geneid | 10096 |
---|---|
ensemblid | ENSG00000115091.12 |
hgncid | 170 |
symbol | ACTR3 |
name | actin related protein 3 |
refseq_nuc | NM_005721.5 |
refseq_prot | NP_005712.1 |
ensembl_nuc | ENST00000263238.7 |
ensembl_prot | ENSP00000263238.2 |
mane_status | MANE Select |
chr | chr2 |
start | 113890089 |
end | 113962596 |
strand | + |
ver | v1.2 |
region | chr2:113890089-113962596 |
region5000 | chr2:113885089-113967596 |
regionname0 | ACTR3_chr2_113890089_113962596 |
regionname5000 | ACTR3_chr2_113885089_113967596 |
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 | 418 | 389 | 87 | 62 | 188 | 12 | 38 | 148 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0002 | 0/0 | 418 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
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 | 1257 | 387 | 86 | 62 | 188 | 11 | 38 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
c0002 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
c0003 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
c0004 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
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 | 0/0 | 5332 | 103 | 19 | 11 | 61 | 0 | 12 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0002 | 0/1 | 5333 | 65 | 2 | 22 | 17 | 7 | 16 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0003 | 1/0 | 5333 | 54 | 4 | 6 | 41 | 1 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0004 | 0/0 | 5334 | 42 | 4 | 1 | 29 | 3 | 5 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0005 | 0/0 | 5332 | 16 | 6 | 2 | 8 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0006 | 0/0 | 5333 | 13 | 7 | 5 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0007 | 0/0 | 5332 | 11 | 11 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0008 | 0/0 | 5333 | 11 | 0 | 10 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0009 | 0/0 | 5333 | 11 | 10 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0010 | 0/0 | 5333 | 6 | 6 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0011 | 0/0 | 5338 | 5 | 0 | 0 | 5 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0012 | 0/0 | 5333 | 5 | 5 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0013 | 0/0 | 5332 | 5 | 4 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0014 | 0/0 | 5333 | 4 | 0 | 0 | 4 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0015 | 0/0 | 5328 | 4 | 4 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0016 | 0/0 | 5334 | 4 | 0 | 0 | 4 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0017 | 0/0 | 5332 | 4 | 0 | 0 | 3 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0018 | 0/0 | 5332 | 3 | 0 | 0 | 3 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0019 | 0/0 | 5333 | 2 | 0 | 1 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0020 | 0/0 | 5334 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0021 | 0/0 | 5332 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0022 | 0/0 | 5334 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0023 | 0/0 | 5333 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0024 | 0/0 | 5332 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0025 | 0/0 | 5333 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0026 | 0/0 | 5333 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0027 | 0/0 | 5333 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0028 | 0/0 | 5333 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0029 | 0/0 | 5333 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0030 | 0/0 | 5333 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0031 | 0/0 | 5332 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0032 | 0/0 | 5332 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0033 | 0/0 | 5332 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0034 | 0/0 | 5332 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0035 | 0/0 | 5332 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0036 | 0/0 | 5334 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0037 | 0/0 | 5332 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0038 | 0/0 | 5333 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
t0039 | 0/0 | 5333 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
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 | 5 | 0 | 1 | 0 | 2 | 2 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0002 | 0/0 | 4 | 1 | 0 | 0 | 3 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0015 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
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 | 1257 | 387 | 86 | 62 | 188 | 11 | 38 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0002 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0003 | 0/0 | 1257 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0002c0004 | 0/0 | 1257 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6588 | 103 | 19 | 11 | 61 | 0 | 12 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0002 | 0/1 | 6589 | 64 | 2 | 22 | 17 | 6 | 16 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0003 | 1/0 | 6589 | 54 | 4 | 6 | 41 | 1 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0004 | 0/0 | 6590 | 42 | 4 | 1 | 29 | 3 | 5 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0005 | 0/0 | 6588 | 16 | 6 | 2 | 8 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0006 | 0/0 | 6589 | 12 | 6 | 5 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0007 | 0/0 | 6588 | 11 | 11 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0008 | 0/0 | 6589 | 11 | 0 | 10 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0009 | 0/0 | 6589 | 11 | 10 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0010 | 0/0 | 6589 | 5 | 5 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0011 | 0/0 | 6594 | 5 | 0 | 0 | 5 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0012 | 0/0 | 6589 | 5 | 5 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0013 | 0/0 | 6588 | 5 | 4 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0014 | 0/0 | 6589 | 4 | 0 | 0 | 4 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0015 | 0/0 | 6584 | 4 | 4 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0016 | 0/0 | 6590 | 4 | 0 | 0 | 4 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0017 | 0/0 | 6588 | 4 | 0 | 0 | 3 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0018 | 0/0 | 6588 | 3 | 0 | 0 | 3 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0019 | 0/0 | 6589 | 2 | 0 | 1 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0020 | 0/0 | 6590 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0021 | 0/0 | 6588 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0022 | 0/0 | 6590 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0023 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0024 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0025 | 0/0 | 6589 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0026 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0027 | 0/0 | 6589 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0028 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0029 | 0/0 | 6589 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0030 | 0/0 | 6589 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0031 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0032 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0033 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0034 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0035 | 0/0 | 6588 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0036 | 0/0 | 6590 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0037 | 0/0 | 6588 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0038 | 0/0 | 6589 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0001t0039 | 0/0 | 6589 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0002t0010 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0001c0003t0002 | 0/0 | 6589 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
a0002c0004t0006 | 0/0 | 6589 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | copy fasta | chr2 | 113885089 | 113967596 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0001g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0002 | 0/0 | 3 | 0 | 0 | 0 | 3 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0015 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0161 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0003 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0012 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0086 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0001 | 0/0 | 5 | 0 | 1 | 0 | 2 | 2 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0004g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0026 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0328 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0332 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0005g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0006g0006 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0006g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0006g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0006g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0006g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0006g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0006g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0006g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0006g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0006g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0007g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0007g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0007g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0007g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0007g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0007g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0007g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0007g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0007g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0008g0005 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0008g0013 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0008g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0008g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0008g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0008g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0008g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0008g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0009g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0009g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0009g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0009g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0009g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0009g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0009g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0009g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0009g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0010g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0010g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0010g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0010g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0011g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0011g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0011g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0011g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0012g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0012g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0012g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0012g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0013g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0013g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0013g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0013g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0013g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0014g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0014g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0014g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0015g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0015g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0015g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0015g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0016g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0016g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0016g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0016g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0017g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0017g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0017g0299 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0017g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0018g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0018g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0018g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0019g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0019g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0020g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0020g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0021g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0021g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0022g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0023g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0024g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0025g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0026g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0027g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0028g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0029g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0030g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0031g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0032g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0033g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0034g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0035g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0036g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0037g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0038g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0001t0039g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0002t0010g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0001c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
a0002c0004t0006g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0001 | EUR | GBR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00140 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | GBR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00140 | hp2 | a0001 | c0001 | t0004 | g0136 | EUR | GBR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00280 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00280 | hp2 | a0001 | c0001 | t0004 | g0001 | EUR | FIN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0304 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0253 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0090 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00544 | hp1 | a0001 | c0001 | t0018 | g0320 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00544 | hp2 | a0001 | c0001 | t0004 | g0049 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00597 | hp1 | a0001 | c0001 | t0004 | g0042 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00609 | hp2 | a0001 | c0001 | t0005 | g0332 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00621 | hp1 | a0001 | c0001 | t0004 | g0048 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00639 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00733 | hp1 | a0001 | c0001 | t0029 | g0095 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00733 | hp2 | a0001 | c0001 | t0002 | g0194 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00735 | hp1 | a0001 | c0001 | t0008 | g0115 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0099 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00738 | hp1 | a0001 | c0001 | t0008 | g0013 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00738 | hp2 | a0001 | c0001 | t0006 | g0226 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00741 | hp1 | a0001 | c0001 | t0006 | g0227 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG00741 | hp2 | a0001 | c0001 | t0008 | g0005 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0109 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0187 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0103 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01070 | hp2 | a0001 | c0001 | t0019 | g0177 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0275 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01099 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0167 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0083 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0241 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01167 | hp1 | a0001 | c0001 | t0005 | g0328 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0101 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0092 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01243 | hp1 | a0001 | c0001 | t0013 | g0216 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01243 | hp2 | a0001 | c0001 | t0009 | g0130 | AMR | PUR | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0037 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01256 | hp2 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0102 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01257 | hp2 | a0001 | c0001 | t0025 | g0162 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01258 | hp1 | a0001 | c0001 | t0006 | g0006 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0094 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01261 | hp1 | a0001 | c0001 | t0008 | g0119 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01261 | hp2 | a0001 | c0001 | t0002 | g0191 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01358 | hp1 | a0001 | c0001 | t0004 | g0001 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01358 | hp2 | a0001 | c0001 | t0003 | g0072 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0169 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0105 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01433 | hp1 | a0001 | c0001 | t0008 | g0013 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0181 | AMR | CLM | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0186 | EUR | IBS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0107 | EUR | IBS | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01884 | hp2 | a0001 | c0001 | t0012 | g0056 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0339 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0116 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01928 | hp2 | a0001 | c0001 | t0008 | g0005 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0270 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01943 | hp2 | a0001 | c0001 | t0008 | g0075 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0178 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01952 | hp2 | a0001 | c0001 | t0008 | g0118 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01981 | hp1 | a0001 | c0001 | t0005 | g0330 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01981 | hp2 | a0001 | c0001 | t0003 | g0012 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01993 | hp1 | a0001 | c0001 | t0008 | g0005 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0189 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0273 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02004 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02027 | hp1 | a0001 | c0001 | t0004 | g0047 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02040 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02055 | hp1 | a0001 | c0001 | t0013 | g0220 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0088 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02056 | hp2 | a0001 | c0001 | t0004 | g0044 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02071 | hp2 | a0001 | c0001 | t0003 | g0084 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0235 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0314 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0087 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02129 | hp2 | a0001 | c0001 | t0019 | g0039 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0319 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02135 | hp2 | a0001 | c0001 | t0005 | g0326 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0327 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02145 | hp2 | a0001 | c0001 | t0004 | g0208 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0269 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02148 | hp2 | a0001 | c0001 | t0008 | g0124 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02165 | hp1 | a0001 | c0001 | t0014 | g0004 | EAS | CDX | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | CDX | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02257 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0240 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02258 | hp1 | a0001 | c0001 | t0009 | g0131 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02258 | hp2 | a0001 | c0001 | t0013 | g0211 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0018 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02280 | hp1 | a0001 | c0001 | t0006 | g0224 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02280 | hp2 | a0001 | c0001 | t0007 | g0349 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0085 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0278 | AMR | PEL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02451 | hp1 | a0001 | c0001 | t0026 | g0002 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02451 | hp2 | a0001 | c0001 | t0013 | g0210 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0140 | EAS | KHV | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0174 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0036 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02615 | hp1 | a0001 | c0001 | t0015 | g0028 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02615 | hp2 | a0001 | c0001 | t0009 | g0111 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02622 | hp1 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02622 | hp2 | a0001 | c0002 | t0010 | g0019 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02647 | hp1 | a0001 | c0001 | t0009 | g0008 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02647 | hp2 | a0001 | c0001 | t0010 | g0199 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0183 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02698 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0206 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0068 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0266 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02723 | hp2 | a0001 | c0001 | t0007 | g0345 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02735 | hp2 | a0001 | c0001 | t0004 | g0153 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02738 | hp1 | a0001 | c0001 | t0004 | g0157 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0192 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0286 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02809 | hp2 | a0001 | c0001 | t0028 | g0058 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02818 | hp1 | a0001 | c0001 | t0015 | g0342 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0060 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02886 | hp2 | a0001 | c0001 | t0010 | g0198 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02895 | hp1 | a0001 | c0001 | t0010 | g0019 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0026 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02896 | hp1 | a0001 | c0001 | t0003 | g0069 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02896 | hp2 | a0001 | c0001 | t0012 | g0055 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0070 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0334 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02965 | hp2 | a0001 | c0001 | t0010 | g0197 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02970 | hp1 | a0001 | c0001 | t0012 | g0057 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02970 | hp2 | a0001 | c0001 | t0010 | g0200 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02976 | hp1 | a0001 | c0001 | t0012 | g0054 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0242 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0305 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0155 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0237 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0230 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03139 | hp2 | a0001 | c0001 | t0007 | g0215 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03195 | hp1 | a0001 | c0001 | t0013 | g0219 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0218 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03209 | hp2 | a0001 | c0001 | t0006 | g0228 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03225 | hp1 | a0001 | c0001 | t0009 | g0128 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03225 | hp2 | a0001 | c0001 | t0006 | g0223 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0164 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0322 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03453 | hp2 | a0001 | c0001 | t0035 | g0352 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0346 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0333 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03516 | hp1 | a0001 | c0001 | t0023 | g0222 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0209 | AFR | ESN | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03540 | hp1 | a0001 | c0001 | t0007 | g0217 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03540 | hp2 | a0001 | c0001 | t0024 | g0348 | AFR | GWD | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0350 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0104 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0050 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0303 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03688 | hp1 | a0001 | c0001 | t0030 | g0113 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0318 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0023 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03704 | hp2 | a0001 | c0001 | t0004 | g0137 | SAS | PJL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03831 | hp2 | a0001 | c0001 | t0036 | g0038 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03834 | hp1 | a0001 | c0001 | t0039 | g0106 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0190 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0065 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0256 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0205 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0193 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0290 | SAS | BEB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0250 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0163 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG04204 | hp1 | a0001 | c0001 | t0017 | g0299 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0001 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0317 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0125 | SAS | STU | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18522 | hp1 | a0001 | c0001 | t0004 | g0207 | AFR | YRI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0347 | AFR | YRI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18612 | hp1 | a0001 | c0001 | t0003 | g0052 | EAS | CHB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0146 | EAS | CHB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | CHB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | CHB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18939 | hp2 | a0001 | c0001 | t0004 | g0144 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18940 | hp1 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18940 | hp2 | a0001 | c0001 | t0004 | g0134 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18941 | hp2 | a0001 | c0001 | t0014 | g0004 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18942 | hp1 | a0001 | c0001 | t0020 | g0149 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18943 | hp1 | a0001 | c0001 | t0004 | g0201 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18945 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18945 | hp2 | a0001 | c0001 | t0011 | g0025 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18947 | hp1 | a0001 | c0001 | t0022 | g0043 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0170 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18948 | hp1 | a0001 | c0001 | t0003 | g0121 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0073 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18953 | hp1 | a0001 | c0001 | t0038 | g0297 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18957 | hp2 | a0001 | c0001 | t0016 | g0151 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18959 | hp1 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18959 | hp2 | a0001 | c0001 | t0004 | g0129 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18960 | hp1 | a0001 | c0001 | t0016 | g0150 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0061 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18961 | hp2 | a0001 | c0001 | t0005 | g0337 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18962 | hp2 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18964 | hp1 | a0001 | c0001 | t0003 | g0117 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18968 | hp1 | a0001 | c0001 | t0004 | g0041 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0267 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0016 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0344 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0123 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18972 | hp2 | a0001 | c0001 | t0005 | g0329 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18973 | hp1 | a0001 | c0001 | t0018 | g0302 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18973 | hp2 | a0001 | c0001 | t0004 | g0046 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18979 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18981 | hp1 | a0001 | c0001 | t0011 | g0025 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18981 | hp2 | a0001 | c0001 | t0016 | g0156 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0045 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18982 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18983 | hp1 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0281 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18986 | hp1 | a0001 | c0001 | t0014 | g0097 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18986 | hp2 | a0001 | c0001 | t0033 | g0024 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18988 | hp1 | a0001 | c0001 | t0003 | g0077 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18988 | hp2 | a0001 | c0001 | t0037 | g0020 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18989 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18989 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0080 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18992 | hp1 | a0001 | c0001 | t0011 | g0306 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18992 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18993 | hp1 | a0001 | c0001 | t0021 | g0298 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18993 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18994 | hp1 | a0001 | c0001 | t0005 | g0340 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18995 | hp1 | a0001 | c0001 | t0017 | g0289 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18997 | hp1 | a0001 | c0001 | t0018 | g0316 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0064 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18998 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18998 | hp2 | a0001 | c0001 | t0031 | g0007 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19000 | hp1 | a0001 | c0001 | t0003 | g0120 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0133 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19002 | hp1 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19002 | hp2 | a0001 | c0001 | t0032 | g0301 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19003 | hp2 | a0001 | c0001 | t0005 | g0336 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19004 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19005 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19005 | hp2 | a0001 | c0001 | t0011 | g0291 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0247 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19006 | hp2 | a0001 | c0001 | t0027 | g0173 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19009 | hp2 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19010 | hp1 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0067 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0014 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19030 | hp2 | a0001 | c0001 | t0009 | g0160 | AFR | LWK | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19043 | hp1 | a0002 | c0004 | t0006 | g0229 | AFR | LWK | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19043 | hp2 | a0001 | c0001 | t0015 | g0343 | AFR | LWK | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19054 | hp1 | a0001 | c0001 | t0003 | g0003 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19055 | hp2 | a0001 | c0001 | t0017 | g0311 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19058 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0100 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0011 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19062 | hp1 | a0001 | c0001 | t0002 | g0093 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19063 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19063 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19065 | hp1 | a0001 | c0001 | t0016 | g0139 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19067 | hp1 | a0001 | c0001 | t0002 | g0168 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19067 | hp2 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19077 | hp1 | a0001 | c0001 | t0005 | g0331 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19077 | hp2 | a0001 | c0001 | t0011 | g0312 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19078 | hp1 | a0001 | c0001 | t0002 | g0091 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19078 | hp2 | a0001 | c0001 | t0021 | g0321 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19080 | hp1 | a0001 | c0001 | t0003 | g0089 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19082 | hp1 | a0001 | c0001 | t0014 | g0108 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19082 | hp2 | a0001 | c0001 | t0003 | g0079 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0114 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19086 | hp1 | a0001 | c0001 | t0017 | g0288 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19086 | hp2 | a0001 | c0001 | t0008 | g0078 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19087 | hp1 | a0001 | c0001 | t0003 | g0195 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19090 | hp2 | a0001 | c0001 | t0004 | g0159 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19091 | hp1 | a0001 | c0001 | t0020 | g0135 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19240 | hp1 | a0001 | c0001 | t0009 | g0059 | AFR | YRI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0221 | AFR | YRI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA20129 | hp1 | a0001 | c0001 | t0005 | g0335 | AFR | ASW | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ASW | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA20752 | hp1 | a0001 | c0003 | t0002 | g0127 | EUR | TSI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA20752 | hp2 | a0001 | c0001 | t0003 | g0196 | EUR | TSI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA20805 | hp1 | a0001 | c0001 | t0006 | g0225 | EUR | TSI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0179 | EUR | TSI | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0203 | SAS | GIH | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0262 | SAS | GIH | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02109 | hp1 | a0001 | c0001 | t0006 | g0231 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02486 | hp1 | a0001 | c0001 | t0007 | g0212 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0015 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG02559 | hp2 | a0001 | c0001 | t0007 | g0213 | AFR | ACB | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03471 | hp1 | a0001 | c0001 | t0012 | g0053 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0338 | AFR | MSL | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG06807 | hp1 | a0001 | c0001 | t0009 | g0132 | AFR | USA | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
HG06807 | hp2 | a0001 | c0001 | t0015 | g0341 | AFR | USA | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0040 | EAS | JPT | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA20300 | hp1 | a0001 | c0001 | t0007 | g0214 | AFR | USA | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
NA20300 | hp2 | a0001 | c0001 | t0034 | g0351 | AFR | USA | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0161 | REF | REF | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0086 | REF | REF | ACTR3_chr2_113885089_113967596 | ACTR3 | chr2 | 113885089 | 113967596 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:113931368
|
A | G | 1 | a0002 | 1 | NA19043.hp1 | missense_variant | MODERATE | c.404A>G | p.Asn135Ser | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/12 | 595/6589 | 404/1257 | 135/418 | chr2 | 113931368 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:113942200
|
T | C | 1 | a0001c0002 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.699T>C | p.Tyr233Tyr | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/12 | 890/6589 | 699/1257 | 233/418 | chr2 | 113942200 | ||
chr2:113951842
|
G | A | 1 | a0001c0003 | 1 | NA20752.hp1 | synonymous_variant | LOW | c.1074G>A | p.Leu358Leu | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/12 | 1265/6589 | 1074/1257 | 358/418 | chr2 | 113951842 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:113890251
|
G | GGCAGCA | 1 | a0001c0001t0011 | 5 | NA18945.hp2 NA18981.hp1 NA18992.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-18_-13dupCAGCAG | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/12 | 12 | INFO_REALIGN_3_PRIME | chr2 | 113890251 | ||||
chr2:113957745
|
A | G | 1 | a0001c0001t0039 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*290A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 290 | chr2 | 113957745 | |||||
chr2:113957753
|
A | G | 2 | a0001c0001t0017a0001c0001t0038 | 5 | HG04204.hp1 NA18953.hp1 NA18995.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*298A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 298 | chr2 | 113957753 | |||||
chr2:113957767
|
T | C | 1 | a0001c0001t0022 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*312T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 312 | chr2 | 113957767 | |||||
chr2:113957867
|
C | CA | 3 | a0001c0001t0006a0001c0001t0023a0002c0004t0006 | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*415dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 416 | INFO_REALIGN_3_PRIME | chr2 | 113957867 | ||||
chr2:113957892
|
A | G | 1 | a0001c0001t0037 | 1 | NA18988.hp2 | 3_prime_UTR_variant | MODIFIER | c.*437A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 437 | chr2 | 113957892 | |||||
chr2:113957899
|
T | C | 1 | a0001c0001t0024 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*444T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 444 | chr2 | 113957899 | |||||
chr2:113957956
|
G | A | 11 | a0001c0001t0002a0001c0001t0012a0001c0001t0014others(8): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*501G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 501 | chr2 | 113957956 | |||||
chr2:113958093
|
G | A | 1 | a0001c0001t0020 | 2 | NA18942.hp1 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*638G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 638 | chr2 | 113958093 | |||||
chr2:113958133
|
G | A | 1 | a0001c0001t0025 | 1 | HG01257.hp2 | 3_prime_UTR_variant | MODIFIER | c.*678G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 678 | chr2 | 113958133 | |||||
chr2:113958173
|
T | C | 1 | a0001c0001t0030 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*718T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 718 | chr2 | 113958173 | |||||
chr2:113958366
|
G | T | 1 | a0001c0001t0016 | 4 | NA18957.hp2 NA18960.hp1 NA18981.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*911G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 911 | chr2 | 113958366 | |||||
chr2:113958407
|
T | C | 1 | a0001c0001t0026 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*952T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 952 | chr2 | 113958407 | |||||
chr2:113958601
|
GT | G | 19 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(16): Show | 174 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
3_prime_UTR_variant | MODIFIER | c.*1158delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1158 | INFO_REALIGN_3_PRIME | chr2 | 113958601 | ||||
chr2:113958613
|
T | A | 3 | a0001c0001t0006a0001c0001t0023a0002c0004t0006 | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1158T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1158 | chr2 | 113958613 | |||||
chr2:113958730
|
T | C | 1 | a0001c0001t0008 | 11 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1275T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1275 | chr2 | 113958730 | |||||
chr2:113958788
|
G | A | 20 | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(17): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
3_prime_UTR_variant | MODIFIER | c.*1333G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1333 | chr2 | 113958788 | |||||
chr2:113958834
|
A | G | 2 | a0001c0001t0026a0001c0001t0029 | 2 | HG00733.hp1 HG02451.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1379A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1379 | chr2 | 113958834 | |||||
chr2:113958871
|
A | G | 3 | a0001c0001t0007a0001c0001t0013a0001c0001t0024 | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1416A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1416 | chr2 | 113958871 | |||||
chr2:113958971
|
T | C | 1 | a0001c0001t0027 | 1 | NA19006.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1516T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1516 | chr2 | 113958971 | |||||
chr2:113959039
|
A | G | 1 | a0001c0001t0005 | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1584A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1584 | chr2 | 113959039 | |||||
chr2:113959343
|
A | C | 8 | a0001c0001t0006a0001c0001t0007a0001c0001t0013others(5): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1888A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1888 | chr2 | 113959343 | |||||
chr2:113959407
|
C | T | 1 | a0001c0001t0033 | 1 | NA18986.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1952C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1952 | chr2 | 113959407 | |||||
chr2:113959408
|
G | A | 1 | a0001c0001t0019 | 2 | HG01070.hp2 HG02129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1953G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 1953 | chr2 | 113959408 | |||||
chr2:113959507
|
G | A | 1 | a0001c0001t0031 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2052G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 2052 | chr2 | 113959507 | |||||
chr2:113960037
|
G | A | 1 | a0001c0001t0029 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2582G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 2582 | chr2 | 113960037 | |||||
chr2:113960225
|
G | C | 1 | a0001c0001t0032 | 1 | NA19002.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2770G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 2770 | chr2 | 113960225 | |||||
chr2:113960324
|
G | A | 2 | a0001c0001t0010a0001c0002t0010 | 6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2869G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 2869 | chr2 | 113960324 | |||||
chr2:113960466
|
A | G | 3 | a0001c0001t0006a0001c0001t0023a0002c0004t0006 | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3011A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3011 | chr2 | 113960466 | |||||
chr2:113960705
|
A | G | 2 | a0001c0001t0034a0001c0001t0035 | 2 | HG03453.hp2 NA20300.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3250A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3250 | chr2 | 113960705 | |||||
chr2:113960731
|
A | G | 1 | a0001c0001t0036 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3276A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3276 | chr2 | 113960731 | |||||
chr2:113960776
|
C | G | 3 | a0001c0001t0006a0001c0001t0023a0002c0004t0006 | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3321C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3321 | chr2 | 113960776 | |||||
chr2:113960794
|
C | T | 3 | a0001c0001t0006a0001c0001t0023a0002c0004t0006 | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*3339C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3339 | chr2 | 113960794 | |||||
chr2:113960895
|
A | G | 1 | a0001c0001t0021 | 2 | NA18993.hp1 NA19078.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3440A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3440 | chr2 | 113960895 | |||||
chr2:113960925
|
A | G | 1 | a0001c0001t0035 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3470A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3470 | chr2 | 113960925 | |||||
chr2:113961316
|
C | G | 6 | a0001c0001t0004a0001c0001t0009a0001c0001t0016others(3): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*3861C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3861 | chr2 | 113961316 | |||||
chr2:113961449
|
A | G | 1 | a0001c0001t0028 | 1 | HG02809.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3994A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 3994 | chr2 | 113961449 | |||||
chr2:113961456
|
C | T | 1 | a0001c0001t0008 | 11 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4001C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4001 | chr2 | 113961456 | |||||
chr2:113961690
|
A | G | 1 | a0001c0001t0023 | 1 | HG03516.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4235A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4235 | chr2 | 113961690 | |||||
chr2:113961782
|
G | A | 1 | a0001c0001t0013 | 5 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4327G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4327 | chr2 | 113961782 | |||||
chr2:113961874
|
A | G | 9 | a0001c0001t0002a0001c0001t0014a0001c0001t0019others(6): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
3_prime_UTR_variant | MODIFIER | c.*4419A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4419 | chr2 | 113961874 | |||||
chr2:113961913
|
CTAAG | C | 1 | a0001c0001t0015 | 4 | HG02615.hp1 HG02818.hp1 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4460_*4463delAAGT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4460 | INFO_REALIGN_3_PRIME | chr2 | 113961913 | ||||
chr2:113962362
|
T | C | 1 | a0001c0001t0018 | 3 | HG00544.hp1 NA18973.hp1 NA18997.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4907T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4907 | chr2 | 113962362 | |||||
chr2:113962402
|
T | C | 1 | a0001c0001t0014 | 4 | HG02165.hp1 NA18941.hp2 NA18986.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4947T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 4947 | chr2 | 113962402 | |||||
chr2:113962555
|
A | AT | 5 | a0001c0001t0004a0001c0001t0016a0001c0001t0020others(2): Show | 50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*5102dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 5103 | INFO_REALIGN_3_PRIME | chr2 | 113962555 | ||||
chr2:113962570
|
C | A | 1 | a0001c0001t0029 | 1 | HG00733.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5115C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 12/12 | 5115 | chr2 | 113962570 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:113890346
|
G | A | 7 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(4): Show | 7 | HG00609.hp1 NA18951.hp1 NA18955.hp1 others(4): Show |
intron_variant | MODIFIER | c.44+23G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890346 | ||||||
chr2:113890359
|
G | A | 1 | a0001c0001t0002g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.44+36G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890359 | ||||||
chr2:113890368
|
A | G | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.44+45A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890368 | ||||||
chr2:113890394
|
C | T | 6 | a0001c0001t0007g0345a0001c0001t0007g0346a0001c0001t0007g0347others(3): Show | 6 | HG02280.hp2 HG02723.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+71C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890394 | ||||||
chr2:113890495
|
C | T | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(20): Show | 25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+172C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890495 | ||||||
chr2:113890504
|
C | T | 111 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(108): Show | 116 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(113): Show |
intron_variant | MODIFIER | c.44+181C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890504 | ||||||
chr2:113890535
|
C | G | 1 | a0001c0001t0001g0325 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.44+212C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113890535 | ||||||
chr2:113891295
|
A | G | 1 | a0001c0001t0035g0352 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.44+972A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891295 | ||||||
chr2:113891323
|
G | T | 165 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(162): Show | 174 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.44+1000G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891323 | ||||||
chr2:113891456
|
AGAGAATA others(4): Show |
A | 1 | a0001c0001t0002g0037 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.44+1134_44+1144del others(11): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891456 | ||||||
chr2:113891499
|
G | C | 165 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(162): Show | 174 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.44+1176G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891499 | ||||||
chr2:113891519
|
G | T | 165 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(162): Show | 174 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.44+1196G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891519 | ||||||
chr2:113891573
|
T | TA | 134 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(131): Show | 141 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.44+1250_44+1251ins others(1): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891573 | ||||||
chr2:113891615
|
C | CT | 6 | a0001c0001t0001g0324a0001c0001t0004g0206a0001c0001t0004g0207others(3): Show | 6 | HG02145.hp2 HG02717.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.44+1302dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113891615 | |||||
chr2:113891643
|
T | C | 1 | a0001c0001t0005g0326 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.44+1320T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891643 | ||||||
chr2:113891790
|
C | T | 2 | a0001c0001t0001g0323a0001c0001t0002g0205 | 2 | HG02015.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.44+1467C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891790 | ||||||
chr2:113891962
|
T | G | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.44+1639T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113891962 | ||||||
chr2:113892328
|
G | A | 165 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(162): Show | 174 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.44+2005G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113892328 | ||||||
chr2:113892589
|
G | A | 1 | a0001c0001t0036g0038 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.44+2266G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113892589 | ||||||
chr2:113892679
|
T | G | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(20): Show | 25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+2356T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113892679 | ||||||
chr2:113892911
|
A | G | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.44+2588A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113892911 | ||||||
chr2:113892992
|
A | G | 1 | a0001c0001t0002g0203 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.44+2669A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113892992 | ||||||
chr2:113893141
|
T | C | 1 | a0001c0001t0019g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.44+2818T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893141 | ||||||
chr2:113893190
|
A | T | 1 | a0001c0001t0002g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.44+2867A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893190 | ||||||
chr2:113893256
|
CG | C | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+2934delG | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893256 | ||||||
chr2:113893288
|
TTTTG | T | 134 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(131): Show | 141 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.44+2985_44+2988del others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113893288 | |||||
chr2:113893388
|
G | C | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+3065G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893388 | ||||||
chr2:113893398
|
A | G | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.44+3075A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893398 | ||||||
chr2:113893468
|
C | A | 165 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(162): Show | 174 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(171): Show |
intron_variant | MODIFIER | c.44+3145C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893468 | ||||||
chr2:113893581
|
C | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.44+3258C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893581 | ||||||
chr2:113893584
|
G | C | 10 | a0001c0001t0004g0040a0001c0001t0004g0041a0001c0001t0004g0042others(7): Show | 10 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(7): Show |
intron_variant | MODIFIER | c.44+3261G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893584 | ||||||
chr2:113893607
|
A | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+3284A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893607 | ||||||
chr2:113893657
|
G | A | 8 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(5): Show | 10 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.44+3334G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893657 | ||||||
chr2:113893783
|
A | T | 1 | a0001c0001t0004g0201 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.44+3460A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893783 | ||||||
chr2:113893807
|
C | T | 1 | a0001c0001t0015g0343 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.44+3484C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893807 | ||||||
chr2:113893827
|
A | G | 6 | a0001c0001t0010g0019a0001c0001t0010g0197a0001c0001t0010g0198others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.44+3504A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893827 | ||||||
chr2:113893851
|
G | A | 1 | a0001c0001t0006g0228 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.44+3528G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893851 | ||||||
chr2:113893949
|
C | T | 1 | a0001c0001t0003g0196 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.44+3626C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113893949 | ||||||
chr2:113894080
|
A | G | 1 | a0001c0001t0001g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.44+3757A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894080 | ||||||
chr2:113894089
|
G | C | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.44+3766G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894089 | ||||||
chr2:113894093
|
C | CT | 6 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0284others(3): Show | 6 | HG01884.hp1 HG02809.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.44+3783dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113894093 | |||||
chr2:113894093
|
CT | C | 51 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(48): Show | 54 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.44+3783delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113894093 | |||||
chr2:113894143
|
G | A | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.44+3820G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894143 | ||||||
chr2:113894175
|
C | T | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.44+3852C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894175 | ||||||
chr2:113894188
|
G | A | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(20): Show | 25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+3865G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894188 | ||||||
chr2:113894279
|
G | T | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.44+3956G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894279 | ||||||
chr2:113894295
|
G | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+3972G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894295 | ||||||
chr2:113894300
|
C | T | 1 | a0001c0001t0002g0194 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.44+3977C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894300 | ||||||
chr2:113894302
|
A | G | 38 | a0001c0001t0002g0018a0001c0001t0002g0050a0001c0001t0002g0161others(35): Show | 39 | HG00438.hp1 HG00733.hp2 HG01069.hp2 others(36): Show |
intron_variant | MODIFIER | c.44+3979A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894302 | ||||||
chr2:113894363
|
G | A | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.44+4040G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894363 | ||||||
chr2:113894434
|
T | C | 1 | a0001c0001t0002g0051 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.44+4111T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894434 | ||||||
chr2:113894552
|
T | C | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.44+4229T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894552 | ||||||
chr2:113894600
|
TTG | T | 51 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(48): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.44+4281_44+4282del others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113894600 | |||||
chr2:113894621
|
G | A | 1 | a0001c0001t0019g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.44+4298G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894621 | ||||||
chr2:113894891
|
C | T | 1 | a0001c0001t0009g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.44+4568C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113894891 | ||||||
chr2:113894980
|
C | CA | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.44+4666dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113894980 | |||||
chr2:113895058
|
T | A | 1 | a0001c0001t0001g0232 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.44+4735T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895058 | ||||||
chr2:113895059
|
T | C | 1 | a0001c0001t0003g0052 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.44+4736T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895059 | ||||||
chr2:113895059
|
T | TC | 33 | a0001c0001t0002g0125a0001c0001t0002g0126a0001c0001t0002g0190others(30): Show | 36 | HG00544.hp2 HG00735.hp1 HG00741.hp2 others(33): Show |
intron_variant | MODIFIER | c.44+4746dupC | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113895059 | |||||
chr2:113895059
|
TC | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 143 | HG00408.hp1 HG00408.hp2 HG00609.hp1 others(140): Show |
intron_variant | MODIFIER | c.44+4746delC | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113895059 | |||||
chr2:113895069
|
C | A | 1 | a0001c0001t0001g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.44+4746C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895069 | ||||||
chr2:113895070
|
A | C | 1 | a0001c0001t0001g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.44+4747A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895070 | ||||||
chr2:113895077
|
T | C | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.44+4754T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895077 | ||||||
chr2:113895493
|
A | ACCC | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.44+5172_44+5174dup others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113895493 | |||||
chr2:113895623
|
G | A | 6 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0012g0055others(3): Show | 6 | HG01884.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.44+5300G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895623 | ||||||
chr2:113895697
|
T | A | 55 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(52): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.44+5374T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895697 | ||||||
chr2:113895706
|
G | A | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(20): Show | 25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+5383G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895706 | ||||||
chr2:113895708
|
G | A | 6 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0012g0055others(3): Show | 6 | HG01884.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.44+5385G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895708 | ||||||
chr2:113895721
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.44+5398C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895721 | ||||||
chr2:113895801
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.44+5478A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895801 | ||||||
chr2:113895808
|
C | T | 1 | a0001c0001t0001g0317 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.44+5485C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113895808 | ||||||
chr2:113895932
|
C | CACTGCAT others(6): Show |
1 | a0001c0001t0002g0189 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.44+5613_44+5625dup others(13): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113895932 | |||||
chr2:113896008
|
GCCA | G | 41 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(38): Show | 44 | HG00408.hp1 HG00544.hp1 HG02015.hp1 others(41): Show |
intron_variant | MODIFIER | c.44+5689_44+5691del others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113896008 | |||||
chr2:113896238
|
A | G | 1 | a0001c0001t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.44+5915A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113896238 | ||||||
chr2:113896294
|
A | T | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.44+5971A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113896294 | ||||||
chr2:113896408
|
A | AGG | 10 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(7): Show | 10 | HG01099.hp1 HG01167.hp2 HG01168.hp1 others(7): Show |
intron_variant | MODIFIER | c.44+6086_44+6087dup others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113896408 | |||||
chr2:113896439
|
C | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+6116C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113896439 | ||||||
chr2:113896625
|
G | A | 1 | a0001c0001t0001g0234 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.44+6302G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113896625 | ||||||
chr2:113896875
|
A | C | 1 | a0001c0001t0002g0110 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.44+6552A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113896875 | ||||||
chr2:113896950
|
G | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.44+6627G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113896950 | ||||||
chr2:113897171
|
G | A | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.44+6848G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897171 | ||||||
chr2:113897373
|
A | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.44+7050A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897373 | ||||||
chr2:113897515
|
GTTATTT | G | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.44+7195_44+7200del others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113897515 | |||||
chr2:113897515
|
GTTATTTT | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(109): Show | 118 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.44+7195_44+7201del others(7): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113897515 | |||||
chr2:113897518
|
A | AT | 13 | a0001c0001t0003g0090a0001c0001t0004g0046a0001c0001t0004g0047others(10): Show | 13 | HG00438.hp2 HG00621.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.44+7221dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113897518 | |||||
chr2:113897518
|
AT | A | 57 | a0001c0001t0002g0188a0001c0001t0002g0203a0001c0001t0003g0003others(54): Show | 68 | HG00735.hp1 HG00738.hp1 HG00741.hp2 others(65): Show |
intron_variant | MODIFIER | c.44+7221delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113897518 | |||||
chr2:113897518
|
ATT | A | 67 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(64): Show | 72 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(69): Show |
intron_variant | MODIFIER | c.44+7220_44+7221del others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113897518 | |||||
chr2:113897522
|
T | A | 4 | a0001c0001t0001g0035a0001c0001t0001g0315a0001c0001t0001g0318others(1): Show | 4 | HG03688.hp2 NA18955.hp1 NA18997.hp1 others(1): Show |
intron_variant | MODIFIER | c.44+7199T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897522 | ||||||
chr2:113897523
|
T | A | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.44+7200T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897523 | ||||||
chr2:113897524
|
T | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(109): Show | 118 | HG00408.hp2 HG00609.hp2 HG00639.hp1 others(115): Show |
intron_variant | MODIFIER | c.44+7201T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897524 | ||||||
chr2:113897525
|
T | A | 1 | a0001c0001t0001g0281 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.44+7202T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897525 | ||||||
chr2:113897613
|
G | A | 2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.44+7290G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897613 | ||||||
chr2:113897652
|
G | A | 1 | a0001c0001t0005g0340 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.44+7329G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897652 | ||||||
chr2:113897827
|
A | G | 5 | a0001c0001t0001g0028a0001c0001t0015g0028a0001c0001t0015g0341others(2): Show | 5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+7504A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113897827 | ||||||
chr2:113898009
|
G | A | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(20): Show | 25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+7686G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898009 | ||||||
chr2:113898024
|
G | A | 55 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(52): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.44+7701G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898024 | ||||||
chr2:113898239
|
A | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.44+7916A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898239 | ||||||
chr2:113898513
|
T | C | 1 | a0001c0001t0003g0062 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.44+8190T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898513 | ||||||
chr2:113898544
|
A | G | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.44+8221A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898544 | ||||||
chr2:113898556
|
T | C | 1 | a0001c0001t0001g0325 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.44+8233T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898556 | ||||||
chr2:113898599
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.44+8276A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898599 | ||||||
chr2:113898698
|
C | T | 1 | a0001c0003t0002g0127 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.44+8375C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898698 | ||||||
chr2:113898725
|
A | T | 1 | a0001c0001t0002g0107 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.44+8402A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898725 | ||||||
chr2:113898751
|
A | G | 1 | a0001c0001t0003g0083 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.44+8428A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898751 | ||||||
chr2:113898878
|
G | A | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.44+8555G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898878 | ||||||
chr2:113898927
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.44+8604T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898927 | ||||||
chr2:113898934
|
G | T | 3 | a0001c0001t0003g0082a0001c0001t0003g0122a0001c0001t0003g0123 | 3 | NA18940.hp1 NA18959.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.44+8611G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113898934 | ||||||
chr2:113899008
|
A | G | 2 | a0001c0001t0004g0047a0001c0001t0004g0048 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.44+8685A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899008 | ||||||
chr2:113899263
|
T | C | 8 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(5): Show | 10 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.44+8940T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899263 | ||||||
chr2:113899295
|
T | G | 1 | a0001c0001t0001g0233 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.44+8972T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899295 | ||||||
chr2:113899327
|
A | G | 55 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(52): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.44+9004A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899327 | ||||||
chr2:113899352
|
A | G | 5 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0192others(2): Show | 5 | HG00733.hp2 HG01069.hp2 HG01517.hp1 others(2): Show |
intron_variant | MODIFIER | c.44+9029A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899352 | ||||||
chr2:113899379
|
T | TA | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.44+9063dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113899379 | |||||
chr2:113899392
|
G | T | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.44+9069G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899392 | ||||||
chr2:113899506
|
G | T | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+9183G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899506 | ||||||
chr2:113899619
|
G | C | 1 | a0001c0001t0001g0029 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.44+9296G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899619 | ||||||
chr2:113899761
|
G | A | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.44+9438G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899761 | ||||||
chr2:113899774
|
T | C | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(20): Show | 25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.44+9451T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899774 | ||||||
chr2:113899808
|
G | A | 2 | a0001c0001t0002g0192a0001c0001t0002g0194 | 2 | HG00733.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.44+9485G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899808 | ||||||
chr2:113899877
|
C | G | 1 | a0001c0001t0001g0317 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.44+9554C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899877 | ||||||
chr2:113899898
|
G | A | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.44+9575G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113899898 | ||||||
chr2:113900340
|
G | A | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.44+10017G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113900340 | ||||||
chr2:113900525
|
G | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+10202G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113900525 | ||||||
chr2:113900676
|
A | G | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.44+10353A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113900676 | ||||||
chr2:113900838
|
G | A | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.44+10515G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113900838 | ||||||
chr2:113901037
|
T | C | 1 | a0001c0001t0004g0208 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.44+10714T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901037 | ||||||
chr2:113901085
|
C | T | 1 | a0001c0001t0021g0321 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.44+10762C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901085 | ||||||
chr2:113901226
|
G | C | 2 | a0001c0001t0012g0056a0001c0001t0012g0057 | 2 | HG01884.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.44+10903G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901226 | ||||||
chr2:113901286
|
A | T | 1 | a0001c0001t0001g0027 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.44+10963A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901286 | ||||||
chr2:113901315
|
G | T | 1 | a0001c0001t0001g0027 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.44+10992G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901315 | ||||||
chr2:113901334
|
G | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+11011G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901334 | ||||||
chr2:113901420
|
A | C | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.44+11097A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901420 | ||||||
chr2:113901507
|
A | G | 4 | a0001c0001t0006g0006a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.44+11184A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901507 | ||||||
chr2:113901568
|
A | C | 3 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0209 | 3 | HG02145.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.44+11245A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901568 | ||||||
chr2:113901633
|
A | G | 132 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(129): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.44+11310A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901633 | ||||||
chr2:113901707
|
T | C | 10 | a0001c0001t0009g0008a0001c0001t0009g0059a0001c0001t0009g0060others(7): Show | 11 | HG01884.hp2 HG02257.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.44+11384T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901707 | ||||||
chr2:113901867
|
A | G | 1 | a0001c0001t0009g0060 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.45-11305A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901867 | ||||||
chr2:113901989
|
A | G | 1 | a0001c0001t0003g0121 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.45-11183A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113901989 | ||||||
chr2:113902061
|
G | A | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-11111G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902061 | ||||||
chr2:113902072
|
A | G | 1 | a0001c0001t0001g0267 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.45-11100A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902072 | ||||||
chr2:113902132
|
C | G | 4 | a0001c0001t0006g0228a0001c0001t0006g0230a0001c0001t0006g0231others(1): Show | 4 | HG02109.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-11040C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902132 | ||||||
chr2:113902137
|
T | A | 1 | a0001c0001t0006g0221 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.45-11035T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902137 | ||||||
chr2:113902146
|
C | A | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45-11026C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902146 | ||||||
chr2:113902257
|
C | T | 1 | a0001c0001t0002g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.45-10915C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902257 | ||||||
chr2:113902304
|
G | A | 1 | a0001c0001t0003g0084 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.45-10868G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902304 | ||||||
chr2:113902377
|
T | C | 1 | a0001c0001t0003g0052 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.45-10795T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902377 | ||||||
chr2:113902387
|
T | C | 116 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(113): Show | 121 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(118): Show |
intron_variant | MODIFIER | c.45-10785T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902387 | ||||||
chr2:113902456
|
A | G | 1 | a0001c0001t0005g0336 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.45-10716A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902456 | ||||||
chr2:113902517
|
T | C | 2 | a0001c0001t0003g0009a0001c0001t0003g0063 | 3 | NA18992.hp2 NA19005.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.45-10655T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902517 | ||||||
chr2:113902599
|
G | GT | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.45-10562dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113902599 | |||||
chr2:113902626
|
G | A | 1 | a0001c0001t0001g0235 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.45-10546G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902626 | ||||||
chr2:113902660
|
C | T | 1 | a0001c0001t0006g0006 | 3 | HG00639.hp1 HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.45-10512C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902660 | ||||||
chr2:113902692
|
C | T | 2 | a0001c0001t0006g0230a0001c0001t0006g0231 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.45-10480C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902692 | ||||||
chr2:113902709
|
C | T | 51 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(48): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.45-10463C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902709 | ||||||
chr2:113902716
|
C | G | 1 | a0001c0001t0001g0277 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.45-10456C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902716 | ||||||
chr2:113902809
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.45-10363A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902809 | ||||||
chr2:113902818
|
T | C | 1 | a0001c0001t0001g0235 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.45-10354T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902818 | ||||||
chr2:113902841
|
C | T | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.45-10331C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902841 | ||||||
chr2:113902846
|
G | A | 1 | a0001c0001t0019g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.45-10326G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113902846 | ||||||
chr2:113903012
|
C | T | 1 | a0001c0001t0002g0051 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.45-10160C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903012 | ||||||
chr2:113903042
|
C | G | 1 | a0001c0001t0019g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.45-10130C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903042 | ||||||
chr2:113903097
|
C | A | 1 | a0001c0001t0019g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.45-10075C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903097 | ||||||
chr2:113903114
|
C | T | 6 | a0001c0001t0010g0019a0001c0001t0010g0197a0001c0001t0010g0198others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-10058C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903114 | ||||||
chr2:113903117
|
G | C | 1 | a0001c0001t0005g0327 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.45-10055G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903117 | ||||||
chr2:113903127
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.45-10045A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903127 | ||||||
chr2:113903173
|
C | T | 1 | a0001c0001t0004g0159 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.45-9999C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903173 | ||||||
chr2:113903192
|
G | A | 2 | a0001c0001t0003g0064a0001c0001t0003g0112 | 2 | NA18997.hp2 NA19063.hp2 |
intron_variant | MODIFIER | c.45-9980G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903192 | ||||||
chr2:113903438
|
C | T | 1 | a0001c0001t0028g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.45-9734C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903438 | ||||||
chr2:113903442
|
C | T | 1 | a0001c0001t0001g0034 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.45-9730C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903442 | ||||||
chr2:113903510
|
C | T | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.45-9662C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903510 | ||||||
chr2:113903537
|
CT | C | 144 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(141): Show | 149 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(146): Show |
intron_variant | MODIFIER | c.45-9618delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113903537 | |||||
chr2:113903537
|
CTT | C | 12 | a0001c0001t0001g0022a0001c0001t0001g0030a0001c0001t0006g0006others(9): Show | 15 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.45-9619_45-9618del others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113903537 | |||||
chr2:113903724
|
C | G | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.45-9448C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903724 | ||||||
chr2:113903836
|
C | T | 1 | a0001c0001t0003g0081 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.45-9336C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903836 | ||||||
chr2:113903957
|
T | C | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-9215T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113903957 | ||||||
chr2:113904020
|
C | T | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45-9152C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904020 | ||||||
chr2:113904032
|
T | C | 3 | a0001c0001t0002g0164a0001c0001t0002g0191a0001c0001t0002g0203 | 3 | HG01261.hp2 HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.45-9140T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904032 | ||||||
chr2:113904051
|
G | A | 5 | a0001c0001t0005g0326a0001c0001t0005g0328a0001c0001t0005g0329others(2): Show | 5 | HG01167.hp1 HG01981.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.45-9121G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904051 | ||||||
chr2:113904081
|
C | G | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.45-9091C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904081 | ||||||
chr2:113904111
|
C | T | 6 | a0001c0001t0003g0014a0001c0001t0003g0061a0001c0001t0003g0079others(3): Show | 7 | NA18946.hp2 NA18960.hp2 NA18991.hp2 others(4): Show |
intron_variant | MODIFIER | c.45-9061C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904111 | ||||||
chr2:113904135
|
C | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-9037C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904135 | ||||||
chr2:113904659
|
A | G | 1 | a0001c0001t0003g0121 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.45-8513A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904659 | ||||||
chr2:113904773
|
G | A | 3 | a0001c0001t0003g0079a0001c0001t0003g0089a0001c0001t0003g0120 | 3 | NA19000.hp1 NA19080.hp1 NA19082.hp2 |
intron_variant | MODIFIER | c.45-8399G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904773 | ||||||
chr2:113904933
|
C | G | 1 | a0001c0001t0001g0314 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.45-8239C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904933 | ||||||
chr2:113904937
|
A | G | 1 | a0001c0001t0009g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.45-8235A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113904937 | ||||||
chr2:113905114
|
C | T | 1 | a0001c0001t0005g0335 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.45-8058C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905114 | ||||||
chr2:113905154
|
T | C | 4 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(1): Show | 4 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-8018T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905154 | ||||||
chr2:113905196
|
G | A | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.45-7976G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905196 | ||||||
chr2:113905275
|
G | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.45-7897G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905275 | ||||||
chr2:113905371
|
A | G | 41 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(38): Show | 46 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.45-7801A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905371 | ||||||
chr2:113905422
|
G | A | 1 | a0001c0001t0002g0193 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.45-7750G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905422 | ||||||
chr2:113905427
|
G | A | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.45-7745G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905427 | ||||||
chr2:113905464
|
C | CA | 6 | a0001c0001t0001g0236a0001c0001t0001g0280a0001c0001t0002g0192others(3): Show | 6 | HG02738.hp2 HG03098.hp2 HG03453.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-7693dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113905464 | |||||
chr2:113905464
|
CA | C | 25 | a0001c0001t0001g0274a0001c0001t0001g0275a0001c0001t0001g0276others(22): Show | 25 | HG01099.hp1 HG01167.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.45-7693delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113905464 | |||||
chr2:113905632
|
G | C | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-7540G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905632 | ||||||
chr2:113905849
|
T | TTAA | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.45-7323_45-7322ins others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905849 | ||||||
chr2:113905965
|
A | G | 2 | a0001c0001t0016g0150a0001c0001t0016g0151 | 2 | NA18957.hp2 NA18960.hp1 |
intron_variant | MODIFIER | c.45-7207A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113905965 | ||||||
chr2:113906378
|
C | G | 1 | a0002c0004t0006g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.45-6794C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113906378 | ||||||
chr2:113906739
|
A | G | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.45-6433A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113906739 | ||||||
chr2:113906852
|
G | A | 51 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(48): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.45-6320G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113906852 | ||||||
chr2:113906899
|
G | A | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45-6273G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113906899 | ||||||
chr2:113906993
|
G | C | 1 | a0001c0001t0001g0315 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.45-6179G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113906993 | ||||||
chr2:113907023
|
A | T | 1 | a0001c0001t0001g0266 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.45-6149A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907023 | ||||||
chr2:113907191
|
A | G | 1 | a0001c0001t0011g0312 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.45-5981A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907191 | ||||||
chr2:113907499
|
T | A | 1 | a0001c0001t0001g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.45-5673T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907499 | ||||||
chr2:113907547
|
C | T | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(29): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.45-5625C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907547 | ||||||
chr2:113907654
|
A | G | 1 | a0001c0001t0006g0224 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.45-5518A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907654 | ||||||
chr2:113907856
|
C | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.45-5316C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907856 | ||||||
chr2:113907971
|
T | A | 6 | a0001c0001t0010g0019a0001c0001t0010g0197a0001c0001t0010g0198others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-5201T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907971 | ||||||
chr2:113907971
|
TC | T | 74 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(71): Show | 79 | HG00408.hp2 HG00639.hp1 HG00738.hp2 others(76): Show |
intron_variant | MODIFIER | c.45-5196delC | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113907971 | |||||
chr2:113907975
|
C | CA | 42 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(39): Show | 45 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(42): Show |
intron_variant | MODIFIER | c.45-5197_45-5196ins others(1): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907975 | ||||||
chr2:113907975
|
C | CAA | 7 | a0001c0001t0001g0031a0001c0001t0001g0290a0001c0001t0011g0291others(4): Show | 7 | HG04184.hp2 NA18995.hp1 NA18997.hp1 others(4): Show |
intron_variant | MODIFIER | c.45-5197_45-5196ins others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907975 | ||||||
chr2:113907976
|
C | A | 70 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(67): Show | 74 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(71): Show |
intron_variant | MODIFIER | c.45-5196C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907976 | ||||||
chr2:113907976
|
C | CA | 24 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0161others(21): Show | 24 | HG01106.hp1 HG01169.hp2 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.45-5170dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113907976 | |||||
chr2:113907976
|
CA | C | 49 | a0001c0001t0002g0110a0001c0001t0002g0188a0001c0001t0003g0074others(46): Show | 54 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(51): Show |
intron_variant | MODIFIER | c.45-5170delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113907976 | |||||
chr2:113907977
|
A | C | 35 | a0001c0001t0002g0015a0001c0001t0002g0037a0001c0001t0002g0103others(32): Show | 41 | HG00733.hp2 HG00738.hp1 HG00741.hp2 others(38): Show |
intron_variant | MODIFIER | c.45-5195A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907977 | ||||||
chr2:113907978
|
A | C | 1 | a0001c0001t0008g0078 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.45-5194A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113907978 | ||||||
chr2:113908003
|
G | A | 6 | a0001c0001t0002g0165a0001c0001t0002g0170a0001c0001t0002g0171others(3): Show | 6 | NA18947.hp2 NA18984.hp1 NA18993.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-5169G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908003 | ||||||
chr2:113908156
|
C | G | 6 | a0001c0001t0007g0217a0001c0001t0013g0210a0001c0001t0013g0211others(3): Show | 6 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-5016C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908156 | ||||||
chr2:113908244
|
G | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-4928G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908244 | ||||||
chr2:113908251
|
G | GT | 8 | a0001c0001t0001g0268a0001c0001t0002g0172a0001c0001t0002g0184others(5): Show | 8 | HG03453.hp2 HG03831.hp2 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.45-4906dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113908251 | |||||
chr2:113908251
|
GT | G | 64 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(61): Show | 69 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.45-4906delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113908251 | |||||
chr2:113908275
|
A | T | 1 | a0001c0001t0010g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.45-4897A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908275 | ||||||
chr2:113908366
|
G | A | 3 | a0001c0001t0006g0223a0001c0001t0006g0224a0001c0001t0023g0222 | 3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.45-4806G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908366 | ||||||
chr2:113908387
|
G | T | 17 | a0001c0001t0004g0040a0001c0001t0004g0041a0001c0001t0004g0042others(14): Show | 17 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(14): Show |
intron_variant | MODIFIER | c.45-4785G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908387 | ||||||
chr2:113908434
|
T | G | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.45-4738T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908434 | ||||||
chr2:113908557
|
A | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.45-4615A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908557 | ||||||
chr2:113908637
|
A | G | 1 | a0001c0001t0015g0342 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.45-4535A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908637 | ||||||
chr2:113908663
|
C | T | 4 | a0001c0001t0004g0206a0001c0001t0004g0207a0001c0001t0004g0208others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-4509C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908663 | ||||||
chr2:113908769
|
C | G | 1 | a0001c0001t0002g0169 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.45-4403C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908769 | ||||||
chr2:113908773
|
C | T | 19 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(16): Show | 19 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.45-4399C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908773 | ||||||
chr2:113908791
|
G | A | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45-4381G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113908791 | ||||||
chr2:113909114
|
T | C | 1 | a0001c0001t0002g0188 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.45-4058T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909114 | ||||||
chr2:113909185
|
A | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.45-3987A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909185 | ||||||
chr2:113909335
|
T | C | 1 | a0001c0001t0004g0129 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.45-3837T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909335 | ||||||
chr2:113909475
|
C | T | 1 | a0001c0001t0036g0038 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.45-3697C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909475 | ||||||
chr2:113909606
|
TTTG | T | 50 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(47): Show | 55 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(52): Show |
intron_variant | MODIFIER | c.45-3551_45-3549del others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113909606 | |||||
chr2:113909609
|
G | T | 10 | a0001c0001t0005g0326a0001c0001t0005g0328a0001c0001t0005g0329others(7): Show | 10 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.45-3563G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909609 | ||||||
chr2:113909621
|
G | GT | 64 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(61): Show | 66 | HG00408.hp2 HG00544.hp1 HG00639.hp2 others(63): Show |
intron_variant | MODIFIER | c.45-3538dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113909621 | |||||
chr2:113909642
|
T | A | 1 | a0001c0001t0012g0056 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.45-3530T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909642 | ||||||
chr2:113909700
|
GAA | G | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.45-3467_45-3466del others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113909700 | |||||
chr2:113909703
|
A | G | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(20): Show | 25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.45-3469A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909703 | ||||||
chr2:113909917
|
C | G | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-3255C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909917 | ||||||
chr2:113909979
|
G | A | 1 | a0001c0001t0004g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.45-3193G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113909979 | ||||||
chr2:113910039
|
G | T | 1 | a0001c0001t0002g0189 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.45-3133G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910039 | ||||||
chr2:113910055
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-3117A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910055 | ||||||
chr2:113910056
|
TG | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.45-3113delG | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113910056 | |||||
chr2:113910139
|
G | T | 1 | a0001c0001t0001g0276 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.45-3033G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910139 | ||||||
chr2:113910147
|
C | T | 1 | a0001c0001t0001g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.45-3025C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910147 | ||||||
chr2:113910236
|
C | G | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.45-2936C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910236 | ||||||
chr2:113910238
|
A | G | 2 | a0001c0001t0003g0085a0001c0001t0003g0116 | 2 | HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.45-2934A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910238 | ||||||
chr2:113910254
|
CAGAGTTT others(2): Show |
C | 19 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(16): Show | 19 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.45-2913_45-2905del others(9): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113910254 | |||||
chr2:113910310
|
C | T | 1 | a0001c0001t0001g0265 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.45-2862C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910310 | ||||||
chr2:113910330
|
G | A | 6 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0012g0055others(3): Show | 6 | HG01884.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.45-2842G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910330 | ||||||
chr2:113910334
|
A | G | 1 | a0001c0001t0010g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.45-2838A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910334 | ||||||
chr2:113910338
|
C | T | 3 | a0001c0001t0001g0027a0001c0001t0001g0338a0001c0001t0001g0339 | 4 | HG01891.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.45-2834C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910338 | ||||||
chr2:113910515
|
T | G | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-2657T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910515 | ||||||
chr2:113910743
|
C | G | 1 | a0001c0001t0001g0030 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.45-2429C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910743 | ||||||
chr2:113910746
|
A | G | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.45-2426A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910746 | ||||||
chr2:113910765
|
A | T | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.45-2407A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910765 | ||||||
chr2:113910837
|
T | C | 1 | a0001c0001t0028g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.45-2335T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910837 | ||||||
chr2:113910907
|
T | A | 3 | a0001c0001t0006g0223a0001c0001t0006g0224a0001c0001t0023g0222 | 3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.45-2265T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113910907 | ||||||
chr2:113911072
|
G | A | 2 | a0001c0001t0004g0133a0001c0001t0004g0134 | 2 | NA18940.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.45-2100G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911072 | ||||||
chr2:113911108
|
A | G | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.45-2064A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911108 | ||||||
chr2:113911115
|
G | A | 1 | a0001c0001t0003g0052 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.45-2057G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911115 | ||||||
chr2:113911227
|
G | A | 1 | a0001c0001t0001g0272 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.45-1945G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911227 | ||||||
chr2:113911294
|
G | GT | 24 | a0001c0001t0001g0285a0001c0001t0001g0325a0001c0001t0002g0192others(21): Show | 24 | HG00735.hp1 HG01243.hp1 HG01884.hp1 others(21): Show |
intron_variant | MODIFIER | c.45-1866dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113911294 | |||||
chr2:113911307
|
A | T | 1 | a0001c0001t0003g0077 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.45-1865A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911307 | ||||||
chr2:113911419
|
C | CT | 116 | a0001c0001t0001g0292a0001c0001t0002g0165a0001c0001t0003g0003others(113): Show | 133 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(130): Show |
intron_variant | MODIFIER | c.45-1735dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113911419 | |||||
chr2:113911419
|
C | CTT | 61 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(58): Show | 65 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.45-1736_45-1735dup others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113911419 | |||||
chr2:113911419
|
C | CTTT | 75 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(72): Show | 78 | HG00408.hp2 HG00609.hp2 HG00639.hp2 others(75): Show |
intron_variant | MODIFIER | c.45-1737_45-1735dup others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113911419 | |||||
chr2:113911419
|
C | CTTTT | 6 | a0001c0001t0001g0264a0001c0001t0001g0267a0001c0001t0001g0268others(3): Show | 6 | HG01884.hp1 HG02148.hp1 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.45-1738_45-1735dup others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113911419 | |||||
chr2:113911442
|
C | T | 1 | a0001c0001t0009g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.45-1730C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911442 | ||||||
chr2:113911475
|
A | C | 1 | a0001c0001t0007g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.45-1697A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911475 | ||||||
chr2:113911524
|
A | G | 1 | a0001c0001t0007g0218 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.45-1648A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911524 | ||||||
chr2:113911542
|
C | A | 1 | a0001c0001t0007g0347 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.45-1630C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911542 | ||||||
chr2:113911609
|
G | A | 1 | a0001c0001t0002g0183 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.45-1563G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911609 | ||||||
chr2:113911780
|
A | T | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.45-1392A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911780 | ||||||
chr2:113911805
|
C | T | 4 | a0001c0001t0006g0228a0001c0001t0006g0230a0001c0001t0006g0231others(1): Show | 4 | HG02109.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.45-1367C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911805 | ||||||
chr2:113911822
|
C | T | 1 | a0001c0001t0003g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.45-1350C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911822 | ||||||
chr2:113911945
|
T | C | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-1227T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113911945 | ||||||
chr2:113912047
|
T | G | 1 | a0001c0001t0004g0145 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.45-1125T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912047 | ||||||
chr2:113912093
|
C | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.45-1079C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912093 | ||||||
chr2:113912129
|
G | C | 51 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(48): Show | 62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.45-1043G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912129 | ||||||
chr2:113912147
|
G | A | 298 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(295): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.45-1025G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912147 | ||||||
chr2:113912184
|
A | AT | 7 | a0001c0001t0003g0064a0001c0001t0006g0006a0001c0001t0006g0225others(4): Show | 9 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(6): Show |
intron_variant | MODIFIER | c.45-977dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113912184 | |||||
chr2:113912241
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG01884.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.45-931A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912241 | ||||||
chr2:113912355
|
A | T | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.45-817A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912355 | ||||||
chr2:113912368
|
C | G | 1 | a0001c0001t0001g0027 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.45-804C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912368 | ||||||
chr2:113912446
|
T | C | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.45-726T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912446 | ||||||
chr2:113912469
|
G | A | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.45-703G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912469 | ||||||
chr2:113912739
|
A | G | 1 | a0001c0001t0002g0161 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.45-433A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912739 | ||||||
chr2:113912889
|
T | C | 3 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0209 | 3 | HG02145.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.45-283T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | chr2 | 113912889 | ||||||
chr2:113912895
|
TAGA | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.45-274_45-272delAA others(1): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113912895 | |||||
chr2:113912917
|
GACCTTGA others(14): Show |
G | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.45-252_45-232delCT others(19): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr2 | 113912917 | |||||
chr2:113913389
|
CTATT | C | 4 | a0001c0001t0006g0006a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+163_100+166del others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913389 | ||||||
chr2:113913530
|
A | G | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.100+303A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913530 | ||||||
chr2:113913560
|
A | T | 1 | a0001c0001t0001g0317 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.100+333A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913560 | ||||||
chr2:113913568
|
A | G | 1 | a0001c0001t0002g0193 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.100+341A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913568 | ||||||
chr2:113913739
|
G | C | 1 | a0001c0001t0007g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.100+512G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913739 | ||||||
chr2:113913785
|
C | G | 1 | a0001c0001t0001g0263 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.100+558C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913785 | ||||||
chr2:113913920
|
G | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.100+693G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913920 | ||||||
chr2:113913955
|
A | G | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(29): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.100+728A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913955 | ||||||
chr2:113913956
|
T | G | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.100+729T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113913956 | ||||||
chr2:113914026
|
C | T | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.100+799C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914026 | ||||||
chr2:113914112
|
A | AT | 355 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(352): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.100+887dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 113914112 | |||||
chr2:113914199
|
A | ATAGGAAT | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.100+973_100+974ins others(7): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 113914199 | |||||
chr2:113914255
|
C | G | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.100+1028C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914255 | ||||||
chr2:113914334
|
C | T | 1 | a0001c0001t0004g0045 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.100+1107C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914334 | ||||||
chr2:113914336
|
G | A | 1 | a0001c0001t0002g0103 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.100+1109G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914336 | ||||||
chr2:113914340
|
C | T | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.100+1113C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914340 | ||||||
chr2:113914350
|
C | T | 1 | a0001c0001t0001g0262 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.100+1123C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914350 | ||||||
chr2:113914351
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.100+1124G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914351 | ||||||
chr2:113914353
|
C | T | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.100+1126C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914353 | ||||||
chr2:113914383
|
C | T | 1 | a0002c0004t0006g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.100+1156C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914383 | ||||||
chr2:113914474
|
G | A | 1 | a0001c0001t0009g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.100+1247G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914474 | ||||||
chr2:113914529
|
C | T | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.100+1302C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914529 | ||||||
chr2:113914614
|
C | CA | 27 | a0001c0001t0001g0028a0001c0001t0002g0164a0001c0001t0003g0063others(24): Show | 30 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.100+1406dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 113914614 | |||||
chr2:113914614
|
C | CAA | 5 | a0001c0001t0001g0027a0001c0001t0001g0338a0001c0001t0001g0339others(2): Show | 6 | HG01891.hp1 HG02559.hp1 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.100+1405_100+1406d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 113914614 | |||||
chr2:113914614
|
CA | C | 128 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(125): Show | 133 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(130): Show |
intron_variant | MODIFIER | c.100+1406delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 113914614 | |||||
chr2:113914630
|
A | AG | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.100+1403_100+1404i others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914630 | ||||||
chr2:113914630
|
A | G | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.100+1403A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914630 | ||||||
chr2:113914727
|
A | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.100+1500A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914727 | ||||||
chr2:113914763
|
A | C | 1 | a0001c0001t0001g0308 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.100+1536A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914763 | ||||||
chr2:113914909
|
A | T | 1 | a0001c0001t0001g0261 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.100+1682A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113914909 | ||||||
chr2:113915013
|
A | T | 267 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(264): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.100+1786A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915013 | ||||||
chr2:113915120
|
G | A | 132 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(129): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.101-1764G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915120 | ||||||
chr2:113915151
|
C | T | 2 | a0001c0001t0002g0092a0001c0001t0002g0101 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.101-1733C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915151 | ||||||
chr2:113915194
|
A | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.101-1690A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915194 | ||||||
chr2:113915231
|
A | G | 1 | a0001c0001t0003g0090 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.101-1653A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915231 | ||||||
chr2:113915307
|
C | T | 3 | a0001c0001t0006g0223a0001c0001t0006g0224a0001c0001t0023g0222 | 3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.101-1577C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915307 | ||||||
chr2:113915336
|
A | G | 358 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(355): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.101-1548A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915336 | ||||||
chr2:113915337
|
A | C | 358 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(355): Show | 389 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(386): Show |
intron_variant | MODIFIER | c.101-1547A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915337 | ||||||
chr2:113915504
|
A | G | 1 | a0001c0001t0001g0307 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.101-1380A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915504 | ||||||
chr2:113915650
|
C | T | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.101-1234C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915650 | ||||||
chr2:113915663
|
G | C | 3 | a0001c0001t0003g0009a0001c0001t0003g0063a0001c0001t0003g0071 | 4 | NA18945.hp1 NA18992.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-1221G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915663 | ||||||
chr2:113915853
|
A | G | 3 | a0001c0001t0002g0091a0001c0001t0002g0100a0001c0001t0002g0110 | 3 | NA19058.hp2 NA19078.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.101-1031A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915853 | ||||||
chr2:113915967
|
A | G | 7 | a0001c0001t0001g0204a0001c0001t0001g0314a0001c0001t0001g0315others(4): Show | 8 | HG02083.hp2 NA18945.hp2 NA18967.hp1 others(5): Show |
intron_variant | MODIFIER | c.101-917A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113915967 | ||||||
chr2:113916099
|
A | T | 132 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(129): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.101-785A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916099 | ||||||
chr2:113916170
|
G | A | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.101-714G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916170 | ||||||
chr2:113916225
|
C | T | 3 | a0001c0001t0006g0223a0001c0001t0006g0224a0001c0001t0023g0222 | 3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.101-659C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916225 | ||||||
chr2:113916237
|
G | A | 1 | a0001c0001t0003g0196 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.101-647G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916237 | ||||||
chr2:113916238
|
T | TAC | 3 | a0001c0001t0003g0010a0001c0001t0003g0064a0001c0001t0003g0112 | 4 | NA18942.hp2 NA18997.hp2 NA19004.hp1 others(1): Show |
intron_variant | MODIFIER | c.101-644_101-643dup others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr2 | 113916238 | |||||
chr2:113916587
|
C | T | 1 | a0001c0001t0019g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.101-297C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916587 | ||||||
chr2:113916591
|
G | T | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.101-293G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916591 | ||||||
chr2:113916618
|
A | G | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.101-266A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916618 | ||||||
chr2:113916847
|
A | C | 1 | a0001c0001t0001g0034 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.101-37A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 2/11 | chr2 | 113916847 | ||||||
chr2:113917099
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+91A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113917099 | ||||||
chr2:113917310
|
CT | C | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.225+309delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113917310 | |||||
chr2:113917333
|
A | G | 1 | a0001c0001t0023g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.225+325A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113917333 | ||||||
chr2:113917679
|
C | T | 41 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(38): Show | 46 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.225+671C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113917679 | ||||||
chr2:113918039
|
A | G | 1 | a0001c0001t0001g0305 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.225+1031A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918039 | ||||||
chr2:113918272
|
G | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.225+1264G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918272 | ||||||
chr2:113918386
|
C | CT | 20 | a0001c0001t0002g0186a0001c0001t0002g0187a0001c0001t0002g0192others(17): Show | 22 | HG00639.hp1 HG00733.hp2 HG00738.hp2 others(19): Show |
intron_variant | MODIFIER | c.225+1393dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113918386 | |||||
chr2:113918386
|
C | CTT | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.225+1392_225+1393d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113918386 | |||||
chr2:113918386
|
CT | C | 13 | a0001c0001t0001g0244a0001c0001t0001g0245a0001c0001t0001g0271others(10): Show | 13 | HG01167.hp2 HG01943.hp2 HG02273.hp1 others(10): Show |
intron_variant | MODIFIER | c.225+1393delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113918386 | |||||
chr2:113918408
|
A | G | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.225+1400A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918408 | ||||||
chr2:113918558
|
G | A | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.225+1550G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918558 | ||||||
chr2:113918639
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.225+1631C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918639 | ||||||
chr2:113918807
|
A | G | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.225+1799A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918807 | ||||||
chr2:113918815
|
T | C | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.225+1807T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113918815 | ||||||
chr2:113919076
|
A | G | 1 | a0001c0001t0002g0168 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.225+2068A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919076 | ||||||
chr2:113919100
|
G | C | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.225+2092G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919100 | ||||||
chr2:113919153
|
T | C | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.225+2145T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919153 | ||||||
chr2:113919173
|
A | G | 11 | a0001c0001t0004g0017a0001c0001t0004g0129a0001c0001t0004g0133others(8): Show | 12 | HG02080.hp1 HG02523.hp2 NA18939.hp2 others(9): Show |
intron_variant | MODIFIER | c.225+2165A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919173 | ||||||
chr2:113919393
|
G | A | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.225+2385G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919393 | ||||||
chr2:113919465
|
A | C | 1 | a0001c0001t0009g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.225+2457A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919465 | ||||||
chr2:113919602
|
A | T | 1 | a0001c0001t0006g0223 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.225+2594A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919602 | ||||||
chr2:113919756
|
A | AT | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.225+2753dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113919756 | |||||
chr2:113919809
|
A | G | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.225+2801A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919809 | ||||||
chr2:113919815
|
GCTCA | G | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.225+2814_225+2817d others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113919815 | |||||
chr2:113919874
|
G | A | 51 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(48): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.225+2866G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919874 | ||||||
chr2:113919969
|
G | A | 19 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(16): Show | 19 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.225+2961G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919969 | ||||||
chr2:113919982
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.225+2974G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919982 | ||||||
chr2:113919999
|
C | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+2991C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113919999 | ||||||
chr2:113920084
|
G | C | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.225+3076G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920084 | ||||||
chr2:113920112
|
T | C | 4 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(1): Show | 4 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.225+3104T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920112 | ||||||
chr2:113920220
|
G | C | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.225+3212G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920220 | ||||||
chr2:113920251
|
T | C | 1 | a0001c0001t0002g0093 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.225+3243T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920251 | ||||||
chr2:113920427
|
T | C | 1 | a0001c0001t0001g0282 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.225+3419T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920427 | ||||||
chr2:113920719
|
T | C | 1 | a0001c0001t0006g0228 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.225+3711T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920719 | ||||||
chr2:113920725
|
T | C | 1 | a0001c0001t0004g0040 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.225+3717T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920725 | ||||||
chr2:113920868
|
T | C | 4 | a0001c0001t0005g0332a0001c0001t0005g0336a0001c0001t0005g0337others(1): Show | 4 | HG00609.hp2 NA18961.hp2 NA18970.hp2 others(1): Show |
intron_variant | MODIFIER | c.225+3860T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920868 | ||||||
chr2:113920976
|
A | G | 1 | a0001c0001t0004g0201 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.225+3968A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113920976 | ||||||
chr2:113921124
|
C | T | 1 | a0001c0001t0007g0347 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.225+4116C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921124 | ||||||
chr2:113921173
|
G | A | 132 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(129): Show | 143 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(140): Show |
intron_variant | MODIFIER | c.225+4165G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921173 | ||||||
chr2:113921318
|
G | GT | 9 | a0001c0001t0001g0259a0001c0001t0001g0260a0001c0001t0001g0317others(6): Show | 9 | HG01109.hp1 HG04184.hp1 HG04228.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+4325dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113921318 | |||||
chr2:113921320
|
T | C | 3 | a0001c0001t0001g0236a0001c0001t0001g0244a0001c0001t0001g0246 | 3 | NA18946.hp1 NA18953.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.225+4312T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921320 | ||||||
chr2:113921408
|
G | C | 1 | a0001c0001t0002g0166 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.225+4400G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921408 | ||||||
chr2:113921603
|
G | A | 2 | a0001c0001t0001g0030a0001c0001t0001g0032 | 2 | NA18951.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.225+4595G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921603 | ||||||
chr2:113921721
|
G | A | 1 | a0001c0001t0010g0200 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.225+4713G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921721 | ||||||
chr2:113921845
|
C | G | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.225+4837C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921845 | ||||||
chr2:113921847
|
G | A | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.225+4839G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921847 | ||||||
chr2:113921874
|
A | G | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.225+4866A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113921874 | ||||||
chr2:113922167
|
A | G | 1 | a0001c0001t0005g0340 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.225+5159A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922167 | ||||||
chr2:113922182
|
T | C | 1 | a0001c0001t0004g0206 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.226-5163T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922182 | ||||||
chr2:113922221
|
C | T | 1 | a0001c0001t0002g0182 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.226-5124C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922221 | ||||||
chr2:113922314
|
A | G | 1 | a0001c0001t0027g0173 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.226-5031A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922314 | ||||||
chr2:113922410
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0015g0028a0001c0001t0015g0341others(2): Show | 5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-4935T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922410 | ||||||
chr2:113922418
|
A | G | 35 | a0001c0001t0004g0017a0001c0001t0004g0040a0001c0001t0004g0041others(32): Show | 36 | HG00544.hp2 HG00597.hp1 HG00621.hp1 others(33): Show |
intron_variant | MODIFIER | c.226-4927A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922418 | ||||||
chr2:113922463
|
C | G | 1 | a0001c0001t0001g0303 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.226-4882C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922463 | ||||||
chr2:113922535
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.226-4810A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922535 | ||||||
chr2:113922640
|
CT | C | 298 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(295): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.226-4702delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113922640 | |||||
chr2:113922668
|
C | T | 1 | a0001c0001t0036g0038 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.226-4677C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922668 | ||||||
chr2:113922845
|
T | C | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.226-4500T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922845 | ||||||
chr2:113922892
|
A | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.226-4453A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113922892 | ||||||
chr2:113923071
|
C | T | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(29): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.226-4274C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923071 | ||||||
chr2:113923181
|
A | G | 1 | a0001c0001t0003g0012 | 2 | HG01099.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.226-4164A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923181 | ||||||
chr2:113923279
|
T | C | 1 | a0001c0001t0008g0118 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.226-4066T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923279 | ||||||
chr2:113923305
|
C | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.226-4040C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923305 | ||||||
chr2:113923318
|
ATTTG | A | 100 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(97): Show | 104 | HG00408.hp2 HG00544.hp1 HG00639.hp1 others(101): Show |
intron_variant | MODIFIER | c.226-3995_226-3992d others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113923318 | |||||
chr2:113923318
|
ATTTGTTT others(1): Show |
A | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.226-3999_226-3992d others(10): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113923318 | |||||
chr2:113923350
|
G | GTTT | 5 | a0001c0001t0001g0028a0001c0001t0015g0028a0001c0001t0015g0341others(2): Show | 5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-3992_226-3990d others(5): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113923350 | |||||
chr2:113923350
|
G | T | 265 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(262): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.226-3995G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923350 | ||||||
chr2:113923351
|
T | A | 4 | a0001c0001t0006g0228a0001c0001t0006g0230a0001c0001t0006g0231others(1): Show | 4 | HG02109.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.226-3994T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923351 | ||||||
chr2:113923422
|
C | T | 2 | a0001c0001t0003g0085a0001c0001t0003g0116 | 2 | HG01928.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.226-3923C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923422 | ||||||
chr2:113923436
|
T | C | 154 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(151): Show | 161 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(158): Show |
intron_variant | MODIFIER | c.226-3909T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923436 | ||||||
chr2:113923490
|
C | T | 1 | a0001c0001t0002g0107 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.226-3855C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923490 | ||||||
chr2:113923626
|
T | C | 298 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(295): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.226-3719T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923626 | ||||||
chr2:113923627
|
G | A | 1 | a0001c0001t0005g0340 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.226-3718G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923627 | ||||||
chr2:113923631
|
G | A | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.226-3714G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923631 | ||||||
chr2:113923699
|
C | T | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.226-3646C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113923699 | ||||||
chr2:113923732
|
CT | C | 119 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(116): Show | 126 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(123): Show |
intron_variant | MODIFIER | c.226-3599delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113923732 | |||||
chr2:113924001
|
G | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.226-3344G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924001 | ||||||
chr2:113924004
|
C | T | 1 | a0001c0001t0032g0301 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.226-3341C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924004 | ||||||
chr2:113924027
|
C | T | 2 | a0001c0001t0004g0047a0001c0001t0004g0048 | 2 | HG00621.hp1 HG02027.hp1 |
intron_variant | MODIFIER | c.226-3318C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924027 | ||||||
chr2:113924054
|
C | CT | 14 | a0001c0001t0003g0080a0001c0001t0006g0006a0001c0001t0006g0221others(11): Show | 16 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.226-3274dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113924054 | |||||
chr2:113924054
|
CT | C | 121 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(118): Show | 127 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.226-3274delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113924054 | |||||
chr2:113924054
|
CTT | C | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.226-3275_226-3274d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113924054 | |||||
chr2:113924081
|
G | A | 112 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(109): Show | 117 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.226-3264G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924081 | ||||||
chr2:113924201
|
C | T | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.226-3144C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924201 | ||||||
chr2:113924228
|
C | T | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.226-3117C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924228 | ||||||
chr2:113924233
|
C | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.226-3112C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924233 | ||||||
chr2:113924423
|
C | T | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.226-2922C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924423 | ||||||
chr2:113924424
|
G | A | 1 | a0001c0001t0009g0131 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.226-2921G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924424 | ||||||
chr2:113924563
|
T | C | 8 | a0001c0001t0002g0015a0001c0001t0002g0094a0001c0001t0002g0102others(5): Show | 9 | HG01069.hp1 HG01070.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.226-2782T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924563 | ||||||
chr2:113924709
|
A | T | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.226-2636A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924709 | ||||||
chr2:113924840
|
C | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.226-2505C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113924840 | ||||||
chr2:113924887
|
C | CTATT | 35 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(32): Show | 40 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(37): Show |
intron_variant | MODIFIER | c.226-2432_226-2429d others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113924887 | |||||
chr2:113924887
|
C | CTATTTAT others(5): Show |
1 | a0001c0001t0002g0104 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.226-2440_226-2429d others(14): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113924887 | |||||
chr2:113924887
|
CTATT | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(126): Show | 134 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(131): Show |
intron_variant | MODIFIER | c.226-2432_226-2429d others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113924887 | |||||
chr2:113925127
|
C | T | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.226-2218C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925127 | ||||||
chr2:113925194
|
C | CT | 10 | a0001c0001t0002g0105a0001c0001t0002g0182a0001c0001t0002g0192others(7): Show | 10 | HG01361.hp2 HG02145.hp2 HG02738.hp2 others(7): Show |
intron_variant | MODIFIER | c.226-2133dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113925194 | |||||
chr2:113925194
|
C | CTT | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.226-2134_226-2133d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113925194 | |||||
chr2:113925194
|
CT | C | 121 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(118): Show | 127 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(124): Show |
intron_variant | MODIFIER | c.226-2133delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113925194 | |||||
chr2:113925195
|
T | C | 11 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(8): Show | 13 | HG00639.hp1 HG00738.hp2 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.226-2150T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925195 | ||||||
chr2:113925303
|
C | T | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.226-2042C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925303 | ||||||
chr2:113925451
|
C | T | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.226-1894C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925451 | ||||||
chr2:113925485
|
C | T | 9 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0290others(6): Show | 10 | HG02015.hp1 HG02056.hp1 HG02071.hp1 others(7): Show |
intron_variant | MODIFIER | c.226-1860C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925485 | ||||||
chr2:113925513
|
A | T | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.226-1832A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925513 | ||||||
chr2:113925559
|
A | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.226-1786A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925559 | ||||||
chr2:113925672
|
A | G | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.226-1673A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925672 | ||||||
chr2:113925728
|
C | G | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.226-1617C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925728 | ||||||
chr2:113925731
|
A | G | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.226-1614A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925731 | ||||||
chr2:113925741
|
G | A | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(20): Show | 25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.226-1604G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925741 | ||||||
chr2:113925937
|
C | T | 81 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(78): Show | 87 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.226-1408C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925937 | ||||||
chr2:113925938
|
G | A | 5 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0225others(2): Show | 7 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.226-1407G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113925938 | ||||||
chr2:113926233
|
C | T | 112 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(109): Show | 117 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.226-1112C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926233 | ||||||
chr2:113926453
|
A | C | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.226-892A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926453 | ||||||
chr2:113926548
|
A | G | 4 | a0001c0001t0006g0006a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.226-797A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926548 | ||||||
chr2:113926729
|
A | G | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.226-616A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926729 | ||||||
chr2:113926774
|
G | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.226-571G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926774 | ||||||
chr2:113926786
|
A | G | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.226-559A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926786 | ||||||
chr2:113926894
|
C | G | 4 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(1): Show | 4 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.226-451C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926894 | ||||||
chr2:113926895
|
AATT | A | 51 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(48): Show | 62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.226-446_226-444del others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr2 | 113926895 | |||||
chr2:113926937
|
G | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.226-408G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113926937 | ||||||
chr2:113927148
|
CATCT | C | 5 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0012g0055others(2): Show | 5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.226-196_226-193del others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113927148 | ||||||
chr2:113927173
|
A | T | 1 | a0001c0001t0023g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.226-172A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113927173 | ||||||
chr2:113927271
|
T | C | 51 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(48): Show | 56 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(53): Show |
intron_variant | MODIFIER | c.226-74T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 3/11 | chr2 | 113927271 | ||||||
chr2:113927535
|
T | C | 1 | a0001c0001t0002g0126 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.336+80T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113927535 | ||||||
chr2:113927680
|
A | T | 1 | a0001c0001t0001g0307 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.336+225A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113927680 | ||||||
chr2:113927699
|
A | C | 3 | a0001c0001t0006g0230a0001c0001t0006g0231a0002c0004t0006g0229 | 3 | HG02109.hp1 HG03130.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.336+244A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113927699 | ||||||
chr2:113927699
|
A | T | 1 | a0001c0001t0006g0228 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.336+244A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113927699 | ||||||
chr2:113927798
|
A | G | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.336+343A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113927798 | ||||||
chr2:113927832
|
A | G | 1 | a0001c0001t0003g0067 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.336+377A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113927832 | ||||||
chr2:113928026
|
AT | A | 19 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(16): Show | 19 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.336+581delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 113928026 | |||||
chr2:113928044
|
C | A | 304 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(301): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.336+589C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928044 | ||||||
chr2:113928133
|
A | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.336+678A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928133 | ||||||
chr2:113928141
|
A | G | 2 | a0001c0001t0004g0045a0001c0001t0004g0049 | 2 | HG00544.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.336+686A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928141 | ||||||
chr2:113928513
|
GGGTTT | G | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.336+1061_336+1065d others(7): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 113928513 | |||||
chr2:113928703
|
AT | A | 351 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(348): Show | 382 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(379): Show |
intron_variant | MODIFIER | c.336+1260delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 113928703 | |||||
chr2:113928773
|
A | G | 1 | a0001c0001t0004g0148 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.336+1318A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928773 | ||||||
chr2:113928857
|
T | C | 3 | a0001c0001t0004g0207a0001c0001t0004g0208a0001c0001t0004g0209 | 3 | HG02145.hp2 HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.336+1402T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928857 | ||||||
chr2:113928879
|
G | A | 1 | a0001c0001t0005g0336 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.336+1424G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928879 | ||||||
chr2:113928884
|
C | T | 1 | a0001c0001t0005g0337 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.336+1429C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928884 | ||||||
chr2:113928946
|
G | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.336+1491G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928946 | ||||||
chr2:113928954
|
A | G | 4 | a0001c0001t0004g0206a0001c0001t0004g0207a0001c0001t0004g0208others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.336+1499A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113928954 | ||||||
chr2:113929108
|
G | A | 2 | a0001c0001t0001g0031a0001c0001t0001g0035 | 2 | NA18955.hp1 NA19068.hp1 |
intron_variant | MODIFIER | c.336+1653G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929108 | ||||||
chr2:113929113
|
A | G | 1 | a0001c0001t0003g0088 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.336+1658A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929113 | ||||||
chr2:113929130
|
G | GT | 116 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(113): Show | 124 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(121): Show |
intron_variant | MODIFIER | c.336+1685dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 113929130 | |||||
chr2:113929130
|
GT | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.336+1685delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 113929130 | |||||
chr2:113929141
|
G | T | 5 | a0001c0001t0017g0288a0001c0001t0017g0289a0001c0001t0017g0299others(2): Show | 5 | HG04204.hp1 NA18953.hp1 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.336+1686G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929141 | ||||||
chr2:113929147
|
G | T | 1 | a0001c0001t0007g0218 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.336+1692G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929147 | ||||||
chr2:113929190
|
T | G | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.336+1735T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929190 | ||||||
chr2:113929192
|
G | A | 1 | a0001c0001t0007g0347 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.336+1737G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929192 | ||||||
chr2:113929289
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.336+1834C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929289 | ||||||
chr2:113929359
|
T | G | 1 | a0001c0001t0001g0238 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.336+1904T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929359 | ||||||
chr2:113929540
|
G | T | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.337-1761G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929540 | ||||||
chr2:113929541
|
C | T | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.337-1760C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929541 | ||||||
chr2:113929551
|
G | C | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.337-1750G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929551 | ||||||
chr2:113929641
|
G | A | 6 | a0001c0001t0002g0174a0001c0001t0002g0186a0001c0001t0002g0187others(3): Show | 6 | HG00733.hp2 HG01069.hp2 HG01517.hp1 others(3): Show |
intron_variant | MODIFIER | c.337-1660G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929641 | ||||||
chr2:113929751
|
A | G | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.337-1550A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929751 | ||||||
chr2:113929826
|
G | A | 1 | a0001c0001t0008g0075 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.337-1475G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929826 | ||||||
chr2:113929861
|
TA | T | 5 | a0001c0001t0002g0018a0001c0001t0002g0169a0001c0001t0002g0181others(2): Show | 6 | HG01361.hp1 HG01433.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-1439delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929861 | ||||||
chr2:113929906
|
T | C | 27 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(24): Show | 29 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(26): Show |
intron_variant | MODIFIER | c.337-1395T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929906 | ||||||
chr2:113929924
|
C | T | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.337-1377C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929924 | ||||||
chr2:113929938
|
C | T | 1 | a0001c0001t0004g0048 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.337-1363C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113929938 | ||||||
chr2:113930004
|
G | A | 355 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(352): Show | 386 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(383): Show |
intron_variant | MODIFIER | c.337-1297G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930004 | ||||||
chr2:113930028
|
T | C | 2 | a0001c0001t0009g0128a0001c0001t0009g0160 | 2 | HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.337-1273T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930028 | ||||||
chr2:113930325
|
A | T | 6 | a0001c0001t0010g0019a0001c0001t0010g0197a0001c0001t0010g0198others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.337-976A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930325 | ||||||
chr2:113930504
|
AT | A | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.337-792delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr2 | 113930504 | |||||
chr2:113930578
|
C | T | 10 | a0001c0001t0009g0008a0001c0001t0009g0059a0001c0001t0009g0060others(7): Show | 11 | HG01884.hp2 HG02257.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.337-723C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930578 | ||||||
chr2:113930798
|
A | C | 1 | a0001c0001t0009g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.337-503A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930798 | ||||||
chr2:113930800
|
A | G | 2 | a0001c0001t0006g0230a0001c0001t0006g0231 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.337-501A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930800 | ||||||
chr2:113930923
|
A | G | 1 | a0001c0001t0001g0324 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.337-378A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930923 | ||||||
chr2:113930961
|
A | G | 3 | a0001c0001t0006g0223a0001c0001t0006g0224a0001c0001t0023g0222 | 3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.337-340A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113930961 | ||||||
chr2:113931090
|
A | T | 16 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(13): Show | 17 | HG01884.hp2 HG01891.hp1 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.337-211A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113931090 | ||||||
chr2:113931139
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.337-162C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 4/11 | chr2 | 113931139 | ||||||
chr2:113931470
|
C | CT | 134 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(131): Show | 141 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(138): Show |
intron_variant | MODIFIER | c.432+87dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113931470 | |||||
chr2:113931906
|
C | T | 1 | a0001c0001t0009g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.432+510C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113931906 | ||||||
chr2:113931969
|
C | A | 1 | a0001c0001t0010g0197 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.432+573C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113931969 | ||||||
chr2:113931979
|
T | A | 1 | a0001c0001t0011g0291 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.432+583T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113931979 | ||||||
chr2:113932034
|
T | C | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.432+638T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932034 | ||||||
chr2:113932124
|
C | T | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.432+728C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932124 | ||||||
chr2:113932292
|
T | C | 3 | a0001c0001t0009g0008a0001c0001t0009g0059a0001c0001t0009g0111 | 4 | HG02257.hp1 HG02615.hp2 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.432+896T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932292 | ||||||
chr2:113932311
|
G | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.432+915G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932311 | ||||||
chr2:113932402
|
A | G | 1 | a0001c0001t0001g0268 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.432+1006A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932402 | ||||||
chr2:113932432
|
A | G | 12 | a0001c0001t0004g0142a0001c0001t0007g0212a0001c0001t0007g0213others(9): Show | 12 | HG02280.hp2 HG02486.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.432+1036A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932432 | ||||||
chr2:113932469
|
C | T | 1 | a0001c0001t0005g0333 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.432+1073C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932469 | ||||||
chr2:113932498
|
G | A | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.432+1102G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932498 | ||||||
chr2:113932645
|
C | T | 1 | a0001c0001t0009g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.432+1249C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932645 | ||||||
chr2:113932696
|
G | A | 5 | a0001c0001t0001g0028a0001c0001t0015g0028a0001c0001t0015g0341others(2): Show | 5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.432+1300G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932696 | ||||||
chr2:113932701
|
T | C | 1 | a0001c0001t0035g0352 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.432+1305T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932701 | ||||||
chr2:113932804
|
T | C | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.432+1408T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932804 | ||||||
chr2:113932807
|
T | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.432+1411T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932807 | ||||||
chr2:113932833
|
G | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.432+1437G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113932833 | ||||||
chr2:113933079
|
G | A | 44 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(41): Show | 49 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(46): Show |
intron_variant | MODIFIER | c.433-1200G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933079 | ||||||
chr2:113933124
|
C | T | 5 | a0001c0001t0005g0026a0001c0001t0005g0327a0001c0001t0005g0333others(2): Show | 6 | HG02145.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.433-1155C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933124 | ||||||
chr2:113933154
|
T | C | 4 | a0001c0001t0009g0130a0001c0001t0009g0131a0001c0001t0009g0132others(1): Show | 4 | HG01243.hp2 HG02258.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.433-1125T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933154 | ||||||
chr2:113933165
|
C | T | 1 | a0001c0001t0003g0114 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.433-1114C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933165 | ||||||
chr2:113933171
|
C | T | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.433-1108C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933171 | ||||||
chr2:113933365
|
C | T | 51 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(48): Show | 62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.433-914C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933365 | ||||||
chr2:113933366
|
G | A | 1 | a0001c0001t0002g0037 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.433-913G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933366 | ||||||
chr2:113933521
|
AAAAG | A | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.433-755_433-752del others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933521 | |||||
chr2:113933650
|
TAAG | T | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.433-628_433-626del others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933650 | ||||||
chr2:113933677
|
A | AT | 67 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(64): Show | 71 | HG00408.hp1 HG00438.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.433-582dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933677 | |||||
chr2:113933677
|
A | ATT | 60 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(57): Show | 62 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(59): Show |
intron_variant | MODIFIER | c.433-583_433-582dup others(2): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933677 | |||||
chr2:113933677
|
A | ATTT | 6 | a0001c0001t0001g0254a0001c0001t0001g0255a0001c0001t0001g0258others(3): Show | 6 | HG03453.hp2 NA18943.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.433-584_433-582dup others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933677 | |||||
chr2:113933677
|
A | ATTTT | 19 | a0001c0001t0006g0221a0001c0001t0006g0223a0001c0001t0006g0224others(16): Show | 19 | HG01243.hp1 HG02258.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.433-585_433-582dup others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933677 | |||||
chr2:113933677
|
A | ATTTTT | 9 | a0001c0001t0006g0006a0001c0001t0006g0226a0001c0001t0006g0228others(6): Show | 11 | HG00639.hp1 HG00738.hp2 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.433-586_433-582dup others(5): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933677 | |||||
chr2:113933677
|
AT | A | 10 | a0001c0001t0002g0103a0001c0001t0003g0121a0001c0001t0004g0140others(7): Show | 10 | HG01070.hp1 HG01884.hp2 HG02523.hp2 others(7): Show |
intron_variant | MODIFIER | c.433-582delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113933677 | |||||
chr2:113933714
|
C | T | 8 | a0001c0001t0002g0015a0001c0001t0002g0094a0001c0001t0002g0102others(5): Show | 9 | HG01069.hp1 HG01070.hp1 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-565C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933714 | ||||||
chr2:113933765
|
C | T | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.433-514C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933765 | ||||||
chr2:113933870
|
C | T | 1 | a0001c0001t0010g0199 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.433-409C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933870 | ||||||
chr2:113933881
|
C | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.433-398C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933881 | ||||||
chr2:113933932
|
G | A | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.433-347G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113933932 | ||||||
chr2:113934029
|
A | G | 1 | a0001c0001t0015g0341 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.433-250A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113934029 | ||||||
chr2:113934232
|
G | GT | 61 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(58): Show | 66 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.433-35dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr2 | 113934232 | |||||
chr2:113934254
|
C | T | 1 | a0001c0001t0003g0066 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.433-25C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 5/11 | chr2 | 113934254 | ||||||
chr2:113934419
|
T | C | 1 | a0001c0001t0003g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+33T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934419 | ||||||
chr2:113934420
|
G | T | 1 | a0001c0001t0003g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+34G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934420 | ||||||
chr2:113934422
|
A | T | 1 | a0001c0001t0003g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+36A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934422 | ||||||
chr2:113934424
|
T | C | 1 | a0001c0001t0003g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+38T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934424 | ||||||
chr2:113934427
|
C | G | 1 | a0001c0001t0003g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+41C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934427 | ||||||
chr2:113934428
|
A | T | 1 | a0001c0001t0003g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+42A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934428 | ||||||
chr2:113934429
|
C | G | 1 | a0001c0001t0003g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+43C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934429 | ||||||
chr2:113934432
|
C | G | 1 | a0001c0001t0003g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+46C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934432 | ||||||
chr2:113934435
|
G | T | 1 | a0001c0001t0003g0082 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.540+49G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934435 | ||||||
chr2:113934583
|
G | A | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.540+197G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934583 | ||||||
chr2:113934658
|
G | A | 1 | a0001c0001t0005g0330 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.540+272G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934658 | ||||||
chr2:113934960
|
A | G | 1 | a0001c0001t0002g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.540+574A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113934960 | ||||||
chr2:113935010
|
A | T | 1 | a0001c0001t0007g0350 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.540+624A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935010 | ||||||
chr2:113935017
|
G | A | 55 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(52): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.540+631G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935017 | ||||||
chr2:113935035
|
C | CT | 51 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(48): Show | 54 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.540+663dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113935035 | |||||
chr2:113935153
|
C | T | 1 | a0001c0001t0009g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.540+767C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935153 | ||||||
chr2:113935237
|
C | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.540+851C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935237 | ||||||
chr2:113935249
|
G | GT | 112 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(109): Show | 117 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.540+864dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113935249 | |||||
chr2:113935254
|
G | T | 1 | a0001c0001t0034g0351 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.540+868G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935254 | ||||||
chr2:113935455
|
A | G | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.540+1069A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935455 | ||||||
chr2:113935543
|
T | A | 1 | a0001c0001t0009g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.540+1157T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935543 | ||||||
chr2:113935564
|
T | C | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.540+1178T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935564 | ||||||
chr2:113935698
|
A | G | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.540+1312A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935698 | ||||||
chr2:113935749
|
G | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.540+1363G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935749 | ||||||
chr2:113935941
|
A | C | 10 | a0001c0001t0005g0326a0001c0001t0005g0328a0001c0001t0005g0329others(7): Show | 10 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.540+1555A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113935941 | ||||||
chr2:113936022
|
G | A | 2 | a0001c0001t0002g0094a0001c0001t0002g0102 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.540+1636G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936022 | ||||||
chr2:113936032
|
C | T | 2 | a0001c0001t0006g0224a0001c0001t0023g0222 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.540+1646C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936032 | ||||||
chr2:113936209
|
C | G | 1 | a0001c0001t0004g0140 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.540+1823C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936209 | ||||||
chr2:113936302
|
C | CA | 52 | a0001c0001t0002g0104a0001c0001t0002g0186a0001c0001t0002g0187others(49): Show | 58 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(55): Show |
intron_variant | MODIFIER | c.540+1938dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | |||||
chr2:113936302
|
C | CAA | 19 | a0001c0001t0002g0037a0001c0001t0002g0192a0001c0001t0004g0044others(16): Show | 19 | HG01256.hp1 HG02056.hp2 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.540+1937_540+1938d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | |||||
chr2:113936302
|
C | CAAA | 13 | a0001c0001t0004g0208a0001c0001t0007g0212a0001c0001t0007g0217others(10): Show | 13 | HG02055.hp1 HG02145.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.540+1936_540+1938d others(5): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | |||||
chr2:113936302
|
C | CAAAA | 6 | a0001c0001t0010g0019a0001c0001t0010g0198a0001c0001t0010g0199others(3): Show | 6 | HG01243.hp1 HG02622.hp2 HG02647.hp2 others(3): Show |
intron_variant | MODIFIER | c.540+1935_540+1938d others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | |||||
chr2:113936302
|
CA | C | 52 | a0001c0001t0001g0028a0001c0001t0001g0235a0001c0001t0001g0238others(49): Show | 54 | HG00639.hp2 HG01106.hp1 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.540+1938delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | |||||
chr2:113936302
|
CAA | C | 108 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(105): Show | 114 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(111): Show |
intron_variant | MODIFIER | c.540+1937_540+1938d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | |||||
chr2:113936302
|
CAAAAAAA others(1): Show |
C | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.540+1931_540+1938d others(10): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936302 | |||||
chr2:113936338
|
G | GT | 4 | a0001c0001t0006g0006a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.540+1953dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113936338 | |||||
chr2:113936349
|
T | G | 304 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(301): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.540+1963T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936349 | ||||||
chr2:113936546
|
A | G | 10 | a0001c0001t0005g0326a0001c0001t0005g0328a0001c0001t0005g0329others(7): Show | 10 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.540+2160A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936546 | ||||||
chr2:113936628
|
A | G | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.540+2242A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936628 | ||||||
chr2:113936632
|
T | C | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.540+2246T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936632 | ||||||
chr2:113936737
|
G | T | 5 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0225others(2): Show | 7 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(4): Show |
intron_variant | MODIFIER | c.540+2351G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936737 | ||||||
chr2:113936871
|
A | G | 1 | a0001c0001t0009g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.540+2485A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936871 | ||||||
chr2:113936980
|
A | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.540+2594A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113936980 | ||||||
chr2:113937087
|
T | G | 2 | a0001c0001t0003g0011a0001c0001t0003g0081 | 3 | NA18962.hp2 NA18989.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.540+2701T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937087 | ||||||
chr2:113937253
|
A | G | 221 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(218): Show | 236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.541-2706A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937253 | ||||||
chr2:113937350
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.541-2609C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937350 | ||||||
chr2:113937479
|
C | G | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.541-2480C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937479 | ||||||
chr2:113937599
|
G | A | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.541-2360G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937599 | ||||||
chr2:113937810
|
G | A | 1 | a0001c0001t0003g0083 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.541-2149G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937810 | ||||||
chr2:113937820
|
A | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.541-2139A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937820 | ||||||
chr2:113937991
|
A | G | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.541-1968A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937991 | ||||||
chr2:113937998
|
C | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.541-1961C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113937998 | ||||||
chr2:113938320
|
C | T | 4 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(1): Show | 4 | HG02486.hp1 HG02559.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.541-1639C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113938320 | ||||||
chr2:113938323
|
TA | T | 6 | a0001c0001t0010g0019a0001c0001t0010g0197a0001c0001t0010g0198others(3): Show | 6 | HG02622.hp2 HG02647.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.541-1634delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113938323 | |||||
chr2:113938340
|
C | T | 2 | a0001c0001t0010g0198a0001c0001t0010g0199 | 2 | HG02647.hp2 HG02886.hp2 |
intron_variant | MODIFIER | c.541-1619C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113938340 | ||||||
chr2:113938358
|
T | C | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.541-1601T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113938358 | ||||||
chr2:113938410
|
CTTTATAA others(3): Show |
C | 3 | a0001c0001t0001g0245a0001c0001t0001g0259a0001c0001t0001g0266 | 3 | HG02723.hp1 HG03195.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.541-1544_541-1535d others(12): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113938410 | |||||
chr2:113938952
|
ATTTG | A | 4 | a0001c0001t0006g0006a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.541-1003_541-1000d others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113938952 | |||||
chr2:113939029
|
C | CT | 11 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(8): Show | 13 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(10): Show |
intron_variant | MODIFIER | c.541-918dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr2 | 113939029 | |||||
chr2:113939141
|
A | C | 1 | a0001c0001t0001g0280 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.541-818A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939141 | ||||||
chr2:113939149
|
G | A | 65 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(62): Show | 67 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(64): Show |
intron_variant | MODIFIER | c.541-810G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939149 | ||||||
chr2:113939273
|
C | A | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.541-686C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939273 | ||||||
chr2:113939273
|
C | T | 2 | a0001c0001t0004g0157a0002c0004t0006g0229 | 2 | HG02738.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.541-686C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939273 | ||||||
chr2:113939321
|
C | T | 1 | a0001c0001t0004g0201 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.541-638C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939321 | ||||||
chr2:113939455
|
C | G | 2 | a0001c0001t0001g0274a0001c0001t0001g0277 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.541-504C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939455 | ||||||
chr2:113939560
|
G | T | 1 | a0001c0001t0001g0308 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.541-399G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939560 | ||||||
chr2:113939669
|
T | C | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.541-290T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939669 | ||||||
chr2:113939788
|
C | G | 55 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(52): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.541-171C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939788 | ||||||
chr2:113939939
|
A | G | 6 | a0001c0001t0004g0001a0001c0001t0004g0136a0001c0001t0004g0137others(3): Show | 10 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.541-20A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 6/11 | chr2 | 113939939 | ||||||
chr2:113940407
|
AT | A | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.684+306delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113940407 | ||||||
chr2:113940761
|
G | T | 1 | a0002c0004t0006g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.684+659G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113940761 | ||||||
chr2:113940820
|
A | AT | 66 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(63): Show | 70 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(67): Show |
intron_variant | MODIFIER | c.684+733dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 113940820 | |||||
chr2:113940820
|
AT | A | 18 | a0001c0001t0002g0178a0001c0001t0007g0212a0001c0001t0007g0213others(15): Show | 18 | HG01243.hp1 HG01952.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.684+733delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 113940820 | |||||
chr2:113940892
|
C | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.684+790C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113940892 | ||||||
chr2:113940932
|
C | T | 1 | a0001c0001t0001g0241 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.684+830C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113940932 | ||||||
chr2:113940935
|
G | A | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.684+833G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113940935 | ||||||
chr2:113940994
|
G | A | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.684+892G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113940994 | ||||||
chr2:113941065
|
C | T | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.684+963C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113941065 | ||||||
chr2:113941114
|
T | C | 19 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(16): Show | 19 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.684+1012T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113941114 | ||||||
chr2:113941344
|
T | C | 1 | a0001c0001t0007g0350 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.685-842T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113941344 | ||||||
chr2:113941402
|
A | G | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.685-784A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113941402 | ||||||
chr2:113941414
|
A | G | 32 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(29): Show | 36 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(33): Show |
intron_variant | MODIFIER | c.685-772A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113941414 | ||||||
chr2:113941691
|
G | A | 5 | a0001c0001t0005g0326a0001c0001t0005g0328a0001c0001t0005g0329others(2): Show | 5 | HG01167.hp1 HG01981.hp1 HG02135.hp2 others(2): Show |
intron_variant | MODIFIER | c.685-495G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | chr2 | 113941691 | ||||||
chr2:113942083
|
GT | G | 24 | a0001c0001t0005g0326a0001c0001t0005g0328a0001c0001t0005g0329others(21): Show | 26 | HG00609.hp2 HG00639.hp1 HG00738.hp2 others(23): Show |
intron_variant | MODIFIER | c.685-91delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr2 | 113942083 | |||||
chr2:113942363
|
A | AT | 11 | a0001c0001t0009g0008a0001c0001t0009g0059a0001c0001t0009g0060others(8): Show | 12 | HG01884.hp2 HG02257.hp1 HG02615.hp2 others(9): Show |
intron_variant | MODIFIER | c.858+12dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113942363 | |||||
chr2:113942453
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.858+94G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113942453 | ||||||
chr2:113942470
|
GTTT | G | 4 | a0001c0001t0004g0206a0001c0001t0004g0207a0001c0001t0004g0208others(1): Show | 4 | HG02145.hp2 HG02717.hp1 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.858+114_858+116del others(3): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113942470 | |||||
chr2:113942478
|
GA | G | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.858+123delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113942478 | |||||
chr2:113942600
|
A | T | 1 | a0001c0001t0003g0116 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.858+241A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113942600 | ||||||
chr2:113943080
|
C | T | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.858+721C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943080 | ||||||
chr2:113943210
|
A | T | 1 | a0001c0001t0004g0137 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.858+851A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943210 | ||||||
chr2:113943275
|
T | C | 47 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(44): Show | 49 | HG00408.hp2 HG01099.hp1 HG01167.hp2 others(46): Show |
intron_variant | MODIFIER | c.858+916T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943275 | ||||||
chr2:113943464
|
A | C | 19 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(16): Show | 19 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.858+1105A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943464 | ||||||
chr2:113943565
|
T | C | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.858+1206T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943565 | ||||||
chr2:113943615
|
A | G | 1 | a0001c0001t0006g0228 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.858+1256A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943615 | ||||||
chr2:113943646
|
A | G | 1 | a0001c0001t0005g0336 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.858+1287A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943646 | ||||||
chr2:113943671
|
G | A | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.858+1312G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943671 | ||||||
chr2:113943770
|
G | A | 1 | a0001c0001t0019g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.858+1411G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943770 | ||||||
chr2:113943802
|
A | G | 55 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(52): Show | 61 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(58): Show |
intron_variant | MODIFIER | c.858+1443A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943802 | ||||||
chr2:113943821
|
C | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | HG01069.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.858+1462C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943821 | ||||||
chr2:113943879
|
G | A | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(20): Show | 25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.858+1520G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943879 | ||||||
chr2:113943892
|
G | A | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.858+1533G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943892 | ||||||
chr2:113943952
|
C | G | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.858+1593C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113943952 | ||||||
chr2:113944200
|
T | C | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.858+1841T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944200 | ||||||
chr2:113944376
|
C | T | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.858+2017C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944376 | ||||||
chr2:113944466
|
G | T | 1 | a0001c0001t0004g0136 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.858+2107G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944466 | ||||||
chr2:113944554
|
C | T | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.858+2195C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944554 | ||||||
chr2:113944580
|
C | G | 4 | a0001c0001t0006g0006a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.858+2221C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944580 | ||||||
chr2:113944584
|
T | TA | 136 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(133): Show | 145 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(142): Show |
intron_variant | MODIFIER | c.858+2253dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113944584 | |||||
chr2:113944584
|
T | TAA | 25 | a0001c0001t0001g0204a0001c0001t0001g0290a0001c0001t0001g0293others(22): Show | 25 | HG00438.hp1 HG01243.hp1 HG01261.hp2 others(22): Show |
intron_variant | MODIFIER | c.858+2252_858+2253d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113944584 | |||||
chr2:113944584
|
T | TAAA | 6 | a0001c0001t0002g0167a0001c0001t0002g0175a0001c0001t0002g0178others(3): Show | 6 | HG01106.hp1 HG01433.hp2 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.858+2251_858+2253d others(5): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113944584 | |||||
chr2:113944584
|
TA | T | 28 | a0001c0001t0001g0020a0001c0001t0001g0027a0001c0001t0001g0028others(25): Show | 29 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(26): Show |
intron_variant | MODIFIER | c.858+2253delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113944584 | |||||
chr2:113944584
|
TAA | T | 54 | a0001c0001t0001g0007a0001c0001t0001g0021a0001c0001t0001g0233others(51): Show | 56 | HG00408.hp2 HG00609.hp2 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.858+2252_858+2253d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113944584 | |||||
chr2:113944622
|
C | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.858+2263C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944622 | ||||||
chr2:113944635
|
G | A | 29 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(26): Show | 31 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.858+2276G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944635 | ||||||
chr2:113944655
|
G | A | 29 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(26): Show | 31 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.858+2296G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944655 | ||||||
chr2:113944692
|
G | A | 1 | a0001c0001t0005g0340 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.858+2333G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944692 | ||||||
chr2:113944923
|
T | C | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.858+2564T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113944923 | ||||||
chr2:113945013
|
C | A | 1 | a0001c0001t0002g0178 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.858+2654C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113945013 | ||||||
chr2:113945014
|
C | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.858+2655C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113945014 | ||||||
chr2:113945160
|
G | A | 4 | a0001c0001t0006g0228a0001c0001t0006g0230a0001c0001t0006g0231others(1): Show | 4 | HG02109.hp1 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.858+2801G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113945160 | ||||||
chr2:113945227
|
A | G | 221 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(218): Show | 236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.858+2868A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113945227 | ||||||
chr2:113945238
|
C | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.858+2879C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113945238 | ||||||
chr2:113945625
|
T | G | 6 | a0001c0001t0004g0001a0001c0001t0004g0136a0001c0001t0004g0137others(3): Show | 10 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(7): Show |
intron_variant | MODIFIER | c.858+3266T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113945625 | ||||||
chr2:113946131
|
A | G | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.858+3772A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946131 | ||||||
chr2:113946257
|
A | G | 2 | a0001c0001t0004g0045a0001c0001t0004g0049 | 2 | HG00544.hp2 NA18982.hp1 |
intron_variant | MODIFIER | c.858+3898A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946257 | ||||||
chr2:113946366
|
G | T | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.858+4007G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946366 | ||||||
chr2:113946389
|
T | C | 1 | a0001c0001t0006g0224 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.858+4030T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946389 | ||||||
chr2:113946501
|
A | G | 1 | a0001c0001t0006g0224 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.858+4142A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946501 | ||||||
chr2:113946733
|
G | T | 3 | a0001c0001t0006g0223a0001c0001t0006g0224a0001c0001t0023g0222 | 3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.858+4374G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946733 | ||||||
chr2:113946745
|
A | G | 1 | a0001c0001t0003g0067 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.858+4386A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946745 | ||||||
chr2:113946765
|
C | T | 32 | a0001c0001t0002g0018a0001c0001t0002g0050a0001c0001t0002g0161others(29): Show | 33 | HG00438.hp1 HG01070.hp2 HG01106.hp1 others(30): Show |
intron_variant | MODIFIER | c.858+4406C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946765 | ||||||
chr2:113946921
|
C | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.859-4558C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113946921 | ||||||
chr2:113947073
|
C | T | 8 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(5): Show | 9 | HG01891.hp1 HG01891.hp2 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.859-4406C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947073 | ||||||
chr2:113947090
|
C | T | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.859-4389C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947090 | ||||||
chr2:113947156
|
C | T | 1 | a0001c0001t0003g0068 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.859-4323C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947156 | ||||||
chr2:113947427
|
G | A | 1 | a0001c0001t0001g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.859-4052G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947427 | ||||||
chr2:113947471
|
G | A | 9 | a0001c0001t0002g0004a0001c0001t0002g0091a0001c0001t0002g0093others(6): Show | 10 | HG02083.hp1 HG02165.hp1 NA18941.hp2 others(7): Show |
intron_variant | MODIFIER | c.859-4008G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947471 | ||||||
chr2:113947509
|
G | A | 1 | a0001c0001t0001g0325 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.859-3970G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947509 | ||||||
chr2:113947517
|
T | C | 1 | a0001c0001t0006g0224 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.859-3962T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947517 | ||||||
chr2:113947572
|
T | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.859-3907T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947572 | ||||||
chr2:113947597
|
C | A | 3 | a0001c0001t0004g0140a0001c0001t0004g0142a0001c0001t0004g0143 | 3 | HG02523.hp2 NA18989.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.859-3882C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947597 | ||||||
chr2:113947633
|
A | T | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.859-3846A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947633 | ||||||
chr2:113947669
|
A | G | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.859-3810A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947669 | ||||||
chr2:113947853
|
A | G | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.859-3626A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947853 | ||||||
chr2:113947897
|
G | A | 6 | a0001c0001t0007g0345a0001c0001t0007g0346a0001c0001t0007g0347others(3): Show | 6 | HG02280.hp2 HG02723.hp2 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.859-3582G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947897 | ||||||
chr2:113947958
|
G | C | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.859-3521G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113947958 | ||||||
chr2:113948092
|
T | C | 1 | a0001c0001t0019g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.859-3387T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948092 | ||||||
chr2:113948118
|
T | G | 1 | a0001c0001t0007g0347 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.859-3361T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948118 | ||||||
chr2:113948153
|
G | A | 1 | a0001c0001t0015g0341 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.859-3326G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948153 | ||||||
chr2:113948187
|
G | T | 7 | a0001c0001t0004g0138a0001c0001t0004g0152a0001c0001t0004g0154others(4): Show | 7 | NA18747.hp2 NA18941.hp1 NA18957.hp2 others(4): Show |
intron_variant | MODIFIER | c.859-3292G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948187 | ||||||
chr2:113948228
|
C | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.859-3251C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948228 | ||||||
chr2:113948376
|
C | T | 5 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0012g0055others(2): Show | 5 | HG01884.hp2 HG02896.hp2 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-3103C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948376 | ||||||
chr2:113948461
|
G | A | 304 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(301): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.859-3018G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948461 | ||||||
chr2:113948959
|
T | G | 1 | a0001c0001t0002g0193 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.859-2520T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948959 | ||||||
chr2:113948973
|
C | CTACTGTC others(3946): Show |
1 | a0001c0001t0001g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3955): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3947): Show |
1 | a0001c0001t0001g0242 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3956): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3943): Show |
2 | a0001c0001t0001g0243a0001c0001t0001g0323 | 2 | HG02015.hp2 NA18948.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3952): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3945): Show |
6 | a0001c0001t0001g0253a0001c0001t0001g0282a0001c0001t0001g0283others(3): Show | 6 | HG00408.hp2 HG01884.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3954): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3947): Show |
1 | a0001c0001t0001g0259 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3956): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3946): Show |
1 | a0001c0001t0001g0266 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3955): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3945): Show |
1 | a0001c0001t0001g0245 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3954): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3944): Show |
9 | a0001c0001t0001g0021a0001c0001t0001g0232a0001c0001t0001g0239others(6): Show | 10 | HG02074.hp1 HG02148.hp1 HG03492.hp1 others(7): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3953): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3945): Show |
2 | a0001c0001t0001g0238a0001c0001t0001g0252 | 2 | HG00639.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3954): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3945): Show |
1 | a0001c0001t0001g0268 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3954): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3944): Show |
1 | a0001c0001t0001g0249 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3953): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3943): Show |
26 | a0001c0001t0001g0007a0001c0001t0001g0233a0001c0001t0001g0236others(23): Show | 27 | HG01099.hp1 HG01167.hp2 HG01169.hp1 others(24): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3952): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3943): Show |
1 | a0001c0001t0001g0254 | 1 | NA18943.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3952): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3943): Show |
1 | a0001c0001t0001g0325 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3952): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3942): Show |
3 | a0001c0001t0001g0235a0001c0001t0001g0276a0001c0001t0001g0278 | 3 | HG01168.hp1 HG02080.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3951): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3944): Show |
1 | a0001c0001t0001g0234 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3953): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3946): Show |
1 | a0001c0001t0001g0241 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3955): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3945): Show |
1 | a0001c0001t0001g0237 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3954): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3939): Show |
2 | a0001c0001t0001g0020a0001c0001t0037g0020 | 2 | NA18988.hp2 NA19063.hp1 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3948): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3947): Show |
1 | a0001c0001t0001g0280 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3956): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3964): Show |
1 | a0001c0001t0001g0303 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3973): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3968): Show |
3 | a0001c0001t0001g0023a0001c0001t0001g0292a0001c0001t0001g0304 | 4 | HG00408.hp1 HG02040.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3977): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3964): Show |
2 | a0001c0001t0001g0294a0001c0001t0001g0300 | 2 | HG02071.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3973): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3962): Show |
12 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0032others(9): Show | 13 | HG02015.hp1 HG02074.hp2 HG02135.hp1 others(10): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3971): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3962): Show |
1 | a0001c0001t0001g0290 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3971): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3964): Show |
1 | a0001c0001t0001g0318 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3973): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3960): Show |
2 | a0001c0001t0017g0299a0001c0001t0038g0297 | 2 | HG04204.hp1 NA18953.hp1 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3969): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3962): Show |
20 | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(17): Show | 21 | HG00544.hp1 HG00609.hp1 HG00621.hp2 others(18): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3971): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3962): Show |
1 | a0001c0001t0001g0033 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3971): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3962): Show |
1 | a0001c0001t0001g0307 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3971): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3963): Show |
1 | a0001c0001t0001g0204 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3972): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3952): Show |
1 | a0001c0001t0007g0214 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3961): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3960): Show |
1 | a0001c0001t0001g0322 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3969): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3962): Show |
1 | a0001c0001t0001g0314 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3971): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3950): Show |
3 | a0001c0001t0013g0216a0001c0001t0013g0219a0001c0001t0013g0220 | 3 | HG01243.hp1 HG02055.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3959): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3949): Show |
1 | a0001c0001t0013g0210 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3958): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3948): Show |
1 | a0001c0001t0013g0211 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3957): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3950): Show |
1 | a0001c0001t0007g0350 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3959): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3950): Show |
1 | a0001c0001t0007g0217 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3959): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3949): Show |
1 | a0001c0001t0007g0215 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3958): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3949): Show |
1 | a0001c0001t0007g0346 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3958): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3948): Show |
2 | a0001c0001t0007g0212a0001c0001t0007g0213 | 2 | HG02486.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3957): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3948): Show |
4 | a0001c0001t0007g0345a0001c0001t0007g0347a0001c0001t0007g0349others(1): Show | 4 | HG02280.hp2 HG02723.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3957): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3941): Show |
1 | a0001c0001t0007g0218 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3950): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3952): Show |
4 | a0001c0001t0005g0026a0001c0001t0005g0333a0001c0001t0005g0334others(1): Show | 5 | HG02622.hp1 HG02895.hp2 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3961): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3952): Show |
2 | a0001c0001t0001g0338a0001c0001t0001g0339 | 2 | HG01891.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3961): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3952): Show |
1 | a0001c0001t0001g0027 | 2 | HG02559.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3961): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3963): Show |
1 | a0001c0001t0001g0310 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3972): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3963): Show |
1 | a0001c0001t0032g0301 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3972): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3953): Show |
2 | a0001c0001t0005g0337a0001c0001t0005g0344 | 2 | NA18961.hp2 NA18970.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3962): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3956): Show |
1 | a0001c0001t0006g0228 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3965): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3954): Show |
1 | a0002c0004t0006g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3963): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3953): Show |
6 | a0001c0001t0005g0326a0001c0001t0005g0328a0001c0001t0005g0330others(3): Show | 6 | HG01167.hp1 HG01981.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3962): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3954): Show |
1 | a0001c0001t0005g0327 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3963): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3953): Show |
1 | a0001c0001t0005g0332 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3962): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3939): Show |
2 | a0001c0001t0004g0207a0001c0001t0004g0209 | 2 | HG03516.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3948): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3953): Show |
2 | a0001c0001t0006g0230a0001c0001t0006g0231 | 2 | HG02109.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3962): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3954): Show |
1 | a0001c0001t0006g0223 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3963): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3955): Show |
4 | a0001c0001t0006g0006a0001c0001t0006g0225a0001c0001t0006g0226others(1): Show | 6 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(3): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3964): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3945): Show |
1 | a0001c0001t0009g0111 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3954): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3939): Show |
36 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(33): Show | 41 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(38): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3948): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3943): Show |
8 | a0001c0001t0009g0008a0001c0001t0009g0059a0001c0001t0009g0060others(5): Show | 9 | HG01243.hp2 HG02257.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3952): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3943): Show |
1 | a0001c0001t0009g0128 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3952): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3955): Show |
1 | a0001c0001t0006g0224 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3964): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3953): Show |
1 | a0001c0001t0006g0221 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3962): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3931): Show |
2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3940): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3940): Show |
1 | a0001c0001t0004g0145 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3949): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3940): Show |
1 | a0001c0001t0004g0147 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3949): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3956): Show |
1 | a0001c0001t0005g0329 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3965): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3940): Show |
2 | a0001c0001t0004g0133a0001c0001t0004g0208 | 2 | HG02145.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3949): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3940): Show |
3 | a0001c0001t0004g0047a0001c0001t0004g0049a0001c0001t0036g0038 | 3 | HG00544.hp2 HG02027.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3949): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3956): Show |
1 | a0001c0001t0023g0222 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.859-2506_859-2505i others(3965): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948973
|
C | CTACTGTC others(3951): Show |
5 | a0001c0001t0001g0028a0001c0001t0015g0028a0001c0001t0015g0341others(2): Show | 5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-2506_859-2505i others(3960): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948973 | ||||||
chr2:113948974
|
A | T | 221 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(218): Show | 236 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.859-2505A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113948974 | ||||||
chr2:113949051
|
C | T | 54 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(51): Show | 60 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(57): Show |
intron_variant | MODIFIER | c.859-2428C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949051 | ||||||
chr2:113949089
|
G | C | 3 | a0001c0001t0001g0247a0001c0001t0001g0268a0001c0001t0001g0281 | 3 | NA18984.hp2 NA18991.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.859-2390G>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949089 | ||||||
chr2:113949377
|
C | CA | 71 | a0001c0001t0002g0091a0001c0001t0002g0186a0001c0001t0002g0192others(68): Show | 79 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(76): Show |
intron_variant | MODIFIER | c.859-2086dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113949377 | |||||
chr2:113949377
|
CA | C | 11 | a0001c0001t0003g0010a0001c0001t0003g0016a0001c0001t0003g0066others(8): Show | 13 | HG02965.hp2 NA18940.hp1 NA18942.hp2 others(10): Show |
intron_variant | MODIFIER | c.859-2086delA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113949377 | |||||
chr2:113949393
|
A | G | 2 | a0001c0001t0001g0256a0001c0001t0001g0270 | 2 | HG01943.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.859-2086A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949393 | ||||||
chr2:113949393
|
AG | A | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.859-2085delG | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949393 | ||||||
chr2:113949394
|
G | A | 4 | a0001c0001t0001g0204a0001c0001t0001g0235a0001c0001t0001g0256others(1): Show | 4 | HG01943.hp1 HG02080.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.859-2085G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949394 | ||||||
chr2:113949394
|
G | GA | 131 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(128): Show | 138 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.859-2074dupA | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113949394 | |||||
chr2:113949397
|
A | G | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.859-2082A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949397 | ||||||
chr2:113949406
|
G | A | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.859-2073G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949406 | ||||||
chr2:113949474
|
A | T | 304 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(301): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.859-2005A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949474 | ||||||
chr2:113949476
|
GTC | G | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.859-1998_859-1997d others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113949476 | |||||
chr2:113949484
|
A | G | 112 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(109): Show | 117 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(114): Show |
intron_variant | MODIFIER | c.859-1995A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949484 | ||||||
chr2:113949668
|
C | T | 1 | a0001c0001t0003g0196 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.859-1811C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949668 | ||||||
chr2:113949810
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0338a0001c0001t0001g0339 | 4 | HG01891.hp1 HG02559.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.859-1669G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949810 | ||||||
chr2:113949970
|
G | A | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.859-1509G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949970 | ||||||
chr2:113949977
|
T | A | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.859-1502T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113949977 | ||||||
chr2:113950023
|
T | C | 1 | a0001c0001t0011g0306 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.859-1456T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950023 | ||||||
chr2:113950118
|
T | C | 5 | a0001c0001t0001g0028a0001c0001t0015g0028a0001c0001t0015g0341others(2): Show | 5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-1361T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950118 | ||||||
chr2:113950144
|
T | C | 77 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(74): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.859-1335T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950144 | ||||||
chr2:113950444
|
C | T | 77 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(74): Show | 82 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(79): Show |
intron_variant | MODIFIER | c.859-1035C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950444 | ||||||
chr2:113950489
|
C | T | 45 | a0001c0001t0004g0001a0001c0001t0004g0017a0001c0001t0004g0040others(42): Show | 50 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(47): Show |
intron_variant | MODIFIER | c.859-990C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950489 | ||||||
chr2:113950530
|
G | T | 1 | a0001c0001t0002g0036 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.859-949G>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950530 | ||||||
chr2:113950716
|
T | C | 1 | a0001c0001t0009g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.859-763T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950716 | ||||||
chr2:113950826
|
AAAAG | A | 71 | a0001c0001t0002g0002a0001c0001t0002g0004a0001c0001t0002g0015others(68): Show | 76 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(73): Show |
intron_variant | MODIFIER | c.859-647_859-644del others(4): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr2 | 113950826 | |||||
chr2:113950833
|
A | G | 1 | a0001c0001t0032g0301 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.859-646A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950833 | ||||||
chr2:113950857
|
C | T | 5 | a0001c0001t0005g0026a0001c0001t0005g0327a0001c0001t0005g0333others(2): Show | 6 | HG02145.hp1 HG02622.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.859-622C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950857 | ||||||
chr2:113950861
|
G | A | 1 | a0001c0001t0004g0143 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.859-618G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950861 | ||||||
chr2:113950954
|
C | T | 2 | a0001c0001t0004g0147a0001c0001t0007g0347 | 2 | HG02040.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.859-525C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113950954 | ||||||
chr2:113951017
|
C | T | 31 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(28): Show | 33 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.859-462C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113951017 | ||||||
chr2:113951021
|
A | G | 3 | a0001c0001t0001g0021a0001c0001t0001g0251a0001c0001t0001g0324 | 4 | NA18944.hp1 NA19057.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.859-458A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113951021 | ||||||
chr2:113951021
|
A | T | 5 | a0001c0001t0001g0272a0001c0001t0001g0274a0001c0001t0001g0275others(2): Show | 5 | HG01099.hp1 HG01167.hp2 HG01168.hp1 others(2): Show |
intron_variant | MODIFIER | c.859-458A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113951021 | ||||||
chr2:113951031
|
C | A | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.859-448C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113951031 | ||||||
chr2:113951151
|
C | T | 298 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(295): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.859-328C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113951151 | ||||||
chr2:113951358
|
A | G | 1 | a0001c0001t0001g0247 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.859-121A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 8/11 | chr2 | 113951358 | ||||||
chr2:113951594
|
T | C | 3 | a0001c0001t0006g0223a0001c0001t0006g0224a0001c0001t0023g0222 | 3 | HG02280.hp1 HG03225.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.951+23T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 9/11 | chr2 | 113951594 | ||||||
chr2:113951899
|
A | T | 135 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(132): Show | 142 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(139): Show |
intron_variant | MODIFIER | c.1077+54A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113951899 | ||||||
chr2:113951963
|
A | G | 1 | a0001c0001t0009g0160 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1077+118A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113951963 | ||||||
chr2:113952011
|
AT | A | 8 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(5): Show | 10 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077+169delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 113952011 | |||||
chr2:113952087
|
A | T | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.1077+242A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952087 | ||||||
chr2:113952104
|
A | G | 5 | a0001c0001t0001g0028a0001c0001t0015g0028a0001c0001t0015g0341others(2): Show | 5 | HG01891.hp2 HG02615.hp1 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.1077+259A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952104 | ||||||
chr2:113952255
|
C | T | 1 | a0001c0001t0001g0305 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1077+410C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952255 | ||||||
chr2:113952290
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0001g0032 | 2 | NA18951.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.1077+445C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952290 | ||||||
chr2:113952448
|
C | T | 2 | a0001c0001t0002g0094a0001c0001t0002g0102 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1077+603C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952448 | ||||||
chr2:113952743
|
C | A | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1077+898C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952743 | ||||||
chr2:113952839
|
C | G | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1077+994C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952839 | ||||||
chr2:113952883
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1077+1038C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952883 | ||||||
chr2:113952941
|
A | C | 2 | a0001c0001t0002g0050a0001c0001t0002g0205 | 2 | HG03654.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1077+1096A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113952941 | ||||||
chr2:113953066
|
C | T | 1 | a0001c0001t0004g0145 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1077+1221C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953066 | ||||||
chr2:113953284
|
G | A | 8 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(5): Show | 10 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077+1439G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953284 | ||||||
chr2:113953352
|
T | C | 7 | a0001c0001t0002g0096a0001c0001t0002g0174a0001c0001t0002g0186others(4): Show | 7 | HG00733.hp2 HG01069.hp2 HG01517.hp1 others(4): Show |
intron_variant | MODIFIER | c.1077+1507T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953352 | ||||||
chr2:113953417
|
C | T | 1 | a0001c0001t0018g0302 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.1077+1572C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953417 | ||||||
chr2:113953516
|
G | A | 1 | a0001c0001t0019g0039 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1077+1671G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953516 | ||||||
chr2:113953533
|
C | G | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.1077+1688C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953533 | ||||||
chr2:113953611
|
C | A | 1 | a0001c0001t0007g0217 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1077+1766C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953611 | ||||||
chr2:113953679
|
GGTGT | G | 51 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(48): Show | 62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1077+1839_1077+184 others(8): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 113953679 | |||||
chr2:113953684
|
G | A | 51 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(48): Show | 62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1077+1839G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953684 | ||||||
chr2:113953685
|
T | A | 51 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(48): Show | 62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1077+1840T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953685 | ||||||
chr2:113953686
|
G | A | 51 | a0001c0001t0003g0003a0001c0001t0003g0009a0001c0001t0003g0010others(48): Show | 62 | HG00438.hp2 HG00735.hp1 HG00738.hp1 others(59): Show |
intron_variant | MODIFIER | c.1077+1841G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953686 | ||||||
chr2:113953687
|
T | TAC | 51 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(48): Show | 54 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.1077+1857_1077+185 others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 113953687 | |||||
chr2:113953687
|
T | TACAC | 3 | a0001c0001t0017g0288a0001c0001t0017g0289a0001c0001t0017g0311 | 3 | NA18995.hp1 NA19055.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.1077+1855_1077+185 others(8): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 113953687 | |||||
chr2:113953736
|
A | G | 1 | a0001c0001t0003g0012 | 2 | HG01099.hp2 HG01981.hp2 |
intron_variant | MODIFIER | c.1078-1887A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953736 | ||||||
chr2:113953853
|
C | T | 2 | a0001c0001t0034g0351a0001c0001t0035g0352 | 2 | HG03453.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1078-1770C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953853 | ||||||
chr2:113953878
|
A | G | 1 | a0002c0004t0006g0229 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1078-1745A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953878 | ||||||
chr2:113953929
|
T | A | 1 | a0001c0001t0001g0308 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.1078-1694T>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953929 | ||||||
chr2:113953946
|
T | G | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(20): Show | 25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1078-1677T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113953946 | ||||||
chr2:113954054
|
G | A | 1 | a0001c0001t0028g0058 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1078-1569G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954054 | ||||||
chr2:113954073
|
G | A | 15 | a0001c0001t0005g0026a0001c0001t0005g0326a0001c0001t0005g0327others(12): Show | 16 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.1078-1550G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954073 | ||||||
chr2:113954141
|
G | A | 1 | a0001c0001t0006g0230 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1078-1482G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954141 | ||||||
chr2:113954302
|
TAA | T | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.1078-1320_1078-131 others(6): Show |
ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954302 | ||||||
chr2:113954333
|
TG | T | 14 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(11): Show | 16 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(13): Show |
intron_variant | MODIFIER | c.1078-1289delG | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954333 | ||||||
chr2:113954347
|
A | G | 6 | a0001c0001t0012g0053a0001c0001t0012g0054a0001c0001t0012g0055others(3): Show | 6 | HG01884.hp2 HG02809.hp2 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1078-1276A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954347 | ||||||
chr2:113954418
|
A | T | 298 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(295): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1078-1205A>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954418 | ||||||
chr2:113954483
|
A | G | 3 | a0001c0001t0001g0281a0001c0001t0034g0351a0001c0001t0035g0352 | 3 | HG03453.hp2 NA18984.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1078-1140A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954483 | ||||||
chr2:113954581
|
A | AT | 15 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(12): Show | 16 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1078-1029dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr2 | 113954581 | |||||
chr2:113954733
|
G | A | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1078-890G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954733 | ||||||
chr2:113954767
|
T | C | 17 | a0001c0001t0007g0212a0001c0001t0007g0213a0001c0001t0007g0214others(14): Show | 17 | HG01243.hp1 HG02055.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1078-856T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954767 | ||||||
chr2:113954810
|
A | C | 1 | a0001c0001t0007g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1078-813A>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113954810 | ||||||
chr2:113955367
|
A | G | 1 | a0001c0001t0002g0185 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1078-256A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113955367 | ||||||
chr2:113955400
|
T | C | 298 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(295): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.1078-223T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113955400 | ||||||
chr2:113955592
|
A | G | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1078-31A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113955592 | ||||||
chr2:113955609
|
A | G | 1 | a0001c0001t0001g0276 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1078-14A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113955609 | ||||||
chr2:113955611
|
G | A | 12 | a0001c0001t0006g0006a0001c0001t0006g0221a0001c0001t0006g0223others(9): Show | 14 | HG00639.hp1 HG00738.hp2 HG00741.hp1 others(11): Show |
intron_variant | MODIFIER | c.1078-12G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 10/11 | chr2 | 113955611 | ||||||
chr2:113955773
|
C | T | 1 | a0001c0001t0007g0345 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1161+67C>T | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113955773 | ||||||
chr2:113955789
|
C | A | 1 | a0001c0001t0002g0202 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1161+83C>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113955789 | ||||||
chr2:113955807
|
G | A | 1 | a0001c0001t0003g0120 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1161+101G>A | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113955807 | ||||||
chr2:113956377
|
A | AT | 17 | a0001c0001t0004g0045a0001c0001t0005g0026a0001c0001t0005g0326others(14): Show | 18 | HG00609.hp2 HG01167.hp1 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.1161+687dupT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 113956377 | |||||
chr2:113956377
|
AT | A | 16 | a0001c0001t0001g0238a0001c0001t0001g0242a0001c0001t0001g0252others(13): Show | 16 | HG00639.hp2 HG00733.hp2 HG01069.hp1 others(13): Show |
intron_variant | MODIFIER | c.1161+687delT | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr2 | 113956377 | |||||
chr2:113956481
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1161+775T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113956481 | ||||||
chr2:113956576
|
C | G | 1 | a0001c0001t0006g0221 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1162-784C>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113956576 | ||||||
chr2:113956803
|
T | C | 166 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(163): Show | 175 | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(172): Show |
intron_variant | MODIFIER | c.1162-557T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113956803 | ||||||
chr2:113956836
|
T | G | 1 | a0001c0001t0001g0263 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1162-524T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113956836 | ||||||
chr2:113956852
|
T | C | 63 | a0001c0001t0001g0007a0001c0001t0001g0020a0001c0001t0001g0021others(60): Show | 65 | HG00408.hp2 HG00639.hp2 HG01099.hp1 others(62): Show |
intron_variant | MODIFIER | c.1162-508T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113956852 | ||||||
chr2:113956866
|
T | G | 23 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0338others(20): Show | 25 | HG00609.hp2 HG01167.hp1 HG01891.hp1 others(22): Show |
intron_variant | MODIFIER | c.1162-494T>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113956866 | ||||||
chr2:113957265
|
T | C | 1 | a0001c0001t0001g0250 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1162-95T>C | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113957265 | ||||||
chr2:113957278
|
A | G | 49 | a0001c0001t0001g0022a0001c0001t0001g0023a0001c0001t0001g0024others(46): Show | 52 | HG00408.hp1 HG00544.hp1 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.1162-82A>G | ACTR3 | ENSG00000115091.12 | transcript | ENST00000263238.7 | protein_coding | 11/11 | chr2 | 113957278 |