geneid | 51380 |
---|---|
ensemblid | ENSG00000139631.20 |
hgncid | 18966 |
symbol | CSAD |
name | cysteine sulfinic acid decarboxylase |
refseq_nuc | NM_001244705.2 |
refseq_prot | NP_001231634.1 |
ensembl_nuc | ENST00000444623.6 |
ensembl_prot | ENSP00000415485.1 |
mane_status | MANE Select |
chr | chr12 |
start | 53157663 |
end | 53180925 |
strand | - |
ver | v1.2 |
region | chr12:53157663-53180925 |
region5000 | chr12:53152663-53185925 |
regionname0 | CSAD_chr12_53157663_53180925 |
regionname5000 | CSAD_chr12_53152663_53185925 |
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 | 1/1 | 493 | 328 | 89 | 41 | 148 | 6 | 42 | 115 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0002 | 0/0 | 493 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0003 | 0/0 | 493 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0004 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0005 | 0/0 | 493 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0006 | 0/0 | 493 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
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 | 1/1 | 1482 | 278 | 82 | 39 | 109 | 5 | 41 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
c0002 | 0/0 | 1482 | 41 | 1 | 1 | 38 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
c0003 | 0/0 | 1482 | 6 | 5 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
c0004 | 0/0 | 1482 | 2 | 1 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
c0005 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
c0006 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
c0007 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
c0008 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
c0009 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
c0010 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
c0011 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
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 | 1/1 | 1133 | 216 | 43 | 37 | 100 | 5 | 29 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0002 | 0/0 | 1133 | 77 | 23 | 6 | 35 | 0 | 13 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0003 | 0/0 | 1133 | 13 | 13 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0004 | 0/0 | 1133 | 6 | 0 | 0 | 6 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0005 | 0/0 | 1133 | 6 | 5 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0006 | 0/0 | 1133 | 5 | 0 | 0 | 5 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0007 | 0/0 | 1133 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0008 | 0/0 | 1133 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0009 | 0/0 | 1133 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0010 | 0/0 | 1133 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0011 | 0/0 | 1133 | 1 | 0 | 0 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0012 | 0/0 | 1133 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0013 | 0/0 | 1133 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0014 | 0/0 | 1133 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
t0015 | 0/0 | 1133 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
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 | 0/1 | 56 | 5 | 11 | 31 | 1 | 7 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0002 | 0/0 | 38 | 1 | 8 | 24 | 0 | 5 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0003 | 0/0 | 18 | 1 | 0 | 17 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0004 | 0/0 | 8 | 2 | 1 | 1 | 0 | 4 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0008 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0010 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0012 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
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 | 1/1 | 1482 | 278 | 82 | 39 | 109 | 5 | 41 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0002 | 0/0 | 1482 | 41 | 1 | 1 | 38 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0003 | 0/0 | 1482 | 6 | 5 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0004 | 0/0 | 1482 | 2 | 1 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0008 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0002c0009 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0002c0010 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0003c0005 | 0/0 | 1482 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0004c0007 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0005c0006 | 0/0 | 1482 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0006c0011 | 0/0 | 1482 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 2614 | 211 | 42 | 35 | 98 | 5 | 29 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0001t0002 | 0/0 | 2614 | 39 | 21 | 4 | 2 | 0 | 12 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0001t0003 | 0/0 | 2614 | 13 | 13 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0001t0004 | 0/0 | 2614 | 6 | 0 | 0 | 6 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0001t0007 | 0/0 | 2614 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0001t0008 | 0/0 | 2614 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0001t0009 | 0/0 | 2614 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0001t0010 | 0/0 | 2614 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0001t0012 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0001t0013 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0001t0014 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0002t0002 | 0/0 | 2614 | 35 | 1 | 1 | 33 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0002t0006 | 0/0 | 2614 | 5 | 0 | 0 | 5 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0002t0011 | 0/0 | 2614 | 1 | 0 | 0 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0003t0005 | 0/0 | 2614 | 6 | 5 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0004t0002 | 0/0 | 2614 | 2 | 1 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0001c0008t0015 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0002c0009t0001 | 0/0 | 2614 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0002c0010t0002 | 0/0 | 2614 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0003c0005t0001 | 0/0 | 2614 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0004c0007t0001 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0005c0006t0001 | 0/0 | 2614 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
a0006c0011t0001 | 0/0 | 2614 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | copy fasta | chr12 | 53152663 | 53185925 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/1 | 56 | 5 | 11 | 31 | 1 | 7 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0002 | 0/0 | 38 | 1 | 8 | 24 | 0 | 5 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0008 | 0/0 | 5 | 0 | 1 | 0 | 1 | 3 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0010 | 0/0 | 4 | 1 | 2 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0011 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0012 | 0/0 | 4 | 1 | 2 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0016 | 0/0 | 3 | 0 | 1 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0017 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0018 | 0/0 | 3 | 1 | 2 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0020 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0031 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0036 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0040 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0104 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0004 | 0/0 | 8 | 2 | 1 | 1 | 0 | 4 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0006 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0013 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0002g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0003g0005 | 0/0 | 7 | 7 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0003g0024 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0003g0025 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0003g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0004g0007 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0004g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0007g0029 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0008g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0009g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0010g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0012g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0013g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0001t0014g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0002g0003 | 0/0 | 18 | 1 | 0 | 17 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0002g0009 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0002g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0006g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0006g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0002t0011g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0003t0005g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0003t0005g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0003t0005g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0003t0005g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0003t0005g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0004t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0004t0002g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0001c0008t0015g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0002c0009t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0002c0010t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0003c0005t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0004c0007t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0005c0006t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
a0006c0011t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0008 | EUR | GBR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0089 | EUR | GBR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | FIN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00323 | hp2 | a0001 | c0002 | t0011 | g0044 | EUR | FIN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0126 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00423 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00438 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00544 | hp1 | a0001 | c0002 | t0002 | g0045 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00558 | hp2 | a0001 | c0002 | t0002 | g0048 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | CHS | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01167 | hp2 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0026 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01255 | hp1 | a0001 | c0003 | t0005 | g0116 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0047 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01346 | hp1 | a0002 | c0010 | t0002 | g0046 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01433 | hp2 | a0005 | c0006 | t0001 | g0086 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01884 | hp1 | a0001 | c0003 | t0005 | g0115 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0051 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01891 | hp2 | a0001 | c0001 | t0008 | g0028 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01981 | hp1 | a0002 | c0009 | t0001 | g0121 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02056 | hp2 | a0001 | c0002 | t0002 | g0043 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02071 | hp1 | a0001 | c0001 | t0004 | g0007 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02071 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0077 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02135 | hp1 | a0001 | c0001 | t0013 | g0096 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0071 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | CDX | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CDX | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02257 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0076 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02280 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | PEL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02523 | hp1 | a0006 | c0011 | t0001 | g0119 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0064 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02622 | hp2 | a0001 | c0003 | t0005 | g0035 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02630 | hp2 | a0001 | c0003 | t0005 | g0035 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0013 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0102 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0142 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02922 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0057 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0054 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0150 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0085 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0149 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03130 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03139 | hp1 | a0001 | c0002 | t0002 | g0003 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0028 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03209 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03209 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0005 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0063 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03453 | hp1 | a0001 | c0004 | t0002 | g0056 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03453 | hp2 | a0001 | c0003 | t0005 | g0118 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0075 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0040 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0132 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0130 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0053 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0070 | AFR | GWD | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03579 | hp2 | a0001 | c0001 | t0007 | g0029 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0012 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0062 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03688 | hp2 | a0001 | c0004 | t0002 | g0066 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0133 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0129 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0004 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0060 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0055 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0059 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | YRI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | YRI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | CHB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18906 | hp1 | a0001 | c0003 | t0005 | g0117 | AFR | YRI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18906 | hp2 | a0001 | c0001 | t0002 | g0014 | AFR | YRI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18944 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18946 | hp2 | a0001 | c0002 | t0006 | g0072 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18948 | hp1 | a0001 | c0008 | t0015 | g0134 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18948 | hp2 | a0004 | c0007 | t0001 | g0088 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18952 | hp1 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18952 | hp2 | a0001 | c0002 | t0002 | g0022 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18954 | hp1 | a0001 | c0001 | t0014 | g0091 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18964 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18965 | hp2 | a0001 | c0002 | t0006 | g0015 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18967 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18973 | hp2 | a0001 | c0002 | t0002 | g0023 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18975 | hp1 | a0001 | c0002 | t0006 | g0015 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18979 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18983 | hp1 | a0001 | c0001 | t0012 | g0095 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0108 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18985 | hp2 | a0001 | c0002 | t0002 | g0021 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18988 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18994 | hp2 | a0001 | c0002 | t0002 | g0041 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18995 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18997 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18997 | hp2 | a0001 | c0002 | t0002 | g0042 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19005 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19011 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | LWK | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0068 | AFR | LWK | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | LWK | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0025 | AFR | LWK | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19056 | hp1 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19058 | hp1 | a0001 | c0002 | t0006 | g0073 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19060 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19062 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19064 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19070 | hp2 | a0001 | c0002 | t0006 | g0015 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19077 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0103 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19082 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19083 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19084 | hp2 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19085 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0007 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19087 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19089 | hp1 | a0001 | c0002 | t0002 | g0003 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19091 | hp2 | a0001 | c0002 | t0002 | g0050 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19240 | hp1 | a0003 | c0005 | t0001 | g0146 | AFR | YRI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0014 | AFR | ASW | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0001 | EUR | TSI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | TSI | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | GIH | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | GIH | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0010 | AMR | CLM | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02109 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0005 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0052 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03471 | hp1 | a0001 | c0001 | t0002 | g0006 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0139 | AFR | MSL | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0030 | AFR | USA | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0098 | AFR | USA | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA18955 | hp2 | a0001 | c0002 | t0002 | g0009 | EAS | JPT | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0004 | AFR | LWK | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0027 | AFR | LWK | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0001 | REF | REF | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0104 | REF | REF | CSAD_chr12_53152663_53185925 | CSAD | chr12 | 53152663 | 53185925 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:53160142
|
C | T | 1 | a0002 | 2 | HG01346.hp1 HG01981.hp1 |
missense_variant | MODERATE | c.1144G>A | p.Asp382Asn | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 14/17 | 1428/2614 | 1144/1482 | 382/493 | chr12 | 53160142 | ||
chr12:53171972
|
C | T | 1 | a0004 | 1 | NA18948.hp2 | missense_variant | MODERATE | c.361G>A | p.Ala121Thr | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 7/17 | 645/2614 | 361/1482 | 121/493 | chr12 | 53171972 | ||
chr12:53172390
|
A | T | 1 | a0005 | 1 | HG01433.hp2 | missense_variant | MODERATE | c.300T>A | p.His100Gln | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/17 | 584/2614 | 300/1482 | 100/493 | chr12 | 53172390 | ||
chr12:53172428
|
G | A | 1 | a0006 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.262C>T | p.Arg88Trp | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/17 | 546/2614 | 262/1482 | 88/493 | chr12 | 53172428 | ||
chr12:53173451
|
A | T | 1 | a0003 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.20T>A | p.Leu7His | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/17 | 304/2614 | 20/1482 | 7/493 | chr12 | 53173451 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:53170081
|
G | A | 2 | a0001c0002a0002c0010 | 42 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(39): Show |
synonymous_variant | LOW | c.693C>T | p.Ala231Ala | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/17 | 977/2614 | 693/1482 | 231/493 | chr12 | 53170081 | ||
chr12:53170473
|
C | T | 1 | a0001c0003 | 6 | HG01255.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
synonymous_variant | LOW | c.597G>A | p.Ala199Ala | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 9/17 | 881/2614 | 597/1482 | 199/493 | chr12 | 53170473 | ||
chr12:53171353
|
C | T | 1 | a0001c0008 | 1 | NA18948.hp1 | synonymous_variant | LOW | c.540G>A | p.Pro180Pro | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/17 | 824/2614 | 540/1482 | 180/493 | chr12 | 53171353 | ||
chr12:53172381
|
G | A | 1 | a0001c0003 | 6 | HG01255.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
synonymous_variant | LOW | c.309C>T | p.Ala103Ala | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/17 | 593/2614 | 309/1482 | 103/493 | chr12 | 53172381 | ||
chr12:53172625
|
C | T | 1 | a0001c0004 | 2 | HG03453.hp1 HG03688.hp2 |
synonymous_variant | LOW | c.150G>A | p.Glu50Glu | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 5/17 | 434/2614 | 150/1482 | 50/493 | chr12 | 53172625 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:53157773
|
G | T | 2 | a0001c0001t0008a0001c0001t0012 | 3 | HG01891.hp2 HG03195.hp1 NA18983.hp1 |
3_prime_UTR_variant | MODIFIER | c.*738C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 738 | chr12 | 53157773 | |||||
chr12:53157814
|
A | G | 1 | a0001c0001t0010 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*697T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 697 | chr12 | 53157814 | |||||
chr12:53157940
|
A | G | 1 | a0001c0001t0004 | 6 | HG02071.hp1 NA18998.hp2 NA19077.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*571T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 571 | chr12 | 53157940 | |||||
chr12:53157986
|
T | C | 1 | a0001c0001t0008 | 2 | HG01891.hp2 HG03195.hp1 |
3_prime_UTR_variant | MODIFIER | c.*525A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 525 | chr12 | 53157986 | |||||
chr12:53158046
|
A | G | 1 | a0001c0001t0007 | 2 | HG03209.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*465T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 465 | chr12 | 53158046 | |||||
chr12:53158076
|
G | C | 1 | a0001c0002t0011 | 1 | HG00323.hp2 | 3_prime_UTR_variant | MODIFIER | c.*435C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 435 | chr12 | 53158076 | |||||
chr12:53158208
|
G | A | 1 | a0001c0003t0005 | 6 | HG01255.hp1 HG01884.hp1 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*303C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 303 | chr12 | 53158208 | |||||
chr12:53158264
|
T | C | 1 | a0001c0001t0013 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*247A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 247 | chr12 | 53158264 | |||||
chr12:53158333
|
A | C | 1 | a0001c0001t0010 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*178T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 178 | chr12 | 53158333 | |||||
chr12:53158356
|
G | A | 1 | a0001c0001t0003 | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*155C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 155 | chr12 | 53158356 | |||||
chr12:53158415
|
C | T | 1 | a0001c0001t0009 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*96G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 96 | chr12 | 53158415 | |||||
chr12:53158467
|
C | A | 1 | a0001c0001t0014 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*44G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 44 | chr12 | 53158467 | |||||
chr12:53158509
|
G | A | 1 | a0001c0008t0015 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 17/17 | 2 | chr12 | 53158509 | |||||
chr12:53180823
|
G | C | 1 | a0001c0002t0006 | 5 | NA18946.hp2 NA18965.hp2 NA18975.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-182C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/17 | 7353 | chr12 | 53180823 | |||||
chr12:53180847
|
A | C | 11 | a0001c0001t0002a0001c0001t0003a0001c0001t0007others(8): Show | 102 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
5_prime_UTR_variant | MODIFIER | c.-206T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/17 | 7377 | chr12 | 53180847 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr12:53158691
|
A | G | 24 | a0001c0001t0002g0049a0001c0001t0003g0005a0001c0001t0003g0024others(21): Show | 58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
splice_region_variant&intron_variant | LOW | c.1309-7T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53158691 | ||||||
chr12:53158877
|
G | T | 77 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(74): Show | 179 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.1309-193C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53158877 | ||||||
chr12:53159128
|
A | C | 1 | a0001c0001t0003g0025 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1309-444T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53159128 | ||||||
chr12:53159448
|
T | C | 18 | a0001c0001t0002g0049a0001c0002t0002g0003a0001c0002t0002g0009others(15): Show | 43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.1308+175A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53159448 | ||||||
chr12:53159469
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1308+154G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53159469 | ||||||
chr12:53159600
|
A | G | 3 | a0001c0001t0002g0013a0001c0001t0002g0051a0001c0001t0002g0065 | 5 | HG01884.hp2 HG02145.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.1308+23T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53159600 | ||||||
chr12:53159615
|
A | T | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | splice_region_variant&intron_variant | LOW | c.1308+8T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 16/16 | chr12 | 53159615 | ||||||
chr12:53159734
|
A | G | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1219-22T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 15/16 | chr12 | 53159734 | ||||||
chr12:53159736
|
G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1219-24C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 15/16 | chr12 | 53159736 | ||||||
chr12:53159811
|
A | G | 1 | a0001c0001t0001g0129 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1218+76T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 15/16 | chr12 | 53159811 | ||||||
chr12:53160045
|
C | T | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.1166+75G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 14/16 | chr12 | 53160045 | ||||||
chr12:53160342
|
T | C | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.967-23A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160342 | ||||||
chr12:53160386
|
T | G | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.967-67A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160386 | ||||||
chr12:53160412
|
T | C | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.967-93A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160412 | ||||||
chr12:53160499
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(14): Show | 65 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(62): Show |
intron_variant | MODIFIER | c.967-180C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160499 | ||||||
chr12:53160568
|
C | A | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.966+195G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160568 | ||||||
chr12:53160578
|
T | TTC | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.966+183_966+184dup others(2): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160578 | ||||||
chr12:53160599
|
G | C | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.966+164C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160599 | ||||||
chr12:53160613
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.966+150G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 13/16 | chr12 | 53160613 | ||||||
chr12:53161256
|
G | C | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.819+17C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 11/16 | chr12 | 53161256 | ||||||
chr12:53161450
|
G | C | 1 | a0001c0001t0001g0152 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.703-61C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53161450 | ||||||
chr12:53161591
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.703-202G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53161591 | ||||||
chr12:53161674
|
A | T | 24 | a0001c0001t0002g0049a0001c0001t0003g0005a0001c0001t0003g0024others(21): Show | 58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.703-285T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53161674 | ||||||
chr12:53161999
|
C | A | 19 | a0001c0001t0002g0049a0001c0001t0007g0029a0001c0002t0002g0003others(16): Show | 45 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(42): Show |
intron_variant | MODIFIER | c.703-610G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53161999 | ||||||
chr12:53162018
|
G | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-629C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162018 | ||||||
chr12:53162089
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.703-700C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162089 | ||||||
chr12:53162168
|
G | C | 1 | a0001c0001t0001g0097 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.703-779C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162168 | ||||||
chr12:53162198
|
G | A | 2 | a0001c0003t0005g0115a0001c0003t0005g0117 | 2 | HG01884.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.703-809C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162198 | ||||||
chr12:53162218
|
A | C | 1 | a0001c0002t0002g0045 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.703-829T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162218 | ||||||
chr12:53162286
|
T | C | 1 | a0001c0001t0002g0061 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.703-897A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162286 | ||||||
chr12:53162338
|
C | T | 2 | a0001c0004t0002g0056a0001c0004t0002g0066 | 2 | HG03453.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.703-949G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162338 | ||||||
chr12:53162503
|
G | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-1114C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162503 | ||||||
chr12:53162568
|
T | G | 1 | a0001c0002t0002g0047 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.703-1179A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162568 | ||||||
chr12:53162629
|
T | C | 1 | a0001c0002t0002g0050 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.703-1240A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162629 | ||||||
chr12:53162701
|
T | C | 1 | a0001c0001t0001g0039 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.703-1312A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162701 | ||||||
chr12:53162764
|
G | GA | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-1376dupT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162764 | ||||||
chr12:53162787
|
C | T | 1 | a0001c0001t0001g0132 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.703-1398G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162787 | ||||||
chr12:53162813
|
G | A | 1 | a0001c0001t0001g0098 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.703-1424C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162813 | ||||||
chr12:53162881
|
G | C | 1 | a0001c0001t0003g0024 | 2 | HG02615.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.703-1492C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162881 | ||||||
chr12:53162966
|
C | A | 1 | a0001c0003t0005g0116 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.703-1577G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162966 | ||||||
chr12:53162991
|
G | A | 18 | a0001c0001t0002g0049a0001c0002t0002g0003a0001c0002t0002g0009others(15): Show | 43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.703-1602C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53162991 | ||||||
chr12:53163017
|
C | T | 1 | a0001c0001t0003g0025 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.703-1628G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163017 | ||||||
chr12:53163061
|
CA | C | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-1673delT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163061 | ||||||
chr12:53163093
|
T | C | 1 | a0001c0001t0001g0099 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.703-1704A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163093 | ||||||
chr12:53163330
|
C | G | 4 | a0001c0001t0002g0006a0001c0001t0002g0014a0001c0001t0002g0068others(1): Show | 10 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.703-1941G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163330 | ||||||
chr12:53163505
|
T | C | 1 | a0001c0001t0001g0100 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.703-2116A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163505 | ||||||
chr12:53163681
|
AAT | A | 4 | a0001c0001t0001g0010a0001c0001t0001g0089a0001c0001t0001g0102others(1): Show | 7 | HG00140.hp2 HG00323.hp1 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.703-2294_703-2293d others(4): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163681 | ||||||
chr12:53163751
|
C | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0080a0001c0001t0001g0114 | 5 | NA18939.hp2 NA18962.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.703-2362G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163751 | ||||||
chr12:53163903
|
T | G | 1 | a0001c0001t0003g0025 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.703-2514A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163903 | ||||||
chr12:53163984
|
G | GTTGTAAG others(9): Show |
1 | a0001c0002t0006g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.703-2596_703-2595i others(18): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163984 | ||||||
chr12:53163985
|
C | T | 1 | a0001c0002t0006g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.703-2596G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163985 | ||||||
chr12:53163986
|
C | A | 1 | a0001c0002t0006g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.703-2597G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53163986 | ||||||
chr12:53164305
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.703-2916G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164305 | ||||||
chr12:53164394
|
T | G | 1 | a0001c0001t0002g0067 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.703-3005A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164394 | ||||||
chr12:53164536
|
A | G | 1 | a0001c0001t0001g0092 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.703-3147T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164536 | ||||||
chr12:53164591
|
G | A | 1 | a0001c0008t0015g0134 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.703-3202C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164591 | ||||||
chr12:53164722
|
C | T | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-3333G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164722 | ||||||
chr12:53164759
|
G | C | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-3370C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164759 | ||||||
chr12:53164909
|
A | T | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-3520T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53164909 | ||||||
chr12:53165040
|
G | C | 1 | a0001c0001t0001g0101 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.703-3651C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165040 | ||||||
chr12:53165202
|
G | T | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-3813C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165202 | ||||||
chr12:53165245
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(74): Show | 179 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(176): Show |
intron_variant | MODIFIER | c.703-3856T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165245 | ||||||
chr12:53165266
|
A | G | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.703-3877T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165266 | ||||||
chr12:53165287
|
A | T | 1 | a0001c0001t0001g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.703-3898T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165287 | ||||||
chr12:53165340
|
C | CA | 8 | a0001c0001t0001g0138a0001c0001t0003g0005a0001c0001t0003g0024others(5): Show | 17 | HG00673.hp2 HG01255.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.703-3952dupT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165340 | ||||||
chr12:53165387
|
G | A | 1 | a0001c0001t0002g0027 | 2 | HG02723.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.703-3998C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165387 | ||||||
chr12:53165400
|
C | G | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.703-4011G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165400 | ||||||
chr12:53165404
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.703-4015A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165404 | ||||||
chr12:53165405
|
G | A | 151 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(148): Show | 333 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(330): Show |
intron_variant | MODIFIER | c.703-4016C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165405 | ||||||
chr12:53165444
|
A | G | 1 | a0001c0001t0008g0028 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.703-4055T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165444 | ||||||
chr12:53165456
|
C | G | 1 | a0001c0001t0003g0053 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.703-4067G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165456 | ||||||
chr12:53165524
|
G | T | 1 | a0001c0001t0002g0060 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.703-4135C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165524 | ||||||
chr12:53165555
|
C | A | 2 | a0001c0004t0002g0056a0001c0004t0002g0066 | 2 | HG03453.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.703-4166G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165555 | ||||||
chr12:53165620
|
G | C | 1 | a0001c0001t0001g0102 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.703-4231C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165620 | ||||||
chr12:53165662
|
C | CA | 10 | a0001c0001t0001g0034a0001c0001t0001g0038a0001c0001t0001g0093others(7): Show | 13 | HG02109.hp1 HG02145.hp1 HG02622.hp1 others(10): Show |
intron_variant | MODIFIER | c.703-4274dupT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165662 | ||||||
chr12:53165662
|
CA | C | 10 | a0001c0001t0001g0033a0001c0001t0001g0037a0001c0001t0001g0074others(7): Show | 12 | HG00323.hp2 HG01081.hp1 HG01099.hp2 others(9): Show |
intron_variant | MODIFIER | c.703-4274delT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165662 | ||||||
chr12:53165703
|
C | A | 2 | a0001c0001t0001g0147a0003c0005t0001g0146 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.703-4314G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165703 | ||||||
chr12:53165820
|
T | C | 1 | a0001c0001t0001g0011 | 4 | HG01891.hp1 HG03098.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+4252A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165820 | ||||||
chr12:53165909
|
T | C | 1 | a0001c0001t0002g0062 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.702+4163A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165909 | ||||||
chr12:53165929
|
T | C | 1 | a0001c0001t0001g0092 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.702+4143A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165929 | ||||||
chr12:53165974
|
T | C | 1 | a0001c0001t0002g0013 | 3 | HG02145.hp2 HG02572.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.702+4098A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165974 | ||||||
chr12:53165989
|
C | T | 1 | a0001c0002t0002g0048 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.702+4083G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53165989 | ||||||
chr12:53166118
|
T | C | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.702+3954A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166118 | ||||||
chr12:53166120
|
A | AG | 24 | a0001c0001t0002g0049a0001c0001t0003g0005a0001c0001t0003g0024others(21): Show | 58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.702+3951dupC | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166120 | ||||||
chr12:53166131
|
C | T | 1 | a0001c0001t0001g0033 | 2 | HG03017.hp1 HG03654.hp1 |
intron_variant | MODIFIER | c.702+3941G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166131 | ||||||
chr12:53166200
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.702+3872G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166200 | ||||||
chr12:53166202
|
C | G | 1 | a0001c0001t0001g0092 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.702+3870G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166202 | ||||||
chr12:53166243
|
C | T | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(145): Show | 328 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.702+3829G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166243 | ||||||
chr12:53166331
|
G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+3741C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166331 | ||||||
chr12:53166659
|
G | C | 1 | a0001c0003t0005g0117 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.702+3413C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166659 | ||||||
chr12:53166711
|
G | A | 2 | a0001c0001t0002g0049a0001c0002t0002g0022 | 3 | HG00423.hp2 NA18949.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.702+3361C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166711 | ||||||
chr12:53166798
|
AAAAACAA others(3): Show |
A | 1 | a0001c0001t0001g0124 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.702+3264_702+3273d others(12): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166798 | ||||||
chr12:53166862
|
A | G | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+3210T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166862 | ||||||
chr12:53166896
|
T | A | 1 | a0001c0001t0001g0106 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.702+3176A>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166896 | ||||||
chr12:53166936
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.702+3136G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166936 | ||||||
chr12:53166936
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.702+3136G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53166936 | ||||||
chr12:53167201
|
T | C | 1 | a0001c0001t0002g0069 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.702+2871A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53167201 | ||||||
chr12:53167267
|
A | G | 2 | a0001c0001t0001g0039a0001c0002t0011g0044 | 3 | HG00323.hp2 HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.702+2805T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53167267 | ||||||
chr12:53167578
|
T | C | 1 | a0001c0002t0006g0073 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.702+2494A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53167578 | ||||||
chr12:53167874
|
G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+2198C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53167874 | ||||||
chr12:53168069
|
C | T | 2 | a0001c0001t0001g0082a0001c0001t0003g0025 | 3 | HG03139.hp2 NA19043.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.702+2003G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168069 | ||||||
chr12:53168394
|
T | C | 1 | a0001c0001t0001g0107 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.702+1678A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168394 | ||||||
chr12:53168402
|
A | C | 1 | a0001c0001t0014g0091 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.702+1670T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168402 | ||||||
chr12:53168418
|
A | C | 1 | a0001c0001t0002g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.702+1654T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168418 | ||||||
chr12:53168516
|
A | G | 3 | a0001c0001t0001g0019a0001c0001t0001g0080a0001c0001t0001g0114 | 5 | NA18939.hp2 NA18962.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+1556T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168516 | ||||||
chr12:53168539
|
C | G | 1 | a0001c0001t0001g0108 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.702+1533G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168539 | ||||||
chr12:53168578
|
T | C | 1 | a0001c0001t0001g0108 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.702+1494A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168578 | ||||||
chr12:53168932
|
C | A | 2 | a0001c0004t0002g0056a0001c0004t0002g0066 | 2 | HG03453.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.702+1140G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53168932 | ||||||
chr12:53169050
|
C | A | 2 | a0001c0001t0001g0020a0001c0001t0001g0144 | 4 | NA18999.hp2 NA19068.hp2 NA19082.hp1 others(1): Show |
intron_variant | MODIFIER | c.702+1022G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169050 | ||||||
chr12:53169063
|
C | T | 2 | a0001c0001t0002g0006a0001c0001t0002g0068 | 6 | HG01109.hp1 HG02109.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.702+1009G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169063 | ||||||
chr12:53169105
|
G | A | 3 | a0001c0001t0001g0019a0001c0001t0001g0080a0001c0001t0001g0114 | 5 | NA18939.hp2 NA18962.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.702+967C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169105 | ||||||
chr12:53169128
|
C | T | 1 | a0001c0001t0001g0090 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.702+944G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169128 | ||||||
chr12:53169147
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.702+925A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169147 | ||||||
chr12:53169209
|
A | G | 27 | a0001c0001t0001g0137a0001c0001t0002g0049a0001c0001t0003g0005others(24): Show | 62 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(59): Show |
intron_variant | MODIFIER | c.702+863T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169209 | ||||||
chr12:53169440
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.702+632A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169440 | ||||||
chr12:53169479
|
CA | C | 33 | a0001c0001t0001g0032a0001c0001t0001g0078a0001c0001t0002g0004others(30): Show | 70 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(67): Show |
intron_variant | MODIFIER | c.702+592delT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169479 | ||||||
chr12:53169495
|
A | T | 1 | a0001c0001t0001g0136 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.702+577T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169495 | ||||||
chr12:53169669
|
C | A | 1 | a0001c0003t0005g0118 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.702+403G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169669 | ||||||
chr12:53169686
|
G | C | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+386C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169686 | ||||||
chr12:53169784
|
CCTTCCAC others(50): Show |
C | 1 | a0001c0001t0001g0110 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.702+231_702+287del others(57): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53169784 | ||||||
chr12:53170008
|
G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+64C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53170008 | ||||||
chr12:53170044
|
A | C | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.702+28T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 10/16 | chr12 | 53170044 | ||||||
chr12:53170144
|
G | A | 2 | a0001c0001t0002g0054a0001c0001t0009g0057 | 2 | HG02922.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.648-18C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 9/16 | chr12 | 53170144 | ||||||
chr12:53170150
|
A | G | 1 | a0001c0002t0002g0021 | 2 | NA18952.hp1 NA18985.hp2 |
intron_variant | MODIFIER | c.648-24T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 9/16 | chr12 | 53170150 | ||||||
chr12:53170373
|
T | G | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.647+50A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 9/16 | chr12 | 53170373 | ||||||
chr12:53170722
|
G | GT | 5 | a0001c0001t0001g0031a0001c0001t0001g0089a0001c0001t0001g0129others(2): Show | 6 | HG00140.hp2 HG03831.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.568-221dupA | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/16 | chr12 | 53170722 | ||||||
chr12:53170722
|
GT | G | 22 | a0001c0001t0001g0111a0001c0001t0002g0049a0001c0001t0003g0005others(19): Show | 55 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(52): Show |
intron_variant | MODIFIER | c.568-221delA | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/16 | chr12 | 53170722 | ||||||
chr12:53170807
|
G | A | 18 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0014others(15): Show | 32 | HG01109.hp1 HG01256.hp2 HG02080.hp1 others(29): Show |
intron_variant | MODIFIER | c.568-305C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/16 | chr12 | 53170807 | ||||||
chr12:53171001
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.567+325C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/16 | chr12 | 53171001 | ||||||
chr12:53171124
|
C | A | 1 | a0001c0002t0002g0048 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.567+202G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/16 | chr12 | 53171124 | ||||||
chr12:53171296
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.567+30G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 8/16 | chr12 | 53171296 | ||||||
chr12:53171449
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG03540.hp2 | splice_region_variant&intron_variant | LOW | c.452-8T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 7/16 | chr12 | 53171449 | ||||||
chr12:53171459
|
C | T | 1 | a0001c0001t0003g0025 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.452-18G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 7/16 | chr12 | 53171459 | ||||||
chr12:53171673
|
T | C | 78 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(75): Show | 180 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(177): Show |
intron_variant | MODIFIER | c.451+209A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 7/16 | chr12 | 53171673 | ||||||
chr12:53171849
|
G | C | 1 | a0001c0001t0001g0113 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.451+33C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 7/16 | chr12 | 53171849 | ||||||
chr12:53172034
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.345-46C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/16 | chr12 | 53172034 | ||||||
chr12:53172171
|
C | G | 2 | a0001c0001t0001g0087a0001c0001t0001g0125 | 2 | HG02135.hp2 NA18747.hp2 |
intron_variant | MODIFIER | c.344+175G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/16 | chr12 | 53172171 | ||||||
chr12:53172243
|
C | G | 1 | a0001c0001t0001g0133 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.344+103G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/16 | chr12 | 53172243 | ||||||
chr12:53172293
|
T | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0080a0001c0001t0001g0114 | 5 | NA18939.hp2 NA18962.hp2 NA18964.hp2 others(2): Show |
intron_variant | MODIFIER | c.344+53A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 6/16 | chr12 | 53172293 | ||||||
chr12:53172707
|
C | T | 24 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0013others(21): Show | 41 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(38): Show |
intron_variant | MODIFIER | c.127-59G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53172707 | ||||||
chr12:53172730
|
C | T | 2 | a0001c0001t0001g0147a0003c0005t0001g0146 | 2 | HG02809.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.127-82G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53172730 | ||||||
chr12:53172930
|
A | T | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0003c0005t0001g0146 | 3 | HG02809.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.127-282T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53172930 | ||||||
chr12:53172934
|
G | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.127-286C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53172934 | ||||||
chr12:53173006
|
G | A | 6 | a0001c0001t0001g0008a0001c0001t0003g0005a0001c0001t0003g0024others(3): Show | 18 | HG00140.hp1 HG01168.hp2 HG02257.hp1 others(15): Show |
intron_variant | MODIFIER | c.126+339C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173006 | ||||||
chr12:53173065
|
G | A | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.126+280C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173065 | ||||||
chr12:53173069
|
G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.126+276C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173069 | ||||||
chr12:53173224
|
G | C | 1 | a0001c0001t0001g0148 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.126+121C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173224 | ||||||
chr12:53173244
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.126+101C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173244 | ||||||
chr12:53173254
|
AG | A | 35 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0139others(32): Show | 72 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(69): Show |
intron_variant | MODIFIER | c.126+90delC | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173254 | ||||||
chr12:53173263
|
G | T | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.126+82C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173263 | ||||||
chr12:53173278
|
GGAAAAAA others(5): Show |
G | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.126+55_126+66delTT others(10): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 4/16 | chr12 | 53173278 | ||||||
chr12:53173822
|
A | G | 1 | a0001c0001t0008g0028 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-49-52T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53173822 | ||||||
chr12:53173863
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0085 | 3 | HG02630.hp1 HG03041.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.-49-93T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53173863 | ||||||
chr12:53173899
|
C | CA | 5 | a0001c0001t0001g0080a0001c0001t0002g0049a0001c0001t0002g0064others(2): Show | 5 | HG01981.hp1 HG02602.hp1 HG03195.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-130dupT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53173899 | ||||||
chr12:53174070
|
C | G | 4 | a0001c0001t0002g0006a0001c0001t0002g0014a0001c0001t0002g0068others(1): Show | 10 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.-49-300G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174070 | ||||||
chr12:53174087
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-49-317C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174087 | ||||||
chr12:53174188
|
CAGCT | C | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-49-422_-49-419del others(4): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174188 | ||||||
chr12:53174307
|
CA | C | 75 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(72): Show | 175 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(172): Show |
intron_variant | MODIFIER | c.-49-538delT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174307 | ||||||
chr12:53174371
|
T | C | 1 | a0001c0001t0001g0122 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-49-601A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174371 | ||||||
chr12:53174426
|
A | G | 1 | a0001c0001t0002g0058 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-49-656T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174426 | ||||||
chr12:53174737
|
A | G | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-49-967T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174737 | ||||||
chr12:53174797
|
T | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0003c0005t0001g0146 | 3 | HG02809.hp1 HG02896.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-49-1027A>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53174797 | ||||||
chr12:53175003
|
A | T | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-49-1233T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175003 | ||||||
chr12:53175013
|
T | C | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-49-1243A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175013 | ||||||
chr12:53175072
|
C | G | 2 | a0001c0004t0002g0056a0001c0004t0002g0066 | 2 | HG03453.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-49-1302G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175072 | ||||||
chr12:53175280
|
G | A | 3 | a0001c0001t0001g0020a0001c0001t0001g0143a0001c0001t0001g0144 | 5 | NA18999.hp2 NA19058.hp2 NA19068.hp2 others(2): Show |
intron_variant | MODIFIER | c.-49-1510C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175280 | ||||||
chr12:53175515
|
T | C | 1 | a0001c0001t0001g0123 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-49-1745A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175515 | ||||||
chr12:53175605
|
G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-49-1835C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175605 | ||||||
chr12:53175703
|
A | G | 1 | a0001c0001t0009g0057 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-49-1933T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175703 | ||||||
chr12:53175759
|
A | C | 1 | a0001c0002t0002g0041 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.-49-1989T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175759 | ||||||
chr12:53175955
|
G | A | 1 | a0001c0001t0001g0124 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.-49-2185C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175955 | ||||||
chr12:53175999
|
C | A | 1 | a0001c0001t0002g0070 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-49-2229G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53175999 | ||||||
chr12:53176069
|
G | A | 1 | a0001c0001t0003g0025 | 2 | HG03139.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-49-2299C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176069 | ||||||
chr12:53176124
|
G | T | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-49-2354C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176124 | ||||||
chr12:53176238
|
C | T | 50 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0013others(47): Show | 102 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(99): Show |
intron_variant | MODIFIER | c.-49-2468G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176238 | ||||||
chr12:53176422
|
C | A | 2 | a0001c0001t0008g0028a0001c0001t0010g0071 | 3 | HG01891.hp2 HG02145.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.-49-2652G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176422 | ||||||
chr12:53176438
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-50+2664C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176438 | ||||||
chr12:53176502
|
G | A | 1 | a0001c0001t0001g0036 | 2 | NA18983.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.-50+2600C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176502 | ||||||
chr12:53176577
|
G | A | 1 | a0001c0001t0001g0125 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.-50+2525C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176577 | ||||||
chr12:53176668
|
G | A | 1 | a0001c0002t0002g0050 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.-50+2434C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176668 | ||||||
chr12:53176731
|
A | T | 1 | a0001c0001t0002g0067 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-50+2371T>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176731 | ||||||
chr12:53176733
|
T | A | 4 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0052others(1): Show | 11 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-50+2369A>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176733 | ||||||
chr12:53176875
|
G | C | 18 | a0001c0001t0002g0049a0001c0002t0002g0003a0001c0002t0002g0009others(15): Show | 43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-50+2227C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53176875 | ||||||
chr12:53177015
|
G | A | 22 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0013others(19): Show | 39 | HG01109.hp1 HG01167.hp2 HG01169.hp1 others(36): Show |
intron_variant | MODIFIER | c.-50+2087C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177015 | ||||||
chr12:53177084
|
G | T | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-50+2018C>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177084 | ||||||
chr12:53177584
|
T | C | 1 | a0001c0001t0001g0145 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-50+1518A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177584 | ||||||
chr12:53177605
|
C | T | 4 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0052others(1): Show | 11 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.-50+1497G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177605 | ||||||
chr12:53177615
|
A | C | 1 | a0001c0001t0001g0082 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.-50+1487T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177615 | ||||||
chr12:53177621
|
A | G | 1 | a0001c0001t0008g0028 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-50+1481T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177621 | ||||||
chr12:53177623
|
C | CTATT | 19 | a0001c0001t0001g0017a0001c0001t0002g0049a0001c0002t0002g0003others(16): Show | 46 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(43): Show |
intron_variant | MODIFIER | c.-50+1475_-50+1478d others(6): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177623 | ||||||
chr12:53177669
|
G | A | 1 | a0001c0001t0001g0126 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-50+1433C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177669 | ||||||
chr12:53177904
|
T | C | 8 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0003g0005others(5): Show | 16 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.-50+1198A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177904 | ||||||
chr12:53177919
|
C | T | 1 | a0001c0001t0002g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.-50+1183G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177919 | ||||||
chr12:53177924
|
G | A | 1 | a0001c0001t0001g0149 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-50+1178C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53177924 | ||||||
chr12:53178049
|
G | A | 1 | a0001c0001t0008g0028 | 2 | HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-50+1053C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178049 | ||||||
chr12:53178076
|
A | C | 18 | a0001c0001t0002g0049a0001c0002t0002g0003a0001c0002t0002g0009others(15): Show | 43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-50+1026T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178076 | ||||||
chr12:53178270
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.-50+832G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178270 | ||||||
chr12:53178316
|
C | A | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-50+786G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178316 | ||||||
chr12:53178317
|
A | C | 1 | a0001c0001t0001g0080 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.-50+785T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178317 | ||||||
chr12:53178340
|
A | G | 1 | a0001c0001t0002g0026 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-50+762T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178340 | ||||||
chr12:53178346
|
T | G | 24 | a0001c0001t0002g0049a0001c0001t0003g0005a0001c0001t0003g0024others(21): Show | 58 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(55): Show |
intron_variant | MODIFIER | c.-50+756A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178346 | ||||||
chr12:53178401
|
A | G | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-50+701T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178401 | ||||||
chr12:53178513
|
C | T | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-50+589G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178513 | ||||||
chr12:53178758
|
C | G | 1 | a0001c0001t0002g0026 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-50+344G>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178758 | ||||||
chr12:53178784
|
CA | C | 18 | a0001c0001t0002g0049a0001c0002t0002g0003a0001c0002t0002g0009others(15): Show | 43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-50+317delT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178784 | ||||||
chr12:53178788
|
AAAAAAT | A | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-50+308_-50+313del others(6): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178788 | ||||||
chr12:53178876
|
T | G | 1 | a0001c0001t0001g0127 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-50+226A>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178876 | ||||||
chr12:53178940
|
G | A | 1 | a0001c0004t0002g0066 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-50+162C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 2/16 | chr12 | 53178940 | ||||||
chr12:53179160
|
A | G | 3 | a0001c0001t0001g0016a0001c0001t0001g0078a0001c0001t0001g0079 | 5 | HG01934.hp2 HG01975.hp2 NA18949.hp1 others(2): Show |
intron_variant | MODIFIER | c.-90-18T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179160 | ||||||
chr12:53179216
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.-90-74G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179216 | ||||||
chr12:53179246
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-90-104G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179246 | ||||||
chr12:53179322
|
G | A | 1 | a0001c0001t0002g0067 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.-90-180C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179322 | ||||||
chr12:53179360
|
T | C | 1 | a0001c0001t0001g0150 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-90-218A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179360 | ||||||
chr12:53179390
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-90-248G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179390 | ||||||
chr12:53179447
|
G | A | 1 | a0001c0001t0001g0128 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-90-305C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179447 | ||||||
chr12:53179555
|
T | A | 2 | a0001c0001t0001g0012a0001c0001t0001g0151 | 5 | HG01074.hp2 HG01081.hp2 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.-90-413A>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179555 | ||||||
chr12:53179621
|
TTTCAATG | T | 5 | a0001c0001t0003g0005a0001c0001t0003g0024a0001c0001t0003g0025others(2): Show | 13 | HG02257.hp1 HG02280.hp1 HG02486.hp2 others(10): Show |
intron_variant | MODIFIER | c.-90-486_-90-480del others(7): Show |
CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179621 | ||||||
chr12:53179653
|
G | A | 1 | a0001c0001t0007g0029 | 2 | HG03209.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-90-511C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179653 | ||||||
chr12:53179670
|
C | CA | 5 | a0001c0001t0002g0006a0001c0001t0002g0014a0001c0001t0002g0068others(2): Show | 11 | HG01109.hp1 HG02109.hp2 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.-90-529dupT | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179670 | ||||||
chr12:53179715
|
G | GT | 77 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(74): Show | 176 | HG00140.hp1 HG00323.hp2 HG00423.hp2 others(173): Show |
intron_variant | MODIFIER | c.-90-574dupA | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179715 | ||||||
chr12:53179842
|
T | C | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG03492.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.-90-700A>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179842 | ||||||
chr12:53179851
|
C | T | 1 | a0001c0001t0001g0075 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-90-709G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53179851 | ||||||
chr12:53180032
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.-91+700C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180032 | ||||||
chr12:53180119
|
A | C | 18 | a0001c0001t0002g0049a0001c0002t0002g0003a0001c0002t0002g0009others(15): Show | 43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-91+613T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180119 | ||||||
chr12:53180185
|
C | A | 1 | a0001c0001t0010g0071 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-91+547G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180185 | ||||||
chr12:53180260
|
G | C | 18 | a0001c0001t0002g0049a0001c0002t0002g0003a0001c0002t0002g0009others(15): Show | 43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-91+472C>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180260 | ||||||
chr12:53180261
|
A | C | 18 | a0001c0001t0002g0049a0001c0002t0002g0003a0001c0002t0002g0009others(15): Show | 43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-91+471T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180261 | ||||||
chr12:53180455
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-91+277T>C | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180455 | ||||||
chr12:53180503
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.-91+229C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180503 | ||||||
chr12:53180549
|
A | C | 1 | a0001c0001t0001g0074 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.-91+183T>G | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180549 | ||||||
chr12:53180554
|
G | A | 1 | a0001c0001t0001g0132 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.-91+178C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180554 | ||||||
chr12:53180582
|
C | T | 18 | a0001c0001t0002g0049a0001c0002t0002g0003a0001c0002t0002g0009others(15): Show | 43 | HG00323.hp2 HG00423.hp2 HG00438.hp2 others(40): Show |
intron_variant | MODIFIER | c.-91+150G>A | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180582 | ||||||
chr12:53180706
|
G | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0012others(25): Show | 78 | HG00140.hp1 HG00438.hp1 HG00609.hp2 others(75): Show |
intron_variant | MODIFIER | c.-91+26C>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180706 | ||||||
chr12:53180708
|
C | A | 3 | a0001c0002t0006g0015a0001c0002t0006g0072a0001c0002t0006g0073 | 5 | NA18946.hp2 NA18965.hp2 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.-91+24G>T | CSAD | ENSG00000139631.20 | transcript | ENST00000444623.6 | protein_coding | 1/16 | chr12 | 53180708 |