112776887
|
A | G | 2 | a0001c0001t0001g0201a0001c0001t0001g0245 | 2 | NA18612.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.531+1150A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776887 | ||||||
chr5:112776895
|
CT | C | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.531+1161delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112776895 | |||||
chr5:112776903
|
G | A | 10 | a0001c0003t0006g0140a0001c0003t0006g0141a0001c0003t0006g0142others(7): Show | 10 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.531+1166G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776903 | ||||||
chr5:112776939
|
A | T | 1 | a0001c0003t0002g0054 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.531+1202A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112776939 | ||||||
chr5:112777158
|
G | A | 38 | a0001c0001t0001g0109a0001c0002t0003g0001a0001c0002t0003g0002others(35): Show | 40 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.531+1421G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777158 | ||||||
chr5:112777254
|
T | C | 31 | a0001c0002t0008g0184a0001c0002t0008g0185a0001c0003t0002g0004others(28): Show | 31 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.531+1517T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777254 | ||||||
chr5:112777415
|
A | G | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.531+1678A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777415 | ||||||
chr5:112777500
|
T | C | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+1763T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777500 | ||||||
chr5:112777559
|
A | G | 2 | a0001c0002t0004g0025a0011c0023t0004g0026 | 2 | HG02647.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.531+1822A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777559 | ||||||
chr5:112777730
|
T | C | 12 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(9): Show | 12 | HG01081.hp1 HG01106.hp2 HG01361.hp1 others(9): Show |
intron_variant | MODIFIER | c.531+1993T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777730 | ||||||
chr5:112777830
|
A | T | 102 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(99): Show | 102 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.531+2093A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777830 | ||||||
chr5:112777981
|
G | A | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.531+2244G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112777981 | ||||||
chr5:112778038
|
C | T | 101 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(98): Show | 101 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(98): Show |
intron_variant | MODIFIER | c.531+2301C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778038 | ||||||
chr5:112778063
|
T | C | 218 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(215): Show | 220 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(217): Show |
intron_variant | MODIFIER | c.531+2326T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778063 | ||||||
chr5:112778075
|
G | A | 101 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(98): Show | 101 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.531+2338G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778075 | ||||||
chr5:112778236
|
C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.531+2499C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778236 | ||||||
chr5:112778262
|
T | A | 13 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(10): Show | 13 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.531+2525T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778262 | ||||||
chr5:112778307
|
C | A | 1 | a0008c0022t0003g0175 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.532-2483C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778307 | ||||||
chr5:112778309
|
A | C | 1 | a0001c0001t0004g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.532-2481A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778309 | ||||||
chr5:112778467
|
TA | T | 10 | a0001c0001t0001g0198a0001c0001t0001g0204a0001c0001t0001g0271others(7): Show | 10 | HG01975.hp1 HG02622.hp2 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.532-2308delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112778467 | |||||
chr5:112778550
|
A | AT | 130 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(127): Show | 130 | HG00609.hp2 HG00639.hp1 HG00673.hp1 others(127): Show |
intron_variant | MODIFIER | c.532-2226dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112778550 | |||||
chr5:112778550
|
A | ATT | 7 | a0001c0001t0001g0225a0001c0001t0001g0230a0001c0001t0001g0231others(4): Show | 7 | HG00642.hp2 HG01074.hp1 HG02071.hp2 others(4): Show |
intron_variant | MODIFIER | c.532-2227_532-2226d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112778550 | |||||
chr5:112778551
|
T | A | 1 | a0001c0003t0002g0104 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.532-2239T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778551 | ||||||
chr5:112778681
|
G | A | 1 | a0001c0002t0004g0013 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.532-2109G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112778681 | ||||||
chr5:112778688
|
A | AGGC | 185 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(182): Show | 187 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(184): Show |
intron_variant | MODIFIER | c.532-2101_532-2100i others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112778688 | |||||
chr5:112779034
|
A | T | 1 | a0001c0010t0007g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.532-1756A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779034 | ||||||
chr5:112779641
|
T | G | 2 | a0001c0002t0003g0161a0001c0002t0003g0162 | 2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.532-1149T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779641 | ||||||
chr5:112779652
|
A | G | 1 | a0003c0006t0001g0262 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.532-1138A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779652 | ||||||
chr5:112779660
|
A | G | 1 | a0001c0002t0003g0159 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.532-1130A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779660 | ||||||
chr5:112779667
|
A | AT | 44 | a0001c0001t0001g0109a0001c0001t0001g0286a0001c0002t0001g0288others(41): Show | 46 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.532-1111dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr5 | 112779667 | |||||
chr5:112779726
|
T | G | 1 | a0001c0001t0001g0214 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.532-1064T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779726 | ||||||
chr5:112779794
|
G | T | 3 | a0001c0002t0005g0126a0001c0002t0005g0127a0001c0002t0005g0128 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.532-996G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779794 | ||||||
chr5:112779795
|
C | T | 3 | a0001c0002t0005g0126a0001c0002t0005g0127a0001c0002t0005g0128 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.532-995C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779795 | ||||||
chr5:112779870
|
C | T | 1 | a0001c0002t0003g0110 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.532-920C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779870 | ||||||
chr5:112779945
|
A | G | 3 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0287 | 3 | HG00639.hp1 HG01358.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.532-845A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112779945 | ||||||
chr5:112780046
|
G | T | 10 | a0001c0008t0002g0095a0001c0008t0002g0112a0001c0008t0002g0130others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.532-744G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112780046 | ||||||
chr5:112780327
|
C | T | 135 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(132): Show | 135 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(132): Show |
intron_variant | MODIFIER | c.532-463C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112780327 | ||||||
chr5:112780372
|
G | A | 188 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(185): Show | 190 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(187): Show |
intron_variant | MODIFIER | c.532-418G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112780372 | ||||||
chr5:112780406
|
T | C | 3 | a0001c0007t0004g0118a0001c0007t0004g0119a0001c0007t0004g0120 | 3 | HG01081.hp1 HG01106.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.532-384T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112780406 | ||||||
chr5:112780758
|
T | C | 2 | a0001c0008t0002g0130a0001c0030t0002g0129 | 2 | HG01891.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.532-32T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 5/15 | chr5 | 112780758 | ||||||
chr5:112780935
|
C | T | 9 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(6): Show | 9 | HG01081.hp1 HG01106.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.645+32C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112780935 | ||||||
chr5:112780953
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.645+50A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112780953 | ||||||
chr5:112780964
|
C | T | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+61C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112780964 | ||||||
chr5:112780981
|
A | G | 1 | a0002c0004t0002g0088 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.645+78A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112780981 | ||||||
chr5:112781032
|
A | C | 29 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(26): Show | 29 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.645+129A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781032 | ||||||
chr5:112781076
|
A | G | 104 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(101): Show | 104 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.645+173A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781076 | ||||||
chr5:112781213
|
C | T | 1 | a0003c0006t0001g0248 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.645+310C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781213 | ||||||
chr5:112781526
|
G | T | 2 | a0001c0002t0003g0001a0014c0021t0003g0166 | 3 | HG00408.hp1 NA18983.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.645+623G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781526 | ||||||
chr5:112781549
|
A | G | 1 | a0001c0003t0002g0030 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.645+646A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781549 | ||||||
chr5:112781763
|
A | AT | 49 | a0001c0001t0001g0109a0001c0001t0001g0282a0001c0001t0001g0286others(46): Show | 51 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(48): Show |
intron_variant | MODIFIER | c.645+875dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112781763 | |||||
chr5:112781763
|
AT | A | 13 | a0001c0001t0001g0233a0001c0001t0001g0250a0001c0003t0006g0140others(10): Show | 13 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.645+875delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112781763 | |||||
chr5:112781831
|
G | C | 2 | a0001c0001t0001g0200a0001c0001t0001g0210 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.645+928G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781831 | ||||||
chr5:112781852
|
C | T | 1 | a0001c0002t0003g0177 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.645+949C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781852 | ||||||
chr5:112781902
|
C | T | 9 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(6): Show | 9 | HG01081.hp1 HG01106.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.645+999C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781902 | ||||||
chr5:112781934
|
A | G | 3 | a0001c0001t0001g0207a0001c0001t0001g0229a0009c0017t0001g0196 | 3 | NA18948.hp2 NA18980.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.645+1031A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781934 | ||||||
chr5:112781935
|
T | C | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.645+1032T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781935 | ||||||
chr5:112781981
|
G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.645+1078G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112781981 | ||||||
chr5:112782074
|
G | A | 1 | a0001c0002t0003g0162 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.645+1171G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782074 | ||||||
chr5:112782077
|
G | A | 8 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(5): Show | 8 | HG02258.hp2 HG02559.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.645+1174G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782077 | ||||||
chr5:112782194
|
A | G | 12 | a0001c0003t0002g0138a0001c0003t0002g0151a0001c0003t0006g0140others(9): Show | 12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.645+1291A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782194 | ||||||
chr5:112782244
|
C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.645+1341C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782244 | ||||||
chr5:112782276
|
C | T | 9 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(6): Show | 9 | HG01081.hp1 HG01106.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.645+1373C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782276 | ||||||
chr5:112782482
|
A | G | 1 | a0001c0003t0002g0068 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.645+1579A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782482 | ||||||
chr5:112782498
|
G | A | 175 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(172): Show | 177 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(174): Show |
intron_variant | MODIFIER | c.645+1595G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782498 | ||||||
chr5:112782556
|
T | G | 1 | a0001c0001t0001g0250 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.645+1653T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782556 | ||||||
chr5:112782582
|
C | T | 1 | a0006c0012t0002g0097 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.645+1679C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782582 | ||||||
chr5:112782583
|
G | A | 1 | a0001c0002t0003g0181 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.645+1680G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782583 | ||||||
chr5:112782641
|
G | A | 79 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(76): Show | 79 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(76): Show |
intron_variant | MODIFIER | c.645+1738G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782641 | ||||||
chr5:112782766
|
A | G | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.645+1863A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782766 | ||||||
chr5:112782852
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.645+1949T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782852 | ||||||
chr5:112782857
|
A | T | 1 | a0001c0001t0004g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.645+1954A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112782857 | ||||||
chr5:112783050
|
G | T | 1 | a0002c0004t0002g0045 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.645+2147G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783050 | ||||||
chr5:112783094
|
G | A | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.645+2191G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783094 | ||||||
chr5:112783225
|
T | A | 1 | a0001c0001t0001g0263 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.645+2322T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783225 | ||||||
chr5:112783259
|
C | T | 95 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(92): Show | 95 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.645+2356C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783259 | ||||||
chr5:112783378
|
A | G | 1 | a0001c0002t0005g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.645+2475A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783378 | ||||||
chr5:112783435
|
T | G | 29 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(26): Show | 29 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.645+2532T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783435 | ||||||
chr5:112783510
|
A | C | 44 | a0001c0001t0001g0109a0001c0001t0001g0241a0001c0001t0001g0286others(41): Show | 46 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(43): Show |
intron_variant | MODIFIER | c.645+2607A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783510 | ||||||
chr5:112783630
|
C | CA | 20 | a0001c0002t0003g0155a0001c0002t0003g0156a0001c0002t0003g0157others(17): Show | 20 | HG01243.hp1 HG02056.hp1 HG02132.hp1 others(17): Show |
intron_variant | MODIFIER | c.645+2745dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112783630 | |||||
chr5:112783765
|
C | CA | 18 | a0001c0001t0004g0116a0001c0002t0003g0001a0001c0002t0003g0155others(15): Show | 19 | HG00408.hp1 HG01243.hp2 HG01891.hp1 others(16): Show |
intron_variant | MODIFIER | c.645+2881dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112783765 | |||||
chr5:112783765
|
CA | C | 32 | a0001c0001t0001g0282a0001c0002t0001g0288a0001c0002t0003g0176others(29): Show | 32 | HG00741.hp2 HG01515.hp1 HG01993.hp2 others(29): Show |
intron_variant | MODIFIER | c.645+2881delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112783765 | |||||
chr5:112783785
|
GAGAA | G | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.645+2889_645+2892d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112783785 | |||||
chr5:112783826
|
C | G | 1 | a0001c0010t0007g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.645+2923C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783826 | ||||||
chr5:112783896
|
A | G | 2 | a0001c0001t0001g0224a0001c0001t0004g0124 | 2 | HG01099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.645+2993A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112783896 | ||||||
chr5:112784460
|
A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.645+3557A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784460 | ||||||
chr5:112784515
|
C | T | 1 | a0001c0003t0002g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.645+3612C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784515 | ||||||
chr5:112784628
|
C | T | 1 | a0001c0002t0008g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.645+3725C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784628 | ||||||
chr5:112784797
|
C | G | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.645+3894C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784797 | ||||||
chr5:112784892
|
C | G | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.645+3989C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784892 | ||||||
chr5:112784913
|
T | C | 1 | a0002c0004t0002g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.645+4010T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784913 | ||||||
chr5:112784944
|
C | A | 1 | a0001c0003t0002g0047 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.645+4041C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112784944 | ||||||
chr5:112785013
|
A | G | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.645+4110A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112785013 | ||||||
chr5:112785557
|
C | T | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.645+4654C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112785557 | ||||||
chr5:112786015
|
A | T | 1 | a0001c0002t0004g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.645+5112A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786015 | ||||||
chr5:112786261
|
G | GT | 41 | a0001c0003t0002g0030a0002c0004t0002g0031a0002c0004t0002g0037others(38): Show | 41 | HG00323.hp2 HG00408.hp2 HG00639.hp2 others(38): Show |
intron_variant | MODIFIER | c.645+5364dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112786261 | |||||
chr5:112786390
|
G | T | 12 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(9): Show | 12 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.645+5487G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786390 | ||||||
chr5:112786687
|
T | G | 1 | a0009c0017t0001g0196 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.646-5759T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786687 | ||||||
chr5:112786835
|
G | C | 103 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(100): Show | 103 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(100): Show |
intron_variant | MODIFIER | c.646-5611G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786835 | ||||||
chr5:112786873
|
C | CCTTTTT | 14 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(11): Show | 14 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.646-5560_646-5555d others(8): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112786873 | |||||
chr5:112786873
|
C | G | 1 | a0001c0003t0006g0144 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.646-5573C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786873 | ||||||
chr5:112786886
|
C | CT | 11 | a0001c0002t0001g0288a0001c0002t0004g0188a0001c0002t0004g0189others(8): Show | 11 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(8): Show |
intron_variant | MODIFIER | c.646-5541dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112786886 | |||||
chr5:112786886
|
C | CTT | 40 | a0001c0001t0001g0241a0001c0001t0001g0286a0001c0002t0001g0289others(37): Show | 42 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.646-5542_646-5541d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112786886 | |||||
chr5:112786890
|
T | C | 1 | a0001c0002t0008g0185 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.646-5556T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786890 | ||||||
chr5:112786906
|
GAGTC | G | 96 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(93): Show | 96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.646-5537_646-5534d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112786906 | |||||
chr5:112786910
|
C | G | 2 | a0001c0001t0001g0205a0001c0001t0001g0257 | 2 | HG01257.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.646-5536C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112786910 | ||||||
chr5:112787168
|
G | A | 17 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(14): Show | 17 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.646-5278G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787168 | ||||||
chr5:112787169
|
T | C | 1 | a0001c0003t0002g0051 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.646-5277T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787169 | ||||||
chr5:112787184
|
G | A | 1 | a0013c0024t0003g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.646-5262G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787184 | ||||||
chr5:112787312
|
G | A | 1 | a0001c0001t0001g0263 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.646-5134G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787312 | ||||||
chr5:112787329
|
A | G | 1 | a0001c0027t0004g0020 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.646-5117A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787329 | ||||||
chr5:112787339
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.646-5107A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787339 | ||||||
chr5:112787448
|
TTCTG | T | 39 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(36): Show | 39 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.646-4996_646-4993d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112787448 | |||||
chr5:112787472
|
G | C | 1 | a0001c0002t0003g0162 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.646-4974G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787472 | ||||||
chr5:112787542
|
C | G | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.646-4904C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787542 | ||||||
chr5:112787967
|
CAT | C | 13 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(10): Show | 13 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.646-4478_646-4477d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787967 | ||||||
chr5:112787993
|
G | A | 1 | a0004c0009t0002g0100 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.646-4453G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112787993 | ||||||
chr5:112788309
|
A | T | 2 | a0001c0001t0001g0224a0001c0001t0004g0124 | 2 | HG01099.hp1 HG01358.hp1 |
intron_variant | MODIFIER | c.646-4137A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788309 | ||||||
chr5:112788415
|
A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.646-4031A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788415 | ||||||
chr5:112788509
|
A | C | 1 | a0001c0002t0003g0176 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.646-3937A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788509 | ||||||
chr5:112788522
|
A | G | 33 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(30): Show | 33 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(30): Show |
intron_variant | MODIFIER | c.646-3924A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788522 | ||||||
chr5:112788590
|
A | G | 1 | a0002c0004t0002g0082 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.646-3856A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788590 | ||||||
chr5:112788672
|
T | C | 218 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(215): Show | 220 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(217): Show |
intron_variant | MODIFIER | c.646-3774T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788672 | ||||||
chr5:112788708
|
C | T | 2 | a0002c0004t0002g0031a0007c0032t0002g0032 | 2 | HG00323.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.646-3738C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788708 | ||||||
chr5:112788783
|
G | C | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-3663G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788783 | ||||||
chr5:112788847
|
A | G | 2 | a0001c0002t0003g0186a0001c0002t0003g0187 | 2 | NA19074.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.646-3599A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788847 | ||||||
chr5:112788883
|
A | G | 1 | a0001c0001t0001g0226 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.646-3563A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112788883 | ||||||
chr5:112789031
|
G | A | 1 | a0001c0003t0002g0066 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.646-3415G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789031 | ||||||
chr5:112789080
|
A | G | 1 | a0001c0031t0002g0074 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.646-3366A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789080 | ||||||
chr5:112789100
|
A | T | 1 | a0001c0001t0001g0239 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.646-3346A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789100 | ||||||
chr5:112789217
|
A | G | 1 | a0001c0003t0002g0086 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.646-3229A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789217 | ||||||
chr5:112789365
|
A | G | 3 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232 | 3 | HG00642.hp2 HG01074.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.646-3081A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789365 | ||||||
chr5:112789600
|
T | A | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.646-2846T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789600 | ||||||
chr5:112789615
|
G | A | 1 | a0001c0002t0015g0191 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.646-2831G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789615 | ||||||
chr5:112789722
|
A | G | 90 | a0001c0001t0001g0122a0001c0001t0001g0286a0001c0001t0004g0116others(87): Show | 92 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(89): Show |
intron_variant | MODIFIER | c.646-2724A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789722 | ||||||
chr5:112789857
|
A | AT | 28 | a0001c0001t0001g0109a0001c0001t0001g0249a0001c0001t0001g0250others(25): Show | 28 | HG00323.hp1 HG00673.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.646-2576dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112789857 | |||||
chr5:112789857
|
AT | A | 38 | a0001c0001t0001g0272a0001c0001t0004g0124a0001c0002t0003g0001others(35): Show | 40 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.646-2576delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112789857 | |||||
chr5:112789946
|
G | A | 16 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(13): Show | 16 | HG02132.hp1 HG02155.hp2 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.646-2500G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789946 | ||||||
chr5:112789996
|
A | G | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.646-2450A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112789996 | ||||||
chr5:112790000
|
C | T | 7 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.646-2446C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112790000 | ||||||
chr5:112790314
|
T | G | 2 | a0001c0001t0001g0269a0001c0002t0013g0003 | 2 | HG02056.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.646-2132T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112790314 | ||||||
chr5:112790586
|
C | G | 1 | a0001c0001t0001g0285 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.646-1860C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112790586 | ||||||
chr5:112790631
|
G | A | 21 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(18): Show | 21 | HG00741.hp2 HG02132.hp1 HG02155.hp2 others(18): Show |
intron_variant | MODIFIER | c.646-1815G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112790631 | ||||||
chr5:112790648
|
T | C | 40 | a0001c0001t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(37): Show | 42 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.646-1798T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112790648 | ||||||
chr5:112791032
|
CAT | C | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.646-1411_646-1410d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112791032 | |||||
chr5:112791118
|
T | G | 1 | a0001c0002t0004g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.646-1328T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791118 | ||||||
chr5:112791156
|
A | AAC | 4 | a0001c0002t0005g0126a0001c0002t0005g0127a0001c0002t0005g0128others(1): Show | 4 | HG02257.hp1 HG02280.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-1272_646-1271d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | INFO_REALIGN_3_PRIME | chr5 | 112791156 | |||||
chr5:112791156
|
A | C | 1 | a0001c0003t0002g0086 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.646-1290A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791156 | ||||||
chr5:112791278
|
C | T | 3 | a0001c0001t0001g0122a0001c0001t0004g0121a0001c0001t0004g0123 | 3 | HG01361.hp1 HG02257.hp2 HG03654.hp2 |
intron_variant | MODIFIER | c.646-1168C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791278 | ||||||
chr5:112791331
|
C | T | 1 | a0002c0004t0002g0044 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.646-1115C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791331 | ||||||
chr5:112791482
|
T | C | 16 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(13): Show | 16 | HG02132.hp1 HG02155.hp2 HG02886.hp2 others(13): Show |
intron_variant | MODIFIER | c.646-964T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791482 | ||||||
chr5:112791566
|
G | T | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.646-880G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791566 | ||||||
chr5:112791633
|
C | T | 2 | a0002c0004t0002g0028a0002c0004t0002g0029 | 2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.646-813C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791633 | ||||||
chr5:112791756
|
G | A | 9 | a0001c0003t0006g0140a0001c0003t0006g0141a0001c0003t0006g0142others(6): Show | 9 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.646-690G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112791756 | ||||||
chr5:112792139
|
G | A | 1 | a0001c0003t0002g0151 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.646-307G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112792139 | ||||||
chr5:112792245
|
C | T | 5 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0164others(2): Show | 5 | HG02071.hp1 NA18612.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.646-201C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 6/15 | chr5 | 112792245 | ||||||
chr5:112792552
|
T | C | 1 | a0001c0002t0004g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.729+23T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792552 | ||||||
chr5:112792617
|
T | C | 12 | a0001c0002t0003g0001a0001c0002t0003g0153a0001c0002t0003g0155others(9): Show | 13 | HG00408.hp1 HG02071.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.729+88T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792617 | ||||||
chr5:112792712
|
C | T | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.729+183C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792712 | ||||||
chr5:112792827
|
T | C | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+298T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792827 | ||||||
chr5:112792867
|
A | G | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.729+338A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792867 | ||||||
chr5:112792960
|
C | T | 1 | a0001c0001t0001g0274 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.729+431C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792960 | ||||||
chr5:112792976
|
A | G | 39 | a0001c0002t0001g0288a0001c0002t0001g0289a0001c0002t0001g0290others(36): Show | 41 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.729+447A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112792976 | ||||||
chr5:112793048
|
C | T | 1 | a0001c0002t0003g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.729+519C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793048 | ||||||
chr5:112793057
|
A | T | 1 | a0001c0003t0002g0101 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.729+528A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793057 | ||||||
chr5:112793146
|
C | T | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.729+617C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793146 | ||||||
chr5:112793373
|
A | G | 14 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(11): Show | 14 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.729+844A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793373 | ||||||
chr5:112793406
|
C | G | 1 | a0001c0029t0002g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.729+877C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793406 | ||||||
chr5:112793497
|
AC | A | 194 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(191): Show | 196 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(193): Show |
intron_variant | MODIFIER | c.729+969delC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793497 | ||||||
chr5:112793532
|
A | C | 1 | a0001c0001t0001g0253 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.729+1003A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793532 | ||||||
chr5:112793968
|
C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.729+1439C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793968 | ||||||
chr5:112793988
|
G | C | 2 | a0001c0001t0004g0246a0001c0001t0004g0247 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.729+1459G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112793988 | ||||||
chr5:112794042
|
TA | T | 29 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(26): Show | 29 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.729+1527delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr5 | 112794042 | |||||
chr5:112794056
|
AG | A | 177 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(174): Show | 179 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(176): Show |
intron_variant | MODIFIER | c.729+1529delG | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr5 | 112794056 | |||||
chr5:112794057
|
G | A | 3 | a0001c0001t0001g0205a0001c0001t0001g0282a0001c0002t0003g0163 | 3 | HG01257.hp2 HG01993.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.729+1528G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794057 | ||||||
chr5:112794183
|
C | G | 2 | a0001c0001t0001g0236a0001c0001t0001g0237 | 2 | HG02071.hp2 HG02132.hp2 |
intron_variant | MODIFIER | c.729+1654C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794183 | ||||||
chr5:112794265
|
G | A | 1 | a0002c0004t0002g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.729+1736G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794265 | ||||||
chr5:112794271
|
A | G | 14 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(11): Show | 14 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.729+1742A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794271 | ||||||
chr5:112794362
|
G | A | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.729+1833G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794362 | ||||||
chr5:112794378
|
C | A | 1 | a0001c0016t0001g0242 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.729+1849C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794378 | ||||||
chr5:112794389
|
C | A | 199 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(196): Show | 201 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(198): Show |
intron_variant | MODIFIER | c.729+1860C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794389 | ||||||
chr5:112794415
|
A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.729+1886A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794415 | ||||||
chr5:112794449
|
A | G | 10 | a0001c0008t0002g0095a0001c0008t0002g0112a0001c0008t0002g0130others(7): Show | 10 | HG01243.hp1 HG01891.hp1 HG02486.hp2 others(7): Show |
intron_variant | MODIFIER | c.729+1920A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794449 | ||||||
chr5:112794580
|
C | T | 5 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0022others(2): Show | 5 | HG01884.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.729+2051C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794580 | ||||||
chr5:112794749
|
T | C | 3 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007 | 3 | HG02486.hp1 HG02559.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.729+2220T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794749 | ||||||
chr5:112794755
|
C | G | 1 | a0007c0032t0002g0032 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.729+2226C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112794755 | ||||||
chr5:112795058
|
G | T | 12 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(9): Show | 12 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.729+2529G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112795058 | ||||||
chr5:112795278
|
G | A | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.729+2749G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112795278 | ||||||
chr5:112795323
|
G | A | 2 | a0002c0004t0002g0087a0002c0004t0002g0088 | 2 | NA19010.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.729+2794G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112795323 | ||||||
chr5:112795522
|
A | G | 23 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(20): Show | 23 | HG01081.hp1 HG01106.hp2 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.729+2993A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112795522 | ||||||
chr5:112795591
|
A | G | 113 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(110): Show | 113 | HG00323.hp1 HG00609.hp2 HG00639.hp1 others(110): Show |
intron_variant | MODIFIER | c.729+3062A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112795591 | ||||||
chr5:112795812
|
G | C | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.729+3283G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112795812 | ||||||
chr5:112796006
|
C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.729+3477C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112796006 | ||||||
chr5:112796090
|
A | G | 105 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(102): Show | 105 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(102): Show |
intron_variant | MODIFIER | c.729+3561A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112796090 | ||||||
chr5:112796262
|
A | G | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.729+3733A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112796262 | ||||||
chr5:112796367
|
C | A | 1 | a0001c0002t0003g0169 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.729+3838C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112796367 | ||||||
chr5:112797010
|
T | A | 3 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0001g0292 | 3 | NA18953.hp2 NA18974.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.730-4269T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797010 | ||||||
chr5:112797139
|
C | T | 1 | a0011c0023t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.730-4140C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797139 | ||||||
chr5:112797202
|
T | G | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.730-4077T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797202 | ||||||
chr5:112797251
|
A | G | 17 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(14): Show | 17 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(14): Show |
intron_variant | MODIFIER | c.730-4028A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797251 | ||||||
chr5:112797267
|
AT | A | 4 | a0001c0003t0002g0056a0001c0003t0002g0058a0001c0003t0002g0059others(1): Show | 4 | HG01106.hp1 HG01169.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.730-4008delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr5 | 112797267 | |||||
chr5:112797311
|
A | C | 1 | a0001c0001t0001g0238 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.730-3968A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797311 | ||||||
chr5:112797393
|
T | C | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.730-3886T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797393 | ||||||
chr5:112797441
|
A | G | 28 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(25): Show | 28 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(25): Show |
intron_variant | MODIFIER | c.730-3838A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797441 | ||||||
chr5:112797487
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.730-3792T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797487 | ||||||
chr5:112797494
|
T | C | 1 | a0001c0002t0009g0131 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.730-3785T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797494 | ||||||
chr5:112797499
|
G | C | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-3780G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797499 | ||||||
chr5:112797787
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.730-3492G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112797787 | ||||||
chr5:112798150
|
A | G | 2 | a0006c0012t0002g0096a0006c0012t0002g0097 | 2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.730-3129A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798150 | ||||||
chr5:112798345
|
G | A | 14 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0023others(11): Show | 14 | HG01243.hp1 HG01884.hp2 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.730-2934G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798345 | ||||||
chr5:112798480
|
A | G | 1 | a0001c0003t0002g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.730-2799A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798480 | ||||||
chr5:112798660
|
T | C | 1 | a0001c0003t0002g0067 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.730-2619T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798660 | ||||||
chr5:112798931
|
C | T | 12 | a0001c0003t0002g0138a0001c0003t0002g0151a0001c0003t0006g0140others(9): Show | 12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.730-2348C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798931 | ||||||
chr5:112798946
|
A | C | 1 | a0001c0001t0001g0214 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.730-2333A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798946 | ||||||
chr5:112798983
|
G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.730-2296G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112798983 | ||||||
chr5:112799133
|
G | A | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.730-2146G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799133 | ||||||
chr5:112799140
|
C | T | 86 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(83): Show | 88 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(85): Show |
intron_variant | MODIFIER | c.730-2139C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799140 | ||||||
chr5:112799183
|
C | CA | 154 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0194others(151): Show | 155 | HG00609.hp1 HG00609.hp2 HG00639.hp1 others(152): Show |
intron_variant | MODIFIER | c.730-2075dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr5 | 112799183 | |||||
chr5:112799183
|
C | CAA | 32 | a0001c0001t0001g0203a0001c0001t0001g0206a0001c0001t0001g0241others(29): Show | 33 | HG00408.hp1 HG00741.hp2 HG01243.hp2 others(30): Show |
intron_variant | MODIFIER | c.730-2076_730-2075d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr5 | 112799183 | |||||
chr5:112799206
|
G | A | 36 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(33): Show | 36 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(33): Show |
intron_variant | MODIFIER | c.730-2073G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799206 | ||||||
chr5:112799255
|
C | G | 1 | a0001c0003t0002g0050 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.730-2024C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799255 | ||||||
chr5:112799370
|
T | C | 289 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(286): Show | 291 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.730-1909T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799370 | ||||||
chr5:112799393
|
G | A | 104 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(101): Show | 104 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(101): Show |
intron_variant | MODIFIER | c.730-1886G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799393 | ||||||
chr5:112799425
|
C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.730-1854C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799425 | ||||||
chr5:112799429
|
C | T | 7 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.730-1850C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799429 | ||||||
chr5:112799484
|
T | C | 24 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(21): Show | 24 | HG01081.hp1 HG01106.hp2 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.730-1795T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799484 | ||||||
chr5:112799498
|
A | G | 1 | a0001c0002t0008g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.730-1781A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799498 | ||||||
chr5:112799529
|
T | C | 15 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(12): Show | 15 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.730-1750T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799529 | ||||||
chr5:112799647
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.730-1632A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799647 | ||||||
chr5:112799800
|
C | T | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.730-1479C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799800 | ||||||
chr5:112799802
|
T | A | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.730-1477T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799802 | ||||||
chr5:112799829
|
C | G | 2 | a0003c0006t0001g0261a0003c0006t0001g0262 | 2 | HG02109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.730-1450C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799829 | ||||||
chr5:112799866
|
C | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.730-1413C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112799866 | ||||||
chr5:112800040
|
A | G | 102 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(99): Show | 102 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.730-1239A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800040 | ||||||
chr5:112800194
|
T | TA | 7 | a0001c0008t0002g0112a0004c0009t0002g0098a0004c0009t0002g0099others(4): Show | 7 | HG01243.hp1 HG02486.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.730-1082dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr5 | 112800194 | |||||
chr5:112800235
|
T | C | 1 | a0001c0014t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.730-1044T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800235 | ||||||
chr5:112800278
|
G | A | 50 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(47): Show | 50 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(47): Show |
intron_variant | MODIFIER | c.730-1001G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800278 | ||||||
chr5:112800507
|
A | G | 102 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(99): Show | 102 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(99): Show |
intron_variant | MODIFIER | c.730-772A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800507 | ||||||
chr5:112800542
|
T | C | 14 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(11): Show | 14 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.730-737T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800542 | ||||||
chr5:112800618
|
T | C | 9 | a0001c0003t0006g0140a0001c0003t0006g0141a0001c0003t0006g0142others(6): Show | 9 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(6): Show |
intron_variant | MODIFIER | c.730-661T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800618 | ||||||
chr5:112800809
|
C | T | 1 | a0001c0002t0003g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.730-470C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800809 | ||||||
chr5:112800865
|
C | A | 1 | a0001c0002t0008g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.730-414C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112800865 | ||||||
chr5:112801040
|
A | G | 1 | a0001c0001t0001g0227 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.730-239A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112801040 | ||||||
chr5:112801250
|
A | T | 7 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.730-29A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 7/15 | chr5 | 112801250 | ||||||
chr5:112801638
|
G | GT | 13 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(10): Show | 13 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.834+263dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112801638 | |||||
chr5:112801652
|
C | A | 7 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(4): Show | 7 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.834+269C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112801652 | ||||||
chr5:112801663
|
A | G | 1 | a0001c0031t0002g0074 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.834+280A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112801663 | ||||||
chr5:112802008
|
A | C | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.834+625A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802008 | ||||||
chr5:112802492
|
G | A | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+1109G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802492 | ||||||
chr5:112802530
|
A | G | 1 | a0001c0014t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.834+1147A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802530 | ||||||
chr5:112802667
|
A | G | 1 | a0001c0008t0002g0095 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.834+1284A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802667 | ||||||
chr5:112802676
|
A | G | 2 | a0001c0002t0009g0125a0001c0002t0009g0131 | 2 | HG01243.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.834+1293A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802676 | ||||||
chr5:112802736
|
A | G | 1 | a0001c0001t0001g0256 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.834+1353A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802736 | ||||||
chr5:112802845
|
A | G | 17 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(14): Show | 17 | HG01081.hp1 HG01106.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.834+1462A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802845 | ||||||
chr5:112802870
|
A | T | 5 | a0001c0003t0002g0101a0001c0003t0002g0103a0001c0003t0002g0104others(2): Show | 5 | HG02818.hp2 HG03041.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.834+1487A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112802870 | ||||||
chr5:112803037
|
G | A | 217 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(214): Show | 219 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(216): Show |
intron_variant | MODIFIER | c.834+1654G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803037 | ||||||
chr5:112803046
|
A | T | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+1663A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803046 | ||||||
chr5:112803094
|
G | T | 1 | a0001c0003t0002g0047 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.834+1711G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803094 | ||||||
chr5:112803161
|
T | G | 1 | a0001c0003t0002g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.834+1778T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803161 | ||||||
chr5:112803191
|
G | C | 181 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(178): Show | 183 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(180): Show |
intron_variant | MODIFIER | c.834+1808G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803191 | ||||||
chr5:112803308
|
A | T | 8 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(5): Show | 8 | HG01358.hp1 HG01361.hp1 HG01981.hp2 others(5): Show |
intron_variant | MODIFIER | c.834+1925A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803308 | ||||||
chr5:112803365
|
A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.834+1982A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803365 | ||||||
chr5:112803401
|
A | G | 1 | a0002c0004t0002g0073 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.834+2018A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803401 | ||||||
chr5:112803694
|
G | A | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+2311G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803694 | ||||||
chr5:112803727
|
A | G | 104 | a0001c0001t0001g0122a0001c0001t0001g0254a0001c0001t0001g0255others(101): Show | 106 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(103): Show |
intron_variant | MODIFIER | c.834+2344A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803727 | ||||||
chr5:112803797
|
T | G | 12 | a0001c0003t0002g0138a0001c0003t0002g0151a0001c0003t0006g0140others(9): Show | 12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.834+2414T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803797 | ||||||
chr5:112803846
|
A | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.834+2463A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803846 | ||||||
chr5:112803953
|
A | G | 1 | a0001c0001t0001g0286 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.834+2570A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803953 | ||||||
chr5:112803990
|
A | G | 12 | a0001c0003t0002g0138a0001c0003t0002g0151a0001c0003t0006g0140others(9): Show | 12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.834+2607A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112803990 | ||||||
chr5:112804048
|
A | G | 101 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(98): Show | 101 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(98): Show |
intron_variant | MODIFIER | c.834+2665A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804048 | ||||||
chr5:112804068
|
A | G | 1 | a0002c0025t0002g0065 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.834+2685A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804068 | ||||||
chr5:112804211
|
G | A | 1 | a0001c0002t0008g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.834+2828G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804211 | ||||||
chr5:112804325
|
A | G | 32 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(29): Show | 32 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.834+2942A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804325 | ||||||
chr5:112804335
|
G | C | 2 | a0001c0003t0002g0048a0001c0019t0002g0078 | 2 | HG02056.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.834+2952G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804335 | ||||||
chr5:112804390
|
A | G | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.834+3007A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804390 | ||||||
chr5:112804415
|
G | A | 1 | a0001c0003t0002g0068 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.834+3032G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804415 | ||||||
chr5:112804538
|
C | G | 12 | a0001c0003t0002g0138a0001c0003t0002g0151a0001c0003t0006g0140others(9): Show | 12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.834+3155C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804538 | ||||||
chr5:112804610
|
C | T | 1 | a0001c0002t0003g0153 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.834+3227C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804610 | ||||||
chr5:112804671
|
C | T | 1 | a0001c0002t0008g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.834+3288C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804671 | ||||||
chr5:112804685
|
A | C | 1 | a0001c0002t0008g0184 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.834+3302A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804685 | ||||||
chr5:112804772
|
T | C | 14 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0208others(11): Show | 14 | HG01071.hp1 HG01975.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.834+3389T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804772 | ||||||
chr5:112804873
|
T | G | 2 | a0001c0001t0001g0199a0001c0001t0001g0244 | 2 | NA18981.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.834+3490T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804873 | ||||||
chr5:112804879
|
G | A | 1 | a0001c0001t0001g0274 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.834+3496G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112804879 | ||||||
chr5:112805052
|
A | G | 8 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0211others(5): Show | 8 | HG01071.hp1 HG01975.hp2 HG02293.hp2 others(5): Show |
intron_variant | MODIFIER | c.834+3669A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805052 | ||||||
chr5:112805075
|
A | G | 11 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.834+3692A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805075 | ||||||
chr5:112805244
|
T | C | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+3861T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805244 | ||||||
chr5:112805417
|
C | G | 2 | a0002c0004t0002g0031a0007c0032t0002g0032 | 2 | HG00323.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.834+4034C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805417 | ||||||
chr5:112805456
|
G | A | 14 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(11): Show | 14 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.834+4073G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805456 | ||||||
chr5:112805602
|
T | C | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.834+4219T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805602 | ||||||
chr5:112805699
|
T | C | 1 | a0001c0002t0003g0168 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.834+4316T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805699 | ||||||
chr5:112805853
|
T | C | 1 | a0001c0002t0003g0159 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.834+4470T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805853 | ||||||
chr5:112805969
|
A | G | 2 | a0001c0003t0002g0048a0001c0019t0002g0078 | 2 | HG02056.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.834+4586A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112805969 | ||||||
chr5:112806012
|
C | G | 1 | a0001c0002t0003g0181 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.834+4629C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806012 | ||||||
chr5:112806116
|
G | A | 13 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(10): Show | 13 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.834+4733G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806116 | ||||||
chr5:112806124
|
C | T | 1 | a0001c0002t0003g0181 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.834+4741C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806124 | ||||||
chr5:112806206
|
G | A | 1 | a0001c0003t0002g0060 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.834+4823G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806206 | ||||||
chr5:112806339
|
T | C | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+4956T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806339 | ||||||
chr5:112806349
|
C | G | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+4966C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806349 | ||||||
chr5:112806552
|
C | CTTTA | 58 | a0001c0001t0001g0122a0001c0001t0001g0201a0001c0001t0001g0204others(55): Show | 58 | HG00609.hp1 HG00642.hp1 HG01074.hp2 others(55): Show |
intron_variant | MODIFIER | c.834+5208_834+5211d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112806552 | |||||
chr5:112806552
|
C | CTTTATTT others(1): Show |
16 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0155others(13): Show | 18 | HG00408.hp1 HG01243.hp2 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.834+5204_834+5211d others(10): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112806552 | |||||
chr5:112806552
|
C | CTTTATTT others(5): Show |
2 | a0001c0002t0004g0019a0001c0002t0004g0024 | 2 | HG02258.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.834+5200_834+5211d others(14): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112806552 | |||||
chr5:112806552
|
CTTTA | C | 54 | a0001c0001t0001g0263a0001c0001t0001g0276a0001c0001t0001g0278others(51): Show | 54 | HG00323.hp2 HG01081.hp2 HG01106.hp1 others(51): Show |
intron_variant | MODIFIER | c.834+5208_834+5211d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112806552 | |||||
chr5:112806552
|
CTTTATTT others(1): Show |
C | 13 | a0001c0001t0001g0210a0001c0002t0004g0188a0001c0002t0004g0189others(10): Show | 13 | HG00323.hp1 HG00741.hp2 HG01070.hp2 others(10): Show |
intron_variant | MODIFIER | c.834+5204_834+5211d others(10): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112806552 | |||||
chr5:112806552
|
CTTTATTT others(9): Show |
C | 2 | a0001c0010t0007g0132a0001c0014t0007g0133 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.834+5196_834+5211d others(18): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112806552 | |||||
chr5:112806579
|
T | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+5196T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806579 | ||||||
chr5:112806583
|
T | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+5200T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806583 | ||||||
chr5:112806587
|
T | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+5204T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806587 | ||||||
chr5:112806591
|
T | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+5208T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806591 | ||||||
chr5:112806722
|
G | T | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+5339G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806722 | ||||||
chr5:112806962
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.834+5579A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112806962 | ||||||
chr5:112807000
|
G | T | 2 | a0001c0001t0001g0198a0001c0001t0001g0209 | 2 | HG00733.hp1 HG02735.hp2 |
intron_variant | MODIFIER | c.834+5617G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807000 | ||||||
chr5:112807136
|
G | GA | 66 | a0001c0001t0001g0218a0001c0001t0001g0228a0001c0001t0001g0255others(63): Show | 68 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.834+5769dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112807136 | |||||
chr5:112807136
|
G | GAA | 7 | a0001c0002t0003g0172a0001c0002t0005g0126a0001c0002t0005g0127others(4): Show | 7 | HG01243.hp2 HG01891.hp2 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.834+5768_834+5769d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112807136 | |||||
chr5:112807188
|
C | T | 3 | a0001c0003t0002g0035a0001c0003t0002g0036a0001c0029t0002g0033 | 3 | HG02451.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.834+5805C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807188 | ||||||
chr5:112807217
|
C | G | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+5834C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807217 | ||||||
chr5:112807312
|
A | G | 8 | a0001c0002t0003g0154a0001c0002t0003g0168a0001c0002t0003g0171others(5): Show | 8 | HG01074.hp2 HG01891.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+5929A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807312 | ||||||
chr5:112807485
|
A | G | 1 | a0011c0023t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.834+6102A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807485 | ||||||
chr5:112807486
|
T | G | 3 | a0001c0007t0004g0118a0001c0007t0004g0119a0001c0007t0004g0120 | 3 | HG01081.hp1 HG01106.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.834+6103T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807486 | ||||||
chr5:112807503
|
T | C | 1 | a0004c0009t0002g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.834+6120T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807503 | ||||||
chr5:112807542
|
T | C | 1 | a0001c0002t0003g0161 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.834+6159T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807542 | ||||||
chr5:112807584
|
C | T | 1 | a0001c0001t0004g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.834+6201C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807584 | ||||||
chr5:112807924
|
G | A | 1 | a0001c0002t0003g0181 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.834+6541G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112807924 | ||||||
chr5:112808008
|
A | G | 1 | a0001c0001t0001g0259 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.834+6625A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808008 | ||||||
chr5:112808048
|
G | T | 1 | a0001c0002t0003g0181 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.834+6665G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808048 | ||||||
chr5:112808090
|
G | A | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+6707G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808090 | ||||||
chr5:112808124
|
C | T | 14 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(11): Show | 14 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.834+6741C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808124 | ||||||
chr5:112808154
|
C | T | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+6771C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808154 | ||||||
chr5:112808163
|
A | T | 35 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0153others(32): Show | 37 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.834+6780A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808163 | ||||||
chr5:112808326
|
A | G | 105 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(102): Show | 105 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(102): Show |
intron_variant | MODIFIER | c.834+6943A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808326 | ||||||
chr5:112808487
|
A | T | 1 | a0001c0002t0004g0188 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.835-7008A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808487 | ||||||
chr5:112808542
|
G | A | 1 | a0001c0003t0002g0062 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.835-6953G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808542 | ||||||
chr5:112808607
|
C | T | 1 | a0001c0003t0002g0035 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.835-6888C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808607 | ||||||
chr5:112808627
|
G | A | 2 | a0006c0012t0002g0096a0006c0012t0002g0097 | 2 | HG03453.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.835-6868G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808627 | ||||||
chr5:112808714
|
A | C | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.835-6781A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808714 | ||||||
chr5:112808747
|
A | T | 99 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(96): Show | 99 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.835-6748A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112808747 | ||||||
chr5:112809197
|
C | CA | 25 | a0001c0001t0001g0235a0001c0002t0003g0154a0001c0002t0003g0168others(22): Show | 25 | HG00642.hp1 HG01074.hp2 HG01243.hp1 others(22): Show |
intron_variant | MODIFIER | c.835-6283dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112809197 | |||||
chr5:112809257
|
T | C | 214 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(211): Show | 216 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(213): Show |
intron_variant | MODIFIER | c.835-6238T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112809257 | ||||||
chr5:112809564
|
C | A | 96 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(93): Show | 96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.835-5931C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112809564 | ||||||
chr5:112809709
|
G | A | 1 | a0001c0014t0007g0133 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.835-5786G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112809709 | ||||||
chr5:112809767
|
C | T | 1 | a0002c0004t0002g0083 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.835-5728C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112809767 | ||||||
chr5:112810420
|
A | G | 81 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(78): Show | 81 | HG00609.hp2 HG00642.hp2 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.835-5075A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810420 | ||||||
chr5:112810484
|
A | G | 19 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(16): Show | 19 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.835-5011A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810484 | ||||||
chr5:112810500
|
T | G | 99 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(96): Show | 99 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.835-4995T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810500 | ||||||
chr5:112810508
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.835-4987C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810508 | ||||||
chr5:112810540
|
G | A | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.835-4955G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810540 | ||||||
chr5:112810567
|
C | T | 7 | a0001c0003t0002g0046a0001c0003t0002g0048a0001c0003t0002g0053others(4): Show | 7 | HG02132.hp1 NA18747.hp1 NA18954.hp1 others(4): Show |
intron_variant | MODIFIER | c.835-4928C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810567 | ||||||
chr5:112810571
|
A | C | 1 | a0001c0001t0001g0269 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.835-4924A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810571 | ||||||
chr5:112810625
|
G | A | 3 | a0001c0003t0002g0035a0001c0003t0002g0036a0001c0029t0002g0033 | 3 | HG02451.hp2 HG03139.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.835-4870G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810625 | ||||||
chr5:112810647
|
T | TA | 12 | a0001c0001t0001g0206a0001c0001t0001g0208a0001c0001t0001g0211others(9): Show | 12 | HG01071.hp1 HG01975.hp2 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-4848_835-4847i others(3): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810647 | ||||||
chr5:112810686
|
A | C | 1 | a0002c0004t0002g0041 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.835-4809A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810686 | ||||||
chr5:112810879
|
G | A | 4 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(1): Show | 4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-4616G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112810879 | ||||||
chr5:112811023
|
TCA | T | 164 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(161): Show | 166 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(163): Show |
intron_variant | MODIFIER | c.835-4457_835-4456d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112811023 | |||||
chr5:112811040
|
A | C | 7 | a0001c0003t0002g0151a0001c0003t0006g0142a0001c0003t0006g0144others(4): Show | 7 | HG02280.hp2 HG02572.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.835-4455A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112811040 | ||||||
chr5:112811074
|
C | A | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.835-4421C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112811074 | ||||||
chr5:112811402
|
A | G | 11 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.835-4093A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112811402 | ||||||
chr5:112811509
|
G | C | 1 | a0001c0001t0001g0205 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.835-3986G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112811509 | ||||||
chr5:112811684
|
G | T | 1 | a0001c0001t0001g0225 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.835-3811G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112811684 | ||||||
chr5:112811944
|
T | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.835-3551T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112811944 | ||||||
chr5:112812055
|
G | A | 1 | a0001c0002t0003g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.835-3440G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812055 | ||||||
chr5:112812075
|
G | C | 3 | a0001c0002t0003g0171a0001c0002t0003g0172a0001c0002t0003g0173 | 3 | HG01074.hp2 HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.835-3420G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812075 | ||||||
chr5:112812106
|
G | C | 3 | a0001c0002t0003g0171a0001c0002t0003g0172a0001c0002t0003g0173 | 3 | HG01074.hp2 HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.835-3389G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812106 | ||||||
chr5:112812209
|
A | G | 4 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(1): Show | 4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-3286A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812209 | ||||||
chr5:112812252
|
T | C | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.835-3243T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812252 | ||||||
chr5:112812454
|
AT | A | 3 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017 | 3 | HG02559.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.835-3038delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112812454 | |||||
chr5:112812535
|
G | A | 1 | a0001c0002t0005g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.835-2960G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812535 | ||||||
chr5:112812626
|
A | G | 1 | a0001c0001t0001g0228 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.835-2869A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812626 | ||||||
chr5:112812934
|
C | G | 1 | a0001c0001t0001g0232 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.835-2561C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812934 | ||||||
chr5:112812976
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.835-2519G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112812976 | ||||||
chr5:112813049
|
G | C | 1 | a0001c0005t0005g0011 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.835-2446G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813049 | ||||||
chr5:112813192
|
A | G | 1 | a0001c0001t0001g0284 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.835-2303A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813192 | ||||||
chr5:112813341
|
G | T | 1 | a0001c0029t0002g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.835-2154G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813341 | ||||||
chr5:112813342
|
C | T | 1 | a0001c0029t0002g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.835-2153C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813342 | ||||||
chr5:112813628
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.835-1867G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813628 | ||||||
chr5:112813752
|
T | TA | 23 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(20): Show | 23 | HG01081.hp1 HG01106.hp2 HG01243.hp1 others(20): Show |
intron_variant | MODIFIER | c.835-1730dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112813752 | |||||
chr5:112813752
|
T | TAA | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.835-1731_835-1730d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr5 | 112813752 | |||||
chr5:112813779
|
A | C | 16 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(13): Show | 16 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.835-1716A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813779 | ||||||
chr5:112813828
|
T | C | 1 | a0001c0003t0002g0048 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.835-1667T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813828 | ||||||
chr5:112813878
|
C | T | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.835-1617C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813878 | ||||||
chr5:112813973
|
T | G | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.835-1522T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112813973 | ||||||
chr5:112814060
|
T | C | 230 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(227): Show | 232 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(229): Show |
intron_variant | MODIFIER | c.835-1435T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814060 | ||||||
chr5:112814230
|
A | G | 91 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(88): Show | 93 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(90): Show |
intron_variant | MODIFIER | c.835-1265A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814230 | ||||||
chr5:112814245
|
A | G | 1 | a0001c0003t0002g0059 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.835-1250A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814245 | ||||||
chr5:112814272
|
C | T | 2 | a0001c0001t0001g0199a0001c0001t0001g0244 | 2 | NA18981.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.835-1223C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814272 | ||||||
chr5:112814289
|
G | A | 1 | a0001c0003t0002g0048 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.835-1206G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814289 | ||||||
chr5:112814352
|
A | G | 16 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(13): Show | 16 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.835-1143A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814352 | ||||||
chr5:112814372
|
A | G | 1 | a0002c0004t0002g0106 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.835-1123A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814372 | ||||||
chr5:112814452
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.835-1043T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814452 | ||||||
chr5:112814546
|
T | G | 1 | a0001c0001t0001g0269 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.835-949T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814546 | ||||||
chr5:112814549
|
A | G | 1 | a0001c0001t0001g0223 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.835-946A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814549 | ||||||
chr5:112814578
|
A | G | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.835-917A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814578 | ||||||
chr5:112814630
|
C | G | 7 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(4): Show | 7 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.835-865C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814630 | ||||||
chr5:112814843
|
G | A | 5 | a0001c0002t0003g0167a0001c0002t0003g0176a0001c0002t0003g0177others(2): Show | 5 | HG00609.hp1 HG02129.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.835-652G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814843 | ||||||
chr5:112814876
|
T | C | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.835-619T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814876 | ||||||
chr5:112814928
|
A | G | 1 | a0001c0001t0001g0240 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.835-567A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112814928 | ||||||
chr5:112815043
|
G | C | 4 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(1): Show | 4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-452G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112815043 | ||||||
chr5:112815184
|
T | G | 1 | a0002c0020t0012g0057 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.835-311T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112815184 | ||||||
chr5:112815188
|
C | T | 1 | a0001c0003t0006g0152 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.835-307C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112815188 | ||||||
chr5:112815236
|
A | T | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.835-259A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112815236 | ||||||
chr5:112815471
|
A | T | 1 | a0001c0001t0001g0258 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.835-24A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112815471 | ||||||
chr5:112815476
|
T | C | 1 | a0006c0012t0002g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.835-19T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 8/15 | chr5 | 112815476 | ||||||
chr5:112815822
|
G | C | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.933+229G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112815822 | ||||||
chr5:112815854
|
G | T | 175 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(172): Show | 177 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(174): Show |
intron_variant | MODIFIER | c.933+261G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112815854 | ||||||
chr5:112816077
|
C | T | 1 | a0001c0003t0002g0068 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.933+484C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816077 | ||||||
chr5:112816314
|
A | G | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.933+721A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816314 | ||||||
chr5:112816436
|
T | C | 1 | a0011c0023t0004g0026 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.933+843T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816436 | ||||||
chr5:112816509
|
T | G | 40 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(37): Show | 40 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(37): Show |
intron_variant | MODIFIER | c.933+916T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816509 | ||||||
chr5:112816529
|
C | G | 1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.933+936C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816529 | ||||||
chr5:112816652
|
G | T | 12 | a0001c0003t0002g0138a0001c0003t0002g0151a0001c0003t0006g0140others(9): Show | 12 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.933+1059G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816652 | ||||||
chr5:112816697
|
G | C | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.933+1104G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816697 | ||||||
chr5:112816761
|
C | G | 2 | a0001c0002t0005g0115a0001c0002t0009g0131 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.933+1168C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816761 | ||||||
chr5:112816825
|
C | G | 5 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(2): Show | 5 | HG01243.hp2 HG02257.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.933+1232C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816825 | ||||||
chr5:112816864
|
T | TTTTA | 7 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(4): Show | 7 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.933+1287_933+1290d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr5 | 112816864 | |||||
chr5:112816952
|
C | T | 174 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(171): Show | 176 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(173): Show |
intron_variant | MODIFIER | c.933+1359C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112816952 | ||||||
chr5:112817133
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.933+1540G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817133 | ||||||
chr5:112817136
|
C | A | 1 | a0001c0002t0003g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.933+1543C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817136 | ||||||
chr5:112817169
|
C | G | 1 | a0001c0002t0004g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.933+1576C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817169 | ||||||
chr5:112817170
|
C | G | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.933+1577C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817170 | ||||||
chr5:112817223
|
C | T | 61 | a0001c0002t0001g0288a0001c0002t0001g0289a0001c0002t0001g0290others(58): Show | 63 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.933+1630C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817223 | ||||||
chr5:112817334
|
T | G | 1 | a0001c0001t0001g0251 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.934-1632T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817334 | ||||||
chr5:112817422
|
C | T | 193 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(190): Show | 195 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(192): Show |
intron_variant | MODIFIER | c.934-1544C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817422 | ||||||
chr5:112817435
|
C | T | 7 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(4): Show | 7 | HG02258.hp1 HG02280.hp1 HG02486.hp1 others(4): Show |
intron_variant | MODIFIER | c.934-1531C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817435 | ||||||
chr5:112817513
|
A | C | 1 | a0001c0001t0001g0202 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.934-1453A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817513 | ||||||
chr5:112817570
|
C | T | 1 | a0002c0004t0002g0045 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.934-1396C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817570 | ||||||
chr5:112817656
|
T | G | 13 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(10): Show | 13 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.934-1310T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817656 | ||||||
chr5:112817686
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.934-1280A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817686 | ||||||
chr5:112817798
|
A | G | 217 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(214): Show | 219 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(216): Show |
intron_variant | MODIFIER | c.934-1168A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817798 | ||||||
chr5:112817831
|
C | G | 14 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(11): Show | 14 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.934-1135C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817831 | ||||||
chr5:112817876
|
T | G | 1 | a0001c0003t0002g0047 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.934-1090T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817876 | ||||||
chr5:112817940
|
A | G | 1 | a0002c0004t0002g0029 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.934-1026A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817940 | ||||||
chr5:112817966
|
A | G | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.934-1000A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817966 | ||||||
chr5:112817968
|
C | T | 193 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(190): Show | 195 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(192): Show |
intron_variant | MODIFIER | c.934-998C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112817968 | ||||||
chr5:112818025
|
T | C | 2 | a0001c0002t0005g0115a0001c0002t0009g0131 | 2 | HG01243.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.934-941T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818025 | ||||||
chr5:112818060
|
T | C | 43 | a0001c0001t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(40): Show | 45 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.934-906T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818060 | ||||||
chr5:112818164
|
C | A | 3 | a0001c0001t0001g0240a0001c0001t0001g0274a0001c0016t0001g0242 | 3 | HG02523.hp2 NA18973.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.934-802C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818164 | ||||||
chr5:112818167
|
T | C | 1 | a0001c0005t0005g0005 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.934-799T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818167 | ||||||
chr5:112818200
|
A | G | 1 | a0001c0002t0003g0154 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.934-766A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818200 | ||||||
chr5:112818299
|
C | G | 213 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(210): Show | 215 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(212): Show |
intron_variant | MODIFIER | c.934-667C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818299 | ||||||
chr5:112818362
|
G | A | 1 | a0002c0004t0002g0069 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.934-604G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818362 | ||||||
chr5:112818454
|
ATAT | A | 193 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(190): Show | 195 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(192): Show |
intron_variant | MODIFIER | c.934-508_934-506del others(3): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr5 | 112818454 | |||||
chr5:112818606
|
T | G | 196 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(193): Show | 198 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(195): Show |
intron_variant | MODIFIER | c.934-360T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818606 | ||||||
chr5:112818688
|
G | C | 1 | a0001c0003t0002g0048 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.934-278G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818688 | ||||||
chr5:112818747
|
A | G | 3 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0267 | 3 | HG00673.hp1 NA19011.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.934-219A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818747 | ||||||
chr5:112818833
|
TG | T | 178 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(175): Show | 180 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(177): Show |
intron_variant | MODIFIER | c.934-132delG | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818833 | ||||||
chr5:112818834
|
G | T | 39 | a0001c0001t0001g0239a0001c0001t0001g0244a0001c0001t0001g0281others(36): Show | 39 | HG01074.hp2 HG01081.hp1 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.934-132G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818834 | ||||||
chr5:112818847
|
C | CG | 98 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(95): Show | 98 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(95): Show |
intron_variant | MODIFIER | c.934-111dupG | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | INFO_REALIGN_3_PRIME | chr5 | 112818847 | |||||
chr5:112818874
|
G | C | 19 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(16): Show | 19 | HG00741.hp2 HG01358.hp1 HG01361.hp1 others(16): Show |
intron_variant | MODIFIER | c.934-92G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 9/15 | chr5 | 112818874 | ||||||
chr5:112819371
|
G | A | 1 | a0002c0004t0002g0083 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1312+27G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819371 | ||||||
chr5:112819480
|
A | G | 7 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(4): Show | 7 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1312+136A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819480 | ||||||
chr5:112819507
|
C | G | 5 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0164others(2): Show | 5 | HG02071.hp1 NA18612.hp1 NA18971.hp2 others(2): Show |
intron_variant | MODIFIER | c.1312+163C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819507 | ||||||
chr5:112819545
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1312+201A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819545 | ||||||
chr5:112819721
|
A | C | 2 | a0001c0003t0002g0103a0001c0003t0002g0104 | 2 | HG03041.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1312+377A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819721 | ||||||
chr5:112819805
|
T | A | 1 | a0001c0002t0003g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1312+461T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819805 | ||||||
chr5:112819807
|
C | G | 213 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(210): Show | 215 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(212): Show |
intron_variant | MODIFIER | c.1312+463C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819807 | ||||||
chr5:112819893
|
C | T | 7 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(4): Show | 7 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1312+549C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112819893 | ||||||
chr5:112820063
|
C | T | 29 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(26): Show | 29 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(26): Show |
intron_variant | MODIFIER | c.1312+719C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820063 | ||||||
chr5:112820096
|
G | C | 197 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(194): Show | 199 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(196): Show |
intron_variant | MODIFIER | c.1312+752G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820096 | ||||||
chr5:112820182
|
G | GAC | 43 | a0001c0001t0001g0219a0001c0001t0001g0226a0001c0001t0001g0229others(40): Show | 43 | HG00639.hp1 HG00642.hp2 HG00741.hp2 others(40): Show |
intron_variant | MODIFIER | c.1312+871_1312+872d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112820182 | |||||
chr5:112820182
|
G | GACAC | 7 | a0001c0002t0005g0126a0001c0002t0005g0127a0001c0002t0005g0128others(4): Show | 7 | HG01081.hp1 HG01106.hp2 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312+869_1312+872d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112820182 | |||||
chr5:112820182
|
GAC | G | 10 | a0001c0001t0001g0109a0001c0001t0001g0234a0001c0002t0003g0163others(7): Show | 10 | HG01496.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1312+871_1312+872d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112820182 | |||||
chr5:112820182
|
GACAC | G | 37 | a0001c0001t0001g0274a0001c0002t0004g0013a0001c0002t0004g0014others(34): Show | 37 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(34): Show |
intron_variant | MODIFIER | c.1312+869_1312+872d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112820182 | |||||
chr5:112820182
|
GACACAC | G | 38 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0075others(35): Show | 40 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1312+867_1312+872d others(8): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112820182 | |||||
chr5:112820321
|
A | G | 3 | a0001c0002t0003g0154a0001c0002t0003g0178a0001c0002t0003g0179 | 3 | HG03471.hp2 HG06807.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1312+977A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820321 | ||||||
chr5:112820425
|
G | A | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1312+1081G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820425 | ||||||
chr5:112820583
|
T | G | 5 | a0001c0002t0003g0001a0001c0002t0003g0155a0001c0002t0003g0156others(2): Show | 6 | HG00408.hp1 HG02155.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1312+1239T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820583 | ||||||
chr5:112820604
|
T | C | 1 | a0001c0003t0002g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1312+1260T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820604 | ||||||
chr5:112820620
|
C | T | 1 | a0001c0019t0002g0078 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1312+1276C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820620 | ||||||
chr5:112820842
|
T | C | 1 | a0001c0001t0001g0283 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1313-1054T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820842 | ||||||
chr5:112820937
|
C | T | 6 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(3): Show | 6 | HG02257.hp1 HG02615.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1313-959C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820937 | ||||||
chr5:112820974
|
A | G | 2 | a0001c0001t0001g0217a0001c0001t0001g0243 | 2 | NA18950.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.1313-922A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820974 | ||||||
chr5:112820979
|
A | T | 1 | a0001c0029t0002g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1313-917A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820979 | ||||||
chr5:112820995
|
C | A | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1313-901C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112820995 | ||||||
chr5:112821030
|
A | AT | 29 | a0001c0001t0001g0122a0001c0001t0001g0199a0001c0001t0001g0244others(26): Show | 29 | HG00741.hp2 HG01358.hp1 HG01361.hp1 others(26): Show |
intron_variant | MODIFIER | c.1313-846dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112821030 | |||||
chr5:112821030
|
AT | A | 15 | a0001c0001t0001g0198a0001c0001t0001g0243a0001c0001t0001g0264others(12): Show | 15 | HG00323.hp1 HG00323.hp2 HG01070.hp2 others(12): Show |
intron_variant | MODIFIER | c.1313-846delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112821030 | |||||
chr5:112821099
|
G | A | 3 | a0001c0002t0005g0126a0001c0002t0005g0127a0001c0002t0005g0128 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1313-797G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821099 | ||||||
chr5:112821166
|
G | C | 76 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0075others(73): Show | 78 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(75): Show |
intron_variant | MODIFIER | c.1313-730G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821166 | ||||||
chr5:112821234
|
G | A | 1 | a0001c0001t0001g0241 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.1313-662G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821234 | ||||||
chr5:112821242
|
G | A | 1 | a0001c0001t0001g0227 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.1313-654G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821242 | ||||||
chr5:112821400
|
C | T | 1 | a0001c0002t0005g0115 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.1313-496C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821400 | ||||||
chr5:112821401
|
G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1313-495G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821401 | ||||||
chr5:112821504
|
G | GT | 20 | a0001c0002t0004g0015a0001c0002t0004g0016a0001c0002t0004g0017others(17): Show | 20 | HG01496.hp1 HG01884.hp1 HG02145.hp2 others(17): Show |
intron_variant | MODIFIER | c.1313-382dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | INFO_REALIGN_3_PRIME | chr5 | 112821504 | |||||
chr5:112821716
|
T | A | 1 | a0002c0004t0002g0043 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1313-180T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 10/15 | chr5 | 112821716 | ||||||
chr5:112822130
|
G | A | 1 | a0001c0005t0011g0008 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1408+139G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112822130 | ||||||
chr5:112822427
|
A | G | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1408+436A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112822427 | ||||||
chr5:112822676
|
G | A | 1 | a0001c0003t0002g0138 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1408+685G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112822676 | ||||||
chr5:112822734
|
G | A | 186 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(183): Show | 188 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(185): Show |
intron_variant | MODIFIER | c.1408+743G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112822734 | ||||||
chr5:112822783
|
A | T | 14 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(11): Show | 14 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(11): Show |
intron_variant | MODIFIER | c.1408+792A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112822783 | ||||||
chr5:112823052
|
A | T | 15 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(12): Show | 15 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(12): Show |
intron_variant | MODIFIER | c.1408+1061A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823052 | ||||||
chr5:112823321
|
C | T | 1 | a0002c0004t0002g0088 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1408+1330C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823321 | ||||||
chr5:112823376
|
G | A | 1 | a0001c0003t0006g0145 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1408+1385G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823376 | ||||||
chr5:112823519
|
T | G | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1408+1528T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823519 | ||||||
chr5:112823593
|
A | G | 11 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1408+1602A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823593 | ||||||
chr5:112823663
|
A | G | 32 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(29): Show | 32 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(29): Show |
intron_variant | MODIFIER | c.1408+1672A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823663 | ||||||
chr5:112823688
|
A | G | 289 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(286): Show | 291 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(288): Show |
intron_variant | MODIFIER | c.1408+1697A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823688 | ||||||
chr5:112823711
|
T | C | 5 | a0001c0002t0003g0001a0001c0002t0003g0155a0001c0002t0003g0156others(2): Show | 6 | HG00408.hp1 HG02155.hp1 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408+1720T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823711 | ||||||
chr5:112823773
|
A | G | 100 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(97): Show | 100 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(97): Show |
intron_variant | MODIFIER | c.1408+1782A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823773 | ||||||
chr5:112823848
|
A | C | 17 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(14): Show | 17 | HG01081.hp1 HG01106.hp2 HG02056.hp1 others(14): Show |
intron_variant | MODIFIER | c.1408+1857A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823848 | ||||||
chr5:112823865
|
A | G | 237 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(234): Show | 239 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(236): Show |
intron_variant | MODIFIER | c.1408+1874A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823865 | ||||||
chr5:112823939
|
C | T | 1 | a0001c0001t0001g0273 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1408+1948C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823939 | ||||||
chr5:112823986
|
A | T | 1 | a0001c0002t0001g0291 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1408+1995A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112823986 | ||||||
chr5:112824207
|
G | A | 1 | a0013c0024t0003g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1408+2216G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824207 | ||||||
chr5:112824208
|
C | A | 1 | a0013c0024t0003g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1408+2217C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824208 | ||||||
chr5:112824277
|
G | A | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1408+2286G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824277 | ||||||
chr5:112824728
|
C | T | 1 | a0001c0002t0005g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1409-2380C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824728 | ||||||
chr5:112824745
|
CTCATTAG others(14): Show |
C | 178 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(175): Show | 180 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(177): Show |
intron_variant | MODIFIER | c.1409-2360_1409-234 others(25): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr5 | 112824745 | |||||
chr5:112824883
|
T | C | 14 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(11): Show | 14 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(11): Show |
intron_variant | MODIFIER | c.1409-2225T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824883 | ||||||
chr5:112824898
|
T | A | 1 | a0001c0002t0009g0125 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1409-2210T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824898 | ||||||
chr5:112824912
|
T | C | 1 | a0001c0002t0003g0164 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1409-2196T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112824912 | ||||||
chr5:112825027
|
A | G | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-2081A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825027 | ||||||
chr5:112825095
|
C | T | 1 | a0004c0009t0002g0099 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1409-2013C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825095 | ||||||
chr5:112825314
|
G | A | 4 | a0001c0002t0003g0153a0001c0002t0003g0160a0001c0002t0003g0164others(1): Show | 4 | HG02071.hp1 NA18612.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-1794G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825314 | ||||||
chr5:112825430
|
C | A | 1 | a0001c0001t0001g0283 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1409-1678C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825430 | ||||||
chr5:112825617
|
C | T | 62 | a0001c0002t0001g0288a0001c0002t0001g0289a0001c0002t0001g0290others(59): Show | 64 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1409-1491C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825617 | ||||||
chr5:112825622
|
C | T | 1 | a0001c0003t0006g0152 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1409-1486C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825622 | ||||||
chr5:112825650
|
G | A | 6 | a0001c0001t0001g0200a0001c0001t0001g0210a0001c0003t0002g0101others(3): Show | 6 | HG02818.hp2 HG02970.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.1409-1458G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825650 | ||||||
chr5:112825693
|
A | G | 1 | a0002c0020t0012g0057 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.1409-1415A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825693 | ||||||
chr5:112825772
|
C | A | 99 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(96): Show | 99 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.1409-1336C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825772 | ||||||
chr5:112825864
|
C | T | 2 | a0001c0002t0005g0128a0001c0003t0002g0048 | 2 | HG02257.hp1 NA18954.hp1 |
intron_variant | MODIFIER | c.1409-1244C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112825864 | ||||||
chr5:112826082
|
C | G | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-1026C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826082 | ||||||
chr5:112826142
|
TC | T | 42 | a0001c0002t0001g0288a0001c0002t0001g0289a0001c0002t0001g0290others(39): Show | 44 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.1409-965delC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826142 | ||||||
chr5:112826208
|
T | C | 2 | a0003c0006t0001g0261a0003c0006t0001g0262 | 2 | HG02109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1409-900T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826208 | ||||||
chr5:112826222
|
G | T | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1409-886G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826222 | ||||||
chr5:112826586
|
T | TA | 6 | a0001c0002t0003g0158a0001c0002t0003g0161a0001c0002t0003g0187others(3): Show | 6 | HG00408.hp2 HG01109.hp1 HG02683.hp2 others(3): Show |
intron_variant | MODIFIER | c.1409-507dupA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr5 | 112826586 | |||||
chr5:112826586
|
TAA | T | 27 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(24): Show | 27 | HG00741.hp2 HG01496.hp2 HG02132.hp1 others(24): Show |
intron_variant | MODIFIER | c.1409-508_1409-507d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr5 | 112826586 | |||||
chr5:112826599
|
AAAC | A | 13 | a0001c0002t0003g0154a0001c0002t0003g0178a0001c0002t0003g0179others(10): Show | 13 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.1409-506_1409-504d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr5 | 112826599 | |||||
chr5:112826600
|
AAC | A | 27 | a0001c0001t0001g0201a0001c0001t0001g0245a0001c0002t0004g0013others(24): Show | 27 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(24): Show |
intron_variant | MODIFIER | c.1409-506_1409-505d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr5 | 112826600 | |||||
chr5:112826601
|
AC | A | 101 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(98): Show | 101 | HG00609.hp2 HG00639.hp1 HG00673.hp1 others(98): Show |
intron_variant | MODIFIER | c.1409-506delC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826601 | ||||||
chr5:112826602
|
C | A | 52 | a0001c0001t0001g0220a0001c0001t0001g0230a0001c0001t0001g0231others(49): Show | 54 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(51): Show |
intron_variant | MODIFIER | c.1409-506C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826602 | ||||||
chr5:112826716
|
A | G | 113 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(110): Show | 113 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.1409-392A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 11/15 | chr5 | 112826716 | ||||||
chr5:112827394
|
T | C | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1548+147T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 12/15 | chr5 | 112827394 | ||||||
chr5:112827537
|
A | G | 1 | a0001c0001t0001g0205 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1548+290A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 12/15 | chr5 | 112827537 | ||||||
chr5:112827541
|
G | GT | 188 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(185): Show | 190 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(187): Show |
intron_variant | MODIFIER | c.1548+297dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr5 | 112827541 | |||||
chr5:112828160
|
C | T | 1 | a0001c0015t0002g0134 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1626+154C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828160 | ||||||
chr5:112828161
|
G | A | 1 | a0001c0001t0001g0221 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1626+155G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828161 | ||||||
chr5:112828292
|
G | A | 4 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(1): Show | 4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1626+286G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828292 | ||||||
chr5:112828305
|
C | G | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1626+299C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828305 | ||||||
chr5:112828457
|
T | A | 1 | a0004c0009t0002g0098 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1627-399T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828457 | ||||||
chr5:112828457
|
TA | T | 192 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(189): Show | 194 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(191): Show |
intron_variant | MODIFIER | c.1627-382delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr5 | 112828457 | |||||
chr5:112828516
|
G | A | 1 | a0001c0001t0001g0260 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1627-340G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828516 | ||||||
chr5:112828541
|
C | T | 185 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(182): Show | 187 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(184): Show |
intron_variant | MODIFIER | c.1627-315C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828541 | ||||||
chr5:112828547
|
G | T | 4 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(1): Show | 4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627-309G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828547 | ||||||
chr5:112828698
|
C | G | 1 | a0001c0001t0001g0233 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1627-158C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828698 | ||||||
chr5:112828763
|
A | C | 4 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(1): Show | 4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1627-93A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828763 | ||||||
chr5:112828830
|
T | A | 1 | a0001c0003t0002g0048 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1627-26T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 13/15 | chr5 | 112828830 | ||||||
chr5:112829050
|
A | G | 3 | a0001c0003t0002g0030a0002c0004t0002g0031a0007c0032t0002g0032 | 3 | HG00323.hp2 HG03688.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1743+78A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829050 | ||||||
chr5:112829140
|
T | G | 1 | a0001c0003t0002g0054 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1743+168T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829140 | ||||||
chr5:112829165
|
G | A | 99 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(96): Show | 99 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(96): Show |
intron_variant | MODIFIER | c.1743+193G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829165 | ||||||
chr5:112829209
|
G | C | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+237G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829209 | ||||||
chr5:112829239
|
A | G | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1743+267A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829239 | ||||||
chr5:112829354
|
C | T | 13 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(10): Show | 13 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.1743+382C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829354 | ||||||
chr5:112829466
|
C | A | 3 | a0001c0002t0005g0126a0001c0002t0005g0127a0001c0002t0005g0128 | 3 | HG02257.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1743+494C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829466 | ||||||
chr5:112829490
|
C | T | 1 | a0001c0002t0003g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1743+518C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829490 | ||||||
chr5:112829678
|
C | T | 5 | a0001c0002t0003g0167a0001c0002t0003g0176a0001c0002t0003g0177others(2): Show | 5 | HG00609.hp1 HG02129.hp1 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.1743+706C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829678 | ||||||
chr5:112829741
|
G | A | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1743+769G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829741 | ||||||
chr5:112829897
|
A | G | 1 | a0001c0029t0002g0033 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1743+925A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829897 | ||||||
chr5:112829931
|
C | T | 4 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+959C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112829931 | ||||||
chr5:112830047
|
A | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1743+1075A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112830047 | ||||||
chr5:112830142
|
CT | C | 4 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(1): Show | 4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+1172delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112830142 | |||||
chr5:112830292
|
G | A | 38 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0075others(35): Show | 40 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(37): Show |
intron_variant | MODIFIER | c.1743+1320G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112830292 | ||||||
chr5:112830334
|
G | A | 4 | a0001c0003t0002g0101a0001c0003t0002g0103a0001c0003t0002g0104others(1): Show | 4 | HG02818.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+1362G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112830334 | ||||||
chr5:112830347
|
AACT | A | 177 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(174): Show | 179 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(176): Show |
intron_variant | MODIFIER | c.1743+1378_1743+138 others(7): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112830347 | |||||
chr5:112830523
|
A | G | 4 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(1): Show | 4 | HG02257.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1743+1551A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112830523 | ||||||
chr5:112830589
|
TACAC | T | 15 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(12): Show | 15 | HG01884.hp2 HG02258.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1743+1621_1743+162 others(8): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112830589 | |||||
chr5:112830874
|
G | A | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1743+1902G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112830874 | ||||||
chr5:112831053
|
G | T | 1 | a0001c0001t0001g0212 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1743+2081G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831053 | ||||||
chr5:112831054
|
C | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1743+2082C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831054 | ||||||
chr5:112831113
|
A | AT | 14 | a0001c0001t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(11): Show | 14 | HG02257.hp1 HG02683.hp2 HG02886.hp2 others(11): Show |
intron_variant | MODIFIER | c.1743+2155dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112831113 | |||||
chr5:112831131
|
A | G | 1 | a0001c0002t0003g0162 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1743+2159A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831131 | ||||||
chr5:112831165
|
G | A | 95 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(92): Show | 95 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(92): Show |
intron_variant | MODIFIER | c.1743+2193G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831165 | ||||||
chr5:112831178
|
G | A | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1743+2206G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831178 | ||||||
chr5:112831198
|
T | C | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1743+2226T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831198 | ||||||
chr5:112831258
|
G | A | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1743+2286G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831258 | ||||||
chr5:112831328
|
T | A | 2 | a0003c0006t0001g0261a0003c0006t0001g0262 | 2 | HG02109.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.1743+2356T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831328 | ||||||
chr5:112831433
|
T | G | 205 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(202): Show | 207 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(204): Show |
intron_variant | MODIFIER | c.1743+2461T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831433 | ||||||
chr5:112831586
|
A | G | 5 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0287others(2): Show | 5 | HG00639.hp1 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1743+2614A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831586 | ||||||
chr5:112831611
|
T | C | 4 | a0001c0003t0002g0056a0001c0003t0002g0058a0001c0003t0002g0059others(1): Show | 4 | HG01106.hp1 HG01169.hp1 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.1743+2639T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831611 | ||||||
chr5:112831782
|
A | G | 1 | a0001c0003t0002g0086 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.1743+2810A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831782 | ||||||
chr5:112831840
|
T | C | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1743+2868T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831840 | ||||||
chr5:112831890
|
T | C | 97 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(94): Show | 97 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(94): Show |
intron_variant | MODIFIER | c.1743+2918T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112831890 | ||||||
chr5:112832124
|
C | T | 177 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(174): Show | 179 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(176): Show |
intron_variant | MODIFIER | c.1744-2827C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832124 | ||||||
chr5:112832217
|
A | G | 1 | a0001c0003t0002g0066 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.1744-2734A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832217 | ||||||
chr5:112832224
|
G | A | 37 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(34): Show | 37 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(34): Show |
intron_variant | MODIFIER | c.1744-2727G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832224 | ||||||
chr5:112832244
|
C | G | 178 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(175): Show | 180 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(177): Show |
intron_variant | MODIFIER | c.1744-2707C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832244 | ||||||
chr5:112832272
|
T | C | 1 | a0001c0003t0002g0036 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1744-2679T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832272 | ||||||
chr5:112832368
|
A | G | 177 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(174): Show | 179 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(176): Show |
intron_variant | MODIFIER | c.1744-2583A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832368 | ||||||
chr5:112832409
|
C | G | 1 | a0001c0001t0001g0274 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1744-2542C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832409 | ||||||
chr5:112832433
|
G | C | 177 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(174): Show | 179 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(176): Show |
intron_variant | MODIFIER | c.1744-2518G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832433 | ||||||
chr5:112832446
|
T | C | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1744-2505T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832446 | ||||||
chr5:112832452
|
C | G | 2 | a0001c0001t0001g0264a0001c0001t0001g0265 | 2 | HG03704.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1744-2499C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832452 | ||||||
chr5:112832576
|
T | C | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744-2375T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832576 | ||||||
chr5:112832622
|
T | C | 1 | a0001c0002t0003g0160 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1744-2329T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832622 | ||||||
chr5:112832645
|
C | T | 1 | a0001c0002t0003g0172 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1744-2306C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832645 | ||||||
chr5:112832708
|
C | T | 2 | a0001c0002t0003g0161a0001c0002t0003g0162 | 2 | HG02683.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.1744-2243C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832708 | ||||||
chr5:112832754
|
C | T | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1744-2197C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832754 | ||||||
chr5:112832875
|
T | A | 1 | a0001c0002t0004g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1744-2076T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112832875 | ||||||
chr5:112833029
|
GT | G | 176 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(173): Show | 178 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(175): Show |
intron_variant | MODIFIER | c.1744-1910delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112833029 | |||||
chr5:112833041
|
T | G | 16 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(13): Show | 16 | HG01884.hp2 HG02145.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.1744-1910T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833041 | ||||||
chr5:112833062
|
T | G | 2 | a0001c0001t0001g0200a0001c0001t0001g0210 | 2 | HG02970.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1744-1889T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833062 | ||||||
chr5:112833123
|
C | G | 2 | a0001c0010t0007g0132a0001c0014t0007g0133 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1744-1828C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833123 | ||||||
chr5:112833153
|
A | G | 12 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1744-1798A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833153 | ||||||
chr5:112833180
|
A | AT | 9 | a0001c0003t0002g0150a0001c0003t0006g0140a0001c0003t0006g0141others(6): Show | 9 | HG00741.hp2 HG02886.hp2 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.1744-1751dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112833180 | |||||
chr5:112833180
|
AT | A | 176 | a0001c0001t0001g0109a0001c0001t0001g0194a0001c0001t0001g0195others(173): Show | 178 | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.1744-1751delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112833180 | |||||
chr5:112833180
|
ATT | A | 8 | a0001c0001t0001g0193a0001c0001t0001g0205a0001c0001t0001g0211others(5): Show | 8 | HG01070.hp1 HG01070.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744-1752_1744-175 others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112833180 | |||||
chr5:112833196
|
T | G | 8 | a0001c0005t0005g0005a0001c0005t0005g0006a0001c0005t0005g0007others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.1744-1755T>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833196 | ||||||
chr5:112833207
|
G | A | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1744-1744G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833207 | ||||||
chr5:112833342
|
C | T | 2 | a0001c0003t0002g0035a0001c0003t0002g0036 | 2 | HG02451.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.1744-1609C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833342 | ||||||
chr5:112833374
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1744-1577G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833374 | ||||||
chr5:112833393
|
G | T | 1 | a0001c0002t0013g0003 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1744-1558G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833393 | ||||||
chr5:112833423
|
C | A | 4 | a0001c0001t0001g0122a0001c0001t0004g0121a0001c0001t0004g0123others(1): Show | 4 | HG01358.hp1 HG01361.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.1744-1528C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833423 | ||||||
chr5:112833434
|
G | GC | 12 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1744-1513dupC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112833434 | |||||
chr5:112833439
|
T | C | 177 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(174): Show | 179 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(176): Show |
intron_variant | MODIFIER | c.1744-1512T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833439 | ||||||
chr5:112833479
|
C | T | 3 | a0001c0010t0007g0027a0001c0010t0007g0132a0001c0014t0007g0133 | 3 | HG02622.hp2 HG03130.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1744-1472C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833479 | ||||||
chr5:112833481
|
G | A | 4 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(1): Show | 4 | HG01496.hp1 HG01884.hp1 HG02630.hp1 others(1): Show |
intron_variant | MODIFIER | c.1744-1470G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833481 | ||||||
chr5:112833828
|
T | A | 215 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(212): Show | 217 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(214): Show |
intron_variant | MODIFIER | c.1744-1123T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833828 | ||||||
chr5:112833927
|
A | G | 64 | a0001c0001t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(61): Show | 66 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1744-1024A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112833927 | ||||||
chr5:112834105
|
A | AT | 24 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(21): Show | 24 | HG00741.hp2 HG01081.hp1 HG01106.hp2 others(21): Show |
intron_variant | MODIFIER | c.1744-836dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112834105 | |||||
chr5:112834193
|
C | G | 43 | a0001c0001t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(40): Show | 45 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1744-758C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834193 | ||||||
chr5:112834200
|
A | G | 2 | a0001c0010t0007g0132a0001c0014t0007g0133 | 2 | HG02622.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1744-751A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834200 | ||||||
chr5:112834238
|
C | CT | 7 | a0001c0008t0002g0130a0001c0030t0002g0129a0002c0004t0002g0043others(4): Show | 7 | HG01891.hp1 HG03486.hp2 HG03654.hp1 others(4): Show |
intron_variant | MODIFIER | c.1744-691dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112834238 | |||||
chr5:112834259
|
TTA | T | 10 | a0001c0001t0001g0193a0001c0001t0001g0200a0001c0001t0001g0208others(7): Show | 10 | HG01070.hp1 HG01243.hp2 HG01256.hp1 others(7): Show |
intron_variant | MODIFIER | c.1744-691_1744-690d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834259 | ||||||
chr5:112834260
|
TA | T | 161 | a0001c0001t0001g0109a0001c0001t0001g0194a0001c0001t0001g0195others(158): Show | 163 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(160): Show |
intron_variant | MODIFIER | c.1744-686delA | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr5 | 112834260 | |||||
chr5:112834261
|
A | T | 7 | a0001c0001t0001g0221a0001c0001t0001g0226a0001c0001t0001g0273others(4): Show | 7 | HG02145.hp2 HG02602.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1744-690A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834261 | ||||||
chr5:112834262
|
A | T | 4 | a0001c0002t0003g0001a0001c0002t0005g0115a0001c0010t0007g0132others(1): Show | 5 | HG00408.hp1 HG02622.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.1744-689A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834262 | ||||||
chr5:112834268
|
G | T | 1 | a0001c0010t0007g0027 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1744-683G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834268 | ||||||
chr5:112834345
|
G | A | 1 | a0001c0001t0001g0284 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1744-606G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834345 | ||||||
chr5:112834588
|
T | A | 24 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0075others(21): Show | 26 | HG00408.hp1 HG00609.hp1 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1744-363T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834588 | ||||||
chr5:112834661
|
G | A | 212 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(209): Show | 214 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(211): Show |
intron_variant | MODIFIER | c.1744-290G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834661 | ||||||
chr5:112834793
|
A | G | 9 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(6): Show | 9 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(6): Show |
intron_variant | MODIFIER | c.1744-158A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834793 | ||||||
chr5:112834840
|
G | A | 2 | a0001c0001t0004g0246a0001c0001t0004g0247 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.1744-111G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 14/15 | chr5 | 112834840 | ||||||
chr5:112835173
|
T | C | 14 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(11): Show | 14 | HG02056.hp1 HG02132.hp1 HG02155.hp2 others(11): Show |
splice_region_variant&intron_variant | LOW | c.1958+8T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835173 | ||||||
chr5:112835198
|
A | G | 2 | a0001c0001t0001g0213a0001c0001t0001g0220 | 2 | NA19070.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.1958+33A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835198 | ||||||
chr5:112835219
|
A | C | 12 | a0001c0002t0005g0115a0001c0002t0005g0126a0001c0002t0005g0127others(9): Show | 12 | HG02145.hp2 HG02257.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.1958+54A>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835219 | ||||||
chr5:112835274
|
A | G | 3 | a0001c0001t0001g0204a0001c0001t0001g0238a0001c0001t0001g0277 | 3 | HG04184.hp1 NA18954.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.1958+109A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835274 | ||||||
chr5:112835400
|
A | G | 43 | a0001c0001t0001g0286a0001c0002t0001g0288a0001c0002t0001g0289others(40): Show | 45 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1958+235A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835400 | ||||||
chr5:112835503
|
C | G | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1958+338C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835503 | ||||||
chr5:112835572
|
A | AT | 79 | a0001c0001t0001g0122a0001c0001t0001g0286a0001c0001t0004g0116others(76): Show | 81 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(78): Show |
intron_variant | MODIFIER | c.1958+425dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112835572 | |||||
chr5:112835572
|
A | ATT | 15 | a0001c0002t0004g0013a0001c0002t0004g0014a0001c0002t0004g0015others(12): Show | 15 | HG01884.hp2 HG02145.hp2 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.1958+424_1958+425d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112835572 | |||||
chr5:112835572
|
A | T | 1 | a0001c0002t0003g0163 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1958+407A>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835572 | ||||||
chr5:112835572
|
AT | A | 112 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(109): Show | 112 | HG00323.hp2 HG00609.hp2 HG00639.hp1 others(109): Show |
intron_variant | MODIFIER | c.1958+425delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112835572 | |||||
chr5:112835747
|
A | G | 1 | a0001c0002t0003g0181 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1958+582A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835747 | ||||||
chr5:112835748
|
T | C | 1 | a0001c0031t0002g0074 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1958+583T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835748 | ||||||
chr5:112835863
|
G | A | 8 | a0001c0002t0004g0188a0001c0002t0004g0189a0001c0002t0004g0190others(5): Show | 8 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(5): Show |
intron_variant | MODIFIER | c.1958+698G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112835863 | ||||||
chr5:112836009
|
C | CT | 6 | a0001c0003t0002g0042a0001c0003t0002g0062a0001c0003t0002g0105others(3): Show | 6 | HG01346.hp1 HG02293.hp1 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958+870dupT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | |||||
chr5:112836009
|
CT | C | 43 | a0001c0002t0003g0001a0001c0002t0003g0002a0001c0002t0003g0075others(40): Show | 45 | HG00408.hp1 HG00609.hp1 HG00642.hp1 others(42): Show |
intron_variant | MODIFIER | c.1958+870delT | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | |||||
chr5:112836009
|
CTT | C | 14 | a0001c0002t0003g0163a0001c0002t0004g0013a0001c0002t0004g0014others(11): Show | 14 | HG00323.hp1 HG01070.hp2 HG01071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1958+869_1958+870d others(4): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | |||||
chr5:112836009
|
CTTT | C | 11 | a0001c0001t0001g0122a0001c0001t0004g0116a0001c0001t0004g0117others(8): Show | 11 | HG01081.hp1 HG01106.hp2 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.1958+868_1958+870d others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | |||||
chr5:112836009
|
CTTTT | C | 9 | a0001c0002t0005g0127a0001c0002t0005g0128a0001c0005t0005g0005others(6): Show | 9 | HG02257.hp1 HG02258.hp1 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1958+867_1958+870d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | |||||
chr5:112836009
|
CTTTTTT | C | 7 | a0001c0003t0002g0135a0001c0003t0002g0136a0001c0003t0002g0137others(4): Show | 7 | HG01496.hp1 HG01884.hp1 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.1958+865_1958+870d others(8): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | |||||
chr5:112836009
|
CTTTTTTT | C | 27 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(24): Show | 27 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(24): Show |
intron_variant | MODIFIER | c.1958+864_1958+870d others(9): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | |||||
chr5:112836009
|
CTTTTTTT others(2): Show |
C | 14 | a0001c0001t0001g0204a0001c0001t0001g0206a0001c0001t0001g0208others(11): Show | 14 | HG01071.hp1 HG01975.hp2 HG02071.hp2 others(11): Show |
intron_variant | MODIFIER | c.1958+862_1958+870d others(11): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | |||||
chr5:112836009
|
CTTTTTTT others(3): Show |
C | 82 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(79): Show | 82 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(79): Show |
intron_variant | MODIFIER | c.1958+861_1958+870d others(12): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836009 | |||||
chr5:112836025
|
TTTTTTTT others(4): Show |
T | 1 | a0001c0001t0001g0218 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1958+863_1958+873d others(13): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836025 | |||||
chr5:112836037
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1958+872T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836037 | ||||||
chr5:112836064
|
G | A | 5 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0287others(2): Show | 5 | HG00639.hp1 HG01358.hp2 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.1958+899G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836064 | ||||||
chr5:112836087
|
C | T | 1 | a0001c0002t0004g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1958+922C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836087 | ||||||
chr5:112836165
|
T | C | 1 | a0001c0008t0002g0095 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1958+1000T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | ||||||
chr5:112836165
|
T | TC | 18 | a0001c0002t0005g0115a0001c0003t0002g0042a0001c0003t0002g0059others(15): Show | 18 | HG01106.hp1 HG01109.hp1 HG01346.hp1 others(15): Show |
intron_variant | MODIFIER | c.1958+1014dupC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | |||||
chr5:112836165
|
T | TCCCCC | 13 | a0001c0002t0004g0014a0001c0002t0004g0015a0001c0002t0004g0018others(10): Show | 13 | HG01884.hp2 HG02155.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.1958+1010_1958+101 others(9): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | |||||
chr5:112836165
|
T | TCCCCCCC others(3): Show |
1 | a0001c0003t0002g0192 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1958+1005_1958+101 others(14): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | |||||
chr5:112836165
|
T | TCCCCCCC others(4): Show |
1 | a0001c0002t0004g0188 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1958+1004_1958+101 others(15): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | |||||
chr5:112836165
|
T | TCCCCCCC others(9): Show |
1 | a0001c0007t0004g0119 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1958+1013_1958+101 others(20): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | |||||
chr5:112836165
|
T | TCCCCCCC others(12): Show |
1 | a0001c0001t0004g0121 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1958+1013_1958+101 others(23): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | |||||
chr5:112836165
|
T | TCCCCCCC others(8): Show |
1 | a0001c0001t0004g0117 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1958+1012_1958+101 others(19): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | |||||
chr5:112836165
|
T | TCCCCCCC others(9): Show |
3 | a0001c0001t0001g0122a0001c0007t0004g0118a0001c0007t0004g0120 | 3 | HG01081.hp1 HG02257.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1958+1012_1958+101 others(20): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | |||||
chr5:112836165
|
T | TCCCCCCC others(11): Show |
1 | a0001c0001t0004g0124 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1958+1012_1958+101 others(22): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | |||||
chr5:112836165
|
T | TCCCCCCC others(12): Show |
1 | a0001c0001t0004g0123 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.1958+1012_1958+101 others(23): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | |||||
chr5:112836165
|
T | TTCCCC | 4 | a0001c0001t0001g0213a0001c0001t0001g0220a0001c0001t0001g0284others(1): Show | 4 | HG01358.hp2 NA19009.hp1 NA19070.hp1 others(1): Show |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(9): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | ||||||
chr5:112836165
|
T | TTCCCCC | 11 | a0001c0001t0001g0223a0001c0001t0001g0229a0001c0001t0001g0233others(8): Show | 11 | HG01346.hp2 HG01981.hp1 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(10): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | ||||||
chr5:112836165
|
T | TTCCCCCC | 34 | a0001c0001t0001g0193a0001c0001t0001g0201a0001c0001t0001g0202others(31): Show | 34 | HG00673.hp2 HG00741.hp1 HG01071.hp1 others(31): Show |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(11): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | ||||||
chr5:112836165
|
T | TTCCCCCC others(1): Show |
21 | a0001c0001t0001g0194a0001c0001t0001g0195a0001c0001t0001g0197others(18): Show | 21 | HG00609.hp2 HG01169.hp2 HG01175.hp1 others(18): Show |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(12): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | ||||||
chr5:112836165
|
T | TTCCCCCC others(2): Show |
14 | a0001c0001t0001g0109a0001c0001t0001g0219a0001c0001t0001g0225others(11): Show | 14 | HG00642.hp2 HG00673.hp1 HG01109.hp2 others(11): Show |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(13): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | ||||||
chr5:112836165
|
T | TTCCCCCC others(3): Show |
4 | a0001c0001t0001g0204a0001c0001t0001g0222a0001c0001t0001g0265others(1): Show | 4 | HG03927.hp2 NA18954.hp2 NA18975.hp1 others(1): Show |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(14): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | ||||||
chr5:112836165
|
T | TTCCCCCC others(4): Show |
2 | a0001c0001t0001g0211a0001c0016t0001g0242 | 2 | HG02523.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.1958+1000_1958+100 others(15): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | ||||||
chr5:112836165
|
T | TTCCCCCC others(5): Show |
1 | a0001c0001t0001g0254 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1958+1000_1958+100 others(16): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | ||||||
chr5:112836165
|
T | TTCCCCCC others(6): Show |
1 | a0001c0001t0001g0278 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.1958+1000_1958+100 others(17): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836165 | ||||||
chr5:112836165
|
TC | T | 40 | a0001c0001t0004g0116a0001c0002t0008g0184a0001c0002t0008g0185others(37): Show | 40 | HG00323.hp2 HG00639.hp2 HG01081.hp2 others(37): Show |
intron_variant | MODIFIER | c.1958+1014delC | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112836165 | |||||
chr5:112836166
|
C | T | 1 | a0003c0006t0001g0248 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1958+1001C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836166 | ||||||
chr5:112836172
|
C | G | 1 | a0001c0001t0001g0233 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.1958+1007C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836172 | ||||||
chr5:112836172
|
C | T | 1 | a0001c0001t0001g0263 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1958+1007C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836172 | ||||||
chr5:112836173
|
C | T | 6 | a0002c0004t0002g0090a0002c0004t0002g0091a0002c0004t0002g0092others(3): Show | 6 | NA18957.hp1 NA18963.hp1 NA18975.hp2 others(3): Show |
intron_variant | MODIFIER | c.1958+1008C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836173 | ||||||
chr5:112836174
|
C | G | 3 | a0001c0003t0002g0150a0005c0013t0002g0148a0005c0013t0002g0149 | 3 | HG02886.hp2 HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1958+1009C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836174 | ||||||
chr5:112836177
|
C | A | 1 | a0001c0001t0001g0275 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1958+1012C>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836177 | ||||||
chr5:112836177
|
C | CT | 27 | a0001c0002t0001g0289a0001c0002t0001g0290a0001c0002t0001g0291others(24): Show | 29 | HG00408.hp1 HG00609.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1958+1012_1958+101 others(5): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836177 | ||||||
chr5:112836177
|
C | G | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1958+1012C>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836177 | ||||||
chr5:112836178
|
C | CTT | 13 | a0001c0002t0001g0288a0001c0002t0003g0153a0001c0002t0003g0154others(10): Show | 13 | HG01891.hp2 HG02071.hp1 HG02155.hp1 others(10): Show |
intron_variant | MODIFIER | c.1958+1013_1958+101 others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836178 | ||||||
chr5:112836178
|
C | T | 27 | a0001c0002t0001g0289a0001c0002t0001g0290a0001c0002t0001g0291others(24): Show | 29 | HG00408.hp1 HG00609.hp1 HG01074.hp2 others(26): Show |
intron_variant | MODIFIER | c.1958+1013C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836178 | ||||||
chr5:112836180
|
G | A | 96 | a0001c0001t0001g0109a0001c0001t0001g0193a0001c0001t0001g0194others(93): Show | 96 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(93): Show |
intron_variant | MODIFIER | c.1958+1015G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836180 | ||||||
chr5:112836186
|
G | A | 15 | a0001c0003t0002g0138a0001c0003t0002g0150a0001c0003t0002g0151others(12): Show | 15 | HG00741.hp2 HG01496.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.1958+1021G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836186 | ||||||
chr5:112836221
|
G | A | 29 | a0001c0003t0002g0004a0001c0003t0002g0046a0001c0003t0002g0047others(26): Show | 29 | HG00741.hp2 HG01496.hp2 HG02056.hp1 others(26): Show |
intron_variant | MODIFIER | c.1958+1056G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836221 | ||||||
chr5:112836522
|
G | A | 187 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(184): Show | 189 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(186): Show |
intron_variant | MODIFIER | c.1959-1031G>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836522 | ||||||
chr5:112836819
|
G | C | 5 | a0001c0001t0001g0276a0001c0001t0001g0279a0001c0001t0001g0280others(2): Show | 5 | HG01981.hp1 HG01993.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.1959-734G>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112836819 | ||||||
chr5:112837010
|
C | T | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1959-543C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112837010 | ||||||
chr5:112837089
|
G | T | 187 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(184): Show | 189 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(186): Show |
intron_variant | MODIFIER | c.1959-464G>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112837089 | ||||||
chr5:112837103
|
C | T | 8 | a0001c0003t0006g0140a0001c0003t0006g0141a0001c0003t0006g0142others(5): Show | 8 | HG00741.hp2 HG02572.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.1959-450C>T | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112837103 | ||||||
chr5:112837186
|
A | G | 1 | a0001c0002t0004g0025 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1959-367A>G | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112837186 | ||||||
chr5:112837233
|
T | C | 113 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(110): Show | 113 | HG00609.hp2 HG00639.hp1 HG00642.hp2 others(110): Show |
intron_variant | MODIFIER | c.1959-320T>C | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112837233 | ||||||
chr5:112837409
|
T | TAGAA | 188 | a0001c0001t0001g0109a0001c0001t0001g0122a0001c0001t0001g0193others(185): Show | 190 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(187): Show |
intron_variant | MODIFIER | c.1959-143_1959-140d others(6): Show |
APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | INFO_REALIGN_3_PRIME | chr5 | 112837409 | |||||
chr5:112837424
|
T | A | 2 | a0001c0002t0008g0184a0001c0002t0008g0185 | 2 | HG02615.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.1959-129T>A | APC | ENSG00000134982.18 | transcript | ENST00000257430.9 | protein_coding | 15/15 | chr5 | 112837424 |