geneid | 10152 |
---|---|
ensemblid | ENSG00000138443.17 |
hgncid | 24011 |
symbol | ABI2 |
name | abl interactor 2 |
refseq_nuc | NM_001375670.1 |
refseq_prot | NP_001362599.1 |
ensembl_nuc | ENST00000261018.12 |
ensembl_prot | ENSP00000261018.9 |
mane_status | MANE Select |
chr | chr2 |
start | 203328394 |
end | 203432169 |
strand | + |
ver | v1.2 |
region | chr2:203328394-203432169 |
region5000 | chr2:203323394-203437169 |
regionname0 | ABI2_chr2_203328394_203432169 |
regionname5000 | ABI2_chr2_203323394_203437169 |
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 | 542 | 320 | 80 | 60 | 140 | 10 | 28 | 106 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
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 | 1629 | 318 | 78 | 60 | 140 | 10 | 28 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
c0002 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 4940 | 90 | 9 | 18 | 48 | 4 | 10 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0002 | 1/0 | 4939 | 73 | 13 | 13 | 38 | 2 | 6 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0003 | 0/0 | 4940 | 38 | 13 | 16 | 3 | 2 | 4 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0004 | 0/0 | 4940 | 23 | 12 | 2 | 8 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0005 | 0/0 | 4940 | 21 | 4 | 3 | 12 | 0 | 2 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0006 | 0/0 | 4940 | 19 | 15 | 4 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0007 | 0/0 | 4944 | 6 | 0 | 0 | 6 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0008 | 0/0 | 4937 | 6 | 0 | 0 | 6 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0009 | 0/0 | 4938 | 4 | 4 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0010 | 0/0 | 4939 | 4 | 0 | 0 | 4 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0011 | 0/0 | 4940 | 3 | 3 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0012 | 0/0 | 4940 | 3 | 0 | 0 | 3 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0013 | 0/0 | 4940 | 2 | 0 | 0 | 2 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0014 | 0/0 | 4940 | 2 | 0 | 0 | 0 | 0 | 2 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0015 | 0/0 | 4939 | 2 | 0 | 1 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0016 | 0/0 | 4939 | 2 | 0 | 0 | 2 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0017 | 0/0 | 4940 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0018 | 0/0 | 4940 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0019 | 0/0 | 4941 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0020 | 0/0 | 4940 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0021 | 0/0 | 4941 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0022 | 0/0 | 4939 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0023 | 0/0 | 4940 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0024 | 0/0 | 4939 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0025 | 0/0 | 4940 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0026 | 0/0 | 4940 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0027 | 0/0 | 4940 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0028 | 0/0 | 4940 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0029 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0030 | 0/0 | 4940 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0031 | 0/0 | 4940 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0032 | 0/0 | 4938 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0033 | 0/0 | 4940 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0034 | 0/0 | 4939 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0035 | 0/0 | 4939 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0036 | 0/0 | 4939 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0037 | 0/0 | 4939 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
t0038 | 0/0 | 4939 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0315 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
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 | 1629 | 318 | 78 | 60 | 140 | 10 | 28 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0002 | 0/0 | 1629 | 2 | 2 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 6568 | 90 | 9 | 18 | 48 | 4 | 10 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0002 | 1/0 | 6567 | 73 | 13 | 13 | 38 | 2 | 6 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0003 | 0/0 | 6568 | 38 | 13 | 16 | 3 | 2 | 4 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0004 | 0/0 | 6568 | 23 | 12 | 2 | 8 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0005 | 0/0 | 6568 | 20 | 3 | 3 | 12 | 0 | 2 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0006 | 0/0 | 6568 | 19 | 15 | 4 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0007 | 0/0 | 6572 | 6 | 0 | 0 | 6 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0008 | 0/0 | 6565 | 6 | 0 | 0 | 6 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0009 | 0/0 | 6566 | 4 | 4 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0010 | 0/0 | 6567 | 4 | 0 | 0 | 4 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0011 | 0/0 | 6568 | 3 | 3 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0012 | 0/0 | 6568 | 3 | 0 | 0 | 3 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0013 | 0/0 | 6568 | 2 | 0 | 0 | 2 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0014 | 0/0 | 6568 | 2 | 0 | 0 | 0 | 0 | 2 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0015 | 0/0 | 6567 | 2 | 0 | 1 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0016 | 0/0 | 6567 | 2 | 0 | 0 | 2 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0017 | 0/0 | 6568 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0018 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0019 | 0/0 | 6569 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0020 | 0/0 | 6568 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0021 | 0/0 | 6569 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0022 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0023 | 0/0 | 6568 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0025 | 0/0 | 6568 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0026 | 0/0 | 6568 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0027 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0028 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0029 | 0/0 | 6566 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0030 | 0/0 | 6568 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0031 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0032 | 0/0 | 6566 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0033 | 0/0 | 6568 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0034 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0035 | 0/0 | 6567 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0036 | 0/0 | 6567 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0037 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0001t0038 | 0/0 | 6567 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0002t0005 | 0/0 | 6568 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
a0001c0002t0024 | 0/0 | 6567 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | copy fasta | chr2 | 203323394 | 203437169 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0315 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0011 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0133 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0003g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0004g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0007g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0007g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0007g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0007g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0007g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0007g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0008g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0008g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0008g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0008g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0008g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0008g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0009g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0009g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0009g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0010g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0010g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0010g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0010g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0011g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0011g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0011g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0012g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0012g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0012g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0013g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0013g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0014g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0014g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0015g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0015g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0016g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0016g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0017g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0018g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0019g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0020g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0021g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0022g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0023g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0025g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0026g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0027g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0028g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0029g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0030g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0031g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0032g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0033g0087 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0034g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0035g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0036g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0037g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0001t0038g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0002t0005g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
a0001c0002t0024g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0244 | EUR | FIN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00280 | hp2 | a0001 | c0001 | t0033 | g0087 | EUR | FIN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0011 | EUR | FIN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0254 | EUR | FIN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0027 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00438 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00621 | hp1 | a0001 | c0001 | t0021 | g0151 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00642 | hp1 | a0001 | c0001 | t0003 | g0199 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00642 | hp2 | a0001 | c0001 | t0003 | g0281 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00673 | hp1 | a0001 | c0001 | t0026 | g0313 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00673 | hp2 | a0001 | c0001 | t0008 | g0030 | EAS | CHS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0216 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00733 | hp2 | a0001 | c0001 | t0006 | g0166 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0294 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00738 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00738 | hp2 | a0001 | c0001 | t0020 | g0122 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0293 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01074 | hp1 | a0001 | c0001 | t0003 | g0188 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0029 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0055 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0279 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01109 | hp1 | a0001 | c0001 | t0006 | g0167 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01167 | hp2 | a0001 | c0001 | t0003 | g0211 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0009 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01168 | hp2 | a0001 | c0001 | t0006 | g0163 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01169 | hp1 | a0001 | c0001 | t0006 | g0164 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0306 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01175 | hp2 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01192 | hp1 | a0001 | c0001 | t0003 | g0282 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0056 | AMR | PUR | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0318 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01255 | hp2 | a0001 | c0001 | t0003 | g0225 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0249 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0054 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01257 | hp1 | a0001 | c0001 | t0005 | g0102 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0269 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01258 | hp1 | a0001 | c0001 | t0005 | g0103 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0286 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0022 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0307 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01433 | hp1 | a0001 | c0001 | t0030 | g0240 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01433 | hp2 | a0001 | c0001 | t0017 | g0252 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0197 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0299 | EUR | IBS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01515 | hp2 | a0001 | c0001 | t0003 | g0195 | EUR | IBS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01516 | hp1 | a0001 | c0001 | t0035 | g0064 | EUR | IBS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01516 | hp2 | a0001 | c0001 | t0003 | g0198 | EUR | IBS | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01884 | hp1 | a0001 | c0001 | t0006 | g0174 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01884 | hp2 | a0001 | c0001 | t0022 | g0319 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0185 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0289 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0309 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0060 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01943 | hp1 | a0001 | c0001 | t0004 | g0121 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0058 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01952 | hp1 | a0001 | c0001 | t0003 | g0310 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01975 | hp1 | a0001 | c0001 | t0015 | g0119 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0016 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0288 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0065 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0263 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0223 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0051 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02040 | hp2 | a0001 | c0001 | t0013 | g0101 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0287 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02055 | hp2 | a0001 | c0001 | t0027 | g0117 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02080 | hp1 | a0001 | c0001 | t0029 | g0096 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0231 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02083 | hp1 | a0001 | c0001 | t0005 | g0106 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02129 | hp1 | a0001 | c0001 | t0004 | g0135 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0127 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02135 | hp2 | a0001 | c0001 | t0005 | g0113 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02145 | hp2 | a0001 | c0001 | t0009 | g0177 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02148 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0076 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02155 | hp1 | a0001 | c0001 | t0005 | g0112 | EAS | CDX | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | CDX | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | CDX | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | CDX | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02258 | hp1 | a0001 | c0001 | t0003 | g0184 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02258 | hp2 | a0001 | c0001 | t0028 | g0168 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0264 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0221 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0021 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02280 | hp2 | a0001 | c0001 | t0006 | g0178 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02293 | hp1 | a0001 | c0001 | t0004 | g0141 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02293 | hp2 | a0001 | c0001 | t0005 | g0105 | AMR | PEL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02451 | hp1 | a0001 | c0001 | t0005 | g0176 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02451 | hp2 | a0001 | c0001 | t0009 | g0159 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0128 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02572 | hp1 | a0001 | c0001 | t0003 | g0209 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02572 | hp2 | a0001 | c0001 | t0006 | g0162 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02622 | hp1 | a0001 | c0001 | t0004 | g0146 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02630 | hp1 | a0001 | c0001 | t0004 | g0143 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02698 | hp1 | a0001 | c0001 | t0003 | g0219 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02717 | hp1 | a0001 | c0001 | t0009 | g0158 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0226 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0208 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02723 | hp2 | a0001 | c0001 | t0004 | g0145 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02809 | hp1 | a0001 | c0001 | t0011 | g0155 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02809 | hp2 | a0001 | c0001 | t0002 | g0020 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0044 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02818 | hp2 | a0001 | c0001 | t0006 | g0001 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02886 | hp1 | a0001 | c0001 | t0004 | g0137 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0210 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02895 | hp1 | a0001 | c0001 | t0009 | g0160 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0165 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02896 | hp1 | a0001 | c0001 | t0006 | g0175 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02896 | hp2 | a0001 | c0001 | t0003 | g0191 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02897 | hp1 | a0001 | c0001 | t0006 | g0150 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02897 | hp2 | a0001 | c0001 | t0003 | g0192 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02970 | hp1 | a0001 | c0001 | t0004 | g0138 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02970 | hp2 | a0001 | c0001 | t0005 | g0099 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0206 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02976 | hp2 | a0001 | c0002 | t0005 | g0116 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03098 | hp1 | a0001 | c0001 | t0006 | g0173 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0148 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03130 | hp1 | a0001 | c0001 | t0004 | g0125 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0170 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03139 | hp2 | a0001 | c0001 | t0011 | g0154 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03195 | hp2 | a0001 | c0001 | t0004 | g0134 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0061 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0144 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0171 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0012 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03491 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0213 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0084 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03516 | hp2 | a0001 | c0001 | t0006 | g0179 | AFR | ESN | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0142 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03540 | hp2 | a0001 | c0001 | t0006 | g0149 | AFR | GWD | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0063 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0204 | AFR | MSL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0261 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03669 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03688 | hp1 | a0001 | c0001 | t0025 | g0266 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03688 | hp2 | a0001 | c0001 | t0003 | g0317 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03710 | hp1 | a0001 | c0001 | t0004 | g0124 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03710 | hp2 | a0001 | c0001 | t0003 | g0220 | SAS | PJL | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03831 | hp1 | a0001 | c0001 | t0005 | g0115 | SAS | BEB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | BEB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03834 | hp1 | a0001 | c0001 | t0036 | g0073 | SAS | BEB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0276 | SAS | BEB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0161 | SAS | BEB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG03942 | hp2 | a0001 | c0001 | t0014 | g0277 | SAS | BEB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0314 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0311 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG04204 | hp1 | a0001 | c0001 | t0023 | g0114 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0041 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0278 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0006 | SAS | STU | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18747 | hp1 | a0001 | c0001 | t0004 | g0129 | EAS | CHB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18747 | hp2 | a0001 | c0001 | t0005 | g0109 | EAS | CHB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18906 | hp1 | a0001 | c0001 | t0002 | g0018 | AFR | YRI | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18906 | hp2 | a0001 | c0001 | t0004 | g0136 | AFR | YRI | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18939 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18940 | hp1 | a0001 | c0001 | t0016 | g0088 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18946 | hp1 | a0001 | c0001 | t0008 | g0034 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18949 | hp2 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18951 | hp1 | a0001 | c0001 | t0007 | g0089 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18960 | hp1 | a0001 | c0001 | t0013 | g0104 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0069 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18962 | hp1 | a0001 | c0001 | t0005 | g0152 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18962 | hp2 | a0001 | c0001 | t0010 | g0066 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18965 | hp1 | a0001 | c0001 | t0005 | g0111 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0285 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18966 | hp1 | a0001 | c0001 | t0004 | g0126 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0189 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18968 | hp1 | a0001 | c0001 | t0012 | g0123 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18968 | hp2 | a0001 | c0001 | t0007 | g0085 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18969 | hp1 | a0001 | c0001 | t0012 | g0131 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18970 | hp1 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18971 | hp1 | a0001 | c0001 | t0007 | g0093 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18971 | hp2 | a0001 | c0001 | t0016 | g0092 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18974 | hp2 | a0001 | c0001 | t0002 | g0043 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18977 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18978 | hp2 | a0001 | c0001 | t0005 | g0156 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0071 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18982 | hp1 | a0001 | c0001 | t0008 | g0003 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18986 | hp2 | a0001 | c0001 | t0010 | g0067 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18988 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18991 | hp1 | a0001 | c0001 | t0002 | g0074 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18992 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18993 | hp1 | a0001 | c0001 | t0005 | g0081 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18995 | hp1 | a0001 | c0001 | t0005 | g0110 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18999 | hp1 | a0001 | c0001 | t0008 | g0045 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0075 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19010 | hp2 | a0001 | c0001 | t0007 | g0091 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19030 | hp1 | a0001 | c0001 | t0018 | g0274 | AFR | LWK | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19030 | hp2 | a0001 | c0001 | t0003 | g0205 | AFR | LWK | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0308 | AFR | LWK | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19043 | hp2 | a0001 | c0001 | t0006 | g0172 | AFR | LWK | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19057 | hp1 | a0001 | c0001 | t0008 | g0040 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0083 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0130 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19066 | hp1 | a0001 | c0001 | t0010 | g0078 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19067 | hp1 | a0001 | c0001 | t0007 | g0007 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19068 | hp1 | a0001 | c0001 | t0038 | g0038 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19068 | hp2 | a0001 | c0001 | t0008 | g0090 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19070 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19077 | hp1 | a0001 | c0001 | t0019 | g0147 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19077 | hp2 | a0001 | c0001 | t0004 | g0217 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19081 | hp1 | a0001 | c0001 | t0007 | g0094 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19081 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19084 | hp2 | a0001 | c0001 | t0012 | g0132 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19085 | hp1 | a0001 | c0001 | t0034 | g0190 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19086 | hp2 | a0001 | c0001 | t0032 | g0039 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19087 | hp1 | a0001 | c0001 | t0010 | g0068 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19087 | hp2 | a0001 | c0001 | t0005 | g0100 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19088 | hp1 | a0001 | c0001 | t0015 | g0120 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0015 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0019 | AFR | YRI | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA19240 | hp2 | a0001 | c0001 | t0031 | g0183 | AFR | YRI | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0193 | EUR | TSI | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0242 | EUR | TSI | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA20905 | hp1 | a0001 | c0001 | t0014 | g0267 | SAS | GIH | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0268 | SAS | GIH | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02109 | hp1 | a0001 | c0001 | t0011 | g0153 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02109 | hp2 | a0001 | c0001 | t0037 | g0320 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0035 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02486 | hp2 | a0001 | c0001 | t0005 | g0098 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0139 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG02559 | hp2 | a0001 | c0001 | t0006 | g0180 | AFR | ACB | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0169 | AFR | USA | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0036 | AFR | USA | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA20300 | hp1 | a0001 | c0002 | t0024 | g0118 | AFR | USA | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0010 | AFR | USA | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0257 | AFR | LWK | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | LWK | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0315 | REF | REF | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0002 | g0133 | REF | REF | ABI2_chr2_203323394_203437169 | ABI2 | chr2 | 203323394 | 203437169 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:203417014
|
G | C | 1 | a0001c0002 | 2 | HG02976.hp2 NA20300.hp1 |
synonymous_variant | LOW | c.1386G>C | p.Val462Val | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/12 | 1507/6567 | 1386/1629 | 462/542 | chr2 | 203417014 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:203328413
|
C | T | 1 | a0001c0001t0038 | 1 | NA19068.hp1 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-102C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/12 | chr2 | 203328413 | ||||||
chr2:203328436
|
C | G | 1 | a0001c0001t0037 | 1 | HG02109.hp2 | 5_prime_UTR_variant | MODIFIER | c.-79C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/12 | 79 | chr2 | 203328436 | |||||
chr2:203427382
|
G | A | 1 | a0001c0001t0017 | 1 | HG01433.hp2 | 3_prime_UTR_variant | MODIFIER | c.*30G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 30 | chr2 | 203427382 | |||||
chr2:203427794
|
T | C | 24 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(21): Show | 182 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*442T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 442 | chr2 | 203427794 | |||||
chr2:203428187
|
T | C | 1 | a0001c0001t0018 | 1 | NA19030.hp1 | 3_prime_UTR_variant | MODIFIER | c.*835T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 835 | chr2 | 203428187 | |||||
chr2:203428373
|
G | A | 1 | a0001c0001t0016 | 2 | NA18940.hp1 NA18971.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1021G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 1021 | chr2 | 203428373 | |||||
chr2:203428422
|
T | G | 1 | a0001c0001t0013 | 2 | HG02040.hp2 NA18960.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1070T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 1070 | chr2 | 203428422 | |||||
chr2:203428582
|
T | C | 2 | a0001c0001t0010a0001c0001t0029 | 5 | HG02080.hp1 NA18962.hp2 NA18986.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1230T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 1230 | chr2 | 203428582 | |||||
chr2:203428846
|
C | T | 1 | a0001c0001t0028 | 1 | HG02258.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1494C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 1494 | chr2 | 203428846 | |||||
chr2:203429341
|
C | T | 1 | a0001c0001t0027 | 1 | HG02055.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1989C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 1989 | chr2 | 203429341 | |||||
chr2:203429380
|
G | C | 1 | a0001c0001t0011 | 3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2028G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2028 | chr2 | 203429380 | |||||
chr2:203429518
|
G | A | 1 | a0001c0001t0012 | 3 | NA18968.hp1 NA18969.hp1 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2166G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2166 | chr2 | 203429518 | |||||
chr2:203429561
|
A | G | 1 | a0001c0001t0036 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2209A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2209 | chr2 | 203429561 | |||||
chr2:203429689
|
A | G | 24 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(21): Show | 182 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(179): Show |
3_prime_UTR_variant | MODIFIER | c.*2337A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2337 | chr2 | 203429689 | |||||
chr2:203429753
|
C | CA | 24 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(21): Show | 192 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(189): Show |
3_prime_UTR_variant | MODIFIER | c.*2418dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2419 | INFO_REALIGN_3_PRIME | chr2 | 203429753 | ||||
chr2:203429753
|
C | CAA | 5 | a0001c0001t0004a0001c0001t0012a0001c0001t0019others(2): Show | 29 | HG00621.hp1 HG00738.hp2 HG01943.hp1 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*2417_*2418dupAA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2419 | INFO_REALIGN_3_PRIME | chr2 | 203429753 | ||||
chr2:203429870
|
C | A | 1 | a0001c0001t0011 | 3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2518C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2518 | chr2 | 203429870 | |||||
chr2:203429885
|
G | A | 1 | a0001c0001t0022 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2533G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2533 | chr2 | 203429885 | |||||
chr2:203429886
|
C | G | 1 | a0001c0001t0022 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2534C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2534 | chr2 | 203429886 | |||||
chr2:203430144
|
G | C | 1 | a0001c0001t0035 | 1 | HG01516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2792G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2792 | chr2 | 203430144 | |||||
chr2:203430169
|
A | G | 2 | a0001c0001t0006a0001c0001t0028 | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*2817A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 2817 | chr2 | 203430169 | |||||
chr2:203430425
|
T | C | 1 | a0001c0001t0022 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3073T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3073 | chr2 | 203430425 | |||||
chr2:203430501
|
C | T | 1 | a0001c0001t0026 | 1 | HG00673.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3149C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3149 | chr2 | 203430501 | |||||
chr2:203430551
|
G | A | 1 | a0001c0001t0030 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3199G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3199 | chr2 | 203430551 | |||||
chr2:203430727
|
G | A | 1 | a0001c0001t0014 | 2 | HG03942.hp2 NA20905.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3375G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3375 | chr2 | 203430727 | |||||
chr2:203430818
|
G | A | 1 | a0001c0001t0022 | 1 | HG01884.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3466G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3466 | chr2 | 203430818 | |||||
chr2:203430937
|
C | A | 1 | a0001c0001t0031 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3585C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3585 | chr2 | 203430937 | |||||
chr2:203430964
|
C | T | 1 | a0001c0001t0025 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3612C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 3612 | chr2 | 203430964 | |||||
chr2:203431568
|
G | GAGCAC | 1 | a0001c0001t0007 | 6 | NA18951.hp1 NA18968.hp2 NA18971.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4226_*4230dupCAGC others(1): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4231 | INFO_REALIGN_3_PRIME | chr2 | 203431568 | ||||
chr2:203431688
|
A | G | 8 | a0001c0001t0005a0001c0001t0011a0001c0001t0013others(5): Show | 30 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*4336A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4336 | chr2 | 203431688 | |||||
chr2:203431696
|
TA | T | 10 | a0001c0001t0004a0001c0001t0009a0001c0001t0012others(7): Show | 38 | HG00738.hp2 HG01884.hp2 HG01943.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*4356delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4356 | INFO_REALIGN_3_PRIME | chr2 | 203431696 | ||||
chr2:203431793
|
A | G | 1 | a0001c0001t0033 | 1 | HG00280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4441A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4441 | chr2 | 203431793 | |||||
chr2:203431822
|
A | C | 1 | a0001c0001t0020 | 1 | HG00738.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4470A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4470 | chr2 | 203431822 | |||||
chr2:203431847
|
G | A | 1 | a0001c0001t0023 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4495G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4495 | chr2 | 203431847 | |||||
chr2:203432022
|
GGA | G | 2 | a0001c0001t0008a0001c0001t0032 | 7 | HG00673.hp2 NA18946.hp1 NA18982.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*4672_*4673delAG | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 12/12 | 4672 | INFO_REALIGN_3_PRIME | chr2 | 203432022 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:203328753
|
G | C | 1 | a0001c0001t0006g0001 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.117+122G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203328753 | ||||||
chr2:203328895
|
T | TCGGCCGC others(3): Show |
1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+267_117+276dup others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203328895 | |||||
chr2:203328926
|
G | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.117+295G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203328926 | ||||||
chr2:203328965
|
T | G | 96 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(93): Show | 96 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.117+334T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203328965 | ||||||
chr2:203328983
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.117+352C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203328983 | ||||||
chr2:203329026
|
C | T | 1 | a0001c0001t0003g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117+395C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329026 | ||||||
chr2:203329314
|
AAT | A | 138 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(135): Show | 138 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.117+684_117+685del others(2): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329314 | ||||||
chr2:203329341
|
A | AT | 193 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(190): Show | 193 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.117+734dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203329341 | |||||
chr2:203329341
|
A | ATT | 36 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0308others(33): Show | 36 | HG00280.hp2 HG00673.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.117+733_117+734dup others(2): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203329341 | |||||
chr2:203329341
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0002g0002 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.117+725_117+734del others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203329341 | |||||
chr2:203329434
|
G | A | 1 | a0001c0001t0006g0001 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.117+803G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329434 | ||||||
chr2:203329470
|
A | G | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.117+839A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329470 | ||||||
chr2:203329621
|
G | T | 1 | a0001c0001t0002g0097 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.117+990G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329621 | ||||||
chr2:203329695
|
T | C | 24 | a0001c0001t0005g0098a0001c0001t0005g0099a0001c0001t0005g0100others(21): Show | 24 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.117+1064T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329695 | ||||||
chr2:203329808
|
C | G | 23 | a0001c0001t0005g0100a0001c0001t0005g0102a0001c0001t0005g0103others(20): Show | 23 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+1177C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329808 | ||||||
chr2:203329957
|
G | C | 1 | a0001c0001t0002g0008 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.117+1326G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329957 | ||||||
chr2:203329959
|
A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+1328A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329959 | ||||||
chr2:203329971
|
A | G | 1 | a0001c0001t0002g0097 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.117+1340A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203329971 | ||||||
chr2:203330095
|
C | G | 1 | a0001c0001t0006g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.117+1464C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203330095 | ||||||
chr2:203330205
|
TGACCC | T | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.117+1577_117+1581d others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203330205 | |||||
chr2:203330361
|
A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+1730A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203330361 | ||||||
chr2:203330392
|
CA | C | 261 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(258): Show | 261 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.117+1780delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203330392 | |||||
chr2:203330392
|
CAA | C | 16 | a0001c0001t0001g0207a0001c0001t0001g0299a0001c0001t0001g0300others(13): Show | 16 | HG01167.hp2 HG01515.hp1 HG02080.hp1 others(13): Show |
intron_variant | MODIFIER | c.117+1779_117+1780d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203330392 | |||||
chr2:203330759
|
G | C | 1 | a0001c0001t0001g0216 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.117+2128G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203330759 | ||||||
chr2:203330869
|
A | G | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+2238A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203330869 | ||||||
chr2:203330940
|
T | G | 189 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.117+2309T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203330940 | ||||||
chr2:203331005
|
T | TAAAGCAT others(159): Show |
1 | a0001c0001t0002g0014 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.117+2386_117+2387i others(168): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331005 | |||||
chr2:203331180
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.117+2549T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203331180 | ||||||
chr2:203331348
|
C | CTTTTTT | 60 | a0001c0001t0001g0186a0001c0001t0001g0207a0001c0001t0001g0218others(57): Show | 60 | HG00642.hp1 HG00733.hp2 HG00735.hp1 others(57): Show |
intron_variant | MODIFIER | c.117+2732_117+2737d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331348 | |||||
chr2:203331348
|
C | CTTTTTTT | 192 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0202others(189): Show | 192 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.117+2731_117+2737d others(9): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331348 | |||||
chr2:203331348
|
C | CTTTTTTT others(1): Show |
33 | a0001c0001t0001g0292a0001c0001t0001g0293a0001c0001t0001g0294others(30): Show | 33 | HG00597.hp1 HG00621.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.117+2730_117+2737d others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331348 | |||||
chr2:203331560
|
T | C | 1 | a0001c0001t0001g0292 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.117+2929T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203331560 | ||||||
chr2:203331560
|
T | G | 17 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.117+2929T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203331560 | ||||||
chr2:203331701
|
G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+3070G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203331701 | ||||||
chr2:203331808
|
CT | C | 11 | a0001c0001t0001g0182a0001c0001t0001g0290a0001c0001t0001g0291others(8): Show | 11 | HG00642.hp1 HG01975.hp1 HG02622.hp2 others(8): Show |
intron_variant | MODIFIER | c.117+3196delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331808 | |||||
chr2:203331808
|
CTT | C | 173 | a0001c0001t0001g0181a0001c0001t0001g0186a0001c0001t0001g0200others(170): Show | 173 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.117+3195_117+3196d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331808 | |||||
chr2:203331808
|
CTTT | C | 6 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0293others(3): Show | 6 | HG00735.hp2 HG00741.hp2 HG03491.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+3194_117+3196d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203331808 | |||||
chr2:203331895
|
C | T | 7 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0197others(4): Show | 7 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+3264C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203331895 | ||||||
chr2:203332020
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.117+3389G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203332020 | ||||||
chr2:203332241
|
A | G | 2 | a0001c0001t0001g0303a0001c0001t0001g0304 | 2 | NA18980.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.117+3610A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203332241 | ||||||
chr2:203332493
|
C | T | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+3862C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203332493 | ||||||
chr2:203332657
|
T | G | 1 | a0001c0001t0015g0120 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.117+4026T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203332657 | ||||||
chr2:203332768
|
G | A | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+4137G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203332768 | ||||||
chr2:203333149
|
A | G | 1 | a0001c0001t0004g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.117+4518A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203333149 | ||||||
chr2:203333580
|
T | G | 96 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(93): Show | 96 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.117+4949T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203333580 | ||||||
chr2:203333938
|
T | C | 1 | a0001c0001t0002g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.117+5307T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203333938 | ||||||
chr2:203333947
|
T | C | 96 | a0001c0001t0001g0182a0001c0001t0001g0200a0001c0001t0001g0201others(93): Show | 96 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.117+5316T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203333947 | ||||||
chr2:203334190
|
C | G | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.117+5559C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334190 | ||||||
chr2:203334230
|
C | T | 1 | a0001c0001t0002g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.117+5599C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334230 | ||||||
chr2:203334280
|
A | G | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.117+5649A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334280 | ||||||
chr2:203334536
|
A | C | 5 | a0001c0001t0010g0066a0001c0001t0010g0067a0001c0001t0010g0068others(2): Show | 5 | HG02080.hp1 NA18962.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+5905A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334536 | ||||||
chr2:203334668
|
A | AT | 178 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(175): Show | 178 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(175): Show |
intron_variant | MODIFIER | c.117+6051dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203334668 | |||||
chr2:203334668
|
A | ATT | 10 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0284others(7): Show | 10 | HG00735.hp2 HG00741.hp2 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.117+6050_117+6051d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203334668 | |||||
chr2:203334854
|
T | C | 1 | a0001c0001t0001g0218 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.117+6223T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334854 | ||||||
chr2:203334877
|
T | C | 96 | a0001c0001t0001g0182a0001c0001t0001g0200a0001c0001t0001g0201others(93): Show | 96 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.117+6246T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334877 | ||||||
chr2:203334982
|
T | C | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.117+6351T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203334982 | ||||||
chr2:203335040
|
G | A | 16 | a0001c0001t0001g0200a0001c0001t0001g0228a0001c0001t0001g0229others(13): Show | 16 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.117+6409G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335040 | ||||||
chr2:203335055
|
T | C | 1 | a0001c0001t0030g0240 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.117+6424T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335055 | ||||||
chr2:203335136
|
T | A | 1 | a0001c0001t0003g0286 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.117+6505T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335136 | ||||||
chr2:203335471
|
C | G | 189 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.117+6840C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335471 | ||||||
chr2:203335550
|
G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+6919G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335550 | ||||||
chr2:203335555
|
G | T | 16 | a0001c0001t0001g0200a0001c0001t0001g0228a0001c0001t0001g0229others(13): Show | 16 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.117+6924G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335555 | ||||||
chr2:203335592
|
A | C | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+6961A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335592 | ||||||
chr2:203335644
|
T | C | 6 | a0001c0001t0005g0102a0001c0001t0005g0103a0001c0001t0005g0105others(3): Show | 6 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+7013T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335644 | ||||||
chr2:203335966
|
A | T | 1 | a0001c0001t0010g0078 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.117+7335A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203335966 | ||||||
chr2:203336050
|
A | G | 3 | a0001c0001t0011g0153a0001c0001t0011g0154a0001c0001t0011g0155 | 3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.117+7419A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336050 | ||||||
chr2:203336122
|
T | G | 1 | a0001c0001t0003g0286 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.117+7491T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336122 | ||||||
chr2:203336250
|
G | A | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.117+7619G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336250 | ||||||
chr2:203336319
|
A | C | 302 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(299): Show | 302 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.117+7688A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336319 | ||||||
chr2:203336342
|
A | G | 96 | a0001c0001t0001g0182a0001c0001t0001g0200a0001c0001t0001g0201others(93): Show | 96 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.117+7711A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336342 | ||||||
chr2:203336546
|
A | C | 1 | a0001c0001t0034g0190 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.117+7915A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336546 | ||||||
chr2:203336560
|
A | G | 302 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(299): Show | 302 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.117+7929A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336560 | ||||||
chr2:203336600
|
T | A | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+7969T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336600 | ||||||
chr2:203336601
|
A | G | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+7970A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336601 | ||||||
chr2:203336832
|
G | C | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.117+8201G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336832 | ||||||
chr2:203336845
|
G | A | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.117+8214G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336845 | ||||||
chr2:203336986
|
G | A | 1 | a0001c0001t0002g0083 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.117+8355G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203336986 | ||||||
chr2:203337541
|
A | T | 1 | a0001c0001t0001g0283 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.117+8910A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337541 | ||||||
chr2:203337746
|
A | G | 1 | a0001c0001t0010g0068 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.117+9115A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337746 | ||||||
chr2:203337899
|
A | C | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9268A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337899 | ||||||
chr2:203337900
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9269C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337900 | ||||||
chr2:203337902
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9271C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337902 | ||||||
chr2:203337903
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9272G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337903 | ||||||
chr2:203337905
|
C | A | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9274C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337905 | ||||||
chr2:203337907
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9276G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337907 | ||||||
chr2:203337908
|
T | G | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9277T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337908 | ||||||
chr2:203337909
|
A | T | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9278A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337909 | ||||||
chr2:203337911
|
T | A | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9280T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337911 | ||||||
chr2:203337912
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9281C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337912 | ||||||
chr2:203337913
|
C | G | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9282C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337913 | ||||||
chr2:203337914
|
C | T | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9283C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337914 | ||||||
chr2:203337915
|
A | T | 1 | a0001c0001t0001g0291 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.117+9284A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337915 | ||||||
chr2:203337945
|
G | T | 1 | a0001c0001t0003g0225 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.117+9314G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203337945 | ||||||
chr2:203338069
|
T | A | 2 | a0001c0001t0003g0203a0001c0001t0034g0190 | 2 | HG00438.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.117+9438T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338069 | ||||||
chr2:203338070
|
A | G | 1 | a0001c0001t0035g0064 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.117+9439A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338070 | ||||||
chr2:203338115
|
G | C | 189 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.117+9484G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338115 | ||||||
chr2:203338315
|
G | C | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.117+9684G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338315 | ||||||
chr2:203338444
|
G | T | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+9813G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338444 | ||||||
chr2:203338453
|
G | C | 2 | a0001c0001t0004g0121a0001c0001t0020g0122 | 2 | HG00738.hp2 HG01943.hp1 |
intron_variant | MODIFIER | c.117+9822G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338453 | ||||||
chr2:203338840
|
T | A | 1 | a0001c0001t0003g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.117+10209T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338840 | ||||||
chr2:203338920
|
GTGTGTGT others(3): Show |
G | 8 | a0001c0001t0005g0100a0001c0001t0005g0113a0001c0001t0005g0152others(5): Show | 8 | HG02109.hp1 HG02135.hp2 HG02809.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+10291_117+1030 others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | |||||
chr2:203338920
|
GTGTGTGT others(17): Show |
G | 2 | a0001c0001t0005g0112a0001c0002t0005g0116 | 2 | HG02155.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.117+10291_117+1031 others(28): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | |||||
chr2:203338920
|
GTGTGTGT others(19): Show |
G | 1 | a0001c0001t0005g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.117+10291_117+1031 others(30): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | |||||
chr2:203338920
|
GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0005g0111 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.117+10291_117+1031 others(32): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | |||||
chr2:203338920
|
GTGTGTGT others(23): Show |
G | 4 | a0001c0001t0005g0105a0001c0001t0005g0109a0001c0001t0005g0110others(1): Show | 4 | HG02293.hp2 NA18747.hp2 NA18960.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+10291_117+1032 others(34): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | |||||
chr2:203338920
|
GTGTGTGT others(27): Show |
G | 2 | a0001c0001t0005g0102a0001c0001t0005g0103 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.117+10291_117+1032 others(38): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | |||||
chr2:203338920
|
GTGTGTGT others(29): Show |
G | 1 | a0001c0001t0013g0101 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.117+10291_117+1032 others(40): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | |||||
chr2:203338920
|
GTGTGTGT others(41): Show |
G | 3 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0001t0021g0151 | 3 | HG00621.hp1 NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.117+10291_117+1033 others(52): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | |||||
chr2:203338920
|
GTGTGTGT others(43): Show |
G | 1 | a0001c0001t0005g0106 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.117+10291_117+1034 others(54): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338920 | |||||
chr2:203338921
|
TGTGTGTG others(35): Show |
T | 1 | a0001c0002t0024g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.117+10291_117+1033 others(46): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338921 | ||||||
chr2:203338922
|
GTGTGTGT others(21): Show |
G | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+10293_117+1032 others(32): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338922 | |||||
chr2:203338922
|
GTGTGTGT others(23): Show |
G | 1 | a0001c0001t0005g0156 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.117+10293_117+1032 others(34): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338922 | |||||
chr2:203338924
|
GTGTGTAT others(13): Show |
G | 1 | a0001c0001t0003g0185 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.117+10295_117+1031 others(24): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338924 | |||||
chr2:203338924
|
GTGTGTAT others(15): Show |
G | 1 | a0001c0001t0003g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.117+10295_117+1031 others(26): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338924 | |||||
chr2:203338924
|
GTGTGTAT others(29): Show |
G | 1 | a0001c0001t0031g0183 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.117+10295_117+1033 others(40): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338924 | |||||
chr2:203338926
|
GTGTATAT others(11): Show |
G | 1 | a0001c0001t0003g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.117+10297_117+1031 others(22): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(13): Show |
G | 1 | a0001c0001t0003g0210 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.117+10297_117+1031 others(24): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(17): Show |
G | 1 | a0001c0001t0003g0199 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.117+10297_117+1032 others(28): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(19): Show |
G | 2 | a0001c0001t0003g0223a0001c0001t0003g0286 | 2 | HG01358.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.117+10297_117+1032 others(30): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(21): Show |
G | 4 | a0001c0001t0003g0192a0001c0001t0003g0222a0001c0001t0003g0309others(1): Show | 4 | HG01928.hp1 HG01952.hp1 HG02148.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+10297_117+1032 others(32): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(23): Show |
G | 3 | a0001c0001t0003g0189a0001c0001t0003g0191a0001c0001t0003g0289 | 3 | HG01891.hp2 HG02896.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.117+10297_117+1032 others(34): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(25): Show |
G | 3 | a0001c0001t0003g0188a0001c0001t0003g0204a0001c0001t0003g0209 | 3 | HG01074.hp1 HG02572.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.117+10297_117+1032 others(36): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(27): Show |
G | 6 | a0001c0001t0003g0206a0001c0001t0003g0208a0001c0001t0003g0211others(3): Show | 6 | HG01167.hp2 HG01255.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+10297_117+1033 others(38): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(31): Show |
G | 9 | a0001c0001t0001g0186a0001c0001t0001g0218a0001c0001t0001g0273others(6): Show | 9 | HG00735.hp2 HG03453.hp1 HG03688.hp2 others(6): Show |
intron_variant | MODIFIER | c.117+10297_117+1033 others(42): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(33): Show |
G | 5 | a0001c0001t0001g0271a0001c0001t0001g0272a0001c0001t0001g0285others(2): Show | 5 | HG01109.hp2 HG01516.hp2 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+10297_117+1033 others(44): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(35): Show |
G | 12 | a0001c0001t0001g0239a0001c0001t0001g0269a0001c0001t0001g0270others(9): Show | 12 | HG00673.hp1 HG00738.hp1 HG01255.hp1 others(9): Show |
intron_variant | MODIFIER | c.117+10297_117+1033 others(46): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(37): Show |
G | 29 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0207others(26): Show | 29 | HG00438.hp1 HG00733.hp1 HG00735.hp1 others(26): Show |
intron_variant | MODIFIER | c.117+10297_117+1034 others(48): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(39): Show |
G | 35 | a0001c0001t0001g0201a0001c0001t0001g0212a0001c0001t0001g0213others(32): Show | 35 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(32): Show |
intron_variant | MODIFIER | c.117+10297_117+1034 others(50): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(41): Show |
G | 7 | a0001c0001t0001g0227a0001c0001t0001g0228a0001c0001t0001g0241others(4): Show | 7 | HG00423.hp1 HG01175.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+10297_117+1034 others(52): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338926
|
GTGTATAT others(43): Show |
G | 1 | a0001c0001t0001g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.117+10297_117+1034 others(54): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338926 | |||||
chr2:203338927
|
TGTATATG others(29): Show |
T | 5 | a0001c0001t0001g0283a0001c0001t0002g0187a0001c0001t0003g0219others(2): Show | 5 | HG02055.hp1 HG02698.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+10297_117+1033 others(40): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338927 | ||||||
chr2:203338928
|
GTATATGT others(31): Show |
G | 2 | a0001c0001t0003g0282a0001c0001t0030g0240 | 2 | HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.117+10303_117+1034 others(42): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338928 | |||||
chr2:203338928
|
GTATATGT others(33): Show |
G | 1 | a0001c0001t0003g0281 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.117+10303_117+1034 others(44): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338928 | |||||
chr2:203338928
|
GTATATGT others(35): Show |
G | 1 | a0001c0001t0001g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.117+10303_117+1034 others(46): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338928 | |||||
chr2:203338928
|
GTATATGT others(37): Show |
G | 4 | a0001c0001t0001g0279a0001c0001t0001g0280a0001c0001t0001g0292others(1): Show | 4 | HG01081.hp2 NA18978.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+10303_117+1034 others(48): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338928 | |||||
chr2:203338928
|
GTATATGT others(39): Show |
G | 3 | a0001c0001t0001g0278a0001c0001t0001g0298a0001c0001t0001g0314 | 3 | HG04115.hp1 HG04228.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.117+10303_117+1034 others(50): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338928 | |||||
chr2:203338930
|
A | G | 24 | a0001c0001t0004g0135a0001c0001t0005g0098a0001c0001t0005g0099others(21): Show | 24 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+10299A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338930 | ||||||
chr2:203338932
|
A | G | 25 | a0001c0001t0001g0224a0001c0001t0004g0135a0001c0001t0005g0098others(22): Show | 25 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(22): Show |
intron_variant | MODIFIER | c.117+10301A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338932 | ||||||
chr2:203338934
|
GTA | G | 3 | a0001c0001t0004g0126a0001c0001t0004g0128a0001c0001t0004g0157 | 3 | HG02523.hp1 NA18966.hp1 NA18988.hp1 |
intron_variant | MODIFIER | c.117+10330_117+1033 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338934 | |||||
chr2:203338934
|
GTATATAT others(43): Show |
G | 1 | a0001c0001t0002g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.117+10328_117+1037 others(54): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338934 | |||||
chr2:203338935
|
T | TATATATA others(19): Show |
1 | a0001c0001t0004g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.117+10329_117+1033 others(30): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338935 | |||||
chr2:203338936
|
A | G | 119 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(116): Show | 119 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.117+10305A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338936 | ||||||
chr2:203338938
|
A | G | 24 | a0001c0001t0002g0062a0001c0001t0002g0063a0001c0001t0005g0098others(21): Show | 24 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+10307A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338938 | ||||||
chr2:203338939
|
TATATATA others(37): Show |
T | 3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0079 | 3 | HG02145.hp1 HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.117+10332_117+1037 others(48): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338939 | |||||
chr2:203338940
|
A | G | 24 | a0001c0001t0002g0017a0001c0001t0002g0061a0001c0001t0004g0148others(21): Show | 24 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(21): Show |
intron_variant | MODIFIER | c.117+10309A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338940 | ||||||
chr2:203338941
|
T | TATATATA others(33): Show |
1 | a0001c0001t0004g0127 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.117+10329_117+1033 others(44): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338941 | |||||
chr2:203338942
|
A | G | 23 | a0001c0001t0002g0017a0001c0001t0004g0148a0001c0001t0005g0099others(20): Show | 23 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.117+10311A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338942 | ||||||
chr2:203338943
|
T | TATATATA others(7): Show |
3 | a0001c0001t0004g0137a0001c0001t0004g0138a0001c0001t0004g0139 | 3 | HG02559.hp1 HG02886.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.117+10325_117+1032 others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338943 | |||||
chr2:203338943
|
T | TATATATA others(31): Show |
1 | a0001c0001t0012g0123 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.117+10327_117+1032 others(42): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338943 | |||||
chr2:203338943
|
TATATATA others(13): Show |
T | 10 | a0001c0001t0002g0025a0001c0001t0002g0026a0001c0001t0002g0084others(7): Show | 10 | HG01168.hp2 HG01169.hp1 HG02895.hp2 others(7): Show |
intron_variant | MODIFIER | c.117+10352_117+1037 others(24): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338943 | |||||
chr2:203338944
|
A | G | 15 | a0001c0001t0005g0099a0001c0001t0006g0001a0001c0001t0006g0149others(12): Show | 15 | HG00733.hp2 HG01109.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.117+10313A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338944 | ||||||
chr2:203338945
|
T | TATATATA others(65): Show |
1 | a0001c0001t0004g0136 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.117+10325_117+1032 others(76): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338945 | |||||
chr2:203338945
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.117+10327_117+1032 others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338945 | |||||
chr2:203338945
|
T | TATATATA others(9): Show |
1 | a0001c0001t0004g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.117+10329_117+1033 others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338945 | |||||
chr2:203338945
|
TATATATA others(11): Show |
T | 8 | a0001c0001t0002g0015a0001c0001t0002g0027a0001c0001t0002g0028others(5): Show | 8 | HG00280.hp2 HG00423.hp2 HG02135.hp1 others(5): Show |
intron_variant | MODIFIER | c.117+10332_117+1034 others(22): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338945 | |||||
chr2:203338946
|
A | G | 9 | a0001c0001t0006g0001a0001c0001t0006g0166a0001c0001t0006g0167others(6): Show | 9 | HG00733.hp2 HG01109.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.117+10315A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338946 | ||||||
chr2:203338947
|
TATATATA others(9): Show |
T | 15 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0029others(12): Show | 15 | HG00597.hp2 HG00673.hp2 HG00733.hp2 others(12): Show |
intron_variant | MODIFIER | c.117+10332_117+1034 others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338947 | |||||
chr2:203338947
|
TATATATA others(29): Show |
T | 1 | a0001c0001t0002g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.117+10332_117+1036 others(40): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338947 | |||||
chr2:203338948
|
A | G | 4 | a0001c0001t0005g0112a0001c0001t0006g0171a0001c0001t0006g0174others(1): Show | 4 | HG01884.hp1 HG02155.hp1 HG02258.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+10317A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338948 | ||||||
chr2:203338949
|
T | TATATATA others(23): Show |
1 | a0001c0001t0020g0122 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.117+10329_117+1033 others(34): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338949 | |||||
chr2:203338949
|
TATATATA others(7): Show |
T | 18 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0012others(15): Show | 18 | HG01884.hp1 HG02486.hp1 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.117+10332_117+1034 others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338949 | |||||
chr2:203338949
|
TATATATA others(27): Show |
T | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.117+10332_117+1036 others(38): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338949 | |||||
chr2:203338950
|
A | G | 2 | a0001c0001t0005g0115a0001c0001t0006g0171 | 2 | HG03225.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.117+10319A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338950 | ||||||
chr2:203338951
|
T | TATATATA others(21): Show |
1 | a0001c0001t0004g0141 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.117+10327_117+1032 others(32): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338951 | |||||
chr2:203338951
|
T | TATATATA others(43): Show |
1 | a0001c0001t0004g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.117+10327_117+1032 others(54): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338951 | |||||
chr2:203338951
|
TATATATA others(5): Show |
T | 23 | a0001c0001t0002g0006a0001c0001t0002g0016a0001c0001t0002g0017others(20): Show | 23 | HG00741.hp1 HG01975.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+10332_117+1034 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338951 | |||||
chr2:203338952
|
A | G | 2 | a0001c0001t0005g0111a0001c0001t0006g0171 | 2 | HG03225.hp2 NA18965.hp1 |
intron_variant | MODIFIER | c.117+10321A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338952 | ||||||
chr2:203338953
|
T | TATATAAA others(91): Show |
1 | a0001c0001t0015g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.117+10327_117+1032 others(102): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338953 | |||||
chr2:203338953
|
T | TATATATA others(27): Show |
1 | a0001c0001t0004g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.117+10329_117+1033 others(38): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338953 | |||||
chr2:203338953
|
T | TATATATA others(35): Show |
1 | a0001c0001t0004g0145 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.117+10331_117+1033 others(46): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338953 | |||||
chr2:203338953
|
TATATATA others(3): Show |
T | 12 | a0001c0001t0002g0010a0001c0001t0002g0011a0001c0001t0002g0014others(9): Show | 12 | HG00323.hp1 HG02040.hp1 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+10332_117+1034 others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338953 | |||||
chr2:203338953
|
TATATATA others(23): Show |
T | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.117+10332_117+1036 others(34): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338953 | |||||
chr2:203338954
|
A | G | 2 | a0001c0001t0005g0109a0001c0001t0005g0110 | 2 | NA18747.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.117+10323A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338954 | ||||||
chr2:203338955
|
T | TATATATA others(81): Show |
1 | a0001c0001t0004g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.117+10331_117+1033 others(92): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338955 | |||||
chr2:203338955
|
TATATATA others(1): Show |
T | 12 | a0001c0001t0002g0008a0001c0001t0002g0052a0001c0001t0002g0053others(9): Show | 12 | HG01081.hp1 HG01256.hp2 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+10332_117+1033 others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338955 | |||||
chr2:203338955
|
TATATATA others(21): Show |
T | 2 | a0001c0001t0002g0021a0001c0001t0003g0080 | 2 | HG01175.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.117+10332_117+1035 others(32): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338955 | |||||
chr2:203338957
|
TATATAA | T | 5 | a0001c0001t0002g0056a0001c0001t0002g0063a0001c0001t0003g0076others(2): Show | 5 | HG01192.hp2 HG02148.hp2 HG03579.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+10332_117+1033 others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338957 | |||||
chr2:203338957
|
TATATAAA others(19): Show |
T | 5 | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0002g0024others(2): Show | 5 | HG00609.hp2 HG01361.hp1 HG02280.hp2 others(2): Show |
intron_variant | MODIFIER | c.117+10332_117+1035 others(30): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338957 | |||||
chr2:203338959
|
T | A | 1 | a0001c0001t0004g0125 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.117+10328T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338959 | ||||||
chr2:203338959
|
TATAA | T | 3 | a0001c0001t0002g0057a0001c0001t0002g0058a0001c0001t0002g0059 | 3 | HG01943.hp2 HG02523.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.117+10332_117+1033 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338959 | |||||
chr2:203338959
|
TATAAATA others(17): Show |
T | 2 | a0001c0001t0006g0149a0001c0001t0006g0162 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.117+10332_117+1035 others(28): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338959 | |||||
chr2:203338961
|
T | A | 4 | a0001c0001t0004g0129a0001c0001t0004g0130a0001c0001t0012g0131others(1): Show | 4 | NA18747.hp1 NA18969.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.117+10330T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338961 | ||||||
chr2:203338961
|
TAAATATA others(15): Show |
T | 2 | a0001c0001t0006g0171a0001c0001t0006g0172 | 2 | HG03225.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.117+10332_117+1035 others(26): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338961 | |||||
chr2:203338963
|
A | T | 60 | a0001c0001t0002g0042a0001c0001t0002g0060a0001c0001t0002g0077others(57): Show | 60 | HG00621.hp2 HG00642.hp1 HG00738.hp2 others(57): Show |
intron_variant | MODIFIER | c.117+10332A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338963 | ||||||
chr2:203338964
|
A | G | 12 | a0001c0001t0006g0001a0001c0001t0006g0150a0001c0001t0006g0163others(9): Show | 12 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.117+10333A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338964 | ||||||
chr2:203338966
|
A | G | 7 | a0001c0001t0006g0150a0001c0001t0006g0165a0001c0001t0006g0169others(4): Show | 7 | HG01884.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.117+10335A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338966 | ||||||
chr2:203338968
|
A | G | 6 | a0001c0001t0006g0150a0001c0001t0006g0165a0001c0001t0006g0169others(3): Show | 6 | HG01884.hp1 HG02895.hp2 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.117+10337A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338968 | ||||||
chr2:203338969
|
T | A | 2 | a0001c0001t0004g0141a0001c0001t0020g0122 | 2 | HG00738.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.117+10338T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338969 | ||||||
chr2:203338970
|
A | G | 3 | a0001c0001t0006g0169a0001c0001t0006g0170a0001c0001t0006g0179 | 3 | HG03130.hp2 HG03516.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.117+10339A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338970 | ||||||
chr2:203338971
|
T | A | 1 | a0001c0001t0004g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.117+10340T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338971 | ||||||
chr2:203338971
|
T | TATATATA others(55): Show |
1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.117+10351_117+1035 others(66): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338971 | |||||
chr2:203338972
|
A | G | 4 | a0001c0001t0001g0182a0001c0001t0005g0107a0001c0001t0005g0108others(1): Show | 4 | HG00621.hp1 HG02622.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+10341A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338972 | ||||||
chr2:203338973
|
T | A | 1 | a0001c0001t0004g0134 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.117+10342T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338973 | ||||||
chr2:203338974
|
A | G | 2 | a0001c0001t0001g0308a0001c0001t0005g0106 | 2 | HG02083.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.117+10343A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338974 | ||||||
chr2:203338975
|
T | A | 5 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0004g0145others(2): Show | 5 | HG01975.hp1 HG02622.hp1 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.117+10344T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338975 | ||||||
chr2:203338977
|
T | A | 1 | a0001c0001t0004g0144 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.117+10346T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338977 | ||||||
chr2:203338983
|
A | AATATATA others(5): Show |
1 | a0001c0001t0004g0121 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.117+10366_117+1037 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | |||||
chr2:203338983
|
A | AATATATA others(7): Show |
1 | a0001c0001t0004g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.117+10364_117+1037 others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | |||||
chr2:203338983
|
A | AATATATA others(19): Show |
1 | a0001c0001t0004g0129 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.117+10369_117+1037 others(30): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | |||||
chr2:203338983
|
A | AATATATA others(39): Show |
1 | a0001c0001t0004g0126 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.117+10371_117+1037 others(50): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | |||||
chr2:203338983
|
A | AATATATA others(59): Show |
1 | a0001c0001t0015g0120 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.117+10371_117+1037 others(70): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | |||||
chr2:203338983
|
A | AATATATA others(99): Show |
1 | a0001c0001t0004g0157 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.117+10371_117+1037 others(110): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | |||||
chr2:203338983
|
A | AATATATA others(41): Show |
3 | a0001c0001t0004g0130a0001c0001t0012g0131a0001c0001t0012g0132 | 3 | NA18969.hp1 NA19064.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.117+10371_117+1037 others(52): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | |||||
chr2:203338983
|
A | AATATATA others(47): Show |
1 | a0001c0001t0004g0128 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.117+10373_117+1037 others(58): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | |||||
chr2:203338983
|
A | AATATATA others(65): Show |
1 | a0001c0001t0004g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.117+10373_117+1037 others(76): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338983 | |||||
chr2:203338983
|
A | T | 287 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(284): Show | 287 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(284): Show |
intron_variant | MODIFIER | c.117+10352A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338983 | ||||||
chr2:203338986
|
A | G | 1 | a0001c0001t0002g0070 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.117+10355A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203338986 | ||||||
chr2:203338993
|
TATATATA others(8): Show |
T | 1 | a0001c0001t0002g0042 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.117+10364_117+1037 others(19): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203338993 | |||||
chr2:203339007
|
T | A | 3 | a0001c0001t0011g0153a0001c0001t0011g0154a0001c0001t0011g0155 | 3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.117+10376T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339007 | ||||||
chr2:203339037
|
A | C | 1 | a0001c0001t0002g0028 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.117+10406A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339037 | ||||||
chr2:203339095
|
G | A | 3 | a0001c0001t0001g0216a0001c0001t0001g0244a0001c0001t0001g0257 | 3 | HG00280.hp1 HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.117+10464G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339095 | ||||||
chr2:203339126
|
A | G | 1 | a0001c0001t0003g0287 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.117+10495A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339126 | ||||||
chr2:203339233
|
G | A | 2 | a0001c0002t0005g0116a0001c0002t0024g0118 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.117+10602G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339233 | ||||||
chr2:203339567
|
C | G | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.117+10936C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339567 | ||||||
chr2:203339592
|
A | G | 23 | a0001c0001t0005g0081a0001c0001t0005g0100a0001c0001t0005g0102others(20): Show | 23 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(20): Show |
intron_variant | MODIFIER | c.117+10961A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339592 | ||||||
chr2:203339593
|
A | G | 1 | a0001c0001t0006g0167 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.117+10962A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339593 | ||||||
chr2:203339749
|
A | G | 319 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(316): Show | 319 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.117+11118A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339749 | ||||||
chr2:203339912
|
C | T | 1 | a0001c0001t0010g0068 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.117+11281C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339912 | ||||||
chr2:203339986
|
A | T | 1 | a0001c0001t0003g0199 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.117+11355A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203339986 | ||||||
chr2:203340170
|
A | T | 319 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(316): Show | 319 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.117+11539A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340170 | ||||||
chr2:203340235
|
G | GTGGGGAG others(3): Show |
1 | a0001c0001t0002g0043 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.117+11613_117+1162 others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203340235 | |||||
chr2:203340284
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.117+11653T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340284 | ||||||
chr2:203340328
|
A | G | 1 | a0001c0001t0002g0024 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.117+11697A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340328 | ||||||
chr2:203340371
|
A | AT | 25 | a0001c0001t0001g0234a0001c0001t0002g0049a0001c0001t0002g0074others(22): Show | 25 | HG00438.hp2 HG00733.hp2 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.117+11753dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203340371 | |||||
chr2:203340393
|
G | A | 4 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+11762G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340393 | ||||||
chr2:203340425
|
G | A | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+11794G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340425 | ||||||
chr2:203340435
|
C | T | 1 | a0001c0001t0004g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.117+11804C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340435 | ||||||
chr2:203340497
|
G | T | 1 | a0001c0001t0002g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.117+11866G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340497 | ||||||
chr2:203340526
|
A | G | 1 | a0001c0001t0004g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.117+11895A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340526 | ||||||
chr2:203340531
|
T | C | 10 | a0001c0001t0001g0140a0001c0001t0004g0136a0001c0001t0004g0137others(7): Show | 10 | HG02293.hp1 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.117+11900T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340531 | ||||||
chr2:203340546
|
C | T | 1 | a0001c0001t0005g0081 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.117+11915C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340546 | ||||||
chr2:203340547
|
G | A | 3 | a0001c0001t0003g0184a0001c0001t0003g0185a0001c0001t0031g0183 | 3 | HG01891.hp1 HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.117+11916G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340547 | ||||||
chr2:203340745
|
C | T | 2 | a0001c0001t0001g0268a0001c0001t0014g0277 | 2 | HG03942.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.117+12114C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340745 | ||||||
chr2:203340824
|
G | GA | 10 | a0001c0001t0001g0245a0001c0001t0002g0056a0001c0001t0003g0191others(7): Show | 10 | HG01192.hp2 HG01257.hp1 HG01258.hp1 others(7): Show |
intron_variant | MODIFIER | c.117+12203dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203340824 | |||||
chr2:203340860
|
T | C | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.117+12229T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203340860 | ||||||
chr2:203341060
|
C | T | 1 | a0001c0001t0004g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.117+12429C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203341060 | ||||||
chr2:203341359
|
G | A | 4 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+12728G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203341359 | ||||||
chr2:203341443
|
A | G | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.117+12812A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203341443 | ||||||
chr2:203341485
|
C | A | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+12854C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203341485 | ||||||
chr2:203341535
|
C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.117+12904C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203341535 | ||||||
chr2:203341718
|
A | C | 2 | a0001c0001t0001g0256a0001c0001t0001g0292 | 2 | NA18978.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.117+13087A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203341718 | ||||||
chr2:203342254
|
C | T | 319 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(316): Show | 319 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.117+13623C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203342254 | ||||||
chr2:203342255
|
A | C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+13624A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203342255 | ||||||
chr2:203342552
|
T | TTTTA | 60 | a0001c0001t0001g0181a0001c0001t0001g0186a0001c0001t0001g0212others(57): Show | 60 | HG00323.hp2 HG00438.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.117+13961_117+1396 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342552 | |||||
chr2:203342552
|
T | TTTTATTT others(1): Show |
85 | a0001c0001t0001g0140a0001c0001t0001g0201a0001c0001t0001g0207others(82): Show | 85 | HG00280.hp1 HG00438.hp2 HG00597.hp1 others(82): Show |
intron_variant | MODIFIER | c.117+13957_117+1396 others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342552 | |||||
chr2:203342552
|
T | TTTTATTT others(5): Show |
25 | a0001c0001t0001g0182a0001c0001t0001g0200a0001c0001t0001g0202others(22): Show | 25 | HG00423.hp1 HG00642.hp2 HG01167.hp1 others(22): Show |
intron_variant | MODIFIER | c.117+13953_117+1396 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342552 | |||||
chr2:203342552
|
TTTTATTT others(1): Show |
T | 6 | a0001c0001t0002g0014a0001c0001t0002g0059a0001c0001t0003g0208others(3): Show | 6 | HG02055.hp2 HG02155.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.117+13957_117+1396 others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342552 | |||||
chr2:203342552
|
TTTTATTT others(5): Show |
T | 2 | a0001c0001t0003g0317a0001c0001t0037g0320 | 2 | HG02109.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.117+13953_117+1396 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342552 | |||||
chr2:203342570
|
T | TTATTTAT others(5): Show |
1 | a0001c0001t0001g0246 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.117+13950_117+1395 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342570 | |||||
chr2:203342679
|
A | G | 2 | a0001c0001t0003g0203a0001c0001t0034g0190 | 2 | HG00438.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.117+14048A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203342679 | ||||||
chr2:203342704
|
T | C | 7 | a0001c0001t0001g0202a0001c0001t0001g0247a0001c0001t0001g0258others(4): Show | 7 | HG01109.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.117+14073T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203342704 | ||||||
chr2:203342733
|
C | T | 1 | a0001c0001t0006g0171 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.117+14102C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203342733 | ||||||
chr2:203342847
|
C | CA | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.117+14217dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203342847 | |||||
chr2:203342860
|
T | C | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+14229T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203342860 | ||||||
chr2:203343083
|
G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+14452G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203343083 | ||||||
chr2:203343256
|
C | T | 1 | a0001c0001t0003g0188 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.117+14625C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203343256 | ||||||
chr2:203343278
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.117+14647C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203343278 | ||||||
chr2:203343310
|
G | C | 3 | a0001c0001t0003g0184a0001c0001t0003g0185a0001c0001t0031g0183 | 3 | HG01891.hp1 HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.117+14679G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203343310 | ||||||
chr2:203343381
|
A | G | 187 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(184): Show | 187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.117+14750A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203343381 | ||||||
chr2:203343959
|
C | A | 4 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+15328C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203343959 | ||||||
chr2:203344043
|
G | C | 185 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(182): Show | 185 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.117+15412G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344043 | ||||||
chr2:203344062
|
T | C | 1 | a0001c0002t0005g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.117+15431T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344062 | ||||||
chr2:203344192
|
A | T | 3 | a0001c0001t0003g0281a0001c0001t0003g0282a0001c0001t0030g0240 | 3 | HG00642.hp2 HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.117+15561A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344192 | ||||||
chr2:203344361
|
A | AT | 21 | a0001c0001t0005g0081a0001c0001t0005g0100a0001c0001t0005g0102others(18): Show | 21 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.117+15739dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344361 | |||||
chr2:203344512
|
A | C | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.117+15881A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344512 | ||||||
chr2:203344540
|
T | TTTG | 8 | a0001c0001t0002g0048a0001c0001t0002g0055a0001c0001t0002g0097others(5): Show | 8 | HG01081.hp1 HG02080.hp1 NA18962.hp2 others(5): Show |
intron_variant | MODIFIER | c.117+15930_117+1593 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344540 | |||||
chr2:203344540
|
TTTG | T | 3 | a0001c0001t0022g0319a0001c0001t0025g0266a0001c0001t0037g0320 | 3 | HG01884.hp2 HG02109.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.117+15930_117+1593 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344540 | |||||
chr2:203344562
|
T | TTG | 91 | a0001c0001t0001g0238a0001c0001t0002g0002a0001c0001t0002g0004others(88): Show | 91 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.117+15932_117+1593 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344562 | |||||
chr2:203344564
|
T | G | 10 | a0001c0001t0001g0140a0001c0001t0004g0136a0001c0001t0004g0137others(7): Show | 10 | HG02293.hp1 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.117+15933T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344564 | ||||||
chr2:203344567
|
G | T | 91 | a0001c0001t0001g0238a0001c0001t0002g0002a0001c0001t0002g0004others(88): Show | 91 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.117+15936G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344567 | ||||||
chr2:203344567
|
GT | G | 208 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(205): Show | 208 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(205): Show |
intron_variant | MODIFIER | c.117+15948delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344567 | |||||
chr2:203344568
|
T | G | 91 | a0001c0001t0001g0238a0001c0001t0002g0002a0001c0001t0002g0004others(88): Show | 91 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.117+15937T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344568 | ||||||
chr2:203344568
|
T | TTTTTG | 15 | a0001c0001t0001g0140a0001c0001t0004g0136a0001c0001t0004g0137others(12): Show | 15 | HG02080.hp1 HG02293.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.117+15941_117+1594 others(9): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344568 | |||||
chr2:203344574
|
T | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+15943T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344574 | ||||||
chr2:203344637
|
G | A | 3 | a0001c0001t0003g0281a0001c0001t0003g0282a0001c0001t0030g0240 | 3 | HG00642.hp2 HG01192.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.117+16006G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344637 | ||||||
chr2:203344815
|
C | T | 2 | a0001c0001t0001g0182a0001c0001t0001g0308 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.117+16184C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344815 | ||||||
chr2:203344918
|
CGCTCTGT others(17): Show |
C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.117+16331_117+1635 others(28): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203344918 | |||||
chr2:203344970
|
C | G | 2 | a0001c0001t0001g0216a0001c0001t0001g0257 | 2 | HG00733.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.117+16339C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203344970 | ||||||
chr2:203345101
|
C | T | 1 | a0001c0001t0004g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.117+16470C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345101 | ||||||
chr2:203345199
|
C | T | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.117+16568C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345199 | ||||||
chr2:203345367
|
C | G | 21 | a0001c0001t0005g0081a0001c0001t0005g0100a0001c0001t0005g0102others(18): Show | 21 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.117+16736C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345367 | ||||||
chr2:203345575
|
A | G | 1 | a0001c0002t0005g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.117+16944A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345575 | ||||||
chr2:203345683
|
A | T | 1 | a0001c0001t0001g0216 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.117+17052A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345683 | ||||||
chr2:203345743
|
A | G | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.117+17112A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345743 | ||||||
chr2:203345963
|
T | A | 1 | a0001c0001t0002g0027 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.117+17332T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345963 | ||||||
chr2:203345969
|
C | T | 1 | a0001c0001t0001g0305 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.117+17338C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203345969 | ||||||
chr2:203346023
|
T | C | 1 | a0001c0001t0004g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.117+17392T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346023 | ||||||
chr2:203346438
|
A | C | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.117+17807A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346438 | ||||||
chr2:203346445
|
C | T | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.117+17814C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346445 | ||||||
chr2:203346509
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.117+17878G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346509 | ||||||
chr2:203346535
|
G | C | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.117+17904G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346535 | ||||||
chr2:203346643
|
T | C | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.117+18012T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346643 | ||||||
chr2:203346754
|
T | C | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.117+18123T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203346754 | ||||||
chr2:203347033
|
A | G | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.117+18402A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203347033 | ||||||
chr2:203347163
|
G | T | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.117+18532G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203347163 | ||||||
chr2:203347235
|
T | G | 3 | a0001c0001t0011g0153a0001c0001t0011g0154a0001c0001t0011g0155 | 3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.117+18604T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203347235 | ||||||
chr2:203347558
|
C | G | 4 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.117+18927C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203347558 | ||||||
chr2:203347768
|
A | G | 187 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(184): Show | 187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.118-19109A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203347768 | ||||||
chr2:203348045
|
A | T | 1 | a0001c0001t0003g0195 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.118-18832A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348045 | ||||||
chr2:203348109
|
C | T | 1 | a0001c0001t0004g0124 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.118-18768C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348109 | ||||||
chr2:203348184
|
T | C | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.118-18693T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348184 | ||||||
chr2:203348257
|
A | T | 1 | a0001c0001t0036g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.118-18620A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348257 | ||||||
chr2:203348496
|
A | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-18381A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348496 | ||||||
chr2:203348510
|
G | A | 1 | a0001c0001t0003g0203 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.118-18367G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348510 | ||||||
chr2:203348584
|
A | G | 3 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160 | 3 | HG02451.hp2 HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.118-18293A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348584 | ||||||
chr2:203348591
|
T | A | 3 | a0001c0001t0001g0255a0001c0001t0001g0296a0001c0001t0004g0217 | 3 | HG00597.hp1 NA19057.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.118-18286T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348591 | ||||||
chr2:203348757
|
C | T | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118-18120C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348757 | ||||||
chr2:203348780
|
T | C | 290 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(287): Show | 290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.118-18097T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348780 | ||||||
chr2:203348862
|
T | A | 1 | a0001c0001t0002g0062 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.118-18015T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348862 | ||||||
chr2:203348920
|
T | G | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118-17957T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203348920 | ||||||
chr2:203348920
|
TTTTG | T | 4 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0079others(1): Show | 4 | HG02109.hp2 HG02145.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-17933_118-1793 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203348920 | |||||
chr2:203349045
|
G | A | 1 | a0001c0001t0002g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.118-17832G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349045 | ||||||
chr2:203349053
|
C | T | 1 | a0001c0001t0015g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.118-17824C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349053 | ||||||
chr2:203349228
|
C | T | 1 | a0001c0001t0014g0267 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.118-17649C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349228 | ||||||
chr2:203349554
|
G | A | 1 | a0001c0001t0001g0285 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.118-17323G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349554 | ||||||
chr2:203349647
|
C | T | 1 | a0001c0001t0002g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.118-17230C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349647 | ||||||
chr2:203349669
|
T | C | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.118-17208T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349669 | ||||||
chr2:203349738
|
A | G | 1 | a0001c0001t0001g0271 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.118-17139A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349738 | ||||||
chr2:203349955
|
C | T | 1 | a0001c0001t0003g0311 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.118-16922C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203349955 | ||||||
chr2:203350003
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.118-16874C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350003 | ||||||
chr2:203350044
|
T | C | 3 | a0001c0001t0001g0255a0001c0001t0001g0296a0001c0001t0004g0217 | 3 | HG00597.hp1 NA19057.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.118-16833T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350044 | ||||||
chr2:203350195
|
A | C | 2 | a0001c0001t0001g0202a0001c0001t0001g0258 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.118-16682A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350195 | ||||||
chr2:203350237
|
C | T | 2 | a0001c0001t0002g0033a0001c0001t0002g0042 | 2 | NA18952.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.118-16640C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350237 | ||||||
chr2:203350248
|
C | T | 7 | a0001c0001t0001g0207a0001c0001t0001g0265a0001c0001t0001g0272others(4): Show | 7 | NA18940.hp2 NA18946.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-16629C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350248 | ||||||
chr2:203350303
|
T | C | 189 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.118-16574T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350303 | ||||||
chr2:203350509
|
G | C | 189 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.118-16368G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350509 | ||||||
chr2:203350540
|
CT | C | 23 | a0001c0001t0001g0212a0001c0001t0001g0269a0001c0001t0001g0272others(20): Show | 23 | HG01167.hp2 HG01168.hp1 HG01168.hp2 others(20): Show |
intron_variant | MODIFIER | c.118-16321delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350540 | |||||
chr2:203350662
|
C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-16215C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350662 | ||||||
chr2:203350688
|
C | A | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.118-16189C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350688 | ||||||
chr2:203350698
|
C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-16179C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350698 | ||||||
chr2:203350759
|
C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-16118C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350759 | ||||||
chr2:203350790
|
G | A | 6 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG00438.hp2 HG00609.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-16087G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350790 | ||||||
chr2:203350862
|
T | TTG | 14 | a0001c0001t0001g0140a0001c0001t0001g0241a0001c0001t0004g0121others(11): Show | 14 | HG00738.hp2 HG01943.hp1 HG02293.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-15986_118-1598 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350862 | |||||
chr2:203350862
|
T | TTGTG | 3 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160 | 3 | HG02451.hp2 HG02717.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.118-15988_118-1598 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350862 | |||||
chr2:203350862
|
TTG | T | 107 | a0001c0001t0001g0216a0001c0001t0001g0242a0001c0001t0001g0248others(104): Show | 107 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.118-15986_118-1598 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350862 | |||||
chr2:203350862
|
TTGTG | T | 4 | a0001c0001t0003g0184a0001c0001t0003g0185a0001c0001t0006g0149others(1): Show | 4 | HG01891.hp1 HG02258.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-15988_118-1598 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350862 | |||||
chr2:203350889
|
TGTGC | T | 33 | a0001c0001t0001g0181a0001c0001t0001g0224a0001c0001t0002g0187others(30): Show | 33 | HG00438.hp1 HG00621.hp1 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.118-15986_118-1598 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350889 | |||||
chr2:203350891
|
T | C | 1 | a0001c0001t0002g0022 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.118-15986T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350891 | ||||||
chr2:203350891
|
TGC | T | 109 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(106): Show | 109 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(106): Show |
intron_variant | MODIFIER | c.118-15977_118-1597 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203350891 | |||||
chr2:203350893
|
C | T | 14 | a0001c0001t0001g0237a0001c0001t0001g0241a0001c0001t0001g0276others(11): Show | 14 | HG01255.hp1 HG01257.hp1 HG01496.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-15984C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350893 | ||||||
chr2:203350895
|
C | T | 7 | a0001c0001t0001g0218a0001c0001t0001g0245a0001c0001t0001g0255others(4): Show | 7 | HG00597.hp1 HG00673.hp1 NA18945.hp1 others(4): Show |
intron_variant | MODIFIER | c.118-15982C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350895 | ||||||
chr2:203350905
|
C | A | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.118-15972C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350905 | ||||||
chr2:203350959
|
T | G | 4 | a0001c0001t0006g0149a0001c0001t0006g0162a0001c0001t0006g0173others(1): Show | 4 | HG02572.hp2 HG02896.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-15918T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350959 | ||||||
chr2:203350964
|
C | A | 1 | a0001c0001t0001g0259 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.118-15913C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203350964 | ||||||
chr2:203351201
|
A | G | 1 | a0001c0001t0002g0063 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.118-15676A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351201 | ||||||
chr2:203351318
|
A | G | 1 | a0001c0001t0002g0193 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.118-15559A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351318 | ||||||
chr2:203351459
|
T | G | 1 | a0001c0001t0008g0034 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.118-15418T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351459 | ||||||
chr2:203351532
|
G | GT | 177 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(174): Show | 177 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(174): Show |
intron_variant | MODIFIER | c.118-15330dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203351532 | |||||
chr2:203351532
|
G | GTT | 13 | a0001c0001t0001g0216a0001c0001t0001g0296a0001c0001t0001g0316others(10): Show | 13 | HG00597.hp1 HG00733.hp1 HG00733.hp2 others(10): Show |
intron_variant | MODIFIER | c.118-15331_118-1533 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203351532 | |||||
chr2:203351657
|
T | C | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118-15220T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351657 | ||||||
chr2:203351755
|
C | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0308 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.118-15122C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351755 | ||||||
chr2:203351798
|
A | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.118-15079A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351798 | ||||||
chr2:203351836
|
G | A | 302 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(299): Show | 302 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.118-15041G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351836 | ||||||
chr2:203351942
|
A | G | 1 | a0001c0001t0003g0220 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.118-14935A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351942 | ||||||
chr2:203351972
|
G | A | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118-14905G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203351972 | ||||||
chr2:203352067
|
G | A | 1 | a0001c0001t0001g0292 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.118-14810G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203352067 | ||||||
chr2:203352256
|
T | A | 1 | a0001c0001t0014g0277 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.118-14621T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203352256 | ||||||
chr2:203352569
|
GA | G | 95 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(92): Show | 95 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.118-14298delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203352569 | |||||
chr2:203353087
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.118-13790A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353087 | ||||||
chr2:203353208
|
T | G | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.118-13669T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353208 | ||||||
chr2:203353296
|
A | C | 1 | a0001c0001t0002g0031 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.118-13581A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353296 | ||||||
chr2:203353434
|
A | AC | 7 | a0001c0001t0001g0278a0001c0001t0002g0002a0001c0001t0002g0075others(4): Show | 7 | HG02027.hp1 HG02055.hp2 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-13439dupC | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203353434 | |||||
chr2:203353698
|
A | C | 1 | a0001c0001t0003g0220 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.118-13179A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353698 | ||||||
chr2:203353699
|
T | C | 1 | a0001c0001t0002g0032 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.118-13178T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353699 | ||||||
chr2:203353737
|
G | A | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.118-13140G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353737 | ||||||
chr2:203353752
|
C | T | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.118-13125C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353752 | ||||||
chr2:203353813
|
C | T | 1 | a0001c0001t0003g0205 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.118-13064C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203353813 | ||||||
chr2:203354100
|
G | A | 1 | a0001c0001t0015g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.118-12777G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354100 | ||||||
chr2:203354125
|
A | G | 1 | a0001c0001t0002g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.118-12752A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354125 | ||||||
chr2:203354150
|
A | G | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.118-12727A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354150 | ||||||
chr2:203354345
|
A | G | 1 | a0001c0001t0006g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.118-12532A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354345 | ||||||
chr2:203354509
|
G | C | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.118-12368G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354509 | ||||||
chr2:203354705
|
TAAG | T | 39 | a0001c0001t0002g0187a0001c0001t0002g0193a0001c0001t0002g0194others(36): Show | 39 | HG00438.hp1 HG00642.hp1 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.118-12167_118-1216 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203354705 | |||||
chr2:203354803
|
A | C | 1 | a0001c0001t0002g0028 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.118-12074A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354803 | ||||||
chr2:203354839
|
A | T | 1 | a0001c0001t0001g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.118-12038A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354839 | ||||||
chr2:203354957
|
T | C | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.118-11920T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203354957 | ||||||
chr2:203355181
|
C | G | 1 | a0001c0001t0002g0006 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.118-11696C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355181 | ||||||
chr2:203355205
|
A | G | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118-11672A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355205 | ||||||
chr2:203355703
|
C | T | 290 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(287): Show | 290 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.118-11174C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355703 | ||||||
chr2:203355704
|
G | A | 4 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-11173G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355704 | ||||||
chr2:203355828
|
T | G | 1 | a0001c0001t0001g0269 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.118-11049T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355828 | ||||||
chr2:203355828
|
TC | T | 17 | a0001c0001t0005g0100a0001c0001t0005g0102a0001c0001t0005g0103others(14): Show | 17 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.118-11048delC | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355828 | ||||||
chr2:203355829
|
C | A | 2 | a0001c0001t0005g0107a0001c0001t0005g0115 | 2 | HG03831.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.118-11048C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355829 | ||||||
chr2:203355829
|
C | CA | 26 | a0001c0001t0002g0015a0001c0001t0002g0022a0001c0001t0002g0035others(23): Show | 26 | HG00738.hp2 HG01361.hp1 HG01891.hp2 others(23): Show |
intron_variant | MODIFIER | c.118-11026dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203355829 | |||||
chr2:203355829
|
C | CAA | 7 | a0001c0001t0006g0164a0001c0001t0006g0167a0001c0001t0006g0172others(4): Show | 7 | HG01109.hp1 HG01169.hp1 HG02109.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-11027_118-1102 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203355829 | |||||
chr2:203355829
|
C | CAAA | 11 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(8): Show | 11 | HG01168.hp2 HG01884.hp1 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.118-11028_118-1102 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203355829 | |||||
chr2:203355829
|
CA | C | 77 | a0001c0001t0001g0182a0001c0001t0001g0200a0001c0001t0001g0201others(74): Show | 77 | HG00280.hp1 HG00423.hp1 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.118-11026delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203355829 | |||||
chr2:203355830
|
A | AAAACTGT others(3): Show |
1 | a0001c0001t0001g0269 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.118-11044_118-1104 others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203355830 | |||||
chr2:203355880
|
G | A | 1 | a0001c0001t0004g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.118-10997G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355880 | ||||||
chr2:203355926
|
T | C | 5 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0208others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-10951T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355926 | ||||||
chr2:203355936
|
A | G | 1 | a0001c0001t0002g0048 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.118-10941A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203355936 | ||||||
chr2:203356052
|
T | C | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.118-10825T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356052 | ||||||
chr2:203356478
|
C | T | 1 | a0001c0001t0001g0300 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.118-10399C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356478 | ||||||
chr2:203356510
|
A | G | 1 | a0001c0001t0033g0087 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.118-10367A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356510 | ||||||
chr2:203356514
|
G | A | 1 | a0001c0001t0002g0010 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.118-10363G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356514 | ||||||
chr2:203356515
|
C | A | 1 | a0001c0001t0021g0151 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.118-10362C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356515 | ||||||
chr2:203356613
|
A | T | 16 | a0001c0001t0001g0200a0001c0001t0001g0228a0001c0001t0001g0229others(13): Show | 16 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.118-10264A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356613 | ||||||
chr2:203356638
|
A | G | 2 | a0001c0001t0001g0256a0001c0001t0001g0292 | 2 | NA18978.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.118-10239A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203356638 | ||||||
chr2:203356848
|
AT | A | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.118-10016delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203356848 | |||||
chr2:203357043
|
ATTT | A | 95 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(92): Show | 95 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.118-9831_118-9829d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203357043 | |||||
chr2:203357100
|
T | A | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.118-9777T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203357100 | ||||||
chr2:203357287
|
T | A | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.118-9590T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203357287 | ||||||
chr2:203357542
|
C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-9335C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203357542 | ||||||
chr2:203357644
|
G | T | 1 | a0001c0001t0008g0090 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.118-9233G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203357644 | ||||||
chr2:203357720
|
G | T | 1 | a0001c0001t0003g0289 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.118-9157G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203357720 | ||||||
chr2:203357757
|
T | G | 1 | a0001c0001t0001g0275 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.118-9120T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203357757 | ||||||
chr2:203357759
|
T | TTTTG | 3 | a0001c0001t0002g0063a0001c0001t0004g0144a0001c0001t0004g0145 | 3 | HG02723.hp2 HG03209.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.118-9093_118-9090d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203357759 | |||||
chr2:203357759
|
TTTTGTTT others(1): Show |
T | 187 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(184): Show | 187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.118-9097_118-9090d others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203357759 | |||||
chr2:203358017
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.118-8860C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358017 | ||||||
chr2:203358071
|
T | G | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118-8806T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358071 | ||||||
chr2:203358071
|
T | TGTGTG | 3 | a0001c0001t0001g0182a0001c0001t0001g0298a0001c0001t0011g0154 | 3 | HG02622.hp2 HG03139.hp2 NA18995.hp2 |
intron_variant | MODIFIER | c.118-8806_118-8805i others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358071 | ||||||
chr2:203358071
|
T | TTG | 65 | a0001c0001t0001g0224a0001c0001t0001g0250a0001c0001t0001g0254others(62): Show | 65 | HG00323.hp1 HG00323.hp2 HG00597.hp2 others(62): Show |
intron_variant | MODIFIER | c.118-8764_118-8763d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | |||||
chr2:203358071
|
T | TTGTG | 24 | a0001c0001t0002g0010a0001c0001t0002g0014a0001c0001t0002g0022others(21): Show | 24 | HG01074.hp2 HG01175.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.118-8766_118-8763d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | |||||
chr2:203358071
|
T | TTGTGTG | 22 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0035others(19): Show | 22 | HG01257.hp1 HG01258.hp1 HG02027.hp1 others(19): Show |
intron_variant | MODIFIER | c.118-8768_118-8763d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | |||||
chr2:203358071
|
T | TTGTGTGT others(1): Show |
12 | a0001c0001t0002g0036a0001c0001t0002g0044a0001c0001t0002g0050others(9): Show | 12 | HG02040.hp2 HG02155.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.118-8770_118-8763d others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | |||||
chr2:203358071
|
T | TTGTGTGT others(3): Show |
8 | a0001c0001t0002g0018a0001c0001t0004g0134a0001c0001t0004g0148others(5): Show | 8 | HG03098.hp2 HG03195.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.118-8772_118-8763d others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | |||||
chr2:203358071
|
T | TTGTGTGT others(5): Show |
10 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0003g0208others(7): Show | 10 | HG00621.hp1 HG02083.hp1 HG02622.hp1 others(7): Show |
intron_variant | MODIFIER | c.118-8774_118-8763d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | |||||
chr2:203358071
|
T | TTGTGTGT others(7): Show |
1 | a0001c0001t0002g0079 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.118-8776_118-8763d others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | |||||
chr2:203358071
|
TTG | T | 80 | a0001c0001t0001g0186a0001c0001t0001g0200a0001c0001t0001g0201others(77): Show | 80 | HG00280.hp1 HG00423.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.118-8764_118-8763d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | |||||
chr2:203358071
|
TTGTG | T | 9 | a0001c0001t0001g0238a0001c0001t0001g0306a0001c0001t0002g0005others(6): Show | 9 | HG00423.hp2 HG01175.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.118-8766_118-8763d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | |||||
chr2:203358071
|
TTGTGTG | T | 20 | a0001c0001t0001g0270a0001c0001t0001g0271a0001c0001t0004g0136others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.118-8768_118-8763d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358071 | |||||
chr2:203358107
|
GTGTGTGT others(5): Show |
G | 1 | a0001c0001t0003g0189 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.118-8766_118-8755d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358107 | |||||
chr2:203358109
|
GTGTGTT | G | 14 | a0001c0001t0003g0199a0001c0001t0003g0221a0001c0001t0003g0222others(11): Show | 14 | HG00642.hp1 HG00642.hp2 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.118-8764_118-8759d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358109 | |||||
chr2:203358109
|
GTGTGTTT others(3): Show |
G | 8 | a0001c0001t0002g0187a0001c0001t0002g0193a0001c0001t0002g0194others(5): Show | 8 | HG00735.hp1 HG00738.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-8764_118-8755d others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358109 | |||||
chr2:203358111
|
GTGTT | G | 3 | a0001c0001t0003g0188a0001c0001t0003g0220a0001c0001t0003g0311 | 3 | HG01074.hp1 HG03710.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.118-8748_118-8745d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358111 | |||||
chr2:203358113
|
GTT | G | 3 | a0001c0001t0003g0309a0001c0001t0005g0176a0001c0002t0024g0118 | 3 | HG01928.hp1 HG02451.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.118-8762_118-8761d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203358113 | |||||
chr2:203358115
|
T | G | 25 | a0001c0001t0001g0298a0001c0001t0003g0191a0001c0001t0003g0192others(22): Show | 25 | HG00738.hp2 HG01884.hp2 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.118-8762T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358115 | ||||||
chr2:203358119
|
T | G | 1 | a0001c0001t0003g0226 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.118-8758T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358119 | ||||||
chr2:203358180
|
T | G | 3 | a0001c0001t0002g0049a0001c0001t0002g0074a0001c0001t0002g0075 | 3 | NA18970.hp1 NA18991.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.118-8697T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358180 | ||||||
chr2:203358234
|
A | G | 5 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0208others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.118-8643A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358234 | ||||||
chr2:203358322
|
A | G | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.118-8555A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358322 | ||||||
chr2:203358466
|
A | C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-8411A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358466 | ||||||
chr2:203358482
|
C | T | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.118-8395C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358482 | ||||||
chr2:203358789
|
C | T | 4 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.118-8088C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203358789 | ||||||
chr2:203359162
|
A | G | 4 | a0001c0001t0006g0169a0001c0001t0006g0170a0001c0001t0006g0174others(1): Show | 4 | HG01884.hp1 HG03130.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-7715A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203359162 | ||||||
chr2:203359845
|
TG | T | 185 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(182): Show | 185 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.118-7023delG | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203359845 | |||||
chr2:203359957
|
C | T | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.118-6920C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203359957 | ||||||
chr2:203359981
|
T | C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-6896T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203359981 | ||||||
chr2:203360013
|
C | G | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.118-6864C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360013 | ||||||
chr2:203360138
|
T | C | 3 | a0001c0001t0003g0184a0001c0001t0003g0185a0001c0001t0031g0183 | 3 | HG01891.hp1 HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.118-6739T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360138 | ||||||
chr2:203360184
|
C | CA | 8 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0032others(5): Show | 8 | HG02145.hp1 HG02145.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.118-6670dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203360184 | |||||
chr2:203360184
|
CA | C | 183 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(180): Show | 183 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.118-6670delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203360184 | |||||
chr2:203360186
|
A | G | 1 | a0001c0001t0002g0057 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.118-6691A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360186 | ||||||
chr2:203360205
|
A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-6672A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360205 | ||||||
chr2:203360377
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.118-6500A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360377 | ||||||
chr2:203360383
|
G | A | 1 | a0001c0001t0005g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.118-6494G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360383 | ||||||
chr2:203360596
|
A | C | 1 | a0001c0001t0004g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.118-6281A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360596 | ||||||
chr2:203360882
|
C | A | 1 | a0001c0001t0002g0097 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.118-5995C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203360882 | ||||||
chr2:203361280
|
G | T | 42 | a0001c0001t0002g0187a0001c0001t0002g0193a0001c0001t0002g0194others(39): Show | 42 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.118-5597G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203361280 | ||||||
chr2:203361339
|
C | T | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.118-5538C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203361339 | ||||||
chr2:203361608
|
A | G | 42 | a0001c0001t0002g0187a0001c0001t0002g0193a0001c0001t0002g0194others(39): Show | 42 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.118-5269A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203361608 | ||||||
chr2:203361827
|
C | T | 1 | a0001c0001t0002g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.118-5050C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203361827 | ||||||
chr2:203361940
|
A | G | 319 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(316): Show | 319 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.118-4937A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203361940 | ||||||
chr2:203362154
|
T | C | 1 | a0001c0001t0002g0097 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.118-4723T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362154 | ||||||
chr2:203362720
|
T | C | 1 | a0001c0001t0001g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118-4157T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362720 | ||||||
chr2:203362721
|
T | A | 1 | a0001c0001t0001g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118-4156T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362721 | ||||||
chr2:203362724
|
T | G | 1 | a0001c0001t0001g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.118-4153T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362724 | ||||||
chr2:203362744
|
C | G | 3 | a0001c0001t0001g0181a0001c0001t0001g0224a0001c0001t0001g0270 | 3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.118-4133C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362744 | ||||||
chr2:203362967
|
A | G | 3 | a0001c0001t0002g0032a0001c0001t0002g0041a0001c0001t0002g0052 | 3 | HG03491.hp2 HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.118-3910A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362967 | ||||||
chr2:203362996
|
A | G | 3 | a0001c0001t0001g0181a0001c0001t0001g0224a0001c0001t0001g0270 | 3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.118-3881A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203362996 | ||||||
chr2:203363152
|
TA | T | 319 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(316): Show | 319 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.118-3716delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203363152 | |||||
chr2:203363202
|
G | A | 1 | a0001c0001t0006g0175 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.118-3675G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363202 | ||||||
chr2:203363334
|
G | A | 4 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0004g0144others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.118-3543G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363334 | ||||||
chr2:203363377
|
C | G | 1 | a0001c0001t0004g0141 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.118-3500C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363377 | ||||||
chr2:203363402
|
T | C | 1 | a0001c0001t0003g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.118-3475T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363402 | ||||||
chr2:203363525
|
C | T | 3 | a0001c0001t0011g0153a0001c0001t0011g0154a0001c0001t0011g0155 | 3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.118-3352C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363525 | ||||||
chr2:203363578
|
T | C | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.118-3299T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363578 | ||||||
chr2:203363787
|
A | G | 1 | a0001c0001t0003g0188 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.118-3090A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363787 | ||||||
chr2:203363859
|
G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-3018G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203363859 | ||||||
chr2:203364043
|
C | T | 1 | a0001c0001t0004g0126 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.118-2834C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203364043 | ||||||
chr2:203364091
|
C | CT | 19 | a0001c0001t0001g0265a0001c0001t0006g0001a0001c0001t0006g0149others(16): Show | 19 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.118-2772dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203364091 | |||||
chr2:203364091
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0002g0079 | 3 | HG02145.hp1 HG02809.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.118-2781_118-2772d others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203364091 | |||||
chr2:203364318
|
TCCTGACC others(16): Show |
T | 1 | a0001c0001t0035g0064 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.118-2555_118-2533d others(25): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203364318 | |||||
chr2:203364474
|
A | G | 1 | a0001c0002t0024g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.118-2403A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203364474 | ||||||
chr2:203364491
|
G | A | 1 | a0001c0001t0001g0218 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.118-2386G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203364491 | ||||||
chr2:203364734
|
AT | A | 28 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0003g0184others(25): Show | 28 | HG01074.hp1 HG01255.hp2 HG01358.hp1 others(25): Show |
intron_variant | MODIFIER | c.118-2128delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203364734 | |||||
chr2:203364749
|
T | C | 95 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(92): Show | 95 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.118-2128T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203364749 | ||||||
chr2:203365089
|
A | G | 2 | a0001c0002t0005g0116a0001c0002t0024g0118 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.118-1788A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365089 | ||||||
chr2:203365224
|
A | T | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.118-1653A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365224 | ||||||
chr2:203365267
|
T | C | 1 | a0001c0001t0002g0036 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.118-1610T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365267 | ||||||
chr2:203365527
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.118-1350T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365527 | ||||||
chr2:203365536
|
T | A | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.118-1341T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365536 | ||||||
chr2:203365572
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0004g0137a0001c0001t0004g0141 | 3 | HG02293.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.118-1305T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365572 | ||||||
chr2:203365622
|
C | CT | 100 | a0001c0001t0002g0004a0001c0001t0002g0005a0001c0001t0002g0006others(97): Show | 100 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(97): Show |
intron_variant | MODIFIER | c.118-1230dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365622 | |||||
chr2:203365622
|
C | CTT | 20 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0017others(17): Show | 20 | HG01109.hp1 HG01168.hp1 HG02027.hp1 others(17): Show |
intron_variant | MODIFIER | c.118-1231_118-1230d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365622 | |||||
chr2:203365622
|
CT | C | 125 | a0001c0001t0001g0181a0001c0001t0001g0186a0001c0001t0001g0200others(122): Show | 125 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.118-1230delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365622 | |||||
chr2:203365622
|
CTT | C | 6 | a0001c0001t0001g0201a0001c0001t0001g0207a0001c0001t0001g0299others(3): Show | 6 | HG01496.hp2 HG01515.hp1 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.118-1231_118-1230d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365622 | |||||
chr2:203365622
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0004g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.118-1240_118-1230d others(13): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365622 | |||||
chr2:203365622
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0011g0153a0001c0001t0011g0154a0001c0001t0011g0155 | 3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.118-1241_118-1230d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365622 | |||||
chr2:203365966
|
A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.118-911A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203365966 | ||||||
chr2:203365974
|
CTTTGTTT others(3): Show |
C | 1 | a0001c0001t0003g0198 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.118-895_118-886del others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203365974 | |||||
chr2:203366055
|
G | A | 1 | a0001c0001t0003g0225 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.118-822G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203366055 | ||||||
chr2:203366406
|
AT | A | 7 | a0001c0001t0001g0207a0001c0001t0001g0265a0001c0001t0001g0272others(4): Show | 7 | NA18940.hp2 NA18946.hp2 NA18951.hp2 others(4): Show |
intron_variant | MODIFIER | c.118-462delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 203366406 | |||||
chr2:203366682
|
T | C | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.118-195T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203366682 | ||||||
chr2:203366692
|
A | G | 1 | a0001c0001t0003g0282 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.118-185A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 1/11 | chr2 | 203366692 | ||||||
chr2:203367088
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0308 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.285+44A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367088 | ||||||
chr2:203367128
|
T | C | 1 | a0001c0001t0001g0297 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.285+84T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367128 | ||||||
chr2:203367323
|
C | CT | 183 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(180): Show | 183 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(180): Show |
intron_variant | MODIFIER | c.285+292dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203367323 | |||||
chr2:203367337
|
A | T | 2 | a0001c0001t0001g0251a0001c0001t0037g0320 | 2 | HG02109.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.285+293A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367337 | ||||||
chr2:203367551
|
T | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+507T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367551 | ||||||
chr2:203367819
|
A | G | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.285+775A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367819 | ||||||
chr2:203367873
|
G | A | 95 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(92): Show | 95 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.285+829G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367873 | ||||||
chr2:203367876
|
C | T | 3 | a0001c0001t0011g0153a0001c0001t0011g0154a0001c0001t0011g0155 | 3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.285+832C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203367876 | ||||||
chr2:203368222
|
C | T | 1 | a0001c0001t0001g0261 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.285+1178C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368222 | ||||||
chr2:203368228
|
T | G | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.285+1184T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368228 | ||||||
chr2:203368585
|
T | G | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+1541T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368585 | ||||||
chr2:203368818
|
A | AT | 6 | a0001c0001t0001g0202a0001c0001t0001g0247a0001c0001t0002g0084others(3): Show | 6 | HG01169.hp2 HG01358.hp2 HG01884.hp2 others(3): Show |
intron_variant | MODIFIER | c.285+1788dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203368818 | |||||
chr2:203368984
|
AT | A | 16 | a0001c0001t0001g0181a0001c0001t0001g0224a0001c0001t0001g0228others(13): Show | 16 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(13): Show |
intron_variant | MODIFIER | c.285+1972delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203368984 | |||||
chr2:203368984
|
ATT | A | 80 | a0001c0001t0001g0186a0001c0001t0001g0201a0001c0001t0001g0214others(77): Show | 80 | HG00597.hp1 HG00609.hp1 HG00642.hp1 others(77): Show |
intron_variant | MODIFIER | c.285+1971_285+1972d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203368984 | |||||
chr2:203368984
|
ATTT | A | 135 | a0001c0001t0001g0182a0001c0001t0001g0200a0001c0001t0001g0202others(132): Show | 135 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(132): Show |
intron_variant | MODIFIER | c.285+1970_285+1972d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203368984 | |||||
chr2:203368984
|
ATTTT | A | 77 | a0001c0001t0001g0140a0001c0001t0001g0272a0001c0001t0002g0004others(74): Show | 77 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(74): Show |
intron_variant | MODIFIER | c.285+1969_285+1972d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203368984 | |||||
chr2:203368985
|
T | A | 4 | a0001c0001t0001g0230a0001c0001t0003g0209a0001c0001t0006g0172others(1): Show | 4 | HG02280.hp2 HG02572.hp1 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+1941T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368985 | ||||||
chr2:203368986
|
T | A | 15 | a0001c0001t0001g0181a0001c0001t0001g0224a0001c0001t0001g0228others(12): Show | 15 | HG00423.hp1 HG00438.hp1 HG00438.hp2 others(12): Show |
intron_variant | MODIFIER | c.285+1942T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368986 | ||||||
chr2:203368987
|
T | A | 77 | a0001c0001t0001g0186a0001c0001t0001g0201a0001c0001t0001g0214others(74): Show | 77 | HG00597.hp1 HG00609.hp1 HG00642.hp1 others(74): Show |
intron_variant | MODIFIER | c.285+1943T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368987 | ||||||
chr2:203368988
|
T | A | 120 | a0001c0001t0001g0182a0001c0001t0001g0200a0001c0001t0001g0202others(117): Show | 120 | HG00280.hp1 HG00323.hp2 HG00597.hp2 others(117): Show |
intron_variant | MODIFIER | c.285+1944T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368988 | ||||||
chr2:203368989
|
T | A | 69 | a0001c0001t0001g0272a0001c0001t0002g0004a0001c0001t0002g0005others(66): Show | 69 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(66): Show |
intron_variant | MODIFIER | c.285+1945T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368989 | ||||||
chr2:203368990
|
T | A | 5 | a0001c0001t0002g0037a0001c0001t0009g0158a0001c0001t0009g0159others(2): Show | 5 | HG01884.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.285+1946T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203368990 | ||||||
chr2:203369054
|
C | T | 1 | a0001c0001t0005g0156 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.285+2010C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369054 | ||||||
chr2:203369150
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.285+2106G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369150 | ||||||
chr2:203369203
|
A | G | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285+2159A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369203 | ||||||
chr2:203369230
|
T | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.285+2186T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369230 | ||||||
chr2:203369357
|
G | A | 1 | a0001c0001t0002g0006 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.285+2313G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369357 | ||||||
chr2:203369385
|
A | G | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.285+2341A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369385 | ||||||
chr2:203369592
|
G | A | 302 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(299): Show | 302 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(299): Show |
intron_variant | MODIFIER | c.285+2548G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369592 | ||||||
chr2:203369774
|
G | T | 1 | a0001c0001t0004g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.285+2730G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369774 | ||||||
chr2:203369913
|
AT | A | 319 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(316): Show | 319 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.285+2881delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203369913 | |||||
chr2:203369937
|
C | T | 2 | a0001c0002t0005g0116a0001c0002t0024g0118 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.285+2893C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203369937 | ||||||
chr2:203370122
|
TTTG | T | 4 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+3080_285+3082d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370122 | |||||
chr2:203370165
|
A | G | 7 | a0001c0001t0005g0106a0001c0001t0005g0109a0001c0001t0005g0110others(4): Show | 7 | HG02083.hp1 HG02135.hp2 HG02155.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+3121A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370165 | ||||||
chr2:203370175
|
T | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0270 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.285+3131T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370175 | ||||||
chr2:203370176
|
C | G | 2 | a0001c0001t0001g0181a0001c0001t0001g0270 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.285+3132C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370176 | ||||||
chr2:203370178
|
T | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0270 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.285+3134T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370178 | ||||||
chr2:203370180
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0270 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.285+3136C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370180 | ||||||
chr2:203370186
|
T | TTC | 23 | a0001c0001t0001g0140a0001c0001t0001g0224a0001c0001t0002g0019others(20): Show | 23 | HG00741.hp1 HG01074.hp2 HG01175.hp2 others(20): Show |
intron_variant | MODIFIER | c.285+3182_285+3183d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
T | TTCTC | 4 | a0001c0001t0002g0058a0001c0001t0004g0135a0001c0001t0004g0139others(1): Show | 4 | HG01943.hp2 HG02129.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.285+3180_285+3183d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
T | TTCTCTC | 7 | a0001c0001t0002g0018a0001c0001t0002g0032a0001c0001t0002g0035others(4): Show | 7 | HG02083.hp1 HG02486.hp1 HG02630.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+3178_285+3183d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
T | TTCTCTCT others(1): Show |
7 | a0001c0001t0004g0141a0001c0001t0004g0146a0001c0001t0005g0081others(4): Show | 7 | HG00621.hp1 HG02293.hp1 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.285+3176_285+3183d others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
T | TTCTCTCT others(3): Show |
7 | a0001c0001t0002g0036a0001c0001t0005g0100a0001c0001t0005g0109others(4): Show | 7 | HG02040.hp2 HG02155.hp1 HG06807.hp2 others(4): Show |
intron_variant | MODIFIER | c.285+3174_285+3183d others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
T | TTCTCTCT others(5): Show |
3 | a0001c0001t0005g0105a0001c0001t0005g0110a0001c0001t0005g0115 | 3 | HG02293.hp2 HG03831.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.285+3172_285+3183d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
T | TTCTCTCT others(9): Show |
2 | a0001c0001t0005g0102a0001c0001t0005g0161 | 2 | HG01257.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.285+3168_285+3183d others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
T | TTCTCTCT others(13): Show |
1 | a0001c0001t0005g0156 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.285+3164_285+3183d others(22): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
TTC | T | 6 | a0001c0001t0001g0246a0001c0001t0001g0295a0001c0001t0001g0318others(3): Show | 6 | HG00673.hp1 HG01255.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.285+3182_285+3183d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
TTCTC | T | 94 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0200others(91): Show | 94 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(91): Show |
intron_variant | MODIFIER | c.285+3180_285+3183d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
TTCTCTC | T | 31 | a0001c0001t0001g0264a0001c0001t0001g0307a0001c0001t0002g0095others(28): Show | 31 | HG00642.hp2 HG00738.hp1 HG01167.hp2 others(28): Show |
intron_variant | MODIFIER | c.285+3178_285+3183d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
TTCTCTCT others(1): Show |
T | 27 | a0001c0001t0001g0201a0001c0001t0001g0218a0001c0001t0001g0293others(24): Show | 27 | HG00733.hp2 HG00735.hp2 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.285+3176_285+3183d others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
TTCTCTCT others(3): Show |
T | 18 | a0001c0001t0001g0186a0001c0001t0001g0212a0001c0001t0001g0213others(15): Show | 18 | HG00280.hp1 HG00733.hp1 HG00735.hp1 others(15): Show |
intron_variant | MODIFIER | c.285+3174_285+3183d others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
TTCTCTCT others(5): Show |
T | 3 | a0001c0001t0003g0203a0001c0001t0010g0066a0001c0001t0034g0190 | 3 | HG00438.hp1 NA18962.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.285+3172_285+3183d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
TTCTCTCT others(9): Show |
T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.285+3168_285+3183d others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370186
|
TTCTCTCT others(11): Show |
T | 2 | a0001c0001t0007g0093a0001c0001t0016g0092 | 2 | NA18971.hp1 NA18971.hp2 |
intron_variant | MODIFIER | c.285+3166_285+3183d others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370186 | |||||
chr2:203370227
|
T | TC | 3 | a0001c0001t0002g0051a0001c0001t0029g0096a0001c0001t0032g0039 | 3 | HG02040.hp1 HG02080.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.285+3183_285+3184i others(3): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370227 | ||||||
chr2:203370227
|
T | TCTCTC | 3 | a0001c0001t0002g0006a0001c0001t0002g0014a0001c0001t0004g0136 | 3 | HG02155.hp2 HG04228.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.285+3183_285+3184i others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370227 | ||||||
chr2:203370227
|
T | TCTCTCTC others(10): Show |
1 | a0001c0001t0005g0103 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.285+3183_285+3184i others(19): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370227 | ||||||
chr2:203370320
|
T | G | 2 | a0001c0001t0006g0149a0001c0001t0006g0162 | 2 | HG02572.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.285+3276T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370320 | ||||||
chr2:203370375
|
AC | A | 10 | a0001c0001t0005g0106a0001c0001t0005g0107a0001c0001t0005g0108others(7): Show | 10 | HG00621.hp1 HG02083.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.285+3333delC | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203370375 | |||||
chr2:203370451
|
G | A | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.285+3407G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370451 | ||||||
chr2:203370654
|
A | G | 1 | a0001c0001t0018g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.285+3610A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370654 | ||||||
chr2:203370753
|
G | A | 187 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(184): Show | 187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.285+3709G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203370753 | ||||||
chr2:203371049
|
A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.285+4005A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371049 | ||||||
chr2:203371163
|
G | A | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.285+4119G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371163 | ||||||
chr2:203371334
|
C | A | 17 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.285+4290C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371334 | ||||||
chr2:203371394
|
A | G | 4 | a0001c0001t0003g0199a0001c0001t0003g0222a0001c0001t0003g0223others(1): Show | 4 | HG00642.hp1 HG01358.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.285+4350A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371394 | ||||||
chr2:203371537
|
A | G | 3 | a0001c0001t0001g0256a0001c0001t0001g0273a0001c0001t0001g0292 | 3 | NA18978.hp1 NA18982.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.285+4493A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371537 | ||||||
chr2:203371596
|
C | A | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.285+4552C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371596 | ||||||
chr2:203371824
|
T | G | 1 | a0001c0001t0002g0019 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.285+4780T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371824 | ||||||
chr2:203371918
|
A | C | 2 | a0001c0001t0002g0022a0001c0001t0002g0029 | 2 | HG01074.hp2 HG01361.hp1 |
intron_variant | MODIFIER | c.285+4874A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371918 | ||||||
chr2:203371941
|
A | T | 289 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(286): Show | 289 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.285+4897A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371941 | ||||||
chr2:203371958
|
C | T | 2 | a0001c0001t0004g0144a0001c0001t0004g0145 | 2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.285+4914C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203371958 | ||||||
chr2:203372019
|
C | T | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+4975C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372019 | ||||||
chr2:203372082
|
G | A | 1 | a0001c0001t0001g0283 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.285+5038G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372082 | ||||||
chr2:203372128
|
C | T | 1 | a0001c0001t0019g0147 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.285+5084C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372128 | ||||||
chr2:203372244
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.285+5200G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372244 | ||||||
chr2:203372245
|
C | G | 2 | a0001c0001t0001g0214a0001c0001t0001g0215 | 2 | NA18949.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.285+5201C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372245 | ||||||
chr2:203372261
|
A | T | 92 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(89): Show | 92 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(89): Show |
intron_variant | MODIFIER | c.285+5217A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372261 | ||||||
chr2:203372291
|
G | A | 3 | a0001c0001t0010g0066a0001c0001t0010g0067a0001c0001t0010g0078 | 3 | NA18962.hp2 NA18986.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.285+5247G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372291 | ||||||
chr2:203372361
|
C | T | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.285+5317C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372361 | ||||||
chr2:203372385
|
C | G | 3 | a0001c0001t0001g0255a0001c0001t0004g0137a0001c0001t0004g0217 | 3 | HG02886.hp1 NA19057.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.285+5341C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372385 | ||||||
chr2:203372417
|
C | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0270 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.285+5373C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372417 | ||||||
chr2:203372418
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0270 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.285+5374C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372418 | ||||||
chr2:203372526
|
C | T | 1 | a0001c0001t0001g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.285+5482C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372526 | ||||||
chr2:203372547
|
C | T | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+5503C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372547 | ||||||
chr2:203372552
|
G | A | 1 | a0001c0001t0001g0251 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.285+5508G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372552 | ||||||
chr2:203372725
|
C | T | 1 | a0001c0001t0001g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.285+5681C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372725 | ||||||
chr2:203372728
|
G | A | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.285+5684G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372728 | ||||||
chr2:203372759
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.285+5715G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372759 | ||||||
chr2:203372812
|
C | T | 185 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(182): Show | 185 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.285+5768C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372812 | ||||||
chr2:203372842
|
T | C | 189 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.285+5798T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372842 | ||||||
chr2:203372865
|
G | A | 3 | a0001c0001t0004g0136a0001c0001t0004g0138a0001c0001t0004g0139 | 3 | HG02559.hp1 HG02970.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.285+5821G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203372865 | ||||||
chr2:203373198
|
T | C | 291 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(288): Show | 291 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.285+6154T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373198 | ||||||
chr2:203373199
|
G | A | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+6155G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373199 | ||||||
chr2:203373245
|
G | A | 1 | a0001c0001t0002g0028 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.285+6201G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373245 | ||||||
chr2:203373246
|
C | T | 1 | a0001c0001t0001g0251 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.285+6202C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373246 | ||||||
chr2:203373247
|
G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+6203G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373247 | ||||||
chr2:203373328
|
C | T | 1 | a0001c0001t0003g0184 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.285+6284C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373328 | ||||||
chr2:203373336
|
G | A | 1 | a0001c0001t0017g0252 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.285+6292G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373336 | ||||||
chr2:203373356
|
G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.285+6312G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373356 | ||||||
chr2:203373496
|
AGGGAGAG others(5): Show |
A | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.285+6464_285+6475d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203373496 | |||||
chr2:203373498
|
G | A | 9 | a0001c0001t0002g0005a0001c0001t0002g0014a0001c0001t0002g0016others(6): Show | 9 | HG00621.hp2 HG00741.hp1 HG01256.hp2 others(6): Show |
intron_variant | MODIFIER | c.285+6454G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373498 | ||||||
chr2:203373533
|
T | C | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.285+6489T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373533 | ||||||
chr2:203373603
|
A | G | 1 | a0001c0001t0003g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.285+6559A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373603 | ||||||
chr2:203373679
|
C | A | 24 | a0001c0001t0003g0188a0001c0001t0003g0191a0001c0001t0003g0192others(21): Show | 24 | HG00642.hp1 HG01074.hp1 HG01255.hp2 others(21): Show |
intron_variant | MODIFIER | c.286-6529C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373679 | ||||||
chr2:203373710
|
T | C | 3 | a0001c0001t0001g0140a0001c0001t0004g0137a0001c0001t0004g0141 | 3 | HG02293.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286-6498T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373710 | ||||||
chr2:203373714
|
C | G | 3 | a0001c0001t0001g0140a0001c0001t0004g0137a0001c0001t0004g0141 | 3 | HG02293.hp1 HG02886.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.286-6494C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373714 | ||||||
chr2:203373748
|
A | G | 1 | a0001c0001t0004g0130 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.286-6460A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373748 | ||||||
chr2:203373766
|
A | T | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.286-6442A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373766 | ||||||
chr2:203373803
|
A | AAGAGCTA others(19): Show |
1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.286-6404_286-6379d others(28): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203373803 | |||||
chr2:203373881
|
G | A | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.286-6327G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373881 | ||||||
chr2:203373973
|
A | G | 1 | a0001c0001t0004g0130 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.286-6235A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203373973 | ||||||
chr2:203374065
|
G | A | 185 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(182): Show | 185 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(182): Show |
intron_variant | MODIFIER | c.286-6143G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374065 | ||||||
chr2:203374222
|
G | C | 23 | a0001c0001t0002g0010a0001c0001t0002g0023a0001c0001t0002g0024others(20): Show | 23 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.286-5986G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374222 | ||||||
chr2:203374227
|
C | T | 1 | a0001c0001t0003g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.286-5981C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374227 | ||||||
chr2:203374316
|
A | G | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.286-5892A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374316 | ||||||
chr2:203374405
|
TAGG | T | 5 | a0001c0001t0002g0016a0001c0001t0002g0047a0001c0001t0002g0054others(2): Show | 5 | HG00741.hp1 HG01256.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-5800_286-5798d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203374405 | |||||
chr2:203374498
|
C | CA | 15 | a0001c0001t0001g0261a0001c0001t0002g0079a0001c0001t0002g0194others(12): Show | 15 | HG00735.hp1 HG01975.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.286-5689dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203374498 | |||||
chr2:203374498
|
C | CAA | 13 | a0001c0001t0004g0121a0001c0001t0004g0127a0001c0001t0004g0128others(10): Show | 13 | HG00738.hp2 HG01943.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.286-5690_286-5689d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203374498 | |||||
chr2:203374530
|
A | G | 1 | a0001c0001t0003g0198 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.286-5678A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374530 | ||||||
chr2:203374567
|
G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286-5641G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374567 | ||||||
chr2:203374943
|
A | G | 2 | a0001c0001t0002g0051a0001c0001t0002g0053 | 2 | HG02040.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.286-5265A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203374943 | ||||||
chr2:203375000
|
G | C | 6 | a0001c0001t0002g0018a0001c0001t0002g0035a0001c0001t0002g0036others(3): Show | 6 | HG02486.hp1 HG02630.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.286-5208G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375000 | ||||||
chr2:203375014
|
C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286-5194C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375014 | ||||||
chr2:203375280
|
T | C | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.286-4928T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375280 | ||||||
chr2:203375661
|
A | G | 1 | a0001c0001t0002g0008 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.286-4547A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375661 | ||||||
chr2:203375911
|
C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.286-4297C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375911 | ||||||
chr2:203375927
|
C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.286-4281C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375927 | ||||||
chr2:203375980
|
A | G | 4 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0004g0144others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-4228A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203375980 | ||||||
chr2:203376168
|
TC | T | 15 | a0001c0001t0003g0188a0001c0001t0003g0199a0001c0001t0003g0219others(12): Show | 15 | HG00642.hp1 HG01074.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.286-4039delC | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203376168 | ||||||
chr2:203376279
|
T | A | 1 | a0001c0001t0001g0300 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.286-3929T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203376279 | ||||||
chr2:203376561
|
C | T | 7 | a0001c0001t0002g0037a0001c0001t0002g0043a0001c0001t0002g0046others(4): Show | 7 | HG02523.hp2 NA18949.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.286-3647C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203376561 | ||||||
chr2:203376733
|
C | CT | 29 | a0001c0001t0001g0285a0001c0001t0002g0023a0001c0001t0002g0025others(26): Show | 29 | HG00609.hp2 HG00621.hp1 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.286-3456dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203376733 | |||||
chr2:203376733
|
C | CTT | 85 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0201others(82): Show | 85 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.286-3457_286-3456d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203376733 | |||||
chr2:203376733
|
C | CTTT | 10 | a0001c0001t0001g0200a0001c0001t0001g0229a0001c0001t0001g0233others(7): Show | 10 | HG01175.hp1 HG02083.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.286-3458_286-3456d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203376733 | |||||
chr2:203376733
|
CT | C | 9 | a0001c0001t0001g0181a0001c0001t0001g0224a0001c0001t0002g0044others(6): Show | 9 | HG01884.hp2 HG02559.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.286-3456delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203376733 | |||||
chr2:203376829
|
G | A | 1 | a0001c0001t0001g0295 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.286-3379G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203376829 | ||||||
chr2:203376916
|
A | G | 93 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.286-3292A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203376916 | ||||||
chr2:203377184
|
A | G | 319 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(316): Show | 319 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(316): Show |
intron_variant | MODIFIER | c.286-3024A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377184 | ||||||
chr2:203377365
|
G | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0270 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.286-2843G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377365 | ||||||
chr2:203377404
|
TTTCATTT others(5): Show |
T | 4 | a0001c0001t0003g0206a0001c0001t0003g0208a0001c0001t0003g0209others(1): Show | 4 | HG02572.hp1 HG02723.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.286-2802_286-2791d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203377404 | |||||
chr2:203377608
|
C | T | 7 | a0001c0001t0002g0037a0001c0001t0002g0043a0001c0001t0002g0046others(4): Show | 7 | HG02523.hp2 NA18949.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.286-2600C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377608 | ||||||
chr2:203377656
|
A | G | 1 | a0001c0001t0002g0031 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.286-2552A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377656 | ||||||
chr2:203377832
|
A | G | 1 | a0001c0001t0002g0069 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.286-2376A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377832 | ||||||
chr2:203377891
|
G | A | 6 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0001t0001g0232others(3): Show | 6 | HG00438.hp2 HG00609.hp1 HG02080.hp2 others(3): Show |
intron_variant | MODIFIER | c.286-2317G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377891 | ||||||
chr2:203377898
|
A | G | 1 | a0001c0001t0001g0305 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.286-2310A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377898 | ||||||
chr2:203377991
|
T | C | 1 | a0001c0001t0003g0317 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.286-2217T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203377991 | ||||||
chr2:203378114
|
T | A | 1 | a0001c0001t0005g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.286-2094T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378114 | ||||||
chr2:203378135
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0270 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.286-2073T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378135 | ||||||
chr2:203378151
|
T | C | 1 | a0001c0001t0002g0006 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.286-2057T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378151 | ||||||
chr2:203378174
|
A | T | 39 | a0001c0001t0002g0187a0001c0001t0002g0193a0001c0001t0002g0194others(36): Show | 39 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.286-2034A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378174 | ||||||
chr2:203378177
|
A | G | 95 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(92): Show | 95 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.286-2031A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378177 | ||||||
chr2:203378207
|
G | A | 26 | a0001c0001t0005g0098a0001c0001t0005g0099a0001c0001t0005g0100others(23): Show | 26 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.286-2001G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378207 | ||||||
chr2:203378236
|
C | A | 5 | a0001c0001t0002g0048a0001c0001t0002g0049a0001c0001t0002g0055others(2): Show | 5 | HG01081.hp1 NA18970.hp1 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-1972C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378236 | ||||||
chr2:203378258
|
A | G | 85 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(82): Show | 85 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(82): Show |
intron_variant | MODIFIER | c.286-1950A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378258 | ||||||
chr2:203378313
|
G | A | 1 | a0001c0001t0001g0306 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.286-1895G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378313 | ||||||
chr2:203378313
|
G | T | 78 | a0001c0001t0001g0181a0001c0001t0001g0224a0001c0001t0001g0248others(75): Show | 78 | HG00438.hp1 HG00621.hp1 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.286-1895G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378313 | ||||||
chr2:203378322
|
A | G | 2 | a0001c0001t0001g0275a0001c0001t0002g0057 | 2 | HG02523.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.286-1886A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378322 | ||||||
chr2:203378333
|
G | C | 2 | a0001c0001t0001g0279a0001c0001t0019g0147 | 2 | HG01081.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.286-1875G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378333 | ||||||
chr2:203378358
|
A | G | 1 | a0001c0001t0008g0040 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.286-1850A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378358 | ||||||
chr2:203378362
|
T | C | 1 | a0001c0001t0008g0040 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.286-1846T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378362 | ||||||
chr2:203378386
|
T | C | 22 | a0001c0001t0001g0228a0001c0001t0002g0197a0001c0001t0006g0001others(19): Show | 22 | HG00423.hp1 HG00733.hp2 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.286-1822T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378386 | ||||||
chr2:203378401
|
A | G | 1 | a0001c0001t0036g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.286-1807A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378401 | ||||||
chr2:203378447
|
A | G | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.286-1761A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378447 | ||||||
chr2:203378865
|
C | T | 1 | a0001c0001t0001g0246 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.286-1343C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203378865 | ||||||
chr2:203379036
|
A | T | 42 | a0001c0001t0002g0187a0001c0001t0002g0193a0001c0001t0002g0194others(39): Show | 42 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.286-1172A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379036 | ||||||
chr2:203379128
|
G | A | 1 | a0001c0001t0001g0250 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.286-1080G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379128 | ||||||
chr2:203379184
|
G | A | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.286-1024G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379184 | ||||||
chr2:203379514
|
C | T | 5 | a0001c0001t0007g0007a0001c0001t0007g0085a0001c0001t0007g0089others(2): Show | 5 | NA18951.hp1 NA18968.hp2 NA19010.hp2 others(2): Show |
intron_variant | MODIFIER | c.286-694C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379514 | ||||||
chr2:203379519
|
C | CT | 5 | a0001c0001t0002g0082a0001c0001t0002g0097a0001c0001t0007g0093others(2): Show | 5 | HG02165.hp2 NA18940.hp1 NA18971.hp1 others(2): Show |
intron_variant | MODIFIER | c.286-688dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 203379519 | |||||
chr2:203379649
|
G | A | 17 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.286-559G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379649 | ||||||
chr2:203379706
|
T | A | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.286-502T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379706 | ||||||
chr2:203379724
|
G | A | 1 | a0001c0001t0002g0065 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.286-484G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379724 | ||||||
chr2:203379894
|
A | G | 1 | a0001c0001t0004g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.286-314A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379894 | ||||||
chr2:203379922
|
T | G | 2 | a0001c0001t0010g0066a0001c0001t0010g0067 | 2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.286-286T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379922 | ||||||
chr2:203379931
|
T | G | 1 | a0001c0001t0005g0113 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.286-277T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 2/11 | chr2 | 203379931 | ||||||
chr2:203380777
|
G | C | 189 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.462+393G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203380777 | ||||||
chr2:203380921
|
C | G | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.462+537C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203380921 | ||||||
chr2:203381163
|
T | G | 1 | a0001c0001t0001g0253 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.462+779T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381163 | ||||||
chr2:203381260
|
A | G | 1 | a0001c0001t0001g0264 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.462+876A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381260 | ||||||
chr2:203381303
|
G | A | 1 | a0001c0001t0023g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.463-886G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381303 | ||||||
chr2:203381303
|
G | T | 1 | a0001c0001t0005g0108 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.463-886G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381303 | ||||||
chr2:203381384
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.463-805T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381384 | ||||||
chr2:203381649
|
T | C | 1 | a0001c0001t0002g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.463-540T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381649 | ||||||
chr2:203381821
|
T | A | 28 | a0001c0001t0005g0081a0001c0001t0005g0098a0001c0001t0005g0099others(25): Show | 28 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(25): Show |
intron_variant | MODIFIER | c.463-368T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381821 | ||||||
chr2:203381999
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.463-190A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203381999 | ||||||
chr2:203382007
|
C | T | 1 | a0001c0001t0018g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.463-182C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 3/11 | chr2 | 203382007 | ||||||
chr2:203382417
|
G | T | 24 | a0001c0001t0005g0100a0001c0001t0005g0102a0001c0001t0005g0103others(21): Show | 24 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.480+211G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203382417 | ||||||
chr2:203382652
|
A | G | 1 | a0001c0001t0004g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.480+446A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203382652 | ||||||
chr2:203382747
|
C | T | 1 | a0001c0001t0006g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.480+541C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203382747 | ||||||
chr2:203382868
|
A | G | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.480+662A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203382868 | ||||||
chr2:203383522
|
A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.480+1316A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203383522 | ||||||
chr2:203383689
|
C | G | 1 | a0001c0002t0024g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.480+1483C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203383689 | ||||||
chr2:203383836
|
T | C | 1 | a0001c0001t0001g0214 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.480+1630T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203383836 | ||||||
chr2:203383842
|
C | T | 1 | a0001c0001t0001g0214 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.480+1636C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203383842 | ||||||
chr2:203383883
|
C | A | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.480+1677C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203383883 | ||||||
chr2:203383949
|
C | G | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.480+1743C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203383949 | ||||||
chr2:203384244
|
A | G | 1 | a0001c0001t0002g0051 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.480+2038A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384244 | ||||||
chr2:203384275
|
C | CTTGTTTT others(5): Show |
21 | a0001c0001t0001g0140a0001c0001t0002g0058a0001c0001t0004g0121others(18): Show | 21 | HG00738.hp2 HG01884.hp2 HG01943.hp1 others(18): Show |
intron_variant | MODIFIER | c.480+2078_480+2089d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384275 | |||||
chr2:203384275
|
CTTGTTT | C | 38 | a0001c0001t0002g0187a0001c0001t0003g0184a0001c0001t0003g0185others(35): Show | 38 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(35): Show |
intron_variant | MODIFIER | c.480+2084_480+2089d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384275 | |||||
chr2:203384284
|
GTTTTTGT others(10): Show |
G | 4 | a0001c0001t0001g0276a0001c0001t0002g0193a0001c0001t0002g0194others(1): Show | 4 | HG00735.hp1 HG01496.hp1 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+2084_480+2100d others(19): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384284 | |||||
chr2:203384285
|
TTTTTG | T | 122 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(119): Show | 122 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.480+2084_480+2088d others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384285 | |||||
chr2:203384286
|
TTTTG | T | 18 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(15): Show | 18 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(15): Show |
intron_variant | MODIFIER | c.480+2084_480+2087d others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384286 | |||||
chr2:203384290
|
G | GTTTTTGT others(6): Show |
7 | a0001c0001t0004g0127a0001c0001t0004g0128a0001c0001t0004g0142others(4): Show | 7 | HG02132.hp2 HG02523.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.480+2089_480+2090i others(15): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384290 | |||||
chr2:203384290
|
G | GTTTTTGT others(5): Show |
1 | a0001c0001t0004g0141 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.480+2089_480+2090i others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384290 | |||||
chr2:203384290
|
G | T | 3 | a0001c0001t0002g0004a0001c0001t0002g0015a0001c0001t0002g0028 | 3 | NA18954.hp2 NA18992.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.480+2084G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384290 | ||||||
chr2:203384290
|
GT | G | 47 | a0001c0001t0002g0002a0001c0001t0002g0005a0001c0001t0002g0006others(44): Show | 47 | HG00280.hp2 HG00323.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.480+2118delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384290 | |||||
chr2:203384291
|
T | TTTTTGTT others(4): Show |
5 | a0001c0001t0004g0148a0001c0001t0009g0158a0001c0001t0009g0159others(2): Show | 5 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+2089_480+2090i others(13): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203384291 | |||||
chr2:203384299
|
T | G | 11 | a0001c0001t0004g0127a0001c0001t0004g0128a0001c0001t0004g0142others(8): Show | 11 | HG02109.hp2 HG02132.hp2 HG02523.hp1 others(8): Show |
intron_variant | MODIFIER | c.480+2093T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384299 | ||||||
chr2:203384300
|
T | G | 57 | a0001c0001t0001g0140a0001c0001t0001g0292a0001c0001t0002g0018others(54): Show | 57 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(54): Show |
intron_variant | MODIFIER | c.480+2094T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384300 | ||||||
chr2:203384300
|
T | TG | 4 | a0001c0001t0002g0008a0001c0001t0002g0046a0001c0001t0003g0072others(1): Show | 4 | NA18949.hp2 NA19003.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+2094_480+2095i others(3): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384300 | ||||||
chr2:203384301
|
T | G | 240 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(237): Show | 240 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(237): Show |
intron_variant | MODIFIER | c.480+2095T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384301 | ||||||
chr2:203384305
|
T | G | 2 | a0001c0001t0019g0147a0001c0001t0022g0319 | 2 | HG01884.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.480+2099T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384305 | ||||||
chr2:203384306
|
T | G | 6 | a0001c0001t0002g0015a0001c0001t0004g0148a0001c0001t0009g0158others(3): Show | 6 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.480+2100T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384306 | ||||||
chr2:203384310
|
T | G | 1 | a0001c0001t0004g0137 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.480+2104T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384310 | ||||||
chr2:203384312
|
T | G | 4 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.480+2106T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384312 | ||||||
chr2:203384313
|
T | G | 139 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(136): Show | 139 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.480+2107T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384313 | ||||||
chr2:203384314
|
T | G | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.480+2108T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384314 | ||||||
chr2:203384317
|
T | G | 187 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(184): Show | 187 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(184): Show |
intron_variant | MODIFIER | c.480+2111T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384317 | ||||||
chr2:203384451
|
T | C | 1 | a0001c0001t0002g0014 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.480+2245T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384451 | ||||||
chr2:203384676
|
A | G | 93 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.480+2470A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384676 | ||||||
chr2:203384810
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.480+2604G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384810 | ||||||
chr2:203384820
|
A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.480+2614A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384820 | ||||||
chr2:203384888
|
G | A | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.480+2682G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203384888 | ||||||
chr2:203385080
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.480+2874G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385080 | ||||||
chr2:203385094
|
A | G | 5 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160others(2): Show | 5 | HG01884.hp2 HG02145.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.480+2888A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385094 | ||||||
chr2:203385139
|
C | CTTTTTT | 36 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0197others(33): Show | 36 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(33): Show |
intron_variant | MODIFIER | c.480+2941_480+2946d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(1): Show |
20 | a0001c0001t0001g0254a0001c0001t0006g0001a0001c0001t0006g0149others(17): Show | 20 | HG00323.hp2 HG00733.hp2 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.480+2939_480+2946d others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0001g0248a0001c0001t0001g0249a0001c0001t0001g0263others(1): Show | 4 | HG01081.hp2 HG01256.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.480+2934_480+2946d others(15): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(9): Show |
2 | a0001c0001t0005g0100a0001c0002t0005g0116 | 2 | HG02976.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.480+2946_480+2947i others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(10): Show |
16 | a0001c0001t0005g0081a0001c0001t0005g0102a0001c0001t0005g0103others(13): Show | 16 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.480+2946_480+2947i others(19): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(11): Show |
10 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0001t0005g0110others(7): Show | 10 | HG02109.hp1 HG02451.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.480+2946_480+2947i others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(12): Show |
1 | a0001c0001t0001g0227 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.480+2946_480+2947i others(21): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(13): Show |
29 | a0001c0001t0001g0186a0001c0001t0001g0201a0001c0001t0001g0215others(26): Show | 29 | HG00280.hp1 HG00673.hp1 HG00733.hp1 others(26): Show |
intron_variant | MODIFIER | c.480+2946_480+2947i others(22): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(14): Show |
33 | a0001c0001t0001g0182a0001c0001t0001g0200a0001c0001t0001g0202others(30): Show | 33 | HG00438.hp2 HG01109.hp2 HG01169.hp2 others(30): Show |
intron_variant | MODIFIER | c.480+2946_480+2947i others(23): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(15): Show |
18 | a0001c0001t0001g0181a0001c0001t0001g0212a0001c0001t0001g0218others(15): Show | 18 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(15): Show |
intron_variant | MODIFIER | c.480+2946_480+2947i others(24): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(16): Show |
8 | a0001c0001t0001g0213a0001c0001t0001g0229a0001c0001t0001g0233others(5): Show | 8 | HG00741.hp2 HG02083.hp2 HG03492.hp2 others(5): Show |
intron_variant | MODIFIER | c.480+2946_480+2947i others(25): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(18): Show |
1 | a0001c0001t0018g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.480+2946_480+2947i others(27): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(19): Show |
3 | a0001c0001t0001g0224a0001c0001t0001g0246a0001c0001t0001g0270 | 3 | HG03139.hp1 HG03195.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.480+2946_480+2947i others(28): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385139
|
C | CTTTTTTT others(20): Show |
1 | a0001c0001t0001g0292 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.480+2946_480+2947i others(29): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385139 | |||||
chr2:203385157
|
C | CAG | 189 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.480+2952_480+2953d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203385157 | |||||
chr2:203385352
|
C | T | 1 | a0001c0001t0005g0152 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.480+3146C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385352 | ||||||
chr2:203385460
|
A | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.480+3254A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385460 | ||||||
chr2:203385693
|
A | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.480+3487A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385693 | ||||||
chr2:203385729
|
C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.480+3523C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385729 | ||||||
chr2:203385750
|
G | T | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.480+3544G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385750 | ||||||
chr2:203385919
|
T | C | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.480+3713T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385919 | ||||||
chr2:203385966
|
T | G | 20 | a0001c0001t0005g0100a0001c0001t0005g0102a0001c0001t0005g0103others(17): Show | 20 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.480+3760T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203385966 | ||||||
chr2:203386174
|
A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.480+3968A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386174 | ||||||
chr2:203386261
|
C | A | 1 | a0001c0001t0003g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.480+4055C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386261 | ||||||
chr2:203386321
|
C | T | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.480+4115C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386321 | ||||||
chr2:203386361
|
G | C | 1 | a0001c0001t0004g0141 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.480+4155G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386361 | ||||||
chr2:203386366
|
C | T | 5 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0293others(2): Show | 5 | HG00735.hp2 HG00741.hp2 HG03491.hp1 others(2): Show |
intron_variant | MODIFIER | c.480+4160C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386366 | ||||||
chr2:203386393
|
G | A | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.480+4187G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386393 | ||||||
chr2:203386430
|
G | GT | 64 | a0001c0001t0001g0182a0001c0001t0001g0228a0001c0001t0001g0229others(61): Show | 64 | HG00423.hp1 HG00438.hp1 HG00597.hp1 others(61): Show |
intron_variant | MODIFIER | c.480+4250dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386430 | |||||
chr2:203386430
|
G | GTT | 7 | a0001c0001t0001g0224a0001c0001t0001g0292a0001c0001t0003g0191others(4): Show | 7 | HG02135.hp2 HG02809.hp1 HG02896.hp2 others(4): Show |
intron_variant | MODIFIER | c.480+4249_480+4250d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386430 | |||||
chr2:203386430
|
G | GTTTTTTT others(2): Show |
7 | a0001c0001t0006g0150a0001c0001t0006g0163a0001c0001t0006g0164others(4): Show | 7 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(4): Show |
intron_variant | MODIFIER | c.480+4242_480+4250d others(11): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386430 | |||||
chr2:203386430
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0006g0162a0001c0001t0006g0173 | 2 | HG02572.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.480+4241_480+4250d others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386430 | |||||
chr2:203386430
|
G | GTTTTTTT others(5): Show |
1 | a0001c0001t0006g0149 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.480+4239_480+4250d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386430 | |||||
chr2:203386430
|
GT | G | 94 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0002g0004others(91): Show | 94 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(91): Show |
intron_variant | MODIFIER | c.480+4250delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386430 | |||||
chr2:203386542
|
T | G | 1 | a0001c0001t0008g0090 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.480+4336T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386542 | ||||||
chr2:203386640
|
C | CT | 52 | a0001c0001t0001g0275a0001c0001t0001g0298a0001c0001t0001g0306others(49): Show | 52 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(49): Show |
intron_variant | MODIFIER | c.481-4389dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203386640 | |||||
chr2:203386657
|
T | C | 1 | a0001c0001t0005g0113 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.481-4389T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386657 | ||||||
chr2:203386747
|
C | T | 3 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0001t0021g0151 | 3 | HG00621.hp1 NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.481-4299C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386747 | ||||||
chr2:203386962
|
C | T | 1 | a0001c0001t0018g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.481-4084C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203386962 | ||||||
chr2:203387056
|
C | CT | 91 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(88): Show | 91 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(88): Show |
intron_variant | MODIFIER | c.481-3970dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203387056 | |||||
chr2:203387056
|
CT | C | 126 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0004others(123): Show | 126 | HG00280.hp2 HG00423.hp2 HG00597.hp2 others(123): Show |
intron_variant | MODIFIER | c.481-3970delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203387056 | |||||
chr2:203387074
|
TTTC | T | 19 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(16): Show | 19 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.481-3971_481-3969d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387074 | ||||||
chr2:203387075
|
TTC | T | 68 | a0001c0001t0002g0187a0001c0001t0002g0193a0001c0001t0002g0194others(65): Show | 68 | HG00438.hp1 HG00621.hp1 HG00642.hp1 others(65): Show |
intron_variant | MODIFIER | c.481-3970_481-3969d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387075 | ||||||
chr2:203387076
|
TC | T | 5 | a0001c0001t0003g0184a0001c0001t0003g0185a0001c0001t0022g0319others(2): Show | 5 | HG01884.hp2 HG01891.hp1 HG02109.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-3966delC | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203387076 | |||||
chr2:203387077
|
C | T | 95 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(92): Show | 95 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.481-3969C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387077 | ||||||
chr2:203387211
|
A | G | 1 | a0001c0001t0006g0171 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.481-3835A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387211 | ||||||
chr2:203387602
|
A | G | 10 | a0001c0001t0001g0140a0001c0001t0004g0136a0001c0001t0004g0137others(7): Show | 10 | HG02293.hp1 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.481-3444A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387602 | ||||||
chr2:203387854
|
G | C | 1 | a0001c0001t0001g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.481-3192G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387854 | ||||||
chr2:203387856
|
C | T | 1 | a0001c0001t0001g0273 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.481-3190C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203387856 | ||||||
chr2:203388185
|
C | T | 16 | a0001c0001t0003g0188a0001c0001t0003g0199a0001c0001t0003g0219others(13): Show | 16 | HG00642.hp1 HG01074.hp1 HG01255.hp2 others(13): Show |
intron_variant | MODIFIER | c.481-2861C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388185 | ||||||
chr2:203388186
|
G | A | 26 | a0001c0001t0005g0098a0001c0001t0005g0099a0001c0001t0005g0100others(23): Show | 26 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.481-2860G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388186 | ||||||
chr2:203388503
|
C | T | 1 | a0001c0001t0013g0104 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.481-2543C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388503 | ||||||
chr2:203388622
|
A | G | 2 | a0001c0001t0001g0212a0001c0001t0001g0213 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.481-2424A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388622 | ||||||
chr2:203388667
|
C | T | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.481-2379C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388667 | ||||||
chr2:203388687
|
T | A | 5 | a0001c0001t0003g0184a0001c0001t0003g0185a0001c0001t0019g0147others(2): Show | 5 | HG01891.hp1 HG02109.hp2 HG02258.hp1 others(2): Show |
intron_variant | MODIFIER | c.481-2359T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388687 | ||||||
chr2:203388693
|
T | A | 2 | a0001c0001t0004g0125a0001c0001t0004g0134 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.481-2353T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388693 | ||||||
chr2:203388885
|
T | C | 9 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0020others(6): Show | 9 | HG02145.hp1 HG02486.hp1 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.481-2161T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388885 | ||||||
chr2:203388944
|
A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.481-2102A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388944 | ||||||
chr2:203388955
|
G | A | 5 | a0001c0001t0003g0205a0001c0001t0003g0206a0001c0001t0003g0208others(2): Show | 5 | HG02572.hp1 HG02723.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.481-2091G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203388955 | ||||||
chr2:203389008
|
T | C | 9 | a0001c0001t0004g0126a0001c0001t0004g0127a0001c0001t0004g0128others(6): Show | 9 | HG02129.hp1 HG02132.hp2 HG02523.hp1 others(6): Show |
intron_variant | MODIFIER | c.481-2038T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203389008 | ||||||
chr2:203389077
|
T | C | 2 | a0001c0001t0006g0001a0001c0001t0028g0168 | 2 | HG02258.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.481-1969T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203389077 | ||||||
chr2:203389189
|
T | C | 1 | a0001c0001t0006g0162 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.481-1857T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203389189 | ||||||
chr2:203389847
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.481-1199G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203389847 | ||||||
chr2:203389850
|
A | C | 1 | a0001c0001t0007g0007 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.481-1196A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203389850 | ||||||
chr2:203389919
|
G | C | 2 | a0001c0001t0003g0209a0001c0001t0003g0210 | 2 | HG02572.hp1 HG02886.hp2 |
intron_variant | MODIFIER | c.481-1127G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203389919 | ||||||
chr2:203390093
|
A | C | 2 | a0001c0001t0010g0066a0001c0001t0010g0067 | 2 | NA18962.hp2 NA18986.hp2 |
intron_variant | MODIFIER | c.481-953A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203390093 | ||||||
chr2:203390257
|
C | T | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.481-789C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203390257 | ||||||
chr2:203390443
|
G | A | 1 | a0001c0002t0024g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.481-603G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203390443 | ||||||
chr2:203390447
|
C | T | 2 | a0001c0002t0005g0116a0001c0002t0024g0118 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.481-599C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203390447 | ||||||
chr2:203390633
|
G | GA | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.481-402dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 203390633 | |||||
chr2:203390716
|
A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.481-330A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 4/11 | chr2 | 203390716 | ||||||
chr2:203391301
|
A | G | 1 | a0001c0001t0002g0025 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.578+158A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203391301 | ||||||
chr2:203391714
|
G | A | 25 | a0001c0001t0005g0081a0001c0001t0005g0100a0001c0001t0005g0102others(22): Show | 25 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(22): Show |
intron_variant | MODIFIER | c.578+571G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203391714 | ||||||
chr2:203391820
|
C | CA | 42 | a0001c0001t0001g0243a0001c0001t0001g0263a0001c0001t0001g0301others(39): Show | 42 | HG00733.hp2 HG00738.hp1 HG01109.hp1 others(39): Show |
intron_variant | MODIFIER | c.578+695dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203391820 | |||||
chr2:203392258
|
C | T | 1 | a0001c0001t0001g0256 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.578+1115C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392258 | ||||||
chr2:203392263
|
G | GCACCACC others(5): Show |
1 | a0001c0001t0001g0228 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.578+1131_578+1132i others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392263 | |||||
chr2:203392275
|
T | C | 1 | a0001c0001t0001g0228 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.578+1132T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392275 | ||||||
chr2:203392275
|
T | TCAC | 62 | a0001c0001t0001g0181a0001c0001t0002g0005a0001c0001t0002g0010others(59): Show | 62 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(59): Show |
intron_variant | MODIFIER | c.578+1171_578+1173d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | |||||
chr2:203392275
|
T | TCACCAC | 52 | a0001c0001t0001g0224a0001c0001t0001g0270a0001c0001t0001g0298others(49): Show | 52 | HG00438.hp1 HG00597.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.578+1168_578+1173d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | |||||
chr2:203392275
|
T | TCACCACC others(2): Show |
47 | a0001c0001t0001g0182a0001c0001t0001g0242a0001c0001t0001g0268others(44): Show | 47 | HG00621.hp1 HG00642.hp1 HG01255.hp2 others(44): Show |
intron_variant | MODIFIER | c.578+1165_578+1173d others(11): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | |||||
chr2:203392275
|
T | TCACCACC others(5): Show |
28 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0214others(25): Show | 28 | HG00323.hp2 HG00735.hp2 HG00741.hp2 others(25): Show |
intron_variant | MODIFIER | c.578+1162_578+1173d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | |||||
chr2:203392275
|
T | TCACCACC others(8): Show |
48 | a0001c0001t0001g0186a0001c0001t0001g0200a0001c0001t0001g0201others(45): Show | 48 | HG00673.hp1 HG00733.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.578+1159_578+1173d others(17): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | |||||
chr2:203392275
|
T | TCACCACC others(11): Show |
17 | a0001c0001t0001g0207a0001c0001t0001g0230a0001c0001t0001g0232others(14): Show | 17 | HG00438.hp2 HG00597.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.578+1156_578+1173d others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | |||||
chr2:203392275
|
T | TCACCACC others(14): Show |
4 | a0001c0001t0001g0243a0001c0001t0001g0265a0001c0001t0001g0276others(1): Show | 4 | HG01515.hp1 HG03834.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.578+1153_578+1173d others(23): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | |||||
chr2:203392275
|
T | TCACCACC others(17): Show |
1 | a0001c0001t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.578+1150_578+1173d others(26): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | |||||
chr2:203392275
|
TCAC | T | 8 | a0001c0001t0001g0140a0001c0001t0002g0002a0001c0001t0002g0009others(5): Show | 8 | HG01168.hp1 HG02027.hp1 HG02109.hp1 others(5): Show |
intron_variant | MODIFIER | c.578+1171_578+1173d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | |||||
chr2:203392275
|
TCACCAC | T | 9 | a0001c0001t0002g0052a0001c0001t0002g0193a0001c0001t0002g0194others(6): Show | 9 | HG00735.hp1 HG01167.hp2 HG01496.hp1 others(6): Show |
intron_variant | MODIFIER | c.578+1168_578+1173d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | |||||
chr2:203392275
|
TCACCACC others(2): Show |
T | 3 | a0001c0001t0004g0148a0001c0001t0005g0098a0001c0001t0005g0099 | 3 | HG02486.hp2 HG02970.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.578+1165_578+1173d others(11): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392275 | |||||
chr2:203392314
|
C | CCAA | 6 | a0001c0001t0002g0002a0001c0001t0002g0009a0001c0001t0002g0016others(3): Show | 6 | HG00609.hp2 HG01168.hp1 HG01975.hp2 others(3): Show |
intron_variant | MODIFIER | c.578+1199_578+1201d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | |||||
chr2:203392314
|
C | CCAACAA | 3 | a0001c0001t0002g0008a0001c0001t0002g0052a0001c0001t0004g0148 | 3 | HG03098.hp2 HG03491.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.578+1196_578+1201d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | |||||
chr2:203392314
|
CCAA | C | 40 | a0001c0001t0001g0140a0001c0001t0002g0005a0001c0001t0002g0011others(37): Show | 40 | HG00323.hp1 HG01074.hp2 HG01081.hp1 others(37): Show |
intron_variant | MODIFIER | c.578+1199_578+1201d others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | |||||
chr2:203392314
|
CCAACAA | C | 20 | a0001c0001t0002g0006a0001c0001t0002g0056a0001c0001t0002g0060others(17): Show | 20 | HG00621.hp1 HG01192.hp2 HG01928.hp2 others(17): Show |
intron_variant | MODIFIER | c.578+1196_578+1201d others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | |||||
chr2:203392314
|
CCAACAAC others(2): Show |
C | 39 | a0001c0001t0001g0181a0001c0001t0002g0084a0001c0001t0002g0193others(36): Show | 39 | HG00438.hp1 HG00642.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.578+1193_578+1201d others(11): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | |||||
chr2:203392314
|
CCAACAAC others(5): Show |
C | 27 | a0001c0001t0001g0218a0001c0001t0001g0224a0001c0001t0001g0231others(24): Show | 27 | HG01433.hp2 HG01891.hp2 HG02055.hp2 others(24): Show |
intron_variant | MODIFIER | c.578+1190_578+1201d others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | |||||
chr2:203392314
|
CCAACAAC others(8): Show |
C | 104 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(101): Show | 104 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.578+1187_578+1201d others(17): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | |||||
chr2:203392314
|
CCAACAAC others(11): Show |
C | 21 | a0001c0001t0001g0201a0001c0001t0001g0202a0001c0001t0001g0247others(18): Show | 21 | HG00673.hp1 HG01081.hp2 HG01167.hp1 others(18): Show |
intron_variant | MODIFIER | c.578+1184_578+1201d others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392314 | |||||
chr2:203392317
|
A | C | 1 | a0001c0001t0001g0245 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.578+1174A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392317 | ||||||
chr2:203392318
|
C | T | 4 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0004g0144others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.578+1175C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392318 | ||||||
chr2:203392320
|
A | C | 5 | a0001c0001t0001g0245a0001c0001t0004g0142a0001c0001t0004g0143others(2): Show | 5 | HG02630.hp1 HG02723.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.578+1177A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392320 | ||||||
chr2:203392323
|
A | C | 1 | a0001c0001t0001g0245 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.578+1180A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392323 | ||||||
chr2:203392326
|
A | C | 1 | a0001c0001t0001g0245 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.578+1183A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392326 | ||||||
chr2:203392329
|
A | C | 1 | a0001c0001t0001g0245 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.578+1186A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392329 | ||||||
chr2:203392332
|
A | C | 1 | a0001c0001t0001g0245 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.578+1189A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392332 | ||||||
chr2:203392335
|
A | C | 1 | a0001c0001t0001g0245 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.578+1192A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392335 | ||||||
chr2:203392500
|
T | G | 21 | a0001c0001t0005g0081a0001c0001t0005g0100a0001c0001t0005g0102others(18): Show | 21 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(18): Show |
intron_variant | MODIFIER | c.578+1357T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392500 | ||||||
chr2:203392529
|
C | G | 1 | a0001c0001t0002g0006 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.578+1386C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392529 | ||||||
chr2:203392900
|
A | G | 1 | a0001c0001t0031g0183 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.578+1757A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392900 | ||||||
chr2:203392950
|
A | G | 1 | a0001c0001t0015g0119 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.579-1750A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392950 | ||||||
chr2:203392967
|
C | CT | 155 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(152): Show | 155 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.579-1723dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 203392967 | |||||
chr2:203392977
|
T | A | 29 | a0001c0001t0001g0140a0001c0001t0004g0121a0001c0001t0004g0124others(26): Show | 29 | HG00738.hp2 HG01943.hp1 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.579-1723T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392977 | ||||||
chr2:203392978
|
A | T | 2 | a0001c0001t0002g0043a0001c0001t0027g0117 | 2 | HG02055.hp2 NA18974.hp2 |
intron_variant | MODIFIER | c.579-1722A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203392978 | ||||||
chr2:203393108
|
T | G | 1 | a0001c0001t0002g0083 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.579-1592T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203393108 | ||||||
chr2:203393110
|
A | G | 3 | a0001c0001t0006g0163a0001c0001t0006g0164a0001c0001t0006g0166 | 3 | HG00733.hp2 HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.579-1590A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203393110 | ||||||
chr2:203393197
|
G | A | 1 | a0001c0002t0024g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.579-1503G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203393197 | ||||||
chr2:203393203
|
C | T | 93 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.579-1497C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203393203 | ||||||
chr2:203393422
|
C | G | 1 | a0001c0001t0003g0195 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.579-1278C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203393422 | ||||||
chr2:203393970
|
T | C | 1 | a0001c0001t0018g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.579-730T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203393970 | ||||||
chr2:203394018
|
T | A | 10 | a0001c0001t0001g0241a0001c0001t0001g0250a0001c0001t0001g0253others(7): Show | 10 | HG00323.hp2 HG01257.hp2 HG01433.hp2 others(7): Show |
intron_variant | MODIFIER | c.579-682T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203394018 | ||||||
chr2:203394163
|
G | A | 1 | a0001c0001t0002g0046 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.579-537G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203394163 | ||||||
chr2:203394400
|
G | GA | 223 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(220): Show | 223 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(220): Show |
intron_variant | MODIFIER | c.579-300_579-299ins others(1): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 5/11 | chr2 | 203394400 | ||||||
chr2:203395306
|
C | T | 1 | a0001c0001t0003g0188 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.726-350C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395306 | ||||||
chr2:203395432
|
A | AAT | 20 | a0001c0001t0001g0224a0001c0001t0004g0137a0001c0001t0004g0146others(17): Show | 20 | HG01257.hp1 HG01258.hp1 HG02040.hp2 others(17): Show |
intron_variant | MODIFIER | c.726-208_726-207dup others(2): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395432 | |||||
chr2:203395432
|
A | AATATAT | 4 | a0001c0001t0005g0098a0001c0001t0009g0158a0001c0001t0009g0159others(1): Show | 4 | HG02451.hp2 HG02486.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-212_726-207dup others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395432 | |||||
chr2:203395432
|
A | AATATATA others(1): Show |
5 | a0001c0001t0001g0202a0001c0001t0001g0247a0001c0001t0001g0253others(2): Show | 5 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-214_726-207dup others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395432 | |||||
chr2:203395432
|
A | AATATATA others(3): Show |
5 | a0001c0001t0001g0241a0001c0001t0001g0285a0001c0001t0001g0296others(2): Show | 5 | HG00597.hp1 HG03688.hp1 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.726-216_726-207dup others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395432 | |||||
chr2:203395432
|
A | AATATATA others(7): Show |
1 | a0001c0001t0001g0246 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.726-220_726-207dup others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395432 | |||||
chr2:203395432
|
A | AATATATA others(15): Show |
1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.726-207_726-206ins others(22): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395432 | |||||
chr2:203395446
|
T | TAC | 5 | a0001c0001t0002g0009a0001c0001t0002g0053a0001c0001t0002g0062others(2): Show | 5 | HG01168.hp1 HG01175.hp2 NA18980.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-209_726-208ins others(2): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395446 | |||||
chr2:203395446
|
T | TACAC | 3 | a0001c0001t0002g0011a0001c0001t0002g0012a0001c0001t0002g0033 | 3 | HG00323.hp1 HG03490.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.726-209_726-208ins others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395446 | |||||
chr2:203395448
|
T | C | 12 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0012others(9): Show | 12 | HG00323.hp1 HG01168.hp1 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.726-208T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395448 | ||||||
chr2:203395448
|
T | TAC | 63 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0005others(60): Show | 63 | HG00423.hp2 HG00609.hp2 HG00673.hp2 others(60): Show |
intron_variant | MODIFIER | c.726-172_726-171dup others(2): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TACAC | 9 | a0001c0001t0001g0278a0001c0001t0002g0015a0001c0001t0002g0019others(6): Show | 9 | HG00621.hp1 HG00621.hp2 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.726-174_726-171dup others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TACACACA others(3): Show |
2 | a0001c0001t0003g0206a0001c0001t0003g0208 | 2 | HG02723.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.726-180_726-171dup others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TACACACA others(5): Show |
2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.726-182_726-171dup others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATACACA others(5): Show |
4 | a0001c0001t0003g0205a0001c0001t0003g0209a0001c0001t0003g0210others(1): Show | 4 | HG01192.hp1 HG02572.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATACACA others(7): Show |
3 | a0001c0001t0003g0225a0001c0001t0003g0317a0001c0001t0027g0117 | 3 | HG01255.hp2 HG02055.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.726-207_726-206ins others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATACACA others(9): Show |
1 | a0001c0001t0003g0288 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.726-207_726-206ins others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATACA others(3): Show |
2 | a0001c0001t0001g0299a0001c0001t0003g0287 | 2 | HG01515.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.726-207_726-206ins others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATACA others(5): Show |
9 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0197others(6): Show | 9 | HG00438.hp1 HG00735.hp1 HG01167.hp2 others(6): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATACA others(7): Show |
10 | a0001c0001t0003g0188a0001c0001t0003g0199a0001c0001t0003g0219others(7): Show | 10 | HG00642.hp1 HG01074.hp1 HG01358.hp1 others(7): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATACA others(9): Show |
5 | a0001c0001t0002g0187a0001c0001t0003g0189a0001c0001t0003g0220others(2): Show | 5 | HG00642.hp2 HG01433.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATACA others(13): Show |
1 | a0001c0001t0034g0190 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.726-207_726-206ins others(20): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(3): Show |
3 | a0001c0001t0001g0245a0001c0001t0001g0304a0001c0001t0001g0316 | 3 | NA18945.hp1 NA18980.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.726-207_726-206ins others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(5): Show |
3 | a0001c0001t0001g0254a0001c0001t0001g0300a0001c0001t0003g0196 | 3 | HG00323.hp2 HG00738.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.726-207_726-206ins others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(7): Show |
3 | a0001c0001t0003g0184a0001c0001t0003g0185a0001c0001t0031g0183 | 3 | HG01891.hp1 HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.726-207_726-206ins others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(3): Show |
10 | a0001c0001t0001g0216a0001c0001t0001g0228a0001c0001t0001g0257others(7): Show | 10 | HG00423.hp1 HG00733.hp1 HG01081.hp2 others(7): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(10): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(5): Show |
8 | a0001c0001t0001g0207a0001c0001t0001g0263a0001c0001t0001g0268others(5): Show | 8 | HG01255.hp1 HG01981.hp1 NA18951.hp2 others(5): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(7): Show |
1 | a0001c0001t0001g0186 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.726-207_726-206ins others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0276 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.726-207_726-206ins others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(5): Show |
33 | a0001c0001t0001g0214a0001c0001t0001g0215a0001c0001t0001g0218others(30): Show | 33 | HG00280.hp1 HG00609.hp1 HG00673.hp1 others(30): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(12): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(7): Show |
11 | a0001c0001t0001g0200a0001c0001t0001g0201a0001c0001t0001g0229others(8): Show | 11 | HG01496.hp2 HG02083.hp2 NA18939.hp2 others(8): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0295 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.726-207_726-206ins others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(7): Show |
5 | a0001c0001t0001g0212a0001c0001t0001g0213a0001c0001t0001g0234others(2): Show | 5 | HG00438.hp2 HG00735.hp2 HG00741.hp2 others(2): Show |
intron_variant | MODIFIER | c.726-207_726-206ins others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(9): Show |
1 | a0001c0001t0001g0308 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.726-207_726-206ins others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
T | TATATATA others(11): Show |
1 | a0001c0001t0001g0182 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.726-207_726-206ins others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395448
|
TAC | T | 25 | a0001c0001t0002g0047a0001c0001t0002g0048a0001c0001t0002g0069others(22): Show | 25 | HG00738.hp2 HG00741.hp1 HG01943.hp1 others(22): Show |
intron_variant | MODIFIER | c.726-172_726-171del others(2): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 203395448 | |||||
chr2:203395450
|
C | T | 55 | a0001c0001t0001g0140a0001c0001t0001g0256a0001c0001t0004g0124others(52): Show | 55 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(52): Show |
intron_variant | MODIFIER | c.726-206C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395450 | ||||||
chr2:203395452
|
C | T | 56 | a0001c0001t0001g0140a0001c0001t0001g0256a0001c0001t0004g0121others(53): Show | 56 | HG00738.hp2 HG01257.hp1 HG01258.hp1 others(53): Show |
intron_variant | MODIFIER | c.726-204C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395452 | ||||||
chr2:203395454
|
C | T | 5 | a0001c0001t0006g0001a0001c0001t0011g0153a0001c0001t0011g0154others(2): Show | 5 | HG02109.hp1 HG02109.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.726-202C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395454 | ||||||
chr2:203395456
|
C | T | 4 | a0001c0001t0011g0153a0001c0001t0011g0154a0001c0001t0011g0155others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-200C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395456 | ||||||
chr2:203395458
|
C | T | 4 | a0001c0001t0011g0153a0001c0001t0011g0154a0001c0001t0011g0155others(1): Show | 4 | HG02109.hp1 HG02109.hp2 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.726-198C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395458 | ||||||
chr2:203395460
|
C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.726-196C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395460 | ||||||
chr2:203395462
|
C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.726-194C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395462 | ||||||
chr2:203395486
|
T | A | 1 | a0001c0001t0002g0074 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.726-170T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395486 | ||||||
chr2:203395543
|
C | T | 2 | a0001c0001t0002g0187a0001c0001t0003g0189 | 2 | NA18952.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.726-113C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 6/11 | chr2 | 203395543 | ||||||
chr2:203395885
|
T | C | 2 | a0001c0001t0001g0181a0001c0001t0001g0270 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.850+105T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 7/11 | chr2 | 203395885 | ||||||
chr2:203396118
|
G | A | 1 | a0001c0001t0005g0152 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.850+338G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 7/11 | chr2 | 203396118 | ||||||
chr2:203396367
|
T | A | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.851-418T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 7/11 | chr2 | 203396367 | ||||||
chr2:203396463
|
A | C | 1 | a0001c0002t0005g0116 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.851-322A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 7/11 | chr2 | 203396463 | ||||||
chr2:203396712
|
T | C | 29 | a0001c0001t0005g0081a0001c0001t0005g0098a0001c0001t0005g0099others(26): Show | 29 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.851-73T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 7/11 | chr2 | 203396712 | ||||||
chr2:203397000
|
G | C | 189 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1033+33G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397000 | ||||||
chr2:203397067
|
G | A | 1 | a0001c0001t0001g0265 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1033+100G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397067 | ||||||
chr2:203397218
|
A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1033+251A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397218 | ||||||
chr2:203397220
|
A | G | 1 | a0001c0001t0002g0082 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1033+253A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397220 | ||||||
chr2:203397264
|
G | C | 1 | a0001c0001t0001g0244 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1033+297G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397264 | ||||||
chr2:203397540
|
C | T | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1033+573C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397540 | ||||||
chr2:203397773
|
C | A | 2 | a0001c0001t0002g0032a0001c0001t0002g0041 | 2 | HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1033+806C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397773 | ||||||
chr2:203397903
|
G | C | 73 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0207others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1033+936G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203397903 | ||||||
chr2:203398313
|
A | G | 4 | a0001c0001t0002g0193a0001c0001t0002g0194a0001c0001t0002g0197others(1): Show | 4 | HG00735.hp1 HG01496.hp1 HG01515.hp2 others(1): Show |
intron_variant | MODIFIER | c.1033+1346A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398313 | ||||||
chr2:203398482
|
T | C | 1 | a0001c0001t0003g0220 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1033+1515T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398482 | ||||||
chr2:203398507
|
G | A | 1 | a0001c0001t0012g0132 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.1033+1540G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398507 | ||||||
chr2:203398632
|
G | A | 1 | a0001c0001t0005g0176 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1033+1665G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398632 | ||||||
chr2:203398645
|
C | T | 1 | a0001c0001t0023g0114 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1033+1678C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398645 | ||||||
chr2:203398693
|
C | T | 1 | a0001c0001t0001g0229 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1033+1726C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398693 | ||||||
chr2:203398757
|
T | C | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1033+1790T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398757 | ||||||
chr2:203398799
|
A | G | 1 | a0001c0001t0002g0011 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1033+1832A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398799 | ||||||
chr2:203398854
|
A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1033+1887A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398854 | ||||||
chr2:203398906
|
G | A | 1 | a0001c0001t0005g0115 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1033+1939G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203398906 | ||||||
chr2:203399533
|
C | T | 1 | a0001c0001t0002g0084 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1033+2566C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203399533 | ||||||
chr2:203399598
|
C | G | 1 | a0001c0001t0004g0134 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1033+2631C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203399598 | ||||||
chr2:203399738
|
CTCCTGAC others(10): Show |
C | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1033+2772_1033+278 others(21): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203399738 | ||||||
chr2:203399890
|
T | A | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1034-2686T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203399890 | ||||||
chr2:203399999
|
C | T | 1 | a0001c0001t0018g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1034-2577C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203399999 | ||||||
chr2:203400079
|
C | CT | 23 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0022others(20): Show | 23 | HG00423.hp2 HG00621.hp2 HG00673.hp2 others(20): Show |
intron_variant | MODIFIER | c.1034-2469dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 203400079 | |||||
chr2:203400079
|
CT | C | 38 | a0001c0001t0001g0275a0001c0001t0001g0290a0001c0001t0001g0291others(35): Show | 38 | HG00738.hp2 HG01192.hp2 HG01928.hp2 others(35): Show |
intron_variant | MODIFIER | c.1034-2469delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 203400079 | |||||
chr2:203400079
|
CTT | C | 17 | a0001c0001t0001g0207a0001c0001t0001g0235a0001c0001t0001g0242others(14): Show | 17 | HG00735.hp2 HG00741.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1034-2470_1034-246 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 203400079 | |||||
chr2:203400079
|
CTTT | C | 111 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(108): Show | 111 | HG00280.hp1 HG00423.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.1034-2471_1034-246 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 203400079 | |||||
chr2:203400079
|
CTTTT | C | 59 | a0001c0001t0001g0181a0001c0001t0001g0212a0001c0001t0001g0239others(56): Show | 59 | HG00323.hp2 HG00621.hp1 HG00642.hp1 others(56): Show |
intron_variant | MODIFIER | c.1034-2472_1034-246 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 203400079 | |||||
chr2:203400115
|
A | T | 1 | a0001c0001t0001g0230 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1034-2461A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203400115 | ||||||
chr2:203400173
|
C | T | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1034-2403C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203400173 | ||||||
chr2:203400679
|
G | C | 1 | a0001c0001t0001g0246 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1034-1897G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203400679 | ||||||
chr2:203401150
|
G | A | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1034-1426G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203401150 | ||||||
chr2:203401207
|
C | T | 189 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1034-1369C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203401207 | ||||||
chr2:203401335
|
C | T | 1 | a0001c0001t0003g0225 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1034-1241C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203401335 | ||||||
chr2:203401362
|
C | T | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1034-1214C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203401362 | ||||||
chr2:203401620
|
T | C | 73 | a0001c0001t0001g0200a0001c0001t0001g0202a0001c0001t0001g0207others(70): Show | 73 | HG00323.hp2 HG00423.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.1034-956T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203401620 | ||||||
chr2:203401770
|
G | A | 3 | a0001c0001t0008g0040a0001c0001t0008g0045a0001c0001t0032g0039 | 3 | NA18999.hp1 NA19057.hp1 NA19086.hp2 |
intron_variant | MODIFIER | c.1034-806G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203401770 | ||||||
chr2:203402159
|
C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1034-417C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402159 | ||||||
chr2:203402171
|
A | G | 15 | a0001c0001t0003g0188a0001c0001t0003g0199a0001c0001t0003g0219others(12): Show | 15 | HG00642.hp1 HG01074.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1034-405A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402171 | ||||||
chr2:203402179
|
C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1034-397C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402179 | ||||||
chr2:203402310
|
C | T | 3 | a0001c0001t0001g0181a0001c0001t0001g0224a0001c0001t0001g0270 | 3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1034-266C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402310 | ||||||
chr2:203402330
|
C | T | 5 | a0001c0001t0010g0066a0001c0001t0010g0067a0001c0001t0010g0068others(2): Show | 5 | HG02080.hp1 NA18962.hp2 NA18986.hp2 others(2): Show |
intron_variant | MODIFIER | c.1034-246C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402330 | ||||||
chr2:203402349
|
A | G | 1 | a0001c0001t0008g0090 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.1034-227A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402349 | ||||||
chr2:203402367
|
A | G | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1034-209A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 8/11 | chr2 | 203402367 | ||||||
chr2:203402769
|
G | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1192+35G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203402769 | ||||||
chr2:203402831
|
G | T | 29 | a0001c0001t0001g0140a0001c0001t0004g0121a0001c0001t0004g0124others(26): Show | 29 | HG00738.hp2 HG01943.hp1 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.1192+97G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203402831 | ||||||
chr2:203403179
|
C | T | 2 | a0001c0001t0006g0172a0001c0001t0006g0178 | 2 | HG02280.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1192+445C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403179 | ||||||
chr2:203403244
|
A | G | 1 | a0001c0001t0003g0072 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.1192+510A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403244 | ||||||
chr2:203403359
|
A | G | 1 | a0001c0001t0003g0220 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1192+625A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403359 | ||||||
chr2:203403475
|
T | C | 4 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192+741T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403475 | ||||||
chr2:203403510
|
A | G | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1192+776A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403510 | ||||||
chr2:203403645
|
T | TTA | 190 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(187): Show | 190 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1192+915_1192+916d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203403645 | |||||
chr2:203403733
|
T | G | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1192+999T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403733 | ||||||
chr2:203403742
|
G | GT | 24 | a0001c0001t0001g0227a0001c0001t0001g0239a0001c0001t0001g0242others(21): Show | 24 | HG00673.hp2 HG01074.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1192+1030dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203403742 | |||||
chr2:203403742
|
G | GTT | 122 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(119): Show | 122 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.1192+1029_1192+103 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203403742 | |||||
chr2:203403742
|
G | GTTT | 50 | a0001c0001t0001g0237a0001c0001t0001g0265a0001c0001t0001g0291others(47): Show | 50 | HG00597.hp1 HG00621.hp1 HG00733.hp2 others(47): Show |
intron_variant | MODIFIER | c.1192+1028_1192+103 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203403742 | |||||
chr2:203403742
|
GT | G | 11 | a0001c0001t0002g0004a0001c0001t0002g0011a0001c0001t0002g0016others(8): Show | 11 | HG00323.hp1 HG00741.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.1192+1030delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203403742 | |||||
chr2:203403782
|
C | T | 93 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1192+1048C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403782 | ||||||
chr2:203403903
|
G | A | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1192+1169G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203403903 | ||||||
chr2:203404031
|
G | A | 1 | a0001c0001t0001g0237 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1192+1297G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404031 | ||||||
chr2:203404032
|
C | T | 1 | a0001c0001t0001g0237 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1192+1298C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404032 | ||||||
chr2:203404033
|
G | A | 1 | a0001c0001t0005g0161 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1192+1299G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404033 | ||||||
chr2:203404102
|
T | G | 1 | a0001c0001t0001g0246 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1192+1368T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404102 | ||||||
chr2:203404109
|
T | C | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1192+1375T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404109 | ||||||
chr2:203404273
|
A | C | 1 | a0001c0001t0001g0250 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1192+1539A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404273 | ||||||
chr2:203404369
|
G | A | 4 | a0001c0001t0010g0066a0001c0001t0010g0067a0001c0001t0010g0068others(1): Show | 4 | NA18962.hp2 NA18986.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.1192+1635G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404369 | ||||||
chr2:203404442
|
A | G | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG00735.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1192+1708A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404442 | ||||||
chr2:203404546
|
C | T | 21 | a0001c0001t0005g0099a0001c0001t0006g0001a0001c0001t0006g0149others(18): Show | 21 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(18): Show |
intron_variant | MODIFIER | c.1192+1812C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404546 | ||||||
chr2:203404547
|
G | C | 2 | a0001c0001t0001g0293a0001c0001t0001g0294 | 2 | HG00735.hp2 HG00741.hp2 |
intron_variant | MODIFIER | c.1192+1813G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404547 | ||||||
chr2:203404700
|
A | G | 3 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0003g0080 | 3 | HG00323.hp1 HG01168.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.1192+1966A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404700 | ||||||
chr2:203404763
|
C | T | 190 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(187): Show | 190 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1192+2029C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404763 | ||||||
chr2:203404764
|
G | A | 10 | a0001c0001t0001g0140a0001c0001t0004g0136a0001c0001t0004g0137others(7): Show | 10 | HG02293.hp1 HG02559.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.1192+2030G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404764 | ||||||
chr2:203404773
|
G | A | 1 | a0001c0001t0002g0086 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1192+2039G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404773 | ||||||
chr2:203404774
|
G | C | 1 | a0001c0001t0001g0227 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1192+2040G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404774 | ||||||
chr2:203404886
|
G | A | 2 | a0001c0001t0004g0125a0001c0001t0004g0134 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1192+2152G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203404886 | ||||||
chr2:203405045
|
C | T | 27 | a0001c0001t0005g0081a0001c0001t0005g0098a0001c0001t0005g0099others(24): Show | 27 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1192+2311C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203405045 | ||||||
chr2:203405197
|
C | A | 1 | a0001c0001t0006g0180 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1192+2463C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203405197 | ||||||
chr2:203405460
|
C | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1192+2726C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203405460 | ||||||
chr2:203405597
|
G | C | 1 | a0001c0001t0001g0224 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1192+2863G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203405597 | ||||||
chr2:203405769
|
A | G | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1192+3035A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203405769 | ||||||
chr2:203405801
|
T | C | 1 | a0001c0001t0005g0100 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1192+3067T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203405801 | ||||||
chr2:203406119
|
G | A | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1192+3385G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406119 | ||||||
chr2:203406141
|
A | C | 3 | a0001c0001t0001g0256a0001c0001t0001g0273a0001c0001t0001g0292 | 3 | NA18978.hp1 NA18982.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.1192+3407A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406141 | ||||||
chr2:203406231
|
G | A | 190 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(187): Show | 190 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1192+3497G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406231 | ||||||
chr2:203406379
|
G | C | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1192+3645G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406379 | ||||||
chr2:203406409
|
A | G | 1 | a0001c0001t0001g0295 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.1192+3675A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406409 | ||||||
chr2:203406448
|
A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1192+3714A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406448 | ||||||
chr2:203406494
|
G | C | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1192+3760G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406494 | ||||||
chr2:203406573
|
G | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0308 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1192+3839G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406573 | ||||||
chr2:203406688
|
A | G | 1 | a0001c0001t0038g0038 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1192+3954A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406688 | ||||||
chr2:203406767
|
G | A | 1 | a0001c0001t0009g0177 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1192+4033G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406767 | ||||||
chr2:203406788
|
C | T | 42 | a0001c0001t0002g0187a0001c0001t0002g0193a0001c0001t0002g0194others(39): Show | 42 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1192+4054C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406788 | ||||||
chr2:203406820
|
C | T | 6 | a0001c0001t0007g0007a0001c0001t0007g0085a0001c0001t0007g0089others(3): Show | 6 | NA18951.hp1 NA18968.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1192+4086C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406820 | ||||||
chr2:203406903
|
T | C | 1 | a0001c0001t0001g0181 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1192+4169T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203406903 | ||||||
chr2:203407338
|
G | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1193-3947G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407338 | ||||||
chr2:203407367
|
C | T | 93 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1193-3918C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407367 | ||||||
chr2:203407630
|
C | G | 1 | a0001c0001t0003g0199 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1193-3655C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407630 | ||||||
chr2:203407717
|
A | G | 17 | a0001c0001t0004g0121a0001c0001t0004g0124a0001c0001t0004g0125others(14): Show | 17 | HG00738.hp2 HG01943.hp1 HG01975.hp1 others(14): Show |
intron_variant | MODIFIER | c.1193-3568A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407717 | ||||||
chr2:203407732
|
A | G | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1193-3553A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407732 | ||||||
chr2:203407733
|
T | C | 8 | a0001c0001t0004g0127a0001c0001t0004g0128a0001c0001t0004g0129others(5): Show | 8 | HG02129.hp1 HG02132.hp2 HG02523.hp1 others(5): Show |
intron_variant | MODIFIER | c.1193-3552T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407733 | ||||||
chr2:203407857
|
A | G | 5 | a0001c0001t0002g0009a0001c0001t0002g0011a0001c0001t0002g0012others(2): Show | 5 | HG00323.hp1 HG01168.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.1193-3428A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407857 | ||||||
chr2:203407963
|
T | G | 2 | a0001c0001t0004g0125a0001c0001t0004g0134 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1193-3322T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203407963 | ||||||
chr2:203408021
|
T | C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1193-3264T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408021 | ||||||
chr2:203408095
|
A | C | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1193-3190A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408095 | ||||||
chr2:203408109
|
C | T | 1 | a0001c0001t0001g0231 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1193-3176C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408109 | ||||||
chr2:203408165
|
CT | C | 191 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(188): Show | 191 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(188): Show |
intron_variant | MODIFIER | c.1193-3106delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408165 | |||||
chr2:203408251
|
C | T | 3 | a0001c0001t0001g0181a0001c0001t0001g0224a0001c0001t0001g0270 | 3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1193-3034C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408251 | ||||||
chr2:203408265
|
C | T | 7 | a0001c0001t0002g0037a0001c0001t0002g0043a0001c0001t0002g0046others(4): Show | 7 | HG02523.hp2 NA18949.hp2 NA18960.hp2 others(4): Show |
intron_variant | MODIFIER | c.1193-3020C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408265 | ||||||
chr2:203408288
|
G | A | 1 | a0001c0001t0001g0279 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1193-2997G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408288 | ||||||
chr2:203408343
|
A | G | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1193-2942A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408343 | ||||||
chr2:203408635
|
T | C | 4 | a0001c0001t0001g0202a0001c0001t0001g0247a0001c0001t0001g0258others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.1193-2650T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408635 | ||||||
chr2:203408788
|
C | G | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1193-2497C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408788 | ||||||
chr2:203408828
|
C | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1193-2457C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408828 | ||||||
chr2:203408829
|
C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1193-2456C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408829 | ||||||
chr2:203408833
|
C | CTTTCTTT others(4): Show |
2 | a0001c0001t0005g0107a0001c0001t0005g0108 | 2 | NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1193-2449_1193-244 others(15): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | |||||
chr2:203408833
|
C | CTTTCTTT others(5): Show |
16 | a0001c0001t0005g0081a0001c0001t0005g0102a0001c0001t0005g0103others(13): Show | 16 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1193-2449_1193-244 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | |||||
chr2:203408833
|
C | CTTTCTTT others(6): Show |
6 | a0001c0001t0005g0100a0001c0001t0005g0115a0001c0001t0005g0156others(3): Show | 6 | HG02109.hp1 HG02809.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1193-2449_1193-244 others(17): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | |||||
chr2:203408833
|
C | CTTTTTTT others(3): Show |
3 | a0001c0001t0001g0212a0001c0001t0001g0236a0001c0001t0006g0164 | 3 | HG01169.hp1 HG03491.hp1 NA18974.hp1 |
intron_variant | MODIFIER | c.1193-2445_1193-243 others(14): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | |||||
chr2:203408833
|
C | CTTTTTTT others(4): Show |
107 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(104): Show | 107 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.1193-2446_1193-243 others(15): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | |||||
chr2:203408833
|
C | CTTTTTTT others(5): Show |
45 | a0001c0001t0001g0202a0001c0001t0001g0215a0001c0001t0001g0224others(42): Show | 45 | HG00423.hp1 HG00438.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.1193-2447_1193-243 others(16): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | |||||
chr2:203408833
|
C | CTTTTTTT others(6): Show |
4 | a0001c0001t0003g0209a0001c0001t0027g0117a0001c0002t0005g0116others(1): Show | 4 | HG02055.hp2 HG02572.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.1193-2448_1193-243 others(17): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | |||||
chr2:203408833
|
C | CTTTTTTT others(7): Show |
1 | a0001c0001t0031g0183 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1193-2449_1193-243 others(18): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | |||||
chr2:203408833
|
C | CTTTTTTT others(8): Show |
1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1193-2450_1193-243 others(19): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203408833 | |||||
chr2:203408878
|
T | C | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1193-2407T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408878 | ||||||
chr2:203408900
|
G | A | 1 | a0001c0001t0036g0073 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1193-2385G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408900 | ||||||
chr2:203408924
|
C | T | 28 | a0001c0001t0001g0140a0001c0001t0004g0121a0001c0001t0004g0124others(25): Show | 28 | HG00738.hp2 HG01943.hp1 HG01975.hp1 others(25): Show |
intron_variant | MODIFIER | c.1193-2361C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408924 | ||||||
chr2:203408995
|
C | T | 1 | a0001c0001t0001g0318 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1193-2290C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408995 | ||||||
chr2:203408996
|
G | C | 1 | a0001c0001t0001g0316 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1193-2289G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203408996 | ||||||
chr2:203409086
|
C | T | 1 | a0001c0001t0001g0233 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.1193-2199C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409086 | ||||||
chr2:203409133
|
C | T | 1 | a0001c0001t0002g0025 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1193-2152C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409133 | ||||||
chr2:203409226
|
A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1193-2059A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409226 | ||||||
chr2:203409589
|
C | T | 1 | a0001c0001t0027g0117 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1193-1696C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409589 | ||||||
chr2:203409595
|
C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1193-1690C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409595 | ||||||
chr2:203409674
|
T | C | 1 | a0001c0001t0001g0307 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1193-1611T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409674 | ||||||
chr2:203409857
|
T | C | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1193-1428T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409857 | ||||||
chr2:203409973
|
G | A | 1 | a0001c0001t0001g0276 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1193-1312G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203409973 | ||||||
chr2:203410194
|
A | T | 1 | a0001c0001t0015g0120 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1193-1091A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203410194 | ||||||
chr2:203410306
|
T | C | 22 | a0001c0001t0005g0081a0001c0001t0005g0100a0001c0001t0005g0102others(19): Show | 22 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1193-979T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203410306 | ||||||
chr2:203410338
|
T | C | 1 | a0001c0001t0016g0092 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1193-947T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203410338 | ||||||
chr2:203410963
|
A | G | 1 | a0001c0001t0003g0220 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1193-322A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | chr2 | 203410963 | ||||||
chr2:203410999
|
TTA | T | 29 | a0001c0001t0001g0140a0001c0001t0004g0121a0001c0001t0004g0124others(26): Show | 29 | HG00738.hp2 HG01943.hp1 HG01975.hp1 others(26): Show |
intron_variant | MODIFIER | c.1193-284_1193-283d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 9/11 | INFO_REALIGN_3_PRIME | chr2 | 203410999 | |||||
chr2:203411604
|
T | C | 93 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1279+233T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203411604 | ||||||
chr2:203411973
|
G | T | 1 | a0001c0001t0001g0251 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1279+602G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203411973 | ||||||
chr2:203412370
|
T | C | 2 | a0001c0001t0003g0221a0001c0001t0003g0288 | 2 | HG01978.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1279+999T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412370 | ||||||
chr2:203412516
|
T | C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1279+1145T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412516 | ||||||
chr2:203412567
|
C | A | 1 | a0001c0001t0025g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1279+1196C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412567 | ||||||
chr2:203412579
|
T | C | 1 | a0001c0001t0003g0225 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1279+1208T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412579 | ||||||
chr2:203412617
|
GT | G | 138 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(135): Show | 138 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1279+1248delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203412617 | |||||
chr2:203412755
|
A | G | 189 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(186): Show | 189 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(186): Show |
intron_variant | MODIFIER | c.1279+1384A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412755 | ||||||
chr2:203412766
|
C | T | 3 | a0001c0001t0005g0107a0001c0001t0005g0108a0001c0001t0021g0151 | 3 | HG00621.hp1 NA18992.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.1279+1395C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412766 | ||||||
chr2:203412885
|
G | C | 190 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(187): Show | 190 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1279+1514G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412885 | ||||||
chr2:203412926
|
C | T | 22 | a0001c0001t0005g0081a0001c0001t0005g0100a0001c0001t0005g0102others(19): Show | 22 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1279+1555C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203412926 | ||||||
chr2:203413068
|
G | A | 27 | a0001c0001t0005g0081a0001c0001t0005g0098a0001c0001t0005g0099others(24): Show | 27 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(24): Show |
intron_variant | MODIFIER | c.1279+1697G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413068 | ||||||
chr2:203413119
|
T | A | 1 | a0001c0001t0004g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1279+1748T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413119 | ||||||
chr2:203413466
|
T | G | 1 | a0001c0001t0001g0254 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1279+2095T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413466 | ||||||
chr2:203413473
|
A | G | 1 | a0001c0001t0001g0254 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1279+2102A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413473 | ||||||
chr2:203413518
|
C | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1279+2147C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413518 | ||||||
chr2:203413527
|
A | G | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1279+2156A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413527 | ||||||
chr2:203413596
|
C | T | 190 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(187): Show | 190 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1279+2225C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413596 | ||||||
chr2:203413651
|
G | A | 4 | a0001c0001t0002g0082a0001c0001t0002g0097a0001c0001t0016g0088others(1): Show | 4 | HG02165.hp2 NA18940.hp1 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.1279+2280G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413651 | ||||||
chr2:203413897
|
C | CCAG | 93 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1279+2527_1279+252 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203413897 | |||||
chr2:203413985
|
T | A | 93 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1279+2614T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203413985 | ||||||
chr2:203414005
|
T | C | 1 | a0001c0001t0018g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1279+2634T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414005 | ||||||
chr2:203414101
|
C | CT | 10 | a0001c0001t0002g0056a0001c0001t0002g0077a0001c0001t0002g0079others(7): Show | 10 | HG00621.hp2 HG01192.hp2 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.1279+2749dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203414101 | |||||
chr2:203414101
|
CT | C | 28 | a0001c0001t0001g0181a0001c0001t0001g0224a0001c0001t0001g0270others(25): Show | 28 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(25): Show |
intron_variant | MODIFIER | c.1279+2749delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203414101 | |||||
chr2:203414101
|
CTT | C | 93 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(90): Show | 93 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.1279+2748_1279+274 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203414101 | |||||
chr2:203414345
|
T | C | 16 | a0001c0001t0001g0200a0001c0001t0001g0228a0001c0001t0001g0229others(13): Show | 16 | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(13): Show |
intron_variant | MODIFIER | c.1280-2563T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414345 | ||||||
chr2:203414393
|
C | T | 1 | a0001c0001t0018g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1280-2515C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414393 | ||||||
chr2:203414442
|
C | A | 190 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(187): Show | 190 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1280-2466C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414442 | ||||||
chr2:203414455
|
C | T | 1 | a0001c0001t0003g0226 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1280-2453C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414455 | ||||||
chr2:203414460
|
C | G | 1 | a0001c0001t0002g0058 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1280-2448C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414460 | ||||||
chr2:203414850
|
A | G | 1 | a0001c0001t0001g0280 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1280-2058A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203414850 | ||||||
chr2:203415148
|
A | G | 3 | a0001c0001t0002g0032a0001c0001t0002g0041a0001c0001t0002g0052 | 3 | HG03491.hp2 HG03669.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.1280-1760A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415148 | ||||||
chr2:203415191
|
T | G | 29 | a0001c0001t0005g0081a0001c0001t0005g0098a0001c0001t0005g0099others(26): Show | 29 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(26): Show |
intron_variant | MODIFIER | c.1280-1717T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415191 | ||||||
chr2:203415339
|
C | T | 1 | a0001c0001t0001g0245 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1280-1569C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415339 | ||||||
chr2:203415345
|
C | T | 3 | a0001c0001t0003g0076a0001c0001t0003g0221a0001c0001t0003g0288 | 3 | HG01978.hp1 HG02148.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1280-1563C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415345 | ||||||
chr2:203415366
|
C | G | 1 | a0001c0001t0003g0204 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1280-1542C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415366 | ||||||
chr2:203415486
|
G | A | 2 | a0001c0001t0004g0125a0001c0001t0004g0134 | 2 | HG03130.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1280-1422G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415486 | ||||||
chr2:203415542
|
G | A | 3 | a0001c0001t0001g0181a0001c0001t0001g0224a0001c0001t0001g0270 | 3 | HG03195.hp1 HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1280-1366G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415542 | ||||||
chr2:203415611
|
C | T | 2 | a0001c0001t0002g0051a0001c0001t0022g0319 | 2 | HG01884.hp2 HG02040.hp1 |
intron_variant | MODIFIER | c.1280-1297C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415611 | ||||||
chr2:203415616
|
C | CA | 63 | a0001c0001t0001g0182a0001c0001t0001g0215a0001c0001t0001g0227others(60): Show | 63 | HG00423.hp2 HG00609.hp2 HG00642.hp1 others(60): Show |
intron_variant | MODIFIER | c.1280-1265dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203415616 | |||||
chr2:203415616
|
C | CAA | 8 | a0001c0001t0002g0002a0001c0001t0003g0188a0001c0001t0003g0220others(5): Show | 8 | HG01074.hp1 HG01358.hp1 HG02027.hp1 others(5): Show |
intron_variant | MODIFIER | c.1280-1266_1280-126 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203415616 | |||||
chr2:203415616
|
C | CAAA | 12 | a0001c0001t0005g0081a0001c0001t0005g0100a0001c0001t0005g0102others(9): Show | 12 | HG01257.hp1 HG01258.hp1 HG02083.hp1 others(9): Show |
intron_variant | MODIFIER | c.1280-1267_1280-126 others(7): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203415616 | |||||
chr2:203415616
|
C | CAAAA | 14 | a0001c0001t0005g0099a0001c0001t0005g0107a0001c0001t0005g0108others(11): Show | 14 | HG00621.hp1 HG02040.hp2 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.1280-1268_1280-126 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203415616 | |||||
chr2:203415616
|
CA | C | 14 | a0001c0001t0001g0224a0001c0001t0001g0232a0001c0001t0001g0242others(11): Show | 14 | HG00609.hp1 HG01496.hp1 HG01975.hp2 others(11): Show |
intron_variant | MODIFIER | c.1280-1265delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203415616 | |||||
chr2:203415616
|
CAAAAAAA others(2): Show |
C | 24 | a0001c0001t0001g0140a0001c0001t0004g0121a0001c0001t0004g0124others(21): Show | 24 | HG00738.hp2 HG01943.hp1 HG01975.hp1 others(21): Show |
intron_variant | MODIFIER | c.1280-1273_1280-126 others(13): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 203415616 | |||||
chr2:203415689
|
A | C | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1280-1219A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415689 | ||||||
chr2:203415817
|
G | A | 2 | a0001c0001t0003g0191a0001c0001t0003g0192 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1280-1091G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415817 | ||||||
chr2:203415879
|
A | G | 188 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(185): Show | 188 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(185): Show |
intron_variant | MODIFIER | c.1280-1029A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415879 | ||||||
chr2:203415929
|
T | A | 138 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(135): Show | 138 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.1280-979T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203415929 | ||||||
chr2:203416040
|
C | T | 1 | a0001c0001t0001g0254 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1280-868C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416040 | ||||||
chr2:203416186
|
A | G | 1 | a0001c0001t0001g0262 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.1280-722A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416186 | ||||||
chr2:203416219
|
C | T | 190 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(187): Show | 190 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(187): Show |
intron_variant | MODIFIER | c.1280-689C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416219 | ||||||
chr2:203416239
|
C | G | 2 | a0001c0001t0001g0276a0001c0001t0001g0318 | 2 | HG01255.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1280-669C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416239 | ||||||
chr2:203416357
|
G | A | 1 | a0001c0001t0025g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1280-551G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416357 | ||||||
chr2:203416397
|
G | A | 42 | a0001c0001t0002g0187a0001c0001t0002g0193a0001c0001t0002g0194others(39): Show | 42 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.1280-511G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416397 | ||||||
chr2:203416440
|
C | T | 2 | a0001c0001t0007g0085a0001c0001t0007g0093 | 2 | NA18968.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1280-468C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416440 | ||||||
chr2:203416538
|
C | T | 2 | a0001c0001t0002g0021a0001c0001t0002g0084 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1280-370C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416538 | ||||||
chr2:203416724
|
G | A | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1280-184G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416724 | ||||||
chr2:203416746
|
G | A | 1 | a0001c0001t0003g0203 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1280-162G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416746 | ||||||
chr2:203416788
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1280-120G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416788 | ||||||
chr2:203416835
|
C | T | 1 | a0001c0001t0004g0135 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1280-73C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 10/11 | chr2 | 203416835 | ||||||
chr2:203417272
|
T | A | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1453+191T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203417272 | ||||||
chr2:203417307
|
G | A | 3 | a0001c0001t0011g0153a0001c0001t0011g0154a0001c0001t0011g0155 | 3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1453+226G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203417307 | ||||||
chr2:203417393
|
A | G | 1 | a0001c0001t0001g0243 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.1453+312A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203417393 | ||||||
chr2:203417564
|
G | A | 3 | a0001c0001t0005g0106a0001c0001t0005g0113a0001c0001t0005g0152 | 3 | HG02083.hp1 HG02135.hp2 NA18962.hp1 |
intron_variant | MODIFIER | c.1453+483G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203417564 | ||||||
chr2:203417815
|
C | T | 1 | a0001c0002t0024g0118 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1453+734C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203417815 | ||||||
chr2:203417944
|
C | T | 1 | a0001c0001t0006g0173 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1453+863C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203417944 | ||||||
chr2:203418193
|
A | C | 4 | a0001c0001t0005g0109a0001c0001t0005g0110a0001c0001t0005g0111others(1): Show | 4 | HG02155.hp1 NA18747.hp2 NA18965.hp1 others(1): Show |
intron_variant | MODIFIER | c.1453+1112A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203418193 | ||||||
chr2:203418596
|
A | G | 1 | a0001c0001t0018g0274 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1453+1515A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203418596 | ||||||
chr2:203418651
|
T | G | 1 | a0001c0001t0025g0266 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1453+1570T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203418651 | ||||||
chr2:203418951
|
A | T | 2 | a0001c0001t0002g0044a0001c0001t0002g0050 | 2 | HG02630.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1453+1870A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203418951 | ||||||
chr2:203419106
|
C | CT | 49 | a0001c0001t0001g0200a0001c0001t0001g0293a0001c0001t0002g0021others(46): Show | 49 | HG00621.hp1 HG00733.hp2 HG00741.hp2 others(46): Show |
intron_variant | MODIFIER | c.1453+2045dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203419106 | |||||
chr2:203419106
|
CT | C | 15 | a0001c0001t0001g0254a0001c0001t0001g0256a0001c0001t0001g0284others(12): Show | 15 | HG00323.hp2 HG01256.hp2 HG01515.hp2 others(12): Show |
intron_variant | MODIFIER | c.1453+2045delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203419106 | |||||
chr2:203419171
|
G | A | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1453+2090G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419171 | ||||||
chr2:203419230
|
C | T | 8 | a0001c0001t0001g0200a0001c0001t0001g0229a0001c0001t0001g0233others(5): Show | 8 | HG02083.hp2 NA18939.hp2 NA18974.hp1 others(5): Show |
intron_variant | MODIFIER | c.1453+2149C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419230 | ||||||
chr2:203419358
|
A | G | 6 | a0001c0001t0007g0007a0001c0001t0007g0085a0001c0001t0007g0089others(3): Show | 6 | NA18951.hp1 NA18968.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1453+2277A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419358 | ||||||
chr2:203419461
|
C | T | 1 | a0001c0001t0002g0024 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1453+2380C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419461 | ||||||
chr2:203419568
|
G | A | 1 | a0001c0001t0002g0075 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1453+2487G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419568 | ||||||
chr2:203419672
|
C | T | 1 | a0001c0001t0002g0017 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1453+2591C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419672 | ||||||
chr2:203419801
|
C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1453+2720C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419801 | ||||||
chr2:203419870
|
C | T | 2 | a0001c0001t0001g0248a0001c0001t0001g0249 | 2 | HG01256.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1453+2789C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419870 | ||||||
chr2:203419913
|
C | A | 22 | a0001c0001t0005g0081a0001c0001t0005g0100a0001c0001t0005g0102others(19): Show | 22 | HG00621.hp1 HG01257.hp1 HG01258.hp1 others(19): Show |
intron_variant | MODIFIER | c.1453+2832C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419913 | ||||||
chr2:203419968
|
A | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1453+2887A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419968 | ||||||
chr2:203419973
|
A | G | 2 | a0001c0001t0008g0030a0001c0001t0008g0034 | 2 | HG00673.hp2 NA18946.hp1 |
intron_variant | MODIFIER | c.1453+2892A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203419973 | ||||||
chr2:203420107
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0308 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1453+3026T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420107 | ||||||
chr2:203420217
|
A | G | 2 | a0001c0001t0003g0309a0001c0001t0003g0310 | 2 | HG01928.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.1453+3136A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420217 | ||||||
chr2:203420304
|
C | T | 1 | a0001c0001t0002g0029 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1453+3223C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420304 | ||||||
chr2:203420316
|
T | TA | 3 | a0001c0001t0002g0023a0001c0001t0002g0024a0001c0001t0002g0027 | 3 | HG00423.hp2 HG00609.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1453+3236dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203420316 | |||||
chr2:203420396
|
CT | C | 8 | a0001c0001t0001g0251a0001c0001t0001g0280a0001c0001t0002g0052others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG03491.hp2 others(5): Show |
intron_variant | MODIFIER | c.1453+3330delT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203420396 | |||||
chr2:203420396
|
CTT | C | 186 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(183): Show | 186 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(183): Show |
intron_variant | MODIFIER | c.1453+3329_1453+333 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203420396 | |||||
chr2:203420600
|
A | G | 1 | a0001c0001t0002g0083 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1453+3519A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420600 | ||||||
chr2:203420684
|
C | T | 1 | a0001c0001t0003g0209 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1453+3603C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420684 | ||||||
chr2:203420718
|
C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1453+3637C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420718 | ||||||
chr2:203420719
|
G | A | 1 | a0001c0001t0002g0031 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1453+3638G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420719 | ||||||
chr2:203420810
|
T | G | 1 | a0001c0001t0003g0196 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1453+3729T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420810 | ||||||
chr2:203420926
|
G | A | 3 | a0001c0001t0002g0049a0001c0001t0002g0074a0001c0001t0002g0075 | 3 | NA18970.hp1 NA18991.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1453+3845G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203420926 | ||||||
chr2:203421051
|
G | A | 39 | a0001c0001t0002g0187a0001c0001t0002g0193a0001c0001t0002g0194others(36): Show | 39 | HG00438.hp1 HG00642.hp1 HG00642.hp2 others(36): Show |
intron_variant | MODIFIER | c.1453+3970G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203421051 | ||||||
chr2:203421096
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1453+4015T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203421096 | ||||||
chr2:203421603
|
T | G | 3 | a0001c0001t0011g0153a0001c0001t0011g0154a0001c0001t0011g0155 | 3 | HG02109.hp1 HG02809.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.1453+4522T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203421603 | ||||||
chr2:203421929
|
G | A | 2 | a0001c0002t0005g0116a0001c0002t0024g0118 | 2 | HG02976.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.1453+4848G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203421929 | ||||||
chr2:203421964
|
C | CA | 39 | a0001c0001t0001g0140a0001c0001t0001g0241a0001c0001t0002g0036others(36): Show | 39 | HG00673.hp2 HG00738.hp2 HG01433.hp1 others(36): Show |
intron_variant | MODIFIER | c.1453+4903dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203421964 | |||||
chr2:203421964
|
C | CAAAA | 13 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(10): Show | 13 | HG00733.hp2 HG01168.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.1453+4900_1453+490 others(8): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203421964 | |||||
chr2:203421964
|
C | CAAAAA | 6 | a0001c0001t0006g0167a0001c0001t0006g0172a0001c0001t0006g0173others(3): Show | 6 | HG01109.hp1 HG02280.hp2 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.1453+4899_1453+490 others(9): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203421964 | |||||
chr2:203421964
|
CA | C | 86 | a0001c0001t0001g0182a0001c0001t0001g0186a0001c0001t0001g0200others(83): Show | 86 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.1453+4903delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203421964 | |||||
chr2:203422126
|
G | A | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1453+5045G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422126 | ||||||
chr2:203422165
|
G | T | 1 | a0001c0001t0004g0142 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1454-5012G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422165 | ||||||
chr2:203422268
|
G | GC | 222 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(219): Show | 222 | HG00280.hp1 HG00323.hp2 HG00423.hp1 others(219): Show |
intron_variant | MODIFIER | c.1454-4909_1454-490 others(5): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422268 | ||||||
chr2:203422285
|
C | T | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1454-4892C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422285 | ||||||
chr2:203422410
|
G | A | 64 | a0001c0001t0001g0140a0001c0001t0001g0224a0001c0001t0001g0241others(61): Show | 64 | HG00280.hp2 HG00621.hp1 HG00738.hp2 others(61): Show |
intron_variant | MODIFIER | c.1454-4767G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422410 | ||||||
chr2:203422411
|
C | T | 1 | a0001c0001t0002g0041 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1454-4766C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422411 | ||||||
chr2:203422492
|
C | T | 1 | a0001c0001t0004g0146 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1454-4685C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422492 | ||||||
chr2:203422554
|
A | G | 2 | a0001c0001t0001g0268a0001c0001t0001g0278 | 2 | HG04228.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1454-4623A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422554 | ||||||
chr2:203422828
|
T | C | 1 | a0001c0001t0006g0178 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1454-4349T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203422828 | ||||||
chr2:203423476
|
A | C | 2 | a0001c0001t0005g0110a0001c0001t0005g0111 | 2 | NA18965.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1454-3701A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423476 | ||||||
chr2:203423477
|
G | T | 2 | a0001c0001t0005g0110a0001c0001t0005g0111 | 2 | NA18965.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.1454-3700G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423477 | ||||||
chr2:203423512
|
G | A | 1 | a0001c0001t0004g0148 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1454-3665G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423512 | ||||||
chr2:203423530
|
A | G | 2 | a0001c0001t0001g0182a0001c0001t0001g0308 | 2 | HG02622.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.1454-3647A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423530 | ||||||
chr2:203423710
|
C | T | 3 | a0001c0001t0001g0182a0001c0001t0001g0246a0001c0001t0001g0308 | 3 | HG02622.hp2 HG03139.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1454-3467C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423710 | ||||||
chr2:203423711
|
G | A | 2 | a0001c0001t0001g0181a0001c0001t0001g0270 | 2 | HG03225.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1454-3466G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423711 | ||||||
chr2:203423714
|
C | A | 6 | a0001c0001t0007g0007a0001c0001t0007g0085a0001c0001t0007g0089others(3): Show | 6 | NA18951.hp1 NA18968.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.1454-3463C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423714 | ||||||
chr2:203423753
|
A | G | 6 | a0001c0001t0006g0001a0001c0001t0006g0163a0001c0001t0006g0164others(3): Show | 6 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1454-3424A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423753 | ||||||
chr2:203423825
|
T | A | 318 | a0001c0001t0001g0140a0001c0001t0001g0181a0001c0001t0001g0182others(315): Show | 318 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(315): Show |
intron_variant | MODIFIER | c.1454-3352T>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423825 | ||||||
chr2:203423979
|
C | G | 1 | a0001c0001t0022g0319 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1454-3198C>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423979 | ||||||
chr2:203423999
|
C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1454-3178C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203423999 | ||||||
chr2:203424079
|
T | G | 4 | a0001c0001t0009g0158a0001c0001t0009g0159a0001c0001t0009g0160others(1): Show | 4 | HG02145.hp2 HG02451.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.1454-3098T>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203424079 | ||||||
chr2:203424091
|
A | G | 17 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(14): Show | 17 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1454-3086A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203424091 | ||||||
chr2:203424635
|
G | C | 1 | a0001c0001t0001g0140 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1454-2542G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203424635 | ||||||
chr2:203425008
|
C | T | 1 | a0001c0001t0003g0195 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1454-2169C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425008 | ||||||
chr2:203425012
|
A | G | 1 | a0001c0001t0004g0143 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1454-2165A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425012 | ||||||
chr2:203425026
|
A | AT | 13 | a0001c0001t0001g0216a0001c0001t0001g0224a0001c0001t0001g0256others(10): Show | 13 | HG00621.hp1 HG00733.hp1 HG01109.hp2 others(10): Show |
intron_variant | MODIFIER | c.1454-2134dupT | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203425026 | |||||
chr2:203425026
|
A | ATT | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1454-2135_1454-213 others(6): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203425026 | |||||
chr2:203425044
|
G | T | 4 | a0001c0001t0004g0142a0001c0001t0004g0143a0001c0001t0004g0144others(1): Show | 4 | HG02630.hp1 HG02723.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1454-2133G>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425044 | ||||||
chr2:203425314
|
T | C | 12 | a0001c0001t0002g0187a0001c0001t0003g0189a0001c0001t0003g0195others(9): Show | 12 | HG00438.hp1 HG00642.hp2 HG00738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1454-1863T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425314 | ||||||
chr2:203425322
|
C | A | 1 | a0001c0001t0002g0048 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1454-1855C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425322 | ||||||
chr2:203425798
|
G | A | 1 | a0001c0001t0002g0060 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.1454-1379G>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425798 | ||||||
chr2:203425806
|
G | C | 15 | a0001c0001t0003g0188a0001c0001t0003g0199a0001c0001t0003g0219others(12): Show | 15 | HG00642.hp1 HG01074.hp1 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.1454-1371G>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425806 | ||||||
chr2:203425935
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1454-1242C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203425935 | ||||||
chr2:203426019
|
C | CA | 51 | a0001c0001t0001g0140a0001c0001t0001g0231a0001c0001t0001g0302others(48): Show | 51 | HG00733.hp2 HG00738.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.1454-1140dupA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203426019 | |||||
chr2:203426040
|
C | A | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1454-1137C>A | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426040 | ||||||
chr2:203426329
|
T | C | 7 | a0001c0001t0008g0003a0001c0001t0008g0030a0001c0001t0008g0034others(4): Show | 7 | HG00673.hp2 NA18946.hp1 NA18982.hp1 others(4): Show |
intron_variant | MODIFIER | c.1454-848T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426329 | ||||||
chr2:203426516
|
T | C | 2 | a0001c0001t0005g0098a0001c0001t0005g0099 | 2 | HG02486.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.1454-661T>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426516 | ||||||
chr2:203426618
|
A | T | 1 | a0001c0001t0002g0047 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1454-559A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426618 | ||||||
chr2:203426677
|
A | T | 1 | a0001c0001t0009g0160 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1454-500A>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426677 | ||||||
chr2:203426785
|
TA | T | 256 | a0001c0001t0001g0181a0001c0001t0001g0182a0001c0001t0001g0186others(253): Show | 256 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.1454-373delA | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203426785 | |||||
chr2:203426785
|
TAA | T | 41 | a0001c0001t0001g0140a0001c0001t0001g0224a0001c0001t0001g0236others(38): Show | 41 | HG00673.hp1 HG00738.hp2 HG01891.hp1 others(38): Show |
intron_variant | MODIFIER | c.1454-374_1454-373d others(4): Show |
ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203426785 | |||||
chr2:203426798
|
A | C | 1 | a0001c0001t0001g0228 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1454-379A>C | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426798 | ||||||
chr2:203426804
|
AC | A | 3 | a0001c0001t0003g0203a0001c0001t0003g0317a0001c0001t0034g0190 | 3 | HG00438.hp1 HG03688.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1454-371delC | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 203426804 | |||||
chr2:203426883
|
A | G | 20 | a0001c0001t0006g0001a0001c0001t0006g0149a0001c0001t0006g0150others(17): Show | 20 | HG00733.hp2 HG01109.hp1 HG01168.hp2 others(17): Show |
intron_variant | MODIFIER | c.1454-294A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426883 | ||||||
chr2:203426890
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1454-287A>G | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203426890 | ||||||
chr2:203427147
|
C | T | 1 | a0001c0001t0037g0320 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1454-30C>T | ABI2 | ENSG00000138443.17 | transcript | ENST00000261018.12 | protein_coding | 11/11 | chr2 | 203427147 |