geneid | 90957 |
---|---|
ensemblid | ENSG00000163214.21 |
hgncid | 20086 |
symbol | DHX57 |
name | DExH-box helicase 57 |
refseq_nuc | NM_198963.3 |
refseq_prot | NP_945314.1 |
ensembl_nuc | ENST00000457308.6 |
ensembl_prot | ENSP00000405111.2 |
mane_status | MANE Select |
chr | chr2 |
start | 38797729 |
end | 38875934 |
strand | - |
ver | v1.2 |
region | chr2:38797729-38875934 |
region5000 | chr2:38792729-38880934 |
regionname0 | DHX57_chr2_38797729_38875934 |
regionname5000 | DHX57_chr2_38792729_38880934 |
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 | 1386 | 135 | 55 | 28 | 34 | 2 | 14 | 29 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002 | 0/0 | 1386 | 126 | 20 | 27 | 58 | 4 | 17 | 43 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0003 | 0/0 | 1386 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0004 | 0/0 | 1385 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0005 | 0/0 | 1386 | 3 | 0 | 0 | 0 | 1 | 2 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0006 | 0/0 | 1386 | 2 | 0 | 1 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0007 | 0/0 | 1386 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0008 | 0/0 | 1386 | 2 | 0 | 2 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0009 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0010 | 0/0 | 1386 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0011 | 0/0 | 1386 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0012 | 0/0 | 1386 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0013 | 0/0 | 1386 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0014 | 0/0 | 1386 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
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 | 4161 | 116 | 42 | 24 | 34 | 2 | 12 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0002 | 0/0 | 4161 | 116 | 17 | 26 | 52 | 4 | 17 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0003 | 0/0 | 4161 | 7 | 4 | 3 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0004 | 0/0 | 4161 | 5 | 5 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0005 | 0/0 | 4161 | 5 | 5 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0006 | 0/0 | 4158 | 3 | 3 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0007 | 0/0 | 4161 | 3 | 0 | 0 | 0 | 1 | 2 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0008 | 0/0 | 4161 | 3 | 0 | 1 | 2 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0009 | 0/0 | 4161 | 3 | 2 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0010 | 0/0 | 4161 | 3 | 0 | 0 | 3 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0011 | 0/0 | 4161 | 2 | 1 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0012 | 0/0 | 4161 | 2 | 0 | 2 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0013 | 0/0 | 4161 | 2 | 2 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0014 | 0/0 | 4161 | 2 | 0 | 1 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0015 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0016 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0017 | 0/0 | 4161 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0018 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0019 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0020 | 0/0 | 4161 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0021 | 0/0 | 4161 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0022 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0023 | 0/0 | 4161 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0024 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0025 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
c0026 | 0/0 | 4161 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
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 | 726 | 123 | 21 | 26 | 55 | 4 | 17 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
t0002 | 0/1 | 724 | 91 | 21 | 25 | 27 | 3 | 14 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
t0003 | 1/0 | 725 | 55 | 40 | 5 | 9 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
t0004 | 0/0 | 726 | 6 | 0 | 3 | 0 | 1 | 2 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
t0005 | 0/0 | 725 | 3 | 1 | 0 | 1 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
t0006 | 0/0 | 727 | 2 | 0 | 0 | 2 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
t0007 | 0/0 | 725 | 2 | 1 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
t0008 | 0/0 | 726 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
t0009 | 0/0 | 726 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
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 | 4161 | 116 | 42 | 24 | 34 | 2 | 12 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0003 | 0/0 | 4161 | 7 | 4 | 3 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0004 | 0/0 | 4161 | 5 | 5 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0011 | 0/0 | 4161 | 2 | 1 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0015 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0017 | 0/0 | 4161 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0019 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0021 | 0/0 | 4161 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0024 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0002 | 0/0 | 4161 | 116 | 17 | 26 | 52 | 4 | 17 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0008 | 0/0 | 4161 | 3 | 0 | 1 | 2 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0009 | 0/0 | 4161 | 3 | 2 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0010 | 0/0 | 4161 | 3 | 0 | 0 | 3 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0022 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0003c0005 | 0/0 | 4161 | 5 | 5 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0004c0006 | 0/0 | 4158 | 3 | 3 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0005c0007 | 0/0 | 4161 | 3 | 0 | 0 | 0 | 1 | 2 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0006c0014 | 0/0 | 4161 | 2 | 0 | 1 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0007c0013 | 0/0 | 4161 | 2 | 2 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0008c0012 | 0/0 | 4161 | 2 | 0 | 2 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0009c0016 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0010c0025 | 0/0 | 4161 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0011c0018 | 0/0 | 4161 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0012c0020 | 0/0 | 4161 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0013c0023 | 0/0 | 4161 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0014c0026 | 0/0 | 4161 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002 | 0/1 | 4884 | 74 | 16 | 20 | 24 | 2 | 11 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0001t0003 | 1/0 | 4885 | 37 | 24 | 3 | 9 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0001t0005 | 0/0 | 4885 | 2 | 0 | 0 | 1 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0001t0007 | 0/0 | 4885 | 2 | 1 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0001t0009 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0003t0001 | 0/0 | 4886 | 7 | 4 | 3 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0004t0003 | 0/0 | 4885 | 5 | 5 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0011t0002 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0011t0003 | 0/0 | 4885 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0015t0005 | 0/0 | 4885 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0017t0002 | 0/0 | 4884 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0019t0002 | 0/0 | 4884 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0021t0001 | 0/0 | 4886 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0001c0024t0003 | 0/0 | 4885 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0002t0001 | 0/0 | 4886 | 107 | 15 | 23 | 50 | 4 | 15 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0002t0003 | 0/0 | 4885 | 2 | 1 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0002t0004 | 0/0 | 4886 | 4 | 0 | 2 | 0 | 0 | 2 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0002t0006 | 0/0 | 4887 | 2 | 0 | 0 | 2 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0002t0008 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0008t0002 | 0/0 | 4884 | 3 | 0 | 1 | 2 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0009t0002 | 0/0 | 4884 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0009t0003 | 0/0 | 4885 | 2 | 2 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0010t0001 | 0/0 | 4886 | 3 | 0 | 0 | 3 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0002c0022t0001 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0003c0005t0002 | 0/0 | 4884 | 4 | 4 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0003c0005t0003 | 0/0 | 4885 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0004c0006t0003 | 0/0 | 4882 | 3 | 3 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0005c0007t0002 | 0/0 | 4884 | 3 | 0 | 0 | 0 | 1 | 2 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0006c0014t0004 | 0/0 | 4886 | 2 | 0 | 1 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0007c0013t0003 | 0/0 | 4885 | 2 | 2 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0008c0012t0002 | 0/0 | 4884 | 2 | 0 | 2 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0009c0016t0001 | 0/0 | 4886 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0010c0025t0001 | 0/0 | 4886 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0011c0018t0001 | 0/0 | 4886 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0012c0020t0003 | 0/0 | 4885 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0013c0023t0001 | 0/0 | 4886 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
a0014c0026t0002 | 0/0 | 4884 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | copy fasta | chr2 | 38792729 | 38880934 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0243 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0246 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0144 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0005g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0005g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0007g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0007g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0001t0009g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0003t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0003t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0003t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0003t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0003t0001g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0003t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0004t0003g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0004t0003g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0004t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0004t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0011t0002g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0011t0003g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0015t0005g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0017t0002g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0019t0002g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0021t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0001c0024t0003g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0006 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0012 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0003g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0004g0276 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0004g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0004g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0004g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0006g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0006g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0002t0008g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0008t0002g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0008t0002g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0008t0002g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0009t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0009t0003g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0009t0003g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0010t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0010t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0010t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0002c0022t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0003c0005t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0003c0005t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0003c0005t0002g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0003c0005t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0003c0005t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0004c0006t0003g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0004c0006t0003g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0004c0006t0003g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0005c0007t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0005c0007t0002g0198 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0005c0007t0002g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0006c0014t0004g0280 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0006c0014t0004g0281 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0007c0013t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0007c0013t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0008c0012t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0008c0012t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0009c0016t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0010c0025t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0011c0018t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0012c0020t0003g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0013c0023t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
a0014c0026t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00323 | hp1 | a0006 | c0014 | t0004 | g0281 | EUR | FIN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00323 | hp2 | a0002 | c0002 | t0001 | g0110 | EUR | FIN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00423 | hp1 | a0002 | c0002 | t0001 | g0027 | EAS | CHS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00423 | hp2 | a0002 | c0002 | t0001 | g0017 | EAS | CHS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00558 | hp1 | a0002 | c0002 | t0001 | g0118 | EAS | CHS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0114 | EAS | CHS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00609 | hp1 | a0002 | c0002 | t0001 | g0090 | EAS | CHS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | CHS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00621 | hp1 | a0002 | c0002 | t0001 | g0088 | EAS | CHS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00621 | hp2 | a0002 | c0002 | t0001 | g0025 | EAS | CHS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00639 | hp2 | a0002 | c0002 | t0001 | g0061 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00673 | hp1 | a0002 | c0010 | t0001 | g0115 | EAS | CHS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0196 | EAS | CHS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00735 | hp1 | a0002 | c0002 | t0001 | g0049 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00735 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00741 | hp1 | a0014 | c0026 | t0002 | g0214 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01070 | hp2 | a0002 | c0002 | t0001 | g0119 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01071 | hp1 | a0002 | c0002 | t0001 | g0131 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01074 | hp1 | a0002 | c0002 | t0004 | g0277 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01074 | hp2 | a0001 | c0003 | t0001 | g0223 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01081 | hp1 | a0002 | c0002 | t0001 | g0105 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01081 | hp2 | a0001 | c0001 | t0002 | g0234 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01099 | hp1 | a0002 | c0002 | t0001 | g0060 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01099 | hp2 | a0001 | c0011 | t0002 | g0220 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01106 | hp1 | a0001 | c0003 | t0001 | g0173 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01106 | hp2 | a0001 | c0001 | t0003 | g0251 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01109 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01109 | hp2 | a0002 | c0002 | t0001 | g0104 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0238 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01167 | hp2 | a0008 | c0012 | t0002 | g0043 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0054 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0242 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01169 | hp1 | a0008 | c0012 | t0002 | g0044 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01169 | hp2 | a0002 | c0002 | t0001 | g0056 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0217 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0042 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01192 | hp2 | a0002 | c0002 | t0001 | g0096 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01243 | hp1 | a0012 | c0020 | t0003 | g0184 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0010 | AMR | PUR | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01256 | hp1 | a0002 | c0002 | t0001 | g0046 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01256 | hp2 | a0001 | c0003 | t0001 | g0219 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0227 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01257 | hp2 | a0002 | c0002 | t0001 | g0063 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01346 | hp1 | a0002 | c0002 | t0001 | g0004 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01346 | hp2 | a0002 | c0002 | t0001 | g0053 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01361 | hp1 | a0002 | c0008 | t0002 | g0094 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01361 | hp2 | a0001 | c0001 | t0007 | g0273 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01433 | hp1 | a0002 | c0002 | t0001 | g0117 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01433 | hp2 | a0006 | c0014 | t0004 | g0280 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01496 | hp1 | a0002 | c0002 | t0001 | g0033 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01496 | hp2 | a0001 | c0001 | t0003 | g0143 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01516 | hp1 | a0002 | c0002 | t0001 | g0005 | EUR | IBS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0248 | EUR | IBS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0006 | EUR | IBS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01517 | hp2 | a0002 | c0002 | t0001 | g0120 | EUR | IBS | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01884 | hp1 | a0011 | c0018 | t0001 | g0009 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01884 | hp2 | a0001 | c0001 | t0003 | g0178 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01891 | hp1 | a0002 | c0002 | t0001 | g0057 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01891 | hp2 | a0001 | c0001 | t0002 | g0162 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01928 | hp2 | a0002 | c0002 | t0003 | g0014 | AMR | PEL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0247 | AMR | PEL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01934 | hp2 | a0002 | c0002 | t0001 | g0018 | AMR | PEL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01943 | hp1 | a0002 | c0002 | t0001 | g0127 | AMR | PEL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0241 | AMR | PEL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01975 | hp1 | a0001 | c0001 | t0002 | g0246 | AMR | PEL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01975 | hp2 | a0002 | c0002 | t0001 | g0019 | AMR | PEL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01978 | hp1 | a0002 | c0002 | t0001 | g0024 | AMR | PEL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01993 | hp1 | a0002 | c0002 | t0001 | g0097 | AMR | PEL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01993 | hp2 | a0001 | c0001 | t0003 | g0174 | AMR | PEL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0159 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02055 | hp2 | a0001 | c0019 | t0002 | g0258 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0107 | EAS | KHV | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02080 | hp2 | a0002 | c0002 | t0001 | g0126 | EAS | KHV | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02135 | hp1 | a0002 | c0002 | t0001 | g0029 | EAS | KHV | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02135 | hp2 | a0002 | c0002 | t0001 | g0035 | EAS | KHV | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02145 | hp1 | a0001 | c0015 | t0005 | g0154 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0156 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0102 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02258 | hp2 | a0001 | c0001 | t0002 | g0254 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02280 | hp1 | a0002 | c0002 | t0001 | g0087 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02280 | hp2 | a0003 | c0005 | t0002 | g0187 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02523 | hp1 | a0002 | c0002 | t0001 | g0113 | EAS | KHV | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | KHV | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02572 | hp1 | a0004 | c0006 | t0003 | g0270 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0041 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02602 | hp2 | a0002 | c0002 | t0001 | g0066 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02615 | hp1 | a0001 | c0001 | t0002 | g0133 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0166 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0135 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02622 | hp2 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0250 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02630 | hp2 | a0002 | c0009 | t0003 | g0047 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02698 | hp1 | a0005 | c0007 | t0002 | g0197 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0038 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02723 | hp1 | a0001 | c0001 | t0003 | g0179 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02723 | hp2 | a0007 | c0013 | t0003 | g0193 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02738 | hp1 | a0002 | c0002 | t0004 | g0276 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0249 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02809 | hp1 | a0001 | c0001 | t0003 | g0149 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0134 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02818 | hp1 | a0003 | c0005 | t0002 | g0188 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02818 | hp2 | a0001 | c0004 | t0003 | g0191 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0275 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02886 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02895 | hp1 | a0001 | c0004 | t0003 | g0192 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02895 | hp2 | a0002 | c0022 | t0001 | g0078 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0160 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02896 | hp2 | a0001 | c0003 | t0001 | g0140 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02897 | hp1 | a0001 | c0004 | t0003 | g0190 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0163 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02922 | hp1 | a0001 | c0001 | t0003 | g0138 | AFR | ESN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0256 | AFR | ESN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0165 | AFR | ESN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02965 | hp2 | a0002 | c0002 | t0001 | g0032 | AFR | ESN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0158 | AFR | ESN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02976 | hp2 | a0002 | c0002 | t0001 | g0030 | AFR | ESN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0062 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03041 | hp1 | a0001 | c0011 | t0003 | g0180 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03041 | hp2 | a0002 | c0002 | t0001 | g0086 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ESN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03130 | hp2 | a0001 | c0001 | t0003 | g0148 | AFR | ESN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03139 | hp1 | a0001 | c0003 | t0001 | g0182 | AFR | ESN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03139 | hp2 | a0002 | c0002 | t0001 | g0048 | AFR | ESN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03209 | hp1 | a0002 | c0002 | t0001 | g0050 | AFR | MSL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0253 | AFR | MSL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03225 | hp1 | a0004 | c0006 | t0003 | g0268 | AFR | MSL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0142 | AFR | MSL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03239 | hp1 | a0002 | c0002 | t0001 | g0100 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03239 | hp2 | a0002 | c0002 | t0004 | g0279 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | MSL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03453 | hp2 | a0003 | c0005 | t0002 | g0189 | AFR | MSL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03486 | hp1 | a0002 | c0002 | t0008 | g0272 | AFR | MSL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03486 | hp2 | a0001 | c0003 | t0001 | g0155 | AFR | MSL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0200 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03491 | hp2 | a0002 | c0002 | t0001 | g0091 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03492 | hp1 | a0002 | c0002 | t0001 | g0055 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03516 | hp1 | a0001 | c0001 | t0003 | g0147 | AFR | ESN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03516 | hp2 | a0001 | c0001 | t0003 | g0001 | AFR | ESN | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03540 | hp1 | a0002 | c0002 | t0001 | g0064 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0141 | AFR | GWD | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03579 | hp1 | a0001 | c0001 | t0003 | g0161 | AFR | MSL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0139 | AFR | MSL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03654 | hp1 | a0002 | c0002 | t0001 | g0039 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0208 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03669 | hp1 | a0001 | c0017 | t0002 | g0207 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03669 | hp2 | a0005 | c0007 | t0002 | g0198 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0215 | SAS | STU | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0103 | SAS | STU | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03704 | hp1 | a0002 | c0002 | t0001 | g0011 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0211 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03710 | hp1 | a0013 | c0023 | t0001 | g0109 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03710 | hp2 | a0002 | c0002 | t0001 | g0080 | SAS | PJL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03834 | hp1 | a0002 | c0002 | t0001 | g0067 | SAS | BEB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0230 | SAS | BEB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0210 | SAS | BEB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03942 | hp2 | a0002 | c0002 | t0001 | g0051 | SAS | BEB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | STU | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG04115 | hp2 | a0002 | c0002 | t0001 | g0065 | SAS | STU | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG04199 | hp1 | a0002 | c0002 | t0001 | g0015 | SAS | STU | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG04199 | hp2 | a0001 | c0021 | t0001 | g0218 | SAS | STU | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18522 | hp1 | a0003 | c0005 | t0002 | g0186 | AFR | YRI | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18522 | hp2 | a0001 | c0001 | t0007 | g0274 | AFR | YRI | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18612 | hp1 | a0002 | c0002 | t0001 | g0101 | EAS | CHB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | CHB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18747 | hp1 | a0002 | c0002 | t0001 | g0074 | EAS | CHB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18747 | hp2 | a0001 | c0001 | t0002 | g0232 | EAS | CHB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18906 | hp1 | a0004 | c0006 | t0003 | g0269 | AFR | YRI | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18906 | hp2 | a0002 | c0002 | t0001 | g0059 | AFR | YRI | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18943 | hp1 | a0002 | c0002 | t0001 | g0083 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0263 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18948 | hp1 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18948 | hp2 | a0002 | c0002 | t0001 | g0072 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18950 | hp2 | a0002 | c0002 | t0001 | g0089 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18951 | hp1 | a0002 | c0002 | t0001 | g0111 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18951 | hp2 | a0001 | c0001 | t0003 | g0204 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0153 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18952 | hp2 | a0002 | c0002 | t0001 | g0092 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18956 | hp1 | a0001 | c0001 | t0003 | g0170 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18956 | hp2 | a0002 | c0002 | t0001 | g0037 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18957 | hp1 | a0002 | c0002 | t0001 | g0098 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0239 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0267 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18964 | hp1 | a0002 | c0002 | t0001 | g0124 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18970 | hp1 | a0002 | c0002 | t0001 | g0129 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18970 | hp2 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18971 | hp1 | a0002 | c0010 | t0001 | g0026 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18971 | hp2 | a0002 | c0002 | t0001 | g0071 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18973 | hp1 | a0002 | c0002 | t0001 | g0130 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18973 | hp2 | a0002 | c0002 | t0001 | g0007 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18979 | hp1 | a0002 | c0002 | t0001 | g0108 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18979 | hp2 | a0002 | c0002 | t0006 | g0084 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18981 | hp1 | a0002 | c0002 | t0001 | g0034 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18981 | hp2 | a0002 | c0002 | t0001 | g0020 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18982 | hp1 | a0001 | c0001 | t0003 | g0175 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18982 | hp2 | a0002 | c0002 | t0001 | g0021 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18983 | hp1 | a0001 | c0001 | t0002 | g0237 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18983 | hp2 | a0002 | c0002 | t0001 | g0261 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18988 | hp1 | a0002 | c0002 | t0001 | g0095 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0245 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18994 | hp1 | a0002 | c0002 | t0001 | g0016 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18994 | hp2 | a0002 | c0002 | t0001 | g0128 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18995 | hp2 | a0002 | c0002 | t0001 | g0077 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18997 | hp1 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18997 | hp2 | a0001 | c0001 | t0003 | g0168 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18999 | hp1 | a0002 | c0002 | t0001 | g0073 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA18999 | hp2 | a0002 | c0002 | t0001 | g0099 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19002 | hp1 | a0002 | c0002 | t0001 | g0069 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19002 | hp2 | a0002 | c0008 | t0002 | g0137 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19003 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19003 | hp2 | a0002 | c0002 | t0001 | g0167 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19006 | hp1 | a0009 | c0016 | t0001 | g0123 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19006 | hp2 | a0001 | c0001 | t0002 | g0264 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19010 | hp1 | a0002 | c0002 | t0001 | g0023 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0265 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19030 | hp1 | a0002 | c0002 | t0001 | g0079 | AFR | LWK | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0164 | AFR | LWK | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19043 | hp1 | a0003 | c0005 | t0003 | g0195 | AFR | LWK | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0252 | AFR | LWK | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19054 | hp1 | a0002 | c0002 | t0006 | g0081 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19054 | hp2 | a0002 | c0002 | t0001 | g0028 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19057 | hp1 | a0002 | c0002 | t0001 | g0070 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19057 | hp2 | a0001 | c0001 | t0005 | g0121 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19060 | hp1 | a0002 | c0002 | t0001 | g0022 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0236 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19062 | hp1 | a0002 | c0010 | t0001 | g0116 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19063 | hp1 | a0002 | c0002 | t0001 | g0112 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19063 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19066 | hp1 | a0002 | c0002 | t0001 | g0125 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19066 | hp2 | a0002 | c0002 | t0001 | g0075 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19068 | hp1 | a0001 | c0001 | t0003 | g0171 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19068 | hp2 | a0002 | c0002 | t0001 | g0082 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19079 | hp1 | a0002 | c0002 | t0001 | g0085 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19079 | hp2 | a0010 | c0025 | t0001 | g0271 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19086 | hp1 | a0002 | c0008 | t0002 | g0136 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19087 | hp2 | a0002 | c0002 | t0001 | g0036 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19088 | hp1 | a0002 | c0002 | t0001 | g0076 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19088 | hp2 | a0002 | c0009 | t0002 | g0093 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0240 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19091 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | JPT | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19240 | hp1 | a0001 | c0004 | t0003 | g0002 | AFR | YRI | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0183 | AFR | YRI | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA20129 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | ASW | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0176 | AFR | ASW | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA20752 | hp1 | a0005 | c0007 | t0002 | g0199 | EUR | TSI | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0213 | EUR | TSI | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0040 | SAS | GIH | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0012 | SAS | GIH | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01123 | hp1 | a0002 | c0002 | t0001 | g0068 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG01123 | hp2 | a0002 | c0002 | t0004 | g0278 | AMR | CLM | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02109 | hp1 | a0001 | c0001 | t0003 | g0177 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02109 | hp2 | a0001 | c0003 | t0001 | g0151 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02486 | hp1 | a0001 | c0001 | t0002 | g0260 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02486 | hp2 | a0002 | c0002 | t0001 | g0106 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02559 | hp1 | a0001 | c0024 | t0003 | g0181 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG02559 | hp2 | a0002 | c0009 | t0003 | g0052 | AFR | ACB | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0152 | AFR | MSL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG03471 | hp2 | a0007 | c0013 | t0003 | g0194 | AFR | MSL | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG06807 | hp1 | a0001 | c0004 | t0003 | g0002 | AFR | USA | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
HG06807 | hp2 | a0002 | c0002 | t0003 | g0031 | AFR | USA | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0008 | AFR | USA | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | USA | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA21309 | hp1 | a0002 | c0002 | t0001 | g0013 | AFR | LWK | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
NA21309 | hp2 | a0001 | c0001 | t0002 | g0255 | AFR | LWK | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0243 | REF | REF | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0144 | REF | REF | DHX57_chr2_38792729_38880934 | DHX57 | chr2 | 38792729 | 38880934 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:38815576
|
T | G | 1 | a0008 | 2 | HG01167.hp2 HG01169.hp1 |
missense_variant | MODERATE | c.3551A>C | p.Glu1184Ala | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/24 | 3705/4885 | 3551/4161 | 1184/1386 | chr2 | 38815576 | ||
chr2:38823216
|
C | T | 1 | a0012 | 1 | HG01243.hp1 | missense_variant | MODERATE | c.3068G>A | p.Arg1023Gln | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/24 | 3222/4885 | 3068/4161 | 1023/1386 | chr2 | 38823216 | ||
chr2:38843014
|
G | A | 1 | a0013 | 1 | HG03710.hp1 | missense_variant | MODERATE | c.2416C>T | p.Arg806Cys | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/24 | 2570/4885 | 2416/4161 | 806/1386 | chr2 | 38843014 | ||
chr2:38848373
|
A | G | 1 | a0007 | 2 | HG02723.hp2 HG03471.hp2 |
missense_variant | MODERATE | c.2060T>C | p.Ile687Thr | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/24 | 2214/4885 | 2060/4161 | 687/1386 | chr2 | 38848373 | ||
chr2:38855202
|
T | C | 5 | a0002a0006a0009others(2): Show | 131 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(128): Show |
missense_variant | MODERATE | c.1760A>G | p.Asn587Ser | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/24 | 1914/4885 | 1760/4161 | 587/1386 | chr2 | 38855202 | ||
chr2:38858776
|
A | G | 1 | a0011 | 1 | HG01884.hp1 | missense_variant | MODERATE | c.1472T>C | p.Val491Ala | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/24 | 1626/4885 | 1472/4161 | 491/1386 | chr2 | 38858776 | ||
chr2:38861113
|
T | C | 2 | a0003a0007 | 7 | HG02280.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
missense_variant | MODERATE | c.1297A>G | p.Ser433Gly | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/24 | 1451/4885 | 1297/4161 | 433/1386 | chr2 | 38861113 | ||
chr2:38861181
|
G | A | 1 | a0006 | 2 | HG00323.hp1 HG01433.hp2 |
missense_variant | MODERATE | c.1229C>T | p.Ser410Phe | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/24 | 1383/4885 | 1229/4161 | 410/1386 | chr2 | 38861181 | ||
chr2:38861527
|
T | C | 1 | a0010 | 1 | NA19079.hp2 | missense_variant | MODERATE | c.883A>G | p.Lys295Glu | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/24 | 1037/4885 | 883/4161 | 295/1386 | chr2 | 38861527 | ||
chr2:38861560
|
T | A | 1 | a0014 | 1 | HG00741.hp1 | stop_gained | HIGH | c.850A>T | p.Arg284* | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/24 | 1004/4885 | 850/4161 | 284/1386 | chr2 | 38861560 | ||
chr2:38863484
|
C | T | 1 | a0009 | 1 | NA19006.hp1 | missense_variant | MODERATE | c.260G>A | p.Arg87His | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 3/24 | 414/4885 | 260/4161 | 87/1386 | chr2 | 38863484 | ||
chr2:38868261
|
C | T | 1 | a0005 | 3 | HG02698.hp1 HG03669.hp2 NA20752.hp1 |
missense_variant | MODERATE | c.145G>A | p.Gly49Ser | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/24 | 299/4885 | 145/4161 | 49/1386 | chr2 | 38868261 | ||
chr2:38868268
|
TCCA | T | 1 | a0004 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
disruptive_inframe_deletion | MODERATE | c.135_137delTGG | p.Gly46del | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/24 | 291/4885 | 135/4161 | 45/1386 | chr2 | 38868268 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:38798413
|
G | A | 10 | a0001c0003a0001c0021a0002c0002others(7): Show | 134 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
synonymous_variant | LOW | c.4047C>T | p.Cys1349Cys | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 24/24 | 4201/4885 | 4047/4161 | 1349/1386 | chr2 | 38798413 | ||
chr2:38802817
|
C | T | 1 | a0001c0004 | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.3915G>A | p.Leu1305Leu | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/24 | 4069/4885 | 3915/4161 | 1305/1386 | chr2 | 38802817 | ||
chr2:38819055
|
C | T | 1 | a0001c0004 | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.3381G>A | p.Ala1127Ala | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 18/24 | 3535/4885 | 3381/4161 | 1127/1386 | chr2 | 38819055 | ||
chr2:38822999
|
A | C | 11 | a0001c0003a0001c0004a0001c0011others(8): Show | 144 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(141): Show |
synonymous_variant | LOW | c.3285T>G | p.Ser1095Ser | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/24 | 3439/4885 | 3285/4161 | 1095/1386 | chr2 | 38822999 | ||
chr2:38826635
|
C | T | 1 | a0001c0019 | 1 | HG02055.hp2 | synonymous_variant | LOW | c.2694G>A | p.Val898Val | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 15/24 | 2848/4885 | 2694/4161 | 898/1386 | chr2 | 38826635 | ||
chr2:38826665
|
T | C | 1 | a0001c0004 | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
synonymous_variant | LOW | c.2664A>G | p.Ser888Ser | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 15/24 | 2818/4885 | 2664/4161 | 888/1386 | chr2 | 38826665 | ||
chr2:38855213
|
A | G | 1 | a0010c0025 | 1 | NA19079.hp2 | synonymous_variant | LOW | c.1749T>C | p.Asp583Asp | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/24 | 1903/4885 | 1749/4161 | 583/1386 | chr2 | 38855213 | ||
chr2:38855228
|
C | T | 1 | a0004c0006 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.1734G>A | p.Pro578Pro | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/24 | 1888/4885 | 1734/4161 | 578/1386 | chr2 | 38855228 | ||
chr2:38855240
|
G | A | 1 | a0004c0006 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.1722C>T | p.Thr574Thr | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/24 | 1876/4885 | 1722/4161 | 574/1386 | chr2 | 38855240 | ||
chr2:38856420
|
T | G | 1 | a0001c0024 | 1 | HG02559.hp1 | synonymous_variant | LOW | c.1629A>C | p.Ser543Ser | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 7/24 | 1783/4885 | 1629/4161 | 543/1386 | chr2 | 38856420 | ||
chr2:38858811
|
C | T | 1 | a0001c0017 | 1 | HG03669.hp1 | synonymous_variant | LOW | c.1437G>A | p.Glu479Glu | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/24 | 1591/4885 | 1437/4161 | 479/1386 | chr2 | 38858811 | ||
chr2:38861432
|
G | A | 1 | a0002c0010 | 3 | HG00673.hp1 NA18971.hp1 NA19062.hp1 |
synonymous_variant | LOW | c.978C>T | p.Pro326Pro | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/24 | 1132/4885 | 978/4161 | 326/1386 | chr2 | 38861432 | ||
chr2:38861558
|
T | C | 1 | a0014c0026 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.852A>G | p.Arg284Arg | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/24 | 1006/4885 | 852/4161 | 284/1386 | chr2 | 38861558 | ||
chr2:38868229
|
A | G | 1 | a0001c0015 | 1 | HG02145.hp1 | synonymous_variant | LOW | c.177T>C | p.Asp59Asp | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/24 | 331/4885 | 177/4161 | 59/1386 | chr2 | 38868229 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:38797843
|
G | GT | 4 | a0001c0001t0005a0001c0001t0009a0001c0015t0005others(1): Show | 6 | HG02145.hp1 HG02886.hp1 HG03654.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*455dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 24/24 | 455 | chr2 | 38797843 | |||||
chr2:38797901
|
G | GA | 13 | a0001c0003t0001a0001c0021t0001a0002c0002t0001others(10): Show | 132 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(129): Show |
3_prime_UTR_variant | MODIFIER | c.*397dupT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 24/24 | 397 | chr2 | 38797901 | |||||
chr2:38797901
|
GA | G | 12 | a0001c0001t0002a0001c0001t0005a0001c0011t0002others(9): Show | 94 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(91): Show |
3_prime_UTR_variant | MODIFIER | c.*397delT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 24/24 | 397 | chr2 | 38797901 | |||||
chr2:38875792
|
T | A | 1 | a0002c0002t0008 | 1 | HG03486.hp1 | 5_prime_UTR_variant | MODIFIER | c.-12A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/24 | 7387 | chr2 | 38875792 | |||||
chr2:38875862
|
G | A | 2 | a0001c0001t0007a0001c0001t0009 | 3 | HG01361.hp2 HG02886.hp1 NA18522.hp2 |
5_prime_UTR_variant | MODIFIER | c.-82C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/24 | 7457 | chr2 | 38875862 | |||||
chr2:38875912
|
G | A | 2 | a0002c0002t0004a0006c0014t0004 | 6 | HG00323.hp1 HG01074.hp1 HG01123.hp2 others(3): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-132C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/24 | chr2 | 38875912 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:38798490
|
A | G | 134 | a0001c0003t0001g0140a0001c0003t0001g0151a0001c0003t0001g0155others(131): Show | 134 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.4018-48T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38798490 | ||||||
chr2:38798795
|
T | C | 1 | a0002c0002t0001g0096 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4018-353A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38798795 | ||||||
chr2:38798799
|
C | T | 131 | a0001c0003t0001g0151a0001c0003t0001g0155a0001c0003t0001g0173others(128): Show | 131 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.4018-357G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38798799 | ||||||
chr2:38798831
|
C | T | 1 | a0002c0002t0001g0092 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.4018-389G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38798831 | ||||||
chr2:38798898
|
G | A | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4018-456C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38798898 | ||||||
chr2:38798900
|
G | A | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4018-458C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38798900 | ||||||
chr2:38798917
|
T | C | 1 | a0002c0002t0001g0089 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.4018-475A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38798917 | ||||||
chr2:38798926
|
T | C | 1 | a0002c0002t0001g0087 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.4018-484A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38798926 | ||||||
chr2:38798930
|
G | C | 5 | a0002c0002t0001g0082a0002c0002t0001g0083a0002c0002t0006g0081others(2): Show | 5 | NA18943.hp1 NA18979.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.4018-488C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38798930 | ||||||
chr2:38798959
|
A | G | 3 | a0002c0002t0001g0082a0002c0002t0001g0083a0010c0025t0001g0271 | 3 | NA18943.hp1 NA19068.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.4018-517T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38798959 | ||||||
chr2:38798970
|
A | G | 1 | a0002c0002t0001g0110 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.4018-528T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38798970 | ||||||
chr2:38799074
|
G | A | 4 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.4018-632C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799074 | ||||||
chr2:38799080
|
A | C | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4018-638T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799080 | ||||||
chr2:38799089
|
C | T | 1 | a0001c0021t0001g0218 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.4018-647G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799089 | ||||||
chr2:38799157
|
G | A | 135 | a0001c0001t0009g0275a0001c0003t0001g0140a0001c0003t0001g0151others(132): Show | 135 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.4018-715C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799157 | ||||||
chr2:38799162
|
G | A | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4018-720C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799162 | ||||||
chr2:38799179
|
T | C | 233 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(230): Show | 235 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.4018-737A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799179 | ||||||
chr2:38799201
|
G | C | 2 | a0001c0001t0003g0176a0002c0009t0003g0047 | 2 | HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4018-759C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799201 | ||||||
chr2:38799220
|
A | C | 1 | a0001c0011t0003g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4018-778T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799220 | ||||||
chr2:38799247
|
T | C | 2 | a0002c0002t0001g0054a0002c0002t0001g0056 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4018-805A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799247 | ||||||
chr2:38799281
|
G | A | 1 | a0002c0002t0001g0034 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.4018-839C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799281 | ||||||
chr2:38799327
|
T | C | 6 | a0002c0002t0001g0018a0002c0002t0001g0096a0002c0002t0001g0097others(3): Show | 6 | HG00673.hp1 HG01192.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.4018-885A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799327 | ||||||
chr2:38799437
|
C | CA | 208 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(205): Show | 209 | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(206): Show |
intron_variant | MODIFIER | c.4018-996dupT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799437 | ||||||
chr2:38799437
|
C | CAA | 13 | a0001c0001t0002g0253a0001c0001t0002g0263a0001c0001t0002g0264others(10): Show | 13 | HG00323.hp2 HG01243.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.4018-997_4018-996d others(4): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799437 | ||||||
chr2:38799500
|
C | G | 1 | a0002c0002t0001g0021 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4018-1058G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799500 | ||||||
chr2:38799562
|
C | G | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4018-1120G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799562 | ||||||
chr2:38799682
|
A | G | 1 | a0002c0002t0001g0107 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.4018-1240T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799682 | ||||||
chr2:38799750
|
C | CA | 138 | a0001c0001t0003g0153a0001c0001t0003g0156a0001c0001t0003g0168others(135): Show | 138 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(135): Show |
intron_variant | MODIFIER | c.4018-1309dupT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799750 | ||||||
chr2:38799750
|
C | CAA | 6 | a0001c0001t0003g0169a0002c0002t0001g0035a0002c0002t0001g0051others(3): Show | 6 | HG00639.hp2 HG02135.hp2 HG03942.hp2 others(3): Show |
intron_variant | MODIFIER | c.4018-1310_4018-130 others(6): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799750 | ||||||
chr2:38799750
|
CA | C | 85 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(82): Show | 86 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.4018-1309delT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799750 | ||||||
chr2:38799944
|
T | G | 1 | a0002c0002t0001g0038 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4018-1502A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799944 | ||||||
chr2:38799962
|
C | A | 16 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(13): Show | 16 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.4018-1520G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799962 | ||||||
chr2:38799966
|
T | A | 1 | a0005c0007t0002g0199 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.4018-1524A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38799966 | ||||||
chr2:38800004
|
A | G | 1 | a0002c0002t0001g0029 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4018-1562T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38800004 | ||||||
chr2:38800059
|
C | G | 1 | a0001c0011t0003g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.4018-1617G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38800059 | ||||||
chr2:38800068
|
C | T | 16 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(13): Show | 16 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.4018-1626G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38800068 | ||||||
chr2:38800185
|
CA | C | 205 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0132others(202): Show | 206 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(203): Show |
intron_variant | MODIFIER | c.4018-1744delT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38800185 | ||||||
chr2:38800227
|
G | C | 2 | a0001c0003t0001g0155a0002c0002t0001g0008 | 2 | HG03486.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.4018-1785C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38800227 | ||||||
chr2:38800285
|
C | G | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.4018-1843G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38800285 | ||||||
chr2:38800505
|
A | G | 16 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(13): Show | 16 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(13): Show |
intron_variant | MODIFIER | c.4018-2063T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38800505 | ||||||
chr2:38801410
|
C | CTATT | 98 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(95): Show | 99 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(96): Show |
intron_variant | MODIFIER | c.4017+1301_4017+130 others(8): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38801410 | ||||||
chr2:38801464
|
C | T | 2 | a0001c0001t0002g0252a0001c0001t0002g0253 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4017+1251G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38801464 | ||||||
chr2:38801478
|
C | T | 2 | a0002c0002t0001g0036a0002c0002t0001g0037 | 2 | NA18956.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.4017+1237G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38801478 | ||||||
chr2:38801625
|
C | T | 2 | a0001c0001t0003g0251a0007c0013t0003g0194 | 2 | HG01106.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4017+1090G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38801625 | ||||||
chr2:38801749
|
C | T | 1 | a0002c0002t0001g0101 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4017+966G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38801749 | ||||||
chr2:38802288
|
CT | C | 119 | a0001c0001t0009g0275a0001c0003t0001g0151a0001c0003t0001g0155others(116): Show | 119 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.4017+426delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38802288 | ||||||
chr2:38802357
|
G | A | 7 | a0001c0003t0001g0223a0002c0002t0001g0102a0002c0002t0001g0103others(4): Show | 7 | HG01070.hp2 HG01074.hp2 HG01081.hp1 others(4): Show |
intron_variant | MODIFIER | c.4017+358C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38802357 | ||||||
chr2:38802377
|
C | A | 2 | a0002c0002t0001g0011a0002c0002t0001g0051 | 2 | HG03704.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.4017+338G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38802377 | ||||||
chr2:38802390
|
C | T | 99 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(96): Show | 101 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.4017+325G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38802390 | ||||||
chr2:38802408
|
G | A | 2 | a0001c0001t0003g0251a0007c0013t0003g0194 | 2 | HG01106.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.4017+307C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38802408 | ||||||
chr2:38802507
|
C | T | 1 | a0001c0001t0003g0177 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.4017+208G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38802507 | ||||||
chr2:38802641
|
T | G | 1 | a0002c0002t0001g0111 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.4017+74A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38802641 | ||||||
chr2:38802672
|
C | T | 1 | a0012c0020t0003g0184 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.4017+43G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 23/23 | chr2 | 38802672 | ||||||
chr2:38802928
|
A | T | 1 | a0002c0002t0003g0014 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.3817-13T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38802928 | ||||||
chr2:38802929
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3817-14G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38802929 | ||||||
chr2:38802932
|
C | T | 133 | a0001c0003t0001g0151a0001c0003t0001g0155a0001c0003t0001g0173others(130): Show | 133 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.3817-17G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38802932 | ||||||
chr2:38803160
|
T | C | 136 | a0001c0003t0001g0140a0001c0003t0001g0151a0001c0003t0001g0155others(133): Show | 136 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.3817-245A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38803160 | ||||||
chr2:38803489
|
A | AT | 9 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(6): Show | 9 | HG01993.hp2 HG02723.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.3817-575dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38803489 | ||||||
chr2:38803489
|
AT | A | 232 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(229): Show | 235 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.3817-575delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38803489 | ||||||
chr2:38803788
|
CT | C | 135 | a0001c0001t0009g0275a0001c0003t0001g0151a0001c0003t0001g0155others(132): Show | 135 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.3817-874delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38803788 | ||||||
chr2:38803954
|
G | T | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3817-1039C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38803954 | ||||||
chr2:38803996
|
G | A | 4 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3817-1081C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38803996 | ||||||
chr2:38804157
|
A | G | 9 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(6): Show | 10 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.3817-1242T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38804157 | ||||||
chr2:38804195
|
A | G | 5 | a0001c0003t0001g0151a0001c0003t0001g0182a0002c0002t0001g0086others(2): Show | 5 | HG02109.hp2 HG02895.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.3817-1280T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38804195 | ||||||
chr2:38804256
|
T | C | 1 | a0001c0001t0002g0262 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.3817-1341A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38804256 | ||||||
chr2:38804320
|
G | A | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3817-1405C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38804320 | ||||||
chr2:38804381
|
T | C | 1 | a0001c0001t0003g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3817-1466A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38804381 | ||||||
chr2:38804448
|
C | G | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3817-1533G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38804448 | ||||||
chr2:38804465
|
G | A | 3 | a0002c0002t0001g0035a0002c0002t0001g0036a0002c0002t0001g0037 | 3 | HG02135.hp2 NA18956.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.3817-1550C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38804465 | ||||||
chr2:38804816
|
G | A | 3 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006 | 3 | HG01346.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.3816+1743C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38804816 | ||||||
chr2:38804834
|
C | G | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3816+1725G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38804834 | ||||||
chr2:38804837
|
G | C | 136 | a0001c0003t0001g0140a0001c0003t0001g0151a0001c0003t0001g0155others(133): Show | 136 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.3816+1722C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38804837 | ||||||
chr2:38805133
|
CA | C | 6 | a0001c0001t0003g0147a0001c0001t0003g0148a0002c0009t0003g0052others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.3816+1425delT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38805133 | ||||||
chr2:38805288
|
C | T | 1 | a0002c0002t0001g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3816+1271G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38805288 | ||||||
chr2:38805434
|
T | C | 1 | a0001c0001t0003g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3816+1125A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38805434 | ||||||
chr2:38805499
|
G | A | 6 | a0001c0001t0003g0147a0001c0001t0003g0148a0002c0009t0003g0052others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.3816+1060C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38805499 | ||||||
chr2:38805561
|
G | C | 135 | a0001c0003t0001g0151a0001c0003t0001g0155a0001c0003t0001g0173others(132): Show | 135 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.3816+998C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38805561 | ||||||
chr2:38805732
|
AT | A | 280 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(277): Show | 283 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(280): Show |
intron_variant | MODIFIER | c.3816+826delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38805732 | ||||||
chr2:38805734
|
T | C | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.3816+825A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38805734 | ||||||
chr2:38805793
|
T | C | 4 | a0002c0002t0001g0089a0002c0002t0001g0099a0002c0002t0001g0124others(1): Show | 4 | NA18950.hp2 NA18964.hp1 NA18999.hp2 others(1): Show |
intron_variant | MODIFIER | c.3816+766A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38805793 | ||||||
chr2:38805840
|
T | C | 2 | a0001c0001t0003g0251a0007c0013t0003g0194 | 2 | HG01106.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3816+719A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38805840 | ||||||
chr2:38805912
|
G | C | 2 | a0002c0002t0001g0032a0002c0002t0003g0031 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.3816+647C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38805912 | ||||||
chr2:38806207
|
C | T | 2 | a0001c0001t0002g0133a0003c0005t0002g0189 | 2 | HG02615.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.3816+352G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38806207 | ||||||
chr2:38806384
|
T | TA | 5 | a0002c0002t0001g0034a0002c0002t0001g0090a0002c0002t0001g0092others(2): Show | 5 | HG00609.hp1 HG01943.hp1 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.3816+174dupT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38806384 | ||||||
chr2:38806448
|
T | C | 74 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(71): Show | 75 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.3816+111A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 22/23 | chr2 | 38806448 | ||||||
chr2:38806768
|
C | T | 6 | a0001c0001t0003g0147a0001c0001t0003g0148a0002c0009t0003g0052others(3): Show | 6 | HG02559.hp2 HG02572.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.3682-75G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38806768 | ||||||
chr2:38806775
|
CCAGTCTT others(3): Show |
C | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3682-92_3682-83del others(10): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38806775 | ||||||
chr2:38806865
|
CT | C | 130 | a0001c0001t0003g0251a0001c0001t0009g0275a0001c0003t0001g0151others(127): Show | 130 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.3682-173delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38806865 | ||||||
chr2:38806922
|
T | A | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3682-229A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38806922 | ||||||
chr2:38807024
|
T | C | 9 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0160others(6): Show | 9 | HG01891.hp2 HG02055.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.3682-331A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807024 | ||||||
chr2:38807059
|
G | GT | 6 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0160others(3): Show | 6 | HG02055.hp1 HG02896.hp1 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.3682-367dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807059 | ||||||
chr2:38807063
|
TG | T | 7 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(4): Show | 7 | HG00639.hp2 NA18943.hp2 NA18961.hp1 others(4): Show |
intron_variant | MODIFIER | c.3682-371delC | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807063 | ||||||
chr2:38807064
|
G | T | 253 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(250): Show | 256 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.3682-371C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807064 | ||||||
chr2:38807072
|
T | G | 136 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(133): Show | 136 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.3682-379A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807072 | ||||||
chr2:38807072
|
T | TG | 5 | a0002c0002t0001g0057a0002c0002t0001g0059a0002c0002t0001g0080others(2): Show | 5 | HG01891.hp1 HG03710.hp1 HG03710.hp2 others(2): Show |
intron_variant | MODIFIER | c.3682-380dupC | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807072 | ||||||
chr2:38807159
|
A | G | 9 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(6): Show | 9 | HG01993.hp2 NA18952.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.3682-466T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807159 | ||||||
chr2:38807420
|
T | C | 264 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(261): Show | 267 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(264): Show |
intron_variant | MODIFIER | c.3682-727A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807420 | ||||||
chr2:38807445
|
C | T | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3682-752G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807445 | ||||||
chr2:38807457
|
A | T | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3682-764T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807457 | ||||||
chr2:38807503
|
G | A | 1 | a0001c0001t0002g0260 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3682-810C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807503 | ||||||
chr2:38807547
|
C | T | 4 | a0002c0002t0001g0007a0002c0002t0001g0035a0002c0002t0001g0036others(1): Show | 4 | HG02135.hp2 NA18956.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.3682-854G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807547 | ||||||
chr2:38807677
|
C | T | 1 | a0002c0002t0001g0117 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3682-984G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807677 | ||||||
chr2:38807716
|
C | T | 1 | a0001c0001t0002g0042 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.3682-1023G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807716 | ||||||
chr2:38807740
|
T | C | 1 | a0002c0002t0001g0015 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.3682-1047A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807740 | ||||||
chr2:38807887
|
C | G | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3682-1194G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807887 | ||||||
chr2:38807898
|
T | G | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3682-1205A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807898 | ||||||
chr2:38807904
|
C | T | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3682-1211G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807904 | ||||||
chr2:38807945
|
C | CT | 17 | a0001c0001t0002g0042a0001c0001t0002g0159a0001c0001t0002g0217others(14): Show | 17 | HG00741.hp2 HG01175.hp2 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.3682-1253dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807945 | ||||||
chr2:38807945
|
CT | C | 110 | a0001c0001t0002g0160a0001c0001t0003g0138a0001c0001t0003g0139others(107): Show | 110 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(107): Show |
intron_variant | MODIFIER | c.3682-1253delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807945 | ||||||
chr2:38807945
|
CTTTTTTT others(4): Show |
C | 1 | a0002c0002t0001g0101 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.3682-1263_3682-125 others(15): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807945 | ||||||
chr2:38807949
|
T | A | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3682-1256A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807949 | ||||||
chr2:38807954
|
T | TG | 4 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3682-1262_3682-126 others(5): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807954 | ||||||
chr2:38807959
|
T | G | 4 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3682-1266A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38807959 | ||||||
chr2:38808017
|
T | C | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3682-1324A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38808017 | ||||||
chr2:38808114
|
T | C | 264 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(261): Show | 267 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(264): Show |
intron_variant | MODIFIER | c.3682-1421A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38808114 | ||||||
chr2:38808153
|
C | T | 2 | a0002c0002t0001g0046a0002c0002t0001g0053 | 2 | HG01256.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.3682-1460G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38808153 | ||||||
chr2:38808194
|
C | T | 1 | a0001c0021t0001g0218 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.3682-1501G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38808194 | ||||||
chr2:38808239
|
C | T | 1 | a0001c0011t0003g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3682-1546G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38808239 | ||||||
chr2:38808273
|
T | G | 136 | a0001c0003t0001g0140a0001c0003t0001g0151a0001c0003t0001g0155others(133): Show | 136 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.3682-1580A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38808273 | ||||||
chr2:38808478
|
A | G | 6 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0160others(3): Show | 6 | HG01891.hp2 HG02055.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.3682-1785T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38808478 | ||||||
chr2:38808488
|
G | A | 8 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.3682-1795C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38808488 | ||||||
chr2:38808503
|
T | C | 1 | a0002c0002t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.3682-1810A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38808503 | ||||||
chr2:38808642
|
A | C | 1 | a0002c0002t0001g0064 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3682-1949T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38808642 | ||||||
chr2:38808906
|
A | G | 261 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(258): Show | 264 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.3682-2213T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38808906 | ||||||
chr2:38808982
|
A | T | 2 | a0001c0001t0007g0273a0001c0001t0007g0274 | 2 | HG01361.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.3682-2289T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38808982 | ||||||
chr2:38809045
|
C | G | 1 | a0002c0002t0001g0019 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.3682-2352G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809045 | ||||||
chr2:38809123
|
C | T | 242 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(239): Show | 245 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(242): Show |
intron_variant | MODIFIER | c.3682-2430G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809123 | ||||||
chr2:38809202
|
C | T | 1 | a0001c0015t0005g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3682-2509G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809202 | ||||||
chr2:38809275
|
G | A | 255 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(252): Show | 258 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.3682-2582C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809275 | ||||||
chr2:38809290
|
A | G | 8 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.3682-2597T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809290 | ||||||
chr2:38809293
|
A | T | 2 | a0001c0001t0003g0251a0007c0013t0003g0194 | 2 | HG01106.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3682-2600T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809293 | ||||||
chr2:38809457
|
T | G | 3 | a0001c0001t0002g0257a0001c0001t0002g0259a0001c0019t0002g0258 | 3 | HG01109.hp1 HG02055.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.3682-2764A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809457 | ||||||
chr2:38809468
|
T | TC | 126 | a0001c0003t0001g0140a0001c0003t0001g0151a0001c0003t0001g0155others(123): Show | 126 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(123): Show |
intron_variant | MODIFIER | c.3682-2776dupG | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809468 | ||||||
chr2:38809468
|
T | TTC | 10 | a0001c0003t0001g0219a0001c0021t0001g0218a0002c0002t0001g0016others(7): Show | 10 | HG00323.hp1 HG00735.hp1 HG01074.hp1 others(7): Show |
intron_variant | MODIFIER | c.3682-2776_3682-277 others(6): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809468 | ||||||
chr2:38809484
|
C | T | 1 | a0002c0002t0001g0118 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3682-2791G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809484 | ||||||
chr2:38809562
|
A | G | 1 | a0001c0015t0005g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3682-2869T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809562 | ||||||
chr2:38809610
|
C | T | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3682-2917G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809610 | ||||||
chr2:38809709
|
C | T | 4 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3682-3016G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809709 | ||||||
chr2:38809823
|
A | G | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3682-3130T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809823 | ||||||
chr2:38809954
|
T | C | 1 | a0002c0002t0001g0111 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.3682-3261A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38809954 | ||||||
chr2:38810019
|
A | G | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3682-3326T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38810019 | ||||||
chr2:38810050
|
C | T | 9 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(6): Show | 9 | HG01993.hp2 NA18952.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.3682-3357G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38810050 | ||||||
chr2:38810200
|
CT | C | 39 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(36): Show | 39 | HG00639.hp2 HG00673.hp2 HG01106.hp2 others(36): Show |
intron_variant | MODIFIER | c.3682-3508delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38810200 | ||||||
chr2:38810248
|
C | G | 2 | a0001c0001t0003g0251a0007c0013t0003g0194 | 2 | HG01106.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3682-3555G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38810248 | ||||||
chr2:38810347
|
C | G | 24 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(21): Show | 25 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(22): Show |
intron_variant | MODIFIER | c.3681+3474G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38810347 | ||||||
chr2:38810671
|
G | A | 94 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(91): Show | 96 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(93): Show |
intron_variant | MODIFIER | c.3681+3150C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38810671 | ||||||
chr2:38810707
|
C | T | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3681+3114G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38810707 | ||||||
chr2:38810838
|
C | T | 2 | a0001c0001t0002g0216a0001c0001t0002g0217 | 2 | HG01175.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.3681+2983G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38810838 | ||||||
chr2:38810892
|
C | T | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3681+2929G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38810892 | ||||||
chr2:38810923
|
T | C | 1 | a0002c0002t0001g0073 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.3681+2898A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38810923 | ||||||
chr2:38810967
|
C | T | 17 | a0002c0002t0001g0018a0002c0002t0001g0020a0002c0002t0001g0022others(14): Show | 17 | HG00423.hp1 HG00558.hp2 HG00621.hp2 others(14): Show |
intron_variant | MODIFIER | c.3681+2854G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38810967 | ||||||
chr2:38811071
|
G | C | 261 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(258): Show | 264 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.3681+2750C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811071 | ||||||
chr2:38811186
|
A | G | 1 | a0001c0001t0002g0225 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3681+2635T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811186 | ||||||
chr2:38811284
|
C | T | 2 | a0001c0001t0003g0251a0007c0013t0003g0194 | 2 | HG01106.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3681+2537G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811284 | ||||||
chr2:38811344
|
C | T | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3681+2477G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811344 | ||||||
chr2:38811583
|
C | T | 100 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(97): Show | 102 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(99): Show |
intron_variant | MODIFIER | c.3681+2238G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811583 | ||||||
chr2:38811591
|
C | G | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+2230G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811591 | ||||||
chr2:38811636
|
T | C | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+2185A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811636 | ||||||
chr2:38811657
|
C | T | 1 | a0001c0015t0005g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3681+2164G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811657 | ||||||
chr2:38811746
|
A | G | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+2075T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811746 | ||||||
chr2:38811776
|
G | A | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+2045C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811776 | ||||||
chr2:38811835
|
A | G | 6 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(3): Show | 6 | HG00639.hp2 NA18943.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.3681+1986T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811835 | ||||||
chr2:38811850
|
A | C | 2 | a0002c0002t0001g0112a0002c0002t0001g0113 | 2 | HG02523.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.3681+1971T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811850 | ||||||
chr2:38811949
|
G | T | 2 | a0001c0001t0003g0147a0001c0001t0003g0148 | 2 | HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3681+1872C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811949 | ||||||
chr2:38811968
|
A | G | 1 | a0002c0002t0001g0011 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.3681+1853T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38811968 | ||||||
chr2:38812081
|
C | G | 1 | a0002c0002t0001g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.3681+1740G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812081 | ||||||
chr2:38812086
|
T | C | 9 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(6): Show | 10 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.3681+1735A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812086 | ||||||
chr2:38812265
|
A | AT | 136 | a0001c0003t0001g0140a0001c0003t0001g0151a0001c0003t0001g0155others(133): Show | 136 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.3681+1555dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812265 | ||||||
chr2:38812295
|
A | G | 3 | a0002c0002t0001g0035a0002c0002t0001g0036a0002c0002t0001g0037 | 3 | HG02135.hp2 NA18956.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.3681+1526T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812295 | ||||||
chr2:38812350
|
G | A | 2 | a0001c0001t0003g0176a0002c0009t0003g0047 | 2 | HG02630.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3681+1471C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812350 | ||||||
chr2:38812582
|
G | A | 1 | a0001c0024t0003g0181 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3681+1239C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812582 | ||||||
chr2:38812626
|
C | T | 2 | a0001c0001t0003g0147a0001c0001t0003g0148 | 2 | HG03130.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.3681+1195G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812626 | ||||||
chr2:38812707
|
A | G | 1 | a0001c0001t0002g0257 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3681+1114T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812707 | ||||||
chr2:38812825
|
G | A | 1 | a0001c0001t0003g0175 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.3681+996C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812825 | ||||||
chr2:38812826
|
C | G | 1 | a0001c0015t0005g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.3681+995G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812826 | ||||||
chr2:38812841
|
C | CTTGTTTG others(1): Show |
39 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(36): Show | 40 | HG00323.hp1 HG00639.hp2 HG01074.hp1 others(37): Show |
intron_variant | MODIFIER | c.3681+972_3681+979d others(10): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812841 | ||||||
chr2:38812841
|
C | CTTGTTTG others(5): Show |
120 | a0001c0003t0001g0155a0001c0003t0001g0173a0001c0003t0001g0219others(117): Show | 121 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(118): Show |
intron_variant | MODIFIER | c.3681+968_3681+979d others(14): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812841 | ||||||
chr2:38812841
|
C | CTTGTTTG others(9): Show |
9 | a0001c0003t0001g0151a0001c0003t0001g0182a0001c0003t0001g0223others(6): Show | 9 | HG01074.hp2 HG01433.hp1 HG02109.hp2 others(6): Show |
intron_variant | MODIFIER | c.3681+964_3681+979d others(18): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812841 | ||||||
chr2:38812841
|
CTTGTTTG others(5): Show |
C | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+968_3681+979d others(14): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812841 | ||||||
chr2:38812852
|
G | GTTTGTTT others(5): Show |
92 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(89): Show | 93 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.3681+968_3681+969i others(14): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812852 | ||||||
chr2:38812933
|
C | T | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3681+888G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812933 | ||||||
chr2:38812959
|
C | T | 241 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(238): Show | 244 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.3681+862G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812959 | ||||||
chr2:38812999
|
C | T | 94 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(91): Show | 95 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.3681+822G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38812999 | ||||||
chr2:38813091
|
C | T | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3681+730G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38813091 | ||||||
chr2:38813126
|
G | A | 1 | a0003c0005t0002g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3681+695C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38813126 | ||||||
chr2:38813204
|
C | T | 1 | a0002c0002t0001g0070 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.3681+617G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38813204 | ||||||
chr2:38813373
|
T | G | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3681+448A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38813373 | ||||||
chr2:38813375
|
AG | A | 6 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(3): Show | 6 | HG00639.hp2 NA18943.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.3681+445delC | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38813375 | ||||||
chr2:38813444
|
C | T | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+377G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38813444 | ||||||
chr2:38813456
|
C | T | 1 | a0001c0001t0002g0260 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.3681+365G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38813456 | ||||||
chr2:38813495
|
C | G | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3681+326G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38813495 | ||||||
chr2:38813533
|
G | C | 1 | a0001c0001t0002g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3681+288C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38813533 | ||||||
chr2:38813671
|
C | T | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3681+150G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38813671 | ||||||
chr2:38813702
|
C | T | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3681+119G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38813702 | ||||||
chr2:38813703
|
G | A | 94 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(91): Show | 95 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(92): Show |
intron_variant | MODIFIER | c.3681+118C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 21/23 | chr2 | 38813703 | ||||||
chr2:38813899
|
T | C | 1 | a0002c0002t0001g0087 | 1 | HG02280.hp1 | splice_region_variant&intron_variant | LOW | c.3607-4A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38813899 | ||||||
chr2:38813999
|
G | A | 1 | a0001c0011t0002g0220 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.3607-104C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38813999 | ||||||
chr2:38814019
|
C | T | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3607-124G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814019 | ||||||
chr2:38814193
|
C | T | 6 | a0002c0002t0001g0018a0002c0002t0001g0096a0002c0002t0001g0097others(3): Show | 6 | HG00673.hp1 HG01192.hp2 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.3607-298G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814193 | ||||||
chr2:38814217
|
C | T | 134 | a0001c0003t0001g0151a0001c0003t0001g0155a0001c0003t0001g0173others(131): Show | 134 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3607-322G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814217 | ||||||
chr2:38814320
|
C | T | 1 | a0001c0001t0003g0178 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3607-425G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814320 | ||||||
chr2:38814322
|
T | C | 74 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(71): Show | 75 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(72): Show |
intron_variant | MODIFIER | c.3607-427A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814322 | ||||||
chr2:38814524
|
T | C | 1 | a0002c0002t0001g0066 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3607-629A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814524 | ||||||
chr2:38814531
|
G | A | 1 | a0002c0002t0001g0130 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.3607-636C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814531 | ||||||
chr2:38814571
|
T | A | 1 | a0002c0002t0001g0061 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3607-676A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814571 | ||||||
chr2:38814638
|
T | C | 264 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(261): Show | 267 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(264): Show |
intron_variant | MODIFIER | c.3607-743A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814638 | ||||||
chr2:38814728
|
G | GT | 142 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(139): Show | 143 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(140): Show |
intron_variant | MODIFIER | c.3606+792dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814728 | ||||||
chr2:38814786
|
G | A | 15 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0200others(12): Show | 16 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.3606+735C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814786 | ||||||
chr2:38814801
|
C | T | 1 | a0002c0002t0001g0103 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.3606+720G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814801 | ||||||
chr2:38814869
|
T | C | 2 | a0002c0002t0001g0054a0002c0002t0001g0056 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.3606+652A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814869 | ||||||
chr2:38814955
|
T | C | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3606+566A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38814955 | ||||||
chr2:38815012
|
G | A | 1 | a0001c0011t0003g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3606+509C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38815012 | ||||||
chr2:38815071
|
C | CT | 55 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(52): Show | 56 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(53): Show |
intron_variant | MODIFIER | c.3606+449dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38815071 | ||||||
chr2:38815071
|
CT | C | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3606+449delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38815071 | ||||||
chr2:38815131
|
A | G | 1 | a0005c0007t0002g0199 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.3606+390T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38815131 | ||||||
chr2:38815354
|
C | T | 134 | a0001c0003t0001g0151a0001c0003t0001g0155a0001c0003t0001g0173others(131): Show | 134 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.3606+167G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38815354 | ||||||
chr2:38815382
|
G | T | 1 | a0002c0002t0001g0086 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3606+139C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38815382 | ||||||
chr2:38815383
|
C | T | 1 | a0002c0002t0001g0086 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.3606+138G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38815383 | ||||||
chr2:38815497
|
G | A | 241 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(238): Show | 244 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.3606+24C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 20/23 | chr2 | 38815497 | ||||||
chr2:38815901
|
C | A | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3472-246G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38815901 | ||||||
chr2:38815940
|
T | C | 6 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(3): Show | 6 | HG00639.hp2 NA18943.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.3472-285A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38815940 | ||||||
chr2:38816017
|
A | G | 1 | a0002c0002t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3472-362T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816017 | ||||||
chr2:38816156
|
C | T | 11 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0160others(8): Show | 11 | HG01891.hp2 HG02055.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3472-501G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816156 | ||||||
chr2:38816185
|
C | A | 2 | a0001c0001t0003g0251a0007c0013t0003g0194 | 2 | HG01106.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.3472-530G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816185 | ||||||
chr2:38816218
|
AT | A | 12 | a0001c0001t0002g0227a0001c0001t0002g0252a0001c0001t0003g0153others(9): Show | 12 | HG01169.hp1 HG01257.hp1 HG01993.hp2 others(9): Show |
intron_variant | MODIFIER | c.3472-564delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816218 | ||||||
chr2:38816246
|
G | C | 15 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(12): Show | 15 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(12): Show |
intron_variant | MODIFIER | c.3472-591C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816246 | ||||||
chr2:38816379
|
C | T | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3472-724G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816379 | ||||||
chr2:38816389
|
A | T | 3 | a0002c0002t0001g0010a0002c0002t0001g0013a0011c0018t0001g0009 | 3 | HG01243.hp2 HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3472-734T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816389 | ||||||
chr2:38816390
|
T | G | 3 | a0002c0002t0001g0010a0002c0002t0001g0013a0011c0018t0001g0009 | 3 | HG01243.hp2 HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3472-735A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816390 | ||||||
chr2:38816403
|
C | T | 1 | a0002c0002t0001g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3472-748G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816403 | ||||||
chr2:38816507
|
C | T | 1 | a0002c0002t0001g0008 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.3472-852G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816507 | ||||||
chr2:38816564
|
G | A | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3472-909C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816564 | ||||||
chr2:38816567
|
A | T | 14 | a0001c0001t0002g0133a0001c0001t0002g0250a0001c0001t0002g0252others(11): Show | 14 | HG01109.hp1 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.3472-912T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816567 | ||||||
chr2:38816609
|
T | C | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3472-954A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816609 | ||||||
chr2:38816669
|
C | A | 1 | a0001c0001t0002g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3472-1014G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816669 | ||||||
chr2:38816712
|
G | A | 1 | a0002c0002t0001g0095 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.3472-1057C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816712 | ||||||
chr2:38816768
|
A | C | 1 | a0002c0002t0001g0119 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.3472-1113T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38816768 | ||||||
chr2:38817141
|
G | A | 260 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(257): Show | 263 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(260): Show |
intron_variant | MODIFIER | c.3472-1486C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38817141 | ||||||
chr2:38817151
|
C | G | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3472-1496G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38817151 | ||||||
chr2:38817285
|
G | C | 13 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(10): Show | 13 | HG01106.hp2 HG01993.hp2 HG02145.hp1 others(10): Show |
intron_variant | MODIFIER | c.3471+1592C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38817285 | ||||||
chr2:38817356
|
C | T | 1 | a0002c0002t0001g0007 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.3471+1521G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38817356 | ||||||
chr2:38817365
|
A | G | 1 | a0001c0001t0002g0255 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.3471+1512T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38817365 | ||||||
chr2:38817540
|
T | A | 1 | a0001c0001t0003g0150 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.3471+1337A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38817540 | ||||||
chr2:38817940
|
G | A | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3471+937C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38817940 | ||||||
chr2:38817961
|
G | C | 1 | a0002c0002t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.3471+916C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38817961 | ||||||
chr2:38817968
|
G | A | 1 | a0001c0003t0001g0155 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3471+909C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38817968 | ||||||
chr2:38817987
|
G | A | 107 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(104): Show | 108 | HG00609.hp2 HG00639.hp1 HG00639.hp2 others(105): Show |
intron_variant | MODIFIER | c.3471+890C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38817987 | ||||||
chr2:38818081
|
T | C | 4 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3471+796A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38818081 | ||||||
chr2:38818170
|
T | C | 6 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(3): Show | 6 | HG00639.hp2 NA18943.hp2 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.3471+707A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38818170 | ||||||
chr2:38818265
|
A | G | 1 | a0002c0002t0001g0046 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3471+612T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38818265 | ||||||
chr2:38818322
|
C | G | 1 | a0001c0001t0003g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.3471+555G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38818322 | ||||||
chr2:38818368
|
T | C | 113 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(110): Show | 115 | HG00323.hp2 HG00423.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.3471+509A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38818368 | ||||||
chr2:38818657
|
A | C | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3471+220T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38818657 | ||||||
chr2:38818712
|
C | T | 3 | a0001c0001t0003g0251a0001c0024t0003g0181a0007c0013t0003g0194 | 3 | HG01106.hp2 HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.3471+165G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38818712 | ||||||
chr2:38818725
|
G | C | 1 | a0014c0026t0002g0214 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3471+152C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38818725 | ||||||
chr2:38818743
|
C | T | 122 | a0001c0001t0002g0217a0001c0001t0002g0224a0001c0003t0001g0155others(119): Show | 122 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.3471+134G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 19/23 | chr2 | 38818743 | ||||||
chr2:38819007
|
C | A | 9 | a0001c0001t0002g0202a0001c0001t0002g0225a0001c0001t0002g0227others(6): Show | 9 | HG00639.hp1 HG00741.hp2 HG01081.hp2 others(6): Show |
intron_variant | MODIFIER | c.3387+42G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 18/23 | chr2 | 38819007 | ||||||
chr2:38819179
|
CT | C | 8 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(5): Show | 9 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.3292-36delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38819179 | ||||||
chr2:38819595
|
A | G | 26 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(23): Show |
intron_variant | MODIFIER | c.3292-451T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38819595 | ||||||
chr2:38819603
|
G | A | 1 | a0002c0002t0001g0021 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.3292-459C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38819603 | ||||||
chr2:38819749
|
T | C | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3292-605A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38819749 | ||||||
chr2:38819865
|
G | A | 3 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266 | 3 | NA19006.hp2 NA19010.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.3292-721C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38819865 | ||||||
chr2:38819918
|
C | A | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.3292-774G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38819918 | ||||||
chr2:38820012
|
C | A | 75 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(72): Show | 76 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.3292-868G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38820012 | ||||||
chr2:38820234
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.3292-1090G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38820234 | ||||||
chr2:38820290
|
G | A | 1 | a0010c0025t0001g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3292-1146C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38820290 | ||||||
chr2:38820435
|
G | T | 1 | a0010c0025t0001g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.3292-1291C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38820435 | ||||||
chr2:38820437
|
C | T | 1 | a0007c0013t0003g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3292-1293G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38820437 | ||||||
chr2:38820512
|
T | C | 258 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(255): Show | 261 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(258): Show |
intron_variant | MODIFIER | c.3292-1368A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38820512 | ||||||
chr2:38820790
|
G | A | 5 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(2): Show | 6 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(3): Show |
intron_variant | MODIFIER | c.3292-1646C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38820790 | ||||||
chr2:38820831
|
G | A | 1 | a0001c0001t0002g0239 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.3292-1687C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38820831 | ||||||
chr2:38820984
|
A | G | 5 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(2): Show | 5 | NA18943.hp2 NA18961.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.3292-1840T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38820984 | ||||||
chr2:38821078
|
C | T | 73 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(70): Show | 74 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.3291+1915G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38821078 | ||||||
chr2:38821294
|
T | G | 10 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(7): Show | 10 | HG01993.hp2 HG02559.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.3291+1699A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38821294 | ||||||
chr2:38821485
|
G | A | 4 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.3291+1508C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38821485 | ||||||
chr2:38821579
|
G | T | 5 | a0002c0002t0001g0025a0002c0002t0001g0113a0002c0002t0001g0114others(2): Show | 5 | HG00558.hp2 HG00621.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.3291+1414C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38821579 | ||||||
chr2:38821580
|
C | G | 5 | a0002c0002t0001g0025a0002c0002t0001g0113a0002c0002t0001g0114others(2): Show | 5 | HG00558.hp2 HG00621.hp2 HG02523.hp1 others(2): Show |
intron_variant | MODIFIER | c.3291+1413G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38821580 | ||||||
chr2:38821625
|
G | A | 75 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(72): Show | 76 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.3291+1368C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38821625 | ||||||
chr2:38821654
|
T | C | 73 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(70): Show | 74 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(71): Show |
intron_variant | MODIFIER | c.3291+1339A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38821654 | ||||||
chr2:38821827
|
G | C | 9 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(6): Show | 9 | HG01993.hp2 NA18952.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.3291+1166C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38821827 | ||||||
chr2:38821981
|
T | G | 1 | a0001c0003t0001g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.3291+1012A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38821981 | ||||||
chr2:38822114
|
C | T | 1 | a0002c0002t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3291+879G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822114 | ||||||
chr2:38822139
|
C | T | 1 | a0002c0009t0003g0047 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.3291+854G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822139 | ||||||
chr2:38822140
|
A | G | 253 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(250): Show | 256 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.3291+853T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822140 | ||||||
chr2:38822145
|
C | T | 1 | a0002c0002t0008g0272 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.3291+848G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822145 | ||||||
chr2:38822435
|
C | T | 1 | a0002c0002t0001g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.3291+558G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822435 | ||||||
chr2:38822459
|
G | A | 96 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(93): Show | 97 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(94): Show |
intron_variant | MODIFIER | c.3291+534C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822459 | ||||||
chr2:38822510
|
T | C | 1 | a0003c0005t0002g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3291+483A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822510 | ||||||
chr2:38822525
|
T | C | 251 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(248): Show | 254 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.3291+468A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822525 | ||||||
chr2:38822598
|
T | G | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3291+395A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822598 | ||||||
chr2:38822647
|
C | T | 2 | a0002c0002t0001g0112a0002c0002t0001g0113 | 2 | HG02523.hp1 NA19063.hp1 |
intron_variant | MODIFIER | c.3291+346G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822647 | ||||||
chr2:38822760
|
G | C | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3291+233C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822760 | ||||||
chr2:38822877
|
G | T | 253 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(250): Show | 256 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.3291+116C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822877 | ||||||
chr2:38822919
|
AT | A | 251 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(248): Show | 254 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.3291+73delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822919 | ||||||
chr2:38822971
|
T | G | 18 | a0002c0002t0001g0021a0002c0002t0001g0023a0002c0002t0001g0074others(15): Show | 18 | HG00558.hp1 HG00621.hp1 HG02080.hp2 others(15): Show |
intron_variant | MODIFIER | c.3291+22A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 17/23 | chr2 | 38822971 | ||||||
chr2:38823360
|
C | T | 1 | a0002c0002t0001g0061 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3015-91G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38823360 | ||||||
chr2:38823481
|
A | G | 9 | a0001c0001t0002g0209a0001c0001t0002g0210a0001c0001t0002g0211others(6): Show | 9 | HG00735.hp2 HG00741.hp1 HG01168.hp2 others(6): Show |
intron_variant | MODIFIER | c.3015-212T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38823481 | ||||||
chr2:38823646
|
A | C | 2 | a0001c0001t0009g0275a0007c0013t0003g0193 | 2 | HG02723.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.3015-377T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38823646 | ||||||
chr2:38823848
|
C | T | 1 | a0001c0019t0002g0258 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.3015-579G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38823848 | ||||||
chr2:38823945
|
A | G | 1 | a0001c0001t0002g0250 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3015-676T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38823945 | ||||||
chr2:38823992
|
C | A | 1 | a0001c0024t0003g0181 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.3015-723G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38823992 | ||||||
chr2:38824013
|
C | CA | 34 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(31): Show | 34 | HG01071.hp1 HG01123.hp1 HG01123.hp2 others(31): Show |
intron_variant | MODIFIER | c.3015-745dupT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38824013 | ||||||
chr2:38824038
|
A | G | 251 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(248): Show | 254 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(251): Show |
intron_variant | MODIFIER | c.3015-769T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38824038 | ||||||
chr2:38824204
|
C | T | 76 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(73): Show | 77 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.3015-935G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38824204 | ||||||
chr2:38824385
|
G | A | 132 | a0001c0003t0001g0155a0001c0003t0001g0173a0001c0003t0001g0182others(129): Show | 132 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.3015-1116C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38824385 | ||||||
chr2:38824660
|
G | T | 242 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(239): Show | 244 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(241): Show |
intron_variant | MODIFIER | c.3014+1187C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38824660 | ||||||
chr2:38824848
|
C | G | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3014+999G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38824848 | ||||||
chr2:38824949
|
C | T | 81 | a0001c0003t0001g0173a0001c0003t0001g0219a0001c0003t0001g0223others(78): Show | 81 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.3014+898G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38824949 | ||||||
chr2:38824965
|
G | A | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.3014+882C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38824965 | ||||||
chr2:38824999
|
G | T | 1 | a0001c0003t0001g0173 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.3014+848C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38824999 | ||||||
chr2:38825181
|
T | G | 1 | a0002c0002t0001g0048 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.3014+666A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38825181 | ||||||
chr2:38825201
|
A | T | 1 | a0002c0002t0001g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.3014+646T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38825201 | ||||||
chr2:38825375
|
T | C | 250 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(247): Show | 253 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.3014+472A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38825375 | ||||||
chr2:38825597
|
C | G | 1 | a0007c0013t0003g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3014+250G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38825597 | ||||||
chr2:38825598
|
C | T | 2 | a0001c0001t0003g0138a0001c0001t0003g0139 | 2 | HG02922.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.3014+249G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38825598 | ||||||
chr2:38825653
|
G | C | 10 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(7): Show | 10 | HG01993.hp2 HG02559.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.3014+194C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38825653 | ||||||
chr2:38825664
|
G | A | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.3014+183C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38825664 | ||||||
chr2:38825741
|
C | T | 10 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(7): Show | 10 | HG01993.hp2 HG02559.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.3014+106G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38825741 | ||||||
chr2:38825762
|
T | C | 1 | a0001c0001t0003g0152 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3014+85A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 16/23 | chr2 | 38825762 | ||||||
chr2:38826055
|
G | C | 9 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(6): Show | 9 | HG01993.hp2 NA18952.hp1 NA18956.hp1 others(6): Show |
splice_region_variant&intron_variant | LOW | c.2814-8C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 15/23 | chr2 | 38826055 | ||||||
chr2:38826188
|
G | C | 1 | a0002c0002t0001g0113 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2814-141C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 15/23 | chr2 | 38826188 | ||||||
chr2:38826368
|
C | T | 1 | a0001c0001t0002g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2813+148G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 15/23 | chr2 | 38826368 | ||||||
chr2:38826403
|
G | C | 134 | a0001c0003t0001g0140a0001c0003t0001g0151a0001c0003t0001g0155others(131): Show | 134 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2813+113C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 15/23 | chr2 | 38826403 | ||||||
chr2:38826423
|
C | T | 1 | a0001c0001t0003g0174 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2813+93G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 15/23 | chr2 | 38826423 | ||||||
chr2:38826425
|
G | A | 1 | a0002c0010t0001g0116 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.2813+91C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 15/23 | chr2 | 38826425 | ||||||
chr2:38826456
|
G | A | 1 | a0003c0005t0003g0195 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2813+60C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 15/23 | chr2 | 38826456 | ||||||
chr2:38826752
|
G | A | 1 | a0002c0002t0001g0070 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2640-63C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38826752 | ||||||
chr2:38826853
|
G | A | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2640-164C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38826853 | ||||||
chr2:38826906
|
G | A | 78 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(75): Show | 79 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(76): Show |
intron_variant | MODIFIER | c.2640-217C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38826906 | ||||||
chr2:38827133
|
A | AAAAAT | 132 | a0001c0001t0003g0143a0001c0003t0001g0155a0001c0003t0001g0173others(129): Show | 132 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.2640-449_2640-445d others(7): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827133 | ||||||
chr2:38827133
|
A | AAAAATAA others(3): Show |
5 | a0001c0003t0001g0151a0002c0002t0001g0086a0002c0002t0001g0089others(2): Show | 5 | HG00558.hp1 HG02109.hp2 HG03041.hp2 others(2): Show |
intron_variant | MODIFIER | c.2640-454_2640-445d others(12): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827133 | ||||||
chr2:38827136
|
A | G | 1 | a0001c0015t0005g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2640-447T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827136 | ||||||
chr2:38827409
|
C | G | 1 | a0007c0013t0003g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2640-720G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827409 | ||||||
chr2:38827477
|
C | T | 10 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(7): Show | 10 | HG01993.hp2 HG02559.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.2640-788G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827477 | ||||||
chr2:38827478
|
T | C | 80 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(77): Show | 81 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.2640-789A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827478 | ||||||
chr2:38827505
|
A | AT | 11 | a0001c0001t0002g0157a0001c0001t0003g0145a0001c0001t0003g0147others(8): Show | 11 | HG02615.hp2 HG02622.hp2 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.2640-817_2640-816i others(3): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827505 | ||||||
chr2:38827505
|
A | T | 1 | a0001c0001t0007g0273 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2640-816T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827505 | ||||||
chr2:38827506
|
AT | A | 31 | a0001c0001t0002g0132a0001c0001t0002g0196a0001c0001t0002g0209others(28): Show | 32 | HG00639.hp2 HG00673.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.2640-818delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827506 | ||||||
chr2:38827506
|
ATAT | A | 87 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0200others(84): Show | 88 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.2640-820_2640-818d others(5): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827506 | ||||||
chr2:38827506
|
ATATAT | A | 7 | a0001c0001t0002g0040a0001c0001t0002g0045a0001c0001t0002g0249others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.2640-822_2640-818d others(7): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827506 | ||||||
chr2:38827507
|
T | A | 114 | a0001c0001t0002g0041a0001c0001t0002g0122a0001c0001t0002g0202others(111): Show | 115 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(112): Show |
intron_variant | MODIFIER | c.2640-818A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827507 | ||||||
chr2:38827509
|
T | A | 134 | a0001c0001t0002g0122a0001c0001t0002g0132a0001c0001t0002g0196others(131): Show | 136 | HG00323.hp1 HG00558.hp2 HG00609.hp2 others(133): Show |
intron_variant | MODIFIER | c.2640-820A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827509 | ||||||
chr2:38827511
|
T | A | 175 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0196others(172): Show | 178 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(175): Show |
intron_variant | MODIFIER | c.2640-822A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827511 | ||||||
chr2:38827513
|
T | A | 105 | a0001c0001t0002g0040a0001c0001t0002g0042a0001c0001t0002g0045others(102): Show | 107 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.2640-824A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827513 | ||||||
chr2:38827515
|
T | A | 23 | a0001c0001t0002g0045a0001c0001t0002g0249a0001c0001t0002g0260others(20): Show | 24 | HG00673.hp1 HG01358.hp1 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.2639+825A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827515 | ||||||
chr2:38827517
|
T | A | 4 | a0001c0001t0003g0139a0001c0001t0003g0176a0001c0001t0003g0177others(1): Show | 4 | HG02109.hp1 HG03579.hp2 NA20129.hp2 others(1): Show |
intron_variant | MODIFIER | c.2639+823A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827517 | ||||||
chr2:38827519
|
T | A | 1 | a0001c0001t0003g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2639+821A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827519 | ||||||
chr2:38827519
|
T | C | 1 | a0002c0009t0003g0052 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.2639+821A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827519 | ||||||
chr2:38827527
|
TATATATA others(3): Show |
T | 2 | a0001c0001t0002g0041a0002c0022t0001g0078 | 2 | HG02602.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.2639+803_2639+812d others(12): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827527 | ||||||
chr2:38827529
|
TATATACA others(1): Show |
T | 14 | a0001c0003t0001g0151a0001c0011t0003g0180a0002c0002t0001g0023others(11): Show | 14 | HG00323.hp1 HG00558.hp2 HG00621.hp2 others(11): Show |
intron_variant | MODIFIER | c.2639+803_2639+810d others(10): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827529 | ||||||
chr2:38827531
|
TATACAC | T | 47 | a0001c0001t0003g0156a0001c0001t0003g0174a0001c0001t0003g0185others(44): Show | 47 | HG00621.hp1 HG01071.hp1 HG01074.hp1 others(44): Show |
intron_variant | MODIFIER | c.2639+803_2639+808d others(8): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827531 | ||||||
chr2:38827533
|
TAC | T | 41 | a0001c0001t0002g0122a0001c0001t0002g0133a0001c0001t0002g0202others(38): Show | 41 | HG00639.hp1 HG00741.hp2 HG01081.hp2 others(38): Show |
intron_variant | MODIFIER | c.2639+805_2639+806d others(4): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827533 | ||||||
chr2:38827533
|
TACAC | T | 101 | a0001c0001t0002g0040a0001c0001t0002g0045a0001c0001t0002g0211others(98): Show | 102 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.2639+803_2639+806d others(6): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827533 | ||||||
chr2:38827535
|
C | T | 48 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0132others(45): Show | 50 | HG00609.hp2 HG00735.hp2 HG00741.hp1 others(47): Show |
intron_variant | MODIFIER | c.2639+805G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827535 | ||||||
chr2:38827537
|
C | T | 89 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(86): Show | 91 | HG00609.hp2 HG00639.hp1 HG00735.hp2 others(88): Show |
intron_variant | MODIFIER | c.2639+803G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827537 | ||||||
chr2:38827561
|
C | T | 254 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(251): Show | 257 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.2639+779G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827561 | ||||||
chr2:38827617
|
C | T | 1 | a0002c0002t0001g0079 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2639+723G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827617 | ||||||
chr2:38827964
|
C | T | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2639+376G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827964 | ||||||
chr2:38827976
|
C | A | 113 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(110): Show | 116 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(113): Show |
intron_variant | MODIFIER | c.2639+364G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38827976 | ||||||
chr2:38828057
|
C | T | 1 | a0002c0002t0001g0018 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2639+283G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38828057 | ||||||
chr2:38828120
|
A | T | 113 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(110): Show | 116 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(113): Show |
intron_variant | MODIFIER | c.2639+220T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38828120 | ||||||
chr2:38828195
|
G | A | 18 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(15): Show | 19 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.2639+145C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 14/23 | chr2 | 38828195 | ||||||
chr2:38828585
|
C | T | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2543-149G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38828585 | ||||||
chr2:38828620
|
G | A | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2543-184C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38828620 | ||||||
chr2:38828655
|
G | A | 1 | a0002c0008t0002g0137 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.2543-219C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38828655 | ||||||
chr2:38828664
|
G | A | 117 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(114): Show | 120 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(117): Show |
intron_variant | MODIFIER | c.2543-228C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38828664 | ||||||
chr2:38828722
|
CA | C | 9 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(6): Show | 9 | HG00735.hp2 HG00741.hp1 HG01167.hp1 others(6): Show |
intron_variant | MODIFIER | c.2543-287delT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38828722 | ||||||
chr2:38828961
|
G | T | 1 | a0001c0001t0002g0250 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2543-525C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38828961 | ||||||
chr2:38829004
|
G | T | 2 | a0001c0024t0003g0181a0007c0013t0003g0194 | 2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2543-568C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829004 | ||||||
chr2:38829147
|
T | G | 82 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(79): Show | 84 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(81): Show |
intron_variant | MODIFIER | c.2543-711A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829147 | ||||||
chr2:38829190
|
G | A | 33 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(30): Show | 34 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(31): Show |
intron_variant | MODIFIER | c.2543-754C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829190 | ||||||
chr2:38829283
|
A | AT | 137 | a0001c0003t0001g0151a0001c0003t0001g0155a0001c0003t0001g0173others(134): Show | 137 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.2543-848dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829283 | ||||||
chr2:38829283
|
AT | A | 39 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(36): Show | 41 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(38): Show |
intron_variant | MODIFIER | c.2543-848delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829283 | ||||||
chr2:38829359
|
G | A | 133 | a0001c0003t0001g0151a0001c0003t0001g0155a0001c0003t0001g0173others(130): Show | 133 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2543-923C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829359 | ||||||
chr2:38829427
|
A | G | 274 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(271): Show | 277 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(274): Show |
intron_variant | MODIFIER | c.2543-991T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829427 | ||||||
chr2:38829448
|
G | T | 113 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(110): Show | 116 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(113): Show |
intron_variant | MODIFIER | c.2543-1012C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829448 | ||||||
chr2:38829459
|
G | C | 10 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(7): Show | 10 | HG01993.hp2 HG02559.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.2543-1023C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829459 | ||||||
chr2:38829492
|
G | A | 9 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(6): Show | 9 | HG01993.hp2 NA18952.hp1 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.2543-1056C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829492 | ||||||
chr2:38829547
|
G | C | 5 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(2): Show | 5 | NA18943.hp2 NA18961.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.2543-1111C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829547 | ||||||
chr2:38829776
|
A | T | 250 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(247): Show | 253 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(250): Show |
intron_variant | MODIFIER | c.2543-1340T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829776 | ||||||
chr2:38829980
|
G | A | 1 | a0001c0001t0002g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2543-1544C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38829980 | ||||||
chr2:38830295
|
A | G | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2543-1859T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38830295 | ||||||
chr2:38830330
|
T | C | 1 | a0001c0001t0003g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2543-1894A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38830330 | ||||||
chr2:38830354
|
A | G | 1 | a0001c0001t0003g0134 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2543-1918T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38830354 | ||||||
chr2:38830427
|
A | T | 2 | a0001c0001t0003g0152a0001c0001t0003g0165 | 2 | HG02965.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.2543-1991T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38830427 | ||||||
chr2:38830461
|
C | T | 1 | a0002c0002t0001g0015 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2543-2025G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38830461 | ||||||
chr2:38830645
|
A | G | 2 | a0002c0002t0001g0089a0002c0002t0001g0099 | 2 | NA18950.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2543-2209T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38830645 | ||||||
chr2:38830905
|
G | A | 113 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(110): Show | 116 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(113): Show |
intron_variant | MODIFIER | c.2543-2469C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38830905 | ||||||
chr2:38830977
|
T | G | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2543-2541A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38830977 | ||||||
chr2:38831318
|
A | C | 1 | a0002c0002t0001g0027 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2543-2882T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831318 | ||||||
chr2:38831322
|
CT | C | 231 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(228): Show | 233 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.2543-2887delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831322 | ||||||
chr2:38831415
|
T | C | 118 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(115): Show | 121 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(118): Show |
intron_variant | MODIFIER | c.2543-2979A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831415 | ||||||
chr2:38831428
|
C | A | 1 | a0003c0005t0002g0189 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2543-2992G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831428 | ||||||
chr2:38831593
|
G | A | 1 | a0007c0013t0003g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2543-3157C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831593 | ||||||
chr2:38831666
|
T | C | 256 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(253): Show | 259 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.2543-3230A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831666 | ||||||
chr2:38831750
|
G | A | 5 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(2): Show | 5 | NA18943.hp2 NA18961.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.2543-3314C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831750 | ||||||
chr2:38831774
|
T | C | 1 | a0002c0002t0001g0016 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.2543-3338A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831774 | ||||||
chr2:38831788
|
C | T | 1 | a0001c0001t0002g0211 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2543-3352G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831788 | ||||||
chr2:38831805
|
T | C | 118 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(115): Show | 121 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(118): Show |
intron_variant | MODIFIER | c.2543-3369A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831805 | ||||||
chr2:38831844
|
C | CA | 142 | a0001c0001t0002g0159a0001c0001t0002g0234a0001c0001t0002g0235others(139): Show | 143 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(140): Show |
intron_variant | MODIFIER | c.2543-3409dupT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831844 | ||||||
chr2:38831844
|
CA | C | 29 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(26): Show | 30 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(27): Show |
intron_variant | MODIFIER | c.2543-3409delT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831844 | ||||||
chr2:38831866
|
A | G | 1 | a0002c0002t0001g0110 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.2543-3430T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831866 | ||||||
chr2:38831886
|
G | A | 114 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(111): Show | 117 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(114): Show |
intron_variant | MODIFIER | c.2543-3450C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831886 | ||||||
chr2:38831892
|
C | T | 2 | a0001c0024t0003g0181a0007c0013t0003g0194 | 2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2543-3456G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38831892 | ||||||
chr2:38832028
|
G | A | 114 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(111): Show | 117 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(114): Show |
intron_variant | MODIFIER | c.2543-3592C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832028 | ||||||
chr2:38832158
|
G | A | 1 | a0001c0001t0002g0132 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2543-3722C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832158 | ||||||
chr2:38832160
|
G | T | 1 | a0002c0002t0001g0128 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.2543-3724C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832160 | ||||||
chr2:38832259
|
G | T | 1 | a0001c0001t0002g0132 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2543-3823C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832259 | ||||||
chr2:38832546
|
TATA | T | 84 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(81): Show | 86 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(83): Show |
intron_variant | MODIFIER | c.2543-4113_2543-411 others(7): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832546 | ||||||
chr2:38832548
|
TATA | T | 132 | a0001c0003t0001g0151a0001c0003t0001g0155a0001c0003t0001g0182others(129): Show | 132 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.2543-4115_2543-411 others(7): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832548 | ||||||
chr2:38832549
|
ATAT | A | 18 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(15): Show | 18 | HG01106.hp1 HG01993.hp2 HG02559.hp1 others(15): Show |
intron_variant | MODIFIER | c.2543-4116_2543-411 others(7): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832549 | ||||||
chr2:38832549
|
ATATT | A | 7 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(4): Show | 8 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.2543-4117_2543-411 others(8): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832549 | ||||||
chr2:38832551
|
A | T | 87 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(84): Show | 89 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(86): Show |
intron_variant | MODIFIER | c.2543-4115T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832551 | ||||||
chr2:38832551
|
ATTT | A | 11 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(8): Show |
intron_variant | MODIFIER | c.2543-4118_2543-411 others(7): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832551 | ||||||
chr2:38832553
|
T | A | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2543-4117A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832553 | ||||||
chr2:38832653
|
C | T | 133 | a0001c0003t0001g0151a0001c0003t0001g0155a0001c0003t0001g0182others(130): Show | 133 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(130): Show |
intron_variant | MODIFIER | c.2543-4217G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832653 | ||||||
chr2:38832912
|
C | T | 1 | a0001c0003t0001g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2543-4476G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832912 | ||||||
chr2:38832936
|
G | C | 72 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(69): Show | 73 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.2543-4500C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832936 | ||||||
chr2:38832981
|
C | CT | 15 | a0001c0001t0002g0236a0001c0001t0002g0249a0001c0001t0003g0153others(12): Show | 15 | HG01106.hp1 HG01978.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.2543-4546dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832981 | ||||||
chr2:38832981
|
CT | C | 13 | a0001c0001t0002g0226a0001c0001t0002g0232a0001c0001t0002g0244others(10): Show | 14 | HG01099.hp1 HG01168.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.2543-4546delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38832981 | ||||||
chr2:38833002
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2543-4566A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38833002 | ||||||
chr2:38833032
|
G | T | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2543-4596C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38833032 | ||||||
chr2:38833037
|
G | A | 111 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(108): Show | 113 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(110): Show |
intron_variant | MODIFIER | c.2543-4601C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38833037 | ||||||
chr2:38833205
|
C | T | 4 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.2542+4626G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38833205 | ||||||
chr2:38833458
|
G | A | 1 | a0002c0002t0003g0014 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2542+4373C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38833458 | ||||||
chr2:38833501
|
C | A | 2 | a0001c0024t0003g0181a0007c0013t0003g0194 | 2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2542+4330G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38833501 | ||||||
chr2:38833614
|
G | A | 35 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(32): Show | 36 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(33): Show |
intron_variant | MODIFIER | c.2542+4217C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38833614 | ||||||
chr2:38834004
|
A | G | 1 | a0001c0001t0002g0267 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.2542+3827T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38834004 | ||||||
chr2:38834127
|
C | T | 2 | a0001c0024t0003g0181a0007c0013t0003g0194 | 2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2542+3704G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38834127 | ||||||
chr2:38834148
|
G | A | 4 | a0001c0003t0001g0151a0001c0003t0001g0182a0002c0002t0001g0086others(1): Show | 4 | HG02109.hp2 HG03041.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2542+3683C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38834148 | ||||||
chr2:38834331
|
C | CA | 28 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(25): Show | 29 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(26): Show |
intron_variant | MODIFIER | c.2542+3499dupT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38834331 | ||||||
chr2:38834331
|
CA | C | 199 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(196): Show | 200 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(197): Show |
intron_variant | MODIFIER | c.2542+3499delT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38834331 | ||||||
chr2:38834346
|
A | G | 2 | a0001c0024t0003g0181a0007c0013t0003g0194 | 2 | HG02559.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.2542+3485T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38834346 | ||||||
chr2:38834380
|
G | T | 1 | a0002c0002t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2542+3451C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38834380 | ||||||
chr2:38834556
|
A | G | 1 | a0001c0001t0002g0196 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2542+3275T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38834556 | ||||||
chr2:38834586
|
A | C | 15 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0200others(12): Show | 16 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2542+3245T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38834586 | ||||||
chr2:38834638
|
A | G | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2542+3193T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38834638 | ||||||
chr2:38834817
|
G | A | 37 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(34): Show | 38 | HG01106.hp1 HG01167.hp2 HG01169.hp1 others(35): Show |
intron_variant | MODIFIER | c.2542+3014C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38834817 | ||||||
chr2:38834938
|
A | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(78): Show | 83 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.2542+2893T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38834938 | ||||||
chr2:38835010
|
T | C | 2 | a0002c0002t0001g0074a0002c0002t0001g0125 | 2 | NA18747.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.2542+2821A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38835010 | ||||||
chr2:38835246
|
G | C | 1 | a0002c0002t0001g0124 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2542+2585C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38835246 | ||||||
chr2:38835386
|
C | T | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2542+2445G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38835386 | ||||||
chr2:38835459
|
T | A | 4 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2542+2372A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38835459 | ||||||
chr2:38835491
|
C | G | 9 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(6): Show | 10 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.2542+2340G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38835491 | ||||||
chr2:38835669
|
G | C | 134 | a0001c0003t0001g0151a0001c0003t0001g0155a0001c0003t0001g0182others(131): Show | 134 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2542+2162C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38835669 | ||||||
chr2:38835734
|
C | T | 16 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(13): Show | 17 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(14): Show |
intron_variant | MODIFIER | c.2542+2097G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38835734 | ||||||
chr2:38835762
|
A | G | 1 | a0007c0013t0003g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2542+2069T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38835762 | ||||||
chr2:38835945
|
C | G | 1 | a0001c0001t0002g0222 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.2542+1886G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38835945 | ||||||
chr2:38836090
|
C | G | 1 | a0002c0002t0001g0261 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2542+1741G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38836090 | ||||||
chr2:38836447
|
A | T | 1 | a0001c0003t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2542+1384T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38836447 | ||||||
chr2:38836649
|
C | G | 1 | a0001c0001t0002g0245 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2542+1182G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38836649 | ||||||
chr2:38836700
|
G | A | 1 | a0001c0001t0002g0159 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2542+1131C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38836700 | ||||||
chr2:38836775
|
C | CA | 20 | a0001c0001t0002g0235a0001c0001t0002g0264a0001c0001t0003g0147others(17): Show | 20 | HG00741.hp2 HG01192.hp2 HG01517.hp1 others(17): Show |
intron_variant | MODIFIER | c.2542+1055dupT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38836775 | ||||||
chr2:38836794
|
A | AG | 70 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0042others(67): Show | 71 | HG00609.hp2 HG00673.hp2 HG00735.hp2 others(68): Show |
intron_variant | MODIFIER | c.2542+1036_2542+103 others(5): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38836794 | ||||||
chr2:38836794
|
A | G | 1 | a0001c0001t0002g0224 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2542+1037T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38836794 | ||||||
chr2:38836884
|
G | C | 72 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(69): Show | 73 | HG00609.hp2 HG00673.hp2 HG00735.hp2 others(70): Show |
intron_variant | MODIFIER | c.2542+947C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38836884 | ||||||
chr2:38837004
|
C | T | 1 | a0001c0003t0001g0219 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2542+827G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837004 | ||||||
chr2:38837073
|
T | C | 3 | a0003c0005t0002g0189a0007c0013t0003g0193a0007c0013t0003g0194 | 3 | HG02723.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2542+758A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837073 | ||||||
chr2:38837266
|
A | G | 1 | a0001c0001t0003g0174 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2542+565T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837266 | ||||||
chr2:38837281
|
G | A | 6 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0045others(3): Show | 6 | HG01167.hp2 HG01169.hp1 HG01358.hp1 others(3): Show |
intron_variant | MODIFIER | c.2542+550C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837281 | ||||||
chr2:38837332
|
C | T | 11 | a0001c0001t0007g0273a0001c0001t0007g0274a0001c0001t0009g0275others(8): Show | 12 | HG01361.hp2 HG02145.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.2542+499G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837332 | ||||||
chr2:38837348
|
C | T | 1 | a0002c0002t0001g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.2542+483G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837348 | ||||||
chr2:38837349
|
G | A | 2 | a0008c0012t0002g0043a0008c0012t0002g0044 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.2542+482C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837349 | ||||||
chr2:38837352
|
A | T | 233 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(230): Show | 235 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.2542+479T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837352 | ||||||
chr2:38837552
|
A | T | 1 | a0002c0002t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2542+279T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837552 | ||||||
chr2:38837611
|
C | CAAAAAAA others(7): Show |
11 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(8): Show | 11 | HG01106.hp1 HG01361.hp2 HG01993.hp2 others(8): Show |
intron_variant | MODIFIER | c.2542+219_2542+220i others(16): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837611 | ||||||
chr2:38837611
|
C | CAAAAAAA others(8): Show |
31 | a0001c0001t0002g0133a0001c0001t0002g0200a0001c0001t0002g0215others(28): Show | 33 | HG01167.hp1 HG01884.hp2 HG02109.hp1 others(30): Show |
intron_variant | MODIFIER | c.2542+219_2542+220i others(17): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837611 | ||||||
chr2:38837611
|
C | CAAAAAAA others(9): Show |
72 | a0001c0001t0002g0003a0001c0001t0002g0042a0001c0001t0002g0122others(69): Show | 73 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.2542+219_2542+220i others(18): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837611 | ||||||
chr2:38837611
|
C | CAAAAAAA others(10): Show |
12 | a0001c0001t0002g0213a0001c0001t0002g0217a0001c0001t0002g0222others(9): Show | 12 | HG01175.hp1 HG01175.hp2 HG01256.hp1 others(9): Show |
intron_variant | MODIFIER | c.2542+219_2542+220i others(19): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837611 | ||||||
chr2:38837611
|
C | CAAAAAAA others(11): Show |
12 | a0002c0002t0001g0028a0002c0002t0001g0053a0002c0002t0001g0054others(9): Show | 12 | HG01070.hp2 HG01168.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.2542+219_2542+220i others(20): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837611 | ||||||
chr2:38837611
|
C | CAAAAAAA others(12): Show |
89 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(86): Show | 89 | HG00323.hp2 HG00423.hp1 HG00558.hp1 others(86): Show |
intron_variant | MODIFIER | c.2542+219_2542+220i others(21): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837611 | ||||||
chr2:38837611
|
C | CAAAAAAA others(13): Show |
24 | a0002c0002t0001g0013a0002c0002t0001g0015a0002c0002t0001g0016others(21): Show | 24 | HG00323.hp1 HG00423.hp2 HG00621.hp1 others(21): Show |
intron_variant | MODIFIER | c.2542+219_2542+220i others(22): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837611 | ||||||
chr2:38837611
|
C | CAAAAAAA others(14): Show |
4 | a0002c0002t0001g0037a0002c0002t0001g0050a0002c0002t0001g0065others(1): Show | 4 | HG02738.hp1 HG03209.hp1 HG04115.hp2 others(1): Show |
intron_variant | MODIFIER | c.2542+219_2542+220i others(23): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837611 | ||||||
chr2:38837611
|
C | CAAAAAAA others(17): Show |
1 | a0002c0002t0001g0099 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.2542+219_2542+220i others(26): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837611 | ||||||
chr2:38837739
|
G | A | 10 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(7): Show | 10 | HG01361.hp2 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2542+92C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 13/23 | chr2 | 38837739 | ||||||
chr2:38838081
|
A | G | 2 | a0005c0007t0002g0198a0005c0007t0002g0199 | 2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2426-134T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38838081 | ||||||
chr2:38838235
|
A | T | 1 | a0001c0003t0001g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2426-288T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38838235 | ||||||
chr2:38838269
|
A | T | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2426-322T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38838269 | ||||||
chr2:38838295
|
C | G | 2 | a0001c0001t0002g0203a0001c0001t0002g0228 | 2 | NA19063.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.2426-348G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38838295 | ||||||
chr2:38838316
|
G | C | 82 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(79): Show | 83 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(80): Show |
intron_variant | MODIFIER | c.2426-369C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38838316 | ||||||
chr2:38838318
|
C | T | 6 | a0002c0002t0001g0088a0002c0002t0001g0101a0002c0002t0001g0125others(3): Show | 6 | HG00621.hp1 HG02080.hp2 NA18612.hp1 others(3): Show |
intron_variant | MODIFIER | c.2426-371G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38838318 | ||||||
chr2:38838329
|
A | G | 232 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(229): Show | 234 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.2426-382T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38838329 | ||||||
chr2:38838507
|
C | G | 144 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(141): Show | 145 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.2426-560G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38838507 | ||||||
chr2:38838565
|
A | C | 1 | a0002c0002t0001g0127 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2426-618T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38838565 | ||||||
chr2:38838587
|
C | A | 144 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(141): Show | 145 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(142): Show |
intron_variant | MODIFIER | c.2426-640G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38838587 | ||||||
chr2:38838873
|
G | A | 1 | a0002c0002t0001g0077 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2426-926C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38838873 | ||||||
chr2:38838940
|
T | C | 3 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266 | 3 | NA19006.hp2 NA19010.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.2426-993A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38838940 | ||||||
chr2:38839239
|
C | T | 8 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(5): Show | 9 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2426-1292G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38839239 | ||||||
chr2:38839557
|
CA | C | 174 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(171): Show | 177 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(174): Show |
intron_variant | MODIFIER | c.2426-1611delT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38839557 | ||||||
chr2:38839614
|
G | C | 3 | a0003c0005t0002g0189a0007c0013t0003g0193a0007c0013t0003g0194 | 3 | HG02723.hp2 HG03453.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2426-1667C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38839614 | ||||||
chr2:38839703
|
G | C | 1 | a0013c0023t0001g0109 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2426-1756C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38839703 | ||||||
chr2:38839705
|
G | A | 1 | a0002c0022t0001g0078 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.2426-1758C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38839705 | ||||||
chr2:38839715
|
G | A | 1 | a0010c0025t0001g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2426-1768C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38839715 | ||||||
chr2:38839719
|
C | CA | 17 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(14): Show | 18 | HG01074.hp1 HG01361.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.2426-1773dupT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38839719 | ||||||
chr2:38839788
|
G | T | 2 | a0002c0002t0001g0011a0002c0002t0001g0012 | 2 | HG03704.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.2426-1841C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38839788 | ||||||
chr2:38840121
|
T | A | 4 | a0003c0005t0002g0186a0003c0005t0002g0187a0003c0005t0002g0188others(1): Show | 4 | HG02280.hp2 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2426-2174A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38840121 | ||||||
chr2:38840159
|
G | C | 1 | a0002c0002t0001g0013 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2426-2212C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38840159 | ||||||
chr2:38840200
|
C | T | 4 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(1): Show | 4 | HG01071.hp1 HG01346.hp1 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.2426-2253G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38840200 | ||||||
chr2:38840227
|
G | T | 129 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(126): Show | 129 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2426-2280C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38840227 | ||||||
chr2:38840322
|
A | C | 1 | a0001c0001t0002g0224 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2426-2375T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38840322 | ||||||
chr2:38840357
|
G | A | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2426-2410C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38840357 | ||||||
chr2:38840573
|
T | A | 1 | a0002c0002t0001g0108 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.2425+2432A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38840573 | ||||||
chr2:38840574
|
A | AAAAC | 149 | a0001c0001t0002g0133a0001c0001t0002g0263a0001c0001t0002g0264others(146): Show | 150 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.2425+2427_2425+243 others(8): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38840574 | ||||||
chr2:38841023
|
G | A | 254 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(251): Show | 257 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(254): Show |
intron_variant | MODIFIER | c.2425+1982C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38841023 | ||||||
chr2:38841108
|
C | T | 129 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(126): Show | 129 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.2425+1897G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38841108 | ||||||
chr2:38841190
|
T | C | 2 | a0001c0001t0002g0259a0001c0019t0002g0258 | 2 | HG01109.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.2425+1815A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38841190 | ||||||
chr2:38841247
|
C | T | 255 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(252): Show | 258 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.2425+1758G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38841247 | ||||||
chr2:38841428
|
C | G | 1 | a0001c0003t0001g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2425+1577G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38841428 | ||||||
chr2:38841732
|
G | A | 8 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(5): Show | 9 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2425+1273C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38841732 | ||||||
chr2:38841954
|
A | G | 2 | a0001c0001t0003g0156a0001c0001t0003g0177 | 2 | HG02109.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.2425+1051T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38841954 | ||||||
chr2:38842016
|
A | T | 1 | a0001c0024t0003g0181 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2425+989T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38842016 | ||||||
chr2:38842106
|
C | T | 10 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(7): Show | 10 | HG01361.hp2 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.2425+899G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38842106 | ||||||
chr2:38842143
|
A | C | 1 | a0002c0002t0006g0084 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2425+862T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38842143 | ||||||
chr2:38842151
|
C | T | 5 | a0002c0002t0004g0276a0002c0002t0004g0277a0002c0002t0004g0279others(2): Show | 5 | HG00323.hp1 HG01074.hp1 HG01433.hp2 others(2): Show |
intron_variant | MODIFIER | c.2425+854G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38842151 | ||||||
chr2:38842224
|
G | A | 4 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2425+781C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38842224 | ||||||
chr2:38842476
|
C | T | 231 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(228): Show | 233 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(230): Show |
intron_variant | MODIFIER | c.2425+529G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38842476 | ||||||
chr2:38842778
|
G | C | 1 | a0004c0006t0003g0270 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.2425+227C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 12/23 | chr2 | 38842778 | ||||||
chr2:38843308
|
C | T | 1 | a0002c0002t0001g0086 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2220-98G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38843308 | ||||||
chr2:38843339
|
C | T | 2 | a0001c0001t0002g0243a0001c0021t0001g0218 | 2 | HG04199.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.2220-129G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38843339 | ||||||
chr2:38843502
|
C | T | 1 | a0002c0002t0001g0100 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2220-292G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38843502 | ||||||
chr2:38843680
|
T | C | 2 | a0001c0001t0007g0273a0001c0001t0007g0274 | 2 | HG01361.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2220-470A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38843680 | ||||||
chr2:38843731
|
G | T | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | HG02698.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.2220-521C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38843731 | ||||||
chr2:38844017
|
T | C | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2220-807A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844017 | ||||||
chr2:38844029
|
G | A | 79 | a0002c0002t0001g0011a0002c0002t0001g0012a0002c0002t0001g0017others(76): Show | 79 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.2220-819C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844029 | ||||||
chr2:38844165
|
T | C | 2 | a0002c0002t0001g0062a0002c0002t0001g0063 | 2 | HG01257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2220-955A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844165 | ||||||
chr2:38844188
|
T | C | 1 | a0002c0002t0001g0118 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2220-978A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844188 | ||||||
chr2:38844194
|
C | T | 76 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(73): Show | 77 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.2220-984G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844194 | ||||||
chr2:38844226
|
C | A | 4 | a0002c0002t0001g0030a0002c0002t0001g0057a0002c0002t0001g0059others(1): Show | 4 | HG01099.hp1 HG01891.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2220-1016G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844226 | ||||||
chr2:38844335
|
TAAAGAAA others(335): Show |
T | 233 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(230): Show | 235 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.2220-1467_2220-112 others(4): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844335 | ||||||
chr2:38844629
|
CAAA | C | 10 | a0001c0001t0002g0160a0001c0001t0002g0163a0001c0001t0003g0145others(7): Show | 10 | HG02572.hp2 HG02622.hp2 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.2220-1422_2220-142 others(7): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844629 | ||||||
chr2:38844629
|
CAAAAAAA others(10): Show |
C | 1 | a0001c0001t0003g0147 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2220-1436_2220-142 others(21): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844629 | ||||||
chr2:38844629
|
CAAAAAAA others(17): Show |
C | 1 | a0001c0003t0001g0151 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2220-1443_2220-142 others(28): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844629 | ||||||
chr2:38844629
|
CAAAAAAA others(18): Show |
C | 1 | a0001c0003t0001g0140 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2220-1444_2220-142 others(29): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844629 | ||||||
chr2:38844629
|
CAAAAAAA others(23): Show |
C | 2 | a0001c0001t0003g0156a0001c0003t0001g0173 | 2 | HG01106.hp1 HG02145.hp2 |
intron_variant | MODIFIER | c.2220-1449_2220-142 others(34): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844629 | ||||||
chr2:38844629
|
CAAAAAAA others(24): Show |
C | 18 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(15): Show | 19 | HG01884.hp2 HG01993.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.2220-1450_2220-142 others(35): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844629 | ||||||
chr2:38844629
|
CAAAAAAA others(25): Show |
C | 1 | a0001c0001t0003g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.2220-1451_2220-142 others(36): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844629 | ||||||
chr2:38844629
|
CAAAAAAA others(27): Show |
C | 1 | a0001c0003t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2220-1453_2220-142 others(38): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844629 | ||||||
chr2:38844679
|
A | C | 15 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0200others(12): Show | 16 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.2220-1469T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844679 | ||||||
chr2:38844815
|
T | C | 1 | a0002c0002t0001g0125 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2220-1605A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844815 | ||||||
chr2:38844846
|
T | C | 3 | a0002c0002t0001g0023a0002c0002t0001g0110a0002c0002t0001g0111 | 3 | HG00323.hp2 NA18951.hp1 NA19010.hp1 |
intron_variant | MODIFIER | c.2220-1636A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844846 | ||||||
chr2:38844936
|
G | A | 4 | a0002c0002t0001g0007a0002c0002t0001g0035a0002c0002t0001g0036others(1): Show | 4 | HG02135.hp2 NA18956.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.2220-1726C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38844936 | ||||||
chr2:38845025
|
T | C | 3 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.2220-1815A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38845025 | ||||||
chr2:38845223
|
A | C | 19 | a0001c0001t0002g0133a0001c0001t0002g0263a0001c0001t0002g0264others(16): Show | 20 | HG01192.hp2 HG01361.hp2 HG01934.hp2 others(17): Show |
intron_variant | MODIFIER | c.2219+1796T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38845223 | ||||||
chr2:38845277
|
A | G | 4 | a0003c0005t0002g0186a0003c0005t0002g0187a0003c0005t0002g0188others(1): Show | 4 | HG02280.hp2 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2219+1742T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38845277 | ||||||
chr2:38845284
|
T | C | 1 | a0002c0002t0001g0112 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.2219+1735A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38845284 | ||||||
chr2:38845459
|
G | C | 16 | a0001c0001t0002g0133a0001c0001t0002g0263a0001c0001t0002g0264others(13): Show | 17 | HG01361.hp2 HG02145.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.2219+1560C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38845459 | ||||||
chr2:38845483
|
A | G | 2 | a0001c0001t0007g0273a0001c0001t0007g0274 | 2 | HG01361.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2219+1536T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38845483 | ||||||
chr2:38845700
|
T | G | 3 | a0002c0002t0001g0010a0002c0002t0001g0013a0011c0018t0001g0009 | 3 | HG01243.hp2 HG01884.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.2219+1319A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38845700 | ||||||
chr2:38845706
|
G | C | 2 | a0002c0002t0001g0062a0002c0002t0001g0063 | 2 | HG01257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.2219+1313C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38845706 | ||||||
chr2:38845819
|
G | T | 16 | a0001c0001t0002g0133a0001c0001t0002g0263a0001c0001t0002g0264others(13): Show | 17 | HG01361.hp2 HG02145.hp1 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.2219+1200C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38845819 | ||||||
chr2:38845832
|
G | A | 1 | a0002c0002t0001g0261 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2219+1187C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38845832 | ||||||
chr2:38845865
|
C | CT | 11 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(8): Show | 12 | HG01361.hp2 HG02145.hp1 HG02615.hp1 others(9): Show |
intron_variant | MODIFIER | c.2219+1153dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38845865 | ||||||
chr2:38845865
|
CT | C | 99 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(96): Show | 101 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(98): Show |
intron_variant | MODIFIER | c.2219+1153delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38845865 | ||||||
chr2:38846112
|
C | T | 1 | a0002c0002t0001g0125 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.2219+907G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38846112 | ||||||
chr2:38846179
|
A | G | 246 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(243): Show | 249 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(246): Show |
intron_variant | MODIFIER | c.2219+840T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38846179 | ||||||
chr2:38846396
|
G | A | 1 | a0001c0001t0003g0179 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2219+623C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38846396 | ||||||
chr2:38846449
|
G | A | 1 | a0002c0002t0001g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.2219+570C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38846449 | ||||||
chr2:38846523
|
T | C | 1 | a0002c0002t0001g0055 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2219+496A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38846523 | ||||||
chr2:38846576
|
C | T | 1 | a0001c0001t0009g0275 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.2219+443G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38846576 | ||||||
chr2:38846616
|
C | CA | 92 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(89): Show | 93 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(90): Show |
intron_variant | MODIFIER | c.2219+402dupT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38846616 | ||||||
chr2:38847006
|
A | G | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2219+13T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 11/23 | chr2 | 38847006 | ||||||
chr2:38847181
|
A | G | 1 | a0001c0001t0007g0274 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2165-108T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/23 | chr2 | 38847181 | ||||||
chr2:38847223
|
G | C | 4 | a0002c0002t0001g0069a0002c0002t0001g0070a0002c0002t0001g0071others(1): Show | 4 | NA18747.hp1 NA18971.hp2 NA19002.hp1 others(1): Show |
intron_variant | MODIFIER | c.2165-150C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/23 | chr2 | 38847223 | ||||||
chr2:38847304
|
T | G | 4 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.2165-231A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/23 | chr2 | 38847304 | ||||||
chr2:38847430
|
A | C | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2165-357T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/23 | chr2 | 38847430 | ||||||
chr2:38847551
|
T | C | 10 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(7): Show | 10 | HG01106.hp1 HG01993.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.2165-478A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/23 | chr2 | 38847551 | ||||||
chr2:38847733
|
G | A | 1 | a0002c0002t0001g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2164+536C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/23 | chr2 | 38847733 | ||||||
chr2:38847951
|
C | T | 1 | a0001c0001t0002g0210 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2164+318G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/23 | chr2 | 38847951 | ||||||
chr2:38847956
|
A | G | 255 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(252): Show | 258 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(255): Show |
intron_variant | MODIFIER | c.2164+313T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/23 | chr2 | 38847956 | ||||||
chr2:38848076
|
CTG | C | 4 | a0002c0002t0001g0082a0002c0002t0001g0083a0002c0002t0001g0085others(1): Show | 4 | NA18943.hp1 NA18979.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.2164+191_2164+192d others(4): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/23 | chr2 | 38848076 | ||||||
chr2:38848154
|
T | C | 1 | a0002c0002t0001g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.2164+115A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/23 | chr2 | 38848154 | ||||||
chr2:38848166
|
G | A | 2 | a0007c0013t0003g0193a0007c0013t0003g0194 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.2164+103C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/23 | chr2 | 38848166 | ||||||
chr2:38848214
|
A | C | 134 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266others(131): Show | 134 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2164+55T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 10/23 | chr2 | 38848214 | ||||||
chr2:38848484
|
G | T | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2031-82C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38848484 | ||||||
chr2:38848523
|
C | T | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2031-121G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38848523 | ||||||
chr2:38848561
|
C | A | 1 | a0002c0002t0001g0057 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2031-159G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38848561 | ||||||
chr2:38848682
|
G | C | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2031-280C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38848682 | ||||||
chr2:38848799
|
C | T | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2031-397G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38848799 | ||||||
chr2:38848803
|
G | A | 1 | a0002c0002t0001g0071 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2031-401C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38848803 | ||||||
chr2:38848810
|
C | T | 1 | a0002c0002t0001g0004 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2031-408G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38848810 | ||||||
chr2:38849333
|
A | C | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2031-931T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38849333 | ||||||
chr2:38849432
|
C | T | 2 | a0002c0002t0001g0089a0002c0002t0001g0099 | 2 | NA18950.hp2 NA18999.hp2 |
intron_variant | MODIFIER | c.2031-1030G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38849432 | ||||||
chr2:38849440
|
G | A | 7 | a0003c0005t0002g0186a0003c0005t0002g0187a0003c0005t0002g0188others(4): Show | 7 | HG02280.hp2 HG02723.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.2031-1038C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38849440 | ||||||
chr2:38849510
|
A | C | 1 | a0001c0015t0005g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2031-1108T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38849510 | ||||||
chr2:38849547
|
TA | T | 106 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(103): Show | 108 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(105): Show |
intron_variant | MODIFIER | c.2031-1146delT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38849547 | ||||||
chr2:38849547
|
TAA | T | 149 | a0001c0001t0002g0133a0001c0001t0002g0263a0001c0001t0002g0264others(146): Show | 150 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(147): Show |
intron_variant | MODIFIER | c.2031-1147_2031-114 others(6): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38849547 | ||||||
chr2:38849702
|
C | T | 1 | a0001c0015t0005g0154 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2031-1300G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38849702 | ||||||
chr2:38849800
|
A | T | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2031-1398T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38849800 | ||||||
chr2:38850178
|
A | G | 148 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(145): Show | 149 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(146): Show |
intron_variant | MODIFIER | c.2031-1776T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38850178 | ||||||
chr2:38850261
|
C | A | 1 | a0002c0002t0001g0071 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.2031-1859G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38850261 | ||||||
chr2:38850305
|
C | G | 1 | a0010c0025t0001g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.2031-1903G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38850305 | ||||||
chr2:38850571
|
T | C | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2031-2169A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38850571 | ||||||
chr2:38850621
|
C | CAT | 256 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(253): Show | 259 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.2031-2221_2031-222 others(6): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38850621 | ||||||
chr2:38850692
|
C | CAGGGAAA | 256 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(253): Show | 259 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.2031-2297_2031-229 others(11): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38850692 | ||||||
chr2:38850702
|
G | A | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.2031-2300C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38850702 | ||||||
chr2:38850906
|
C | T | 8 | a0001c0001t0003g0001a0001c0001t0003g0138a0001c0001t0003g0139others(5): Show | 9 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.2031-2504G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38850906 | ||||||
chr2:38850935
|
G | A | 1 | a0001c0001t0002g0250 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2031-2533C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38850935 | ||||||
chr2:38850961
|
C | T | 1 | a0002c0002t0001g0051 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2031-2559G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38850961 | ||||||
chr2:38851049
|
C | T | 4 | a0003c0005t0002g0186a0003c0005t0002g0187a0003c0005t0002g0188others(1): Show | 4 | HG02280.hp2 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.2031-2647G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38851049 | ||||||
chr2:38851213
|
A | G | 2 | a0001c0001t0002g0205a0001c0001t0002g0206 | 2 | NA18950.hp1 NA18970.hp2 |
intron_variant | MODIFIER | c.2031-2811T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38851213 | ||||||
chr2:38851632
|
T | C | 21 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(18): Show | 21 | HG01106.hp2 HG01109.hp1 HG01167.hp2 others(18): Show |
intron_variant | MODIFIER | c.2030+2422A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38851632 | ||||||
chr2:38851735
|
T | A | 2 | a0001c0001t0002g0252a0001c0001t0002g0253 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.2030+2319A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38851735 | ||||||
chr2:38851822
|
G | C | 11 | a0002c0002t0001g0018a0002c0002t0001g0025a0002c0002t0001g0096others(8): Show | 11 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(8): Show |
intron_variant | MODIFIER | c.2030+2232C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38851822 | ||||||
chr2:38851956
|
G | A | 1 | a0002c0002t0001g0015 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.2030+2098C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38851956 | ||||||
chr2:38851963
|
C | G | 2 | a0001c0001t0002g0160a0001c0001t0002g0163 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.2030+2091G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38851963 | ||||||
chr2:38852069
|
A | G | 1 | a0002c0002t0001g0057 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2030+1985T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38852069 | ||||||
chr2:38852130
|
T | C | 134 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266others(131): Show | 134 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.2030+1924A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38852130 | ||||||
chr2:38852175
|
C | T | 4 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(1): Show | 4 | HG01192.hp1 HG01358.hp1 HG02602.hp1 others(1): Show |
intron_variant | MODIFIER | c.2030+1879G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38852175 | ||||||
chr2:38852192
|
C | CA | 10 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(7): Show | 10 | HG01106.hp1 HG01993.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.2030+1861_2030+186 others(5): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38852192 | ||||||
chr2:38852336
|
C | CT | 72 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(69): Show | 73 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.2030+1717dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38852336 | ||||||
chr2:38852336
|
CT | C | 136 | a0001c0001t0002g0260a0001c0001t0002g0264a0001c0001t0002g0265others(133): Show | 136 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(133): Show |
intron_variant | MODIFIER | c.2030+1717delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38852336 | ||||||
chr2:38852547
|
T | A | 1 | a0001c0001t0003g0145 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.2030+1507A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38852547 | ||||||
chr2:38852605
|
AT | A | 10 | a0001c0001t0002g0163a0001c0001t0002g0206a0001c0001t0002g0266others(7): Show | 10 | HG01169.hp1 HG01169.hp2 HG02897.hp2 others(7): Show |
intron_variant | MODIFIER | c.2030+1448delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38852605 | ||||||
chr2:38852689
|
A | G | 3 | a0001c0001t0002g0158a0001c0001t0002g0159a0001c0001t0002g0164 | 3 | HG02055.hp1 HG02976.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2030+1365T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38852689 | ||||||
chr2:38852854
|
G | A | 3 | a0002c0002t0004g0276a0002c0002t0004g0277a0002c0002t0004g0279 | 3 | HG01074.hp1 HG02738.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.2030+1200C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38852854 | ||||||
chr2:38852891
|
C | T | 1 | a0001c0001t0002g0225 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.2030+1163G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38852891 | ||||||
chr2:38853044
|
G | GTTTTC | 3 | a0001c0001t0002g0267a0001c0001t0007g0273a0001c0001t0007g0274 | 3 | HG01361.hp2 NA18522.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.2030+1005_2030+100 others(9): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853044 | ||||||
chr2:38853044
|
G | GTTTTCTT others(3): Show |
54 | a0001c0001t0002g0263a0001c0003t0001g0219a0001c0003t0001g0223others(51): Show | 55 | HG00558.hp2 HG00621.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.2030+1000_2030+100 others(14): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853044 | ||||||
chr2:38853044
|
G | GTTTTCTT others(8): Show |
98 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(95): Show | 100 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.2030+995_2030+1009 others(18): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853044 | ||||||
chr2:38853044
|
G | GTTTTCTT others(13): Show |
62 | a0001c0001t0002g0122a0001c0001t0002g0132a0001c0001t0002g0196others(59): Show | 62 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(59): Show |
intron_variant | MODIFIER | c.2030+990_2030+1009 others(23): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853044 | ||||||
chr2:38853044
|
G | GTTTTCTT others(18): Show |
20 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0203others(17): Show | 20 | HG01099.hp1 HG01106.hp2 HG01109.hp1 others(17): Show |
intron_variant | MODIFIER | c.2030+985_2030+1009 others(28): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853044 | ||||||
chr2:38853044
|
G | GTTTTCTT others(23): Show |
5 | a0001c0001t0002g0205a0001c0001t0002g0206a0002c0002t0001g0013others(2): Show | 5 | HG02723.hp2 NA18950.hp1 NA18970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2030+1009_2030+101 others(34): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853044 | ||||||
chr2:38853044
|
G | GTTTTCTT others(28): Show |
5 | a0001c0001t0002g0133a0001c0001t0002g0239a0001c0001t0003g0134others(2): Show | 5 | HG02615.hp1 HG02809.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.2030+1009_2030+101 others(39): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853044 | ||||||
chr2:38853044
|
G | GTTTTCTT others(33): Show |
2 | a0001c0001t0002g0260a0001c0001t0003g0135 | 2 | HG02486.hp1 HG02622.hp1 |
intron_variant | MODIFIER | c.2030+1009_2030+101 others(44): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853044 | ||||||
chr2:38853212
|
C | G | 1 | a0002c0002t0001g0027 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.2030+842G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853212 | ||||||
chr2:38853224
|
AT | A | 233 | a0001c0001t0002g0003a0001c0001t0002g0045a0001c0001t0002g0122others(230): Show | 235 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.2030+829delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853224 | ||||||
chr2:38853241
|
T | C | 1 | a0002c0002t0001g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2030+813A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853241 | ||||||
chr2:38853331
|
C | G | 1 | a0001c0001t0005g0121 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2030+723G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853331 | ||||||
chr2:38853360
|
C | G | 10 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(7): Show | 11 | HG01361.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.2030+694G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853360 | ||||||
chr2:38853372
|
C | A | 1 | a0002c0002t0001g0113 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.2030+682G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853372 | ||||||
chr2:38853887
|
A | C | 1 | a0001c0003t0001g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2030+167T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853887 | ||||||
chr2:38853911
|
T | C | 5 | a0003c0005t0002g0186a0003c0005t0002g0187a0003c0005t0002g0188others(2): Show | 5 | HG02280.hp2 HG02818.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.2030+143A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 9/23 | chr2 | 38853911 | ||||||
chr2:38854188
|
G | A | 1 | a0001c0001t0003g0165 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1906-10C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854188 | ||||||
chr2:38854211
|
T | C | 2 | a0002c0002t0001g0025a0002c0002t0001g0114 | 2 | HG00558.hp2 HG00621.hp2 |
intron_variant | MODIFIER | c.1906-33A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854211 | ||||||
chr2:38854481
|
C | T | 2 | a0002c0002t0001g0010a0011c0018t0001g0009 | 2 | HG01243.hp2 HG01884.hp1 |
intron_variant | MODIFIER | c.1906-303G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854481 | ||||||
chr2:38854556
|
G | GT | 17 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(14): Show | 18 | HG01167.hp2 HG01169.hp1 HG01192.hp1 others(15): Show |
intron_variant | MODIFIER | c.1906-379dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854556 | ||||||
chr2:38854561
|
T | G | 1 | a0001c0003t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1906-383A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854561 | ||||||
chr2:38854563
|
T | TG | 5 | a0002c0002t0001g0079a0002c0002t0001g0085a0002c0002t0001g0120others(2): Show | 5 | HG01361.hp1 HG01517.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.1906-386_1906-385i others(3): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854563 | ||||||
chr2:38854564
|
T | G | 125 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(122): Show | 125 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1906-386A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854564 | ||||||
chr2:38854564
|
T | TG | 61 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0196others(58): Show | 62 | HG00609.hp2 HG00621.hp1 HG00639.hp1 others(59): Show |
intron_variant | MODIFIER | c.1906-387_1906-386i others(3): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854564 | ||||||
chr2:38854565
|
T | G | 4 | a0003c0005t0002g0186a0003c0005t0002g0187a0003c0005t0002g0188others(1): Show | 4 | HG02280.hp2 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1906-387A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854565 | ||||||
chr2:38854566
|
T | G | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1906-388A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854566 | ||||||
chr2:38854569
|
T | G | 1 | a0002c0002t0001g0075 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.1906-391A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854569 | ||||||
chr2:38854592
|
G | C | 131 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(128): Show | 131 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1906-414C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854592 | ||||||
chr2:38854707
|
G | A | 2 | a0002c0002t0001g0005a0002c0002t0001g0006 | 2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.1905+350C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854707 | ||||||
chr2:38854722
|
T | C | 278 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(275): Show | 281 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(278): Show |
intron_variant | MODIFIER | c.1905+335A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854722 | ||||||
chr2:38854770
|
C | T | 7 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(4): Show | 7 | NA18952.hp1 NA18956.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.1905+287G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854770 | ||||||
chr2:38854851
|
C | A | 17 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(14): Show | 17 | HG01106.hp2 HG01109.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1905+206G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854851 | ||||||
chr2:38854853
|
C | T | 10 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(7): Show | 10 | HG01106.hp1 HG01993.hp2 NA18952.hp1 others(7): Show |
intron_variant | MODIFIER | c.1905+204G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854853 | ||||||
chr2:38854854
|
G | A | 1 | a0001c0001t0002g0164 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1905+203C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854854 | ||||||
chr2:38854879
|
AAAATATT others(3): Show |
A | 1 | a0002c0002t0001g0261 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.1905+168_1905+177d others(12): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 8/23 | chr2 | 38854879 | ||||||
chr2:38855354
|
TA | T | 3 | a0001c0001t0002g0260a0007c0013t0003g0193a0007c0013t0003g0194 | 3 | HG02486.hp1 HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.1710-103delT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 7/23 | chr2 | 38855354 | ||||||
chr2:38855437
|
CCAATCAA others(5): Show |
C | 58 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0132others(55): Show | 59 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.1710-197_1710-186d others(14): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 7/23 | chr2 | 38855437 | ||||||
chr2:38855534
|
C | T | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1710-282G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 7/23 | chr2 | 38855534 | ||||||
chr2:38855552
|
A | C | 5 | a0002c0002t0001g0007a0002c0002t0001g0034a0002c0002t0001g0035others(2): Show | 5 | HG02135.hp2 NA18956.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.1710-300T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 7/23 | chr2 | 38855552 | ||||||
chr2:38855826
|
G | A | 17 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(14): Show | 17 | HG01106.hp2 HG01109.hp1 HG01167.hp2 others(14): Show |
intron_variant | MODIFIER | c.1709+514C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 7/23 | chr2 | 38855826 | ||||||
chr2:38855857
|
G | A | 1 | a0001c0003t0001g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1709+483C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 7/23 | chr2 | 38855857 | ||||||
chr2:38855905
|
T | C | 1 | a0002c0002t0001g0016 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1709+435A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 7/23 | chr2 | 38855905 | ||||||
chr2:38856087
|
C | G | 233 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(230): Show | 235 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1709+253G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 7/23 | chr2 | 38856087 | ||||||
chr2:38856487
|
A | G | 1 | a0002c0002t0001g0065 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1588-26T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38856487 | ||||||
chr2:38856503
|
C | CT | 8 | a0001c0001t0002g0203a0001c0001t0002g0225a0001c0001t0002g0260others(5): Show | 8 | HG01071.hp1 HG01358.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.1588-43dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38856503 | ||||||
chr2:38856503
|
CT | C | 6 | a0001c0001t0002g0246a0001c0011t0003g0180a0002c0002t0001g0088others(3): Show | 6 | HG00621.hp1 HG01975.hp1 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1588-43delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38856503 | ||||||
chr2:38856507
|
T | C | 11 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(8): Show | 11 | HG01106.hp1 HG01993.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1588-46A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38856507 | ||||||
chr2:38856592
|
T | C | 1 | a0002c0002t0001g0076 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.1588-131A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38856592 | ||||||
chr2:38856670
|
T | G | 65 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0132others(62): Show | 66 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.1588-209A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38856670 | ||||||
chr2:38856801
|
G | A | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1588-340C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38856801 | ||||||
chr2:38856898
|
T | C | 70 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0132others(67): Show | 71 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(68): Show |
intron_variant | MODIFIER | c.1588-437A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38856898 | ||||||
chr2:38857150
|
A | G | 65 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0132others(62): Show | 66 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(63): Show |
intron_variant | MODIFIER | c.1588-689T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857150 | ||||||
chr2:38857438
|
A | G | 4 | a0003c0005t0002g0186a0003c0005t0002g0187a0003c0005t0002g0188others(1): Show | 4 | HG02280.hp2 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1588-977T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857438 | ||||||
chr2:38857465
|
C | G | 129 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(126): Show | 129 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1588-1004G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857465 | ||||||
chr2:38857469
|
T | C | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1588-1008A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857469 | ||||||
chr2:38857494
|
A | C | 2 | a0001c0001t0002g0243a0001c0021t0001g0218 | 2 | HG04199.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1588-1033T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857494 | ||||||
chr2:38857615
|
G | A | 75 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(72): Show | 76 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(73): Show |
intron_variant | MODIFIER | c.1587+1046C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857615 | ||||||
chr2:38857634
|
G | C | 4 | a0001c0001t0002g0260a0003c0005t0003g0195a0007c0013t0003g0193others(1): Show | 4 | HG02486.hp1 HG02723.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.1587+1027C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857634 | ||||||
chr2:38857711
|
T | G | 7 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(4): Show | 7 | NA18943.hp2 NA18961.hp1 NA19002.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+950A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857711 | ||||||
chr2:38857807
|
G | A | 10 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(7): Show | 11 | HG01361.hp2 HG02615.hp1 HG02622.hp1 others(8): Show |
intron_variant | MODIFIER | c.1587+854C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857807 | ||||||
chr2:38857829
|
G | C | 1 | a0001c0003t0001g0223 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.1587+832C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857829 | ||||||
chr2:38857846
|
A | G | 2 | a0001c0001t0002g0216a0001c0001t0002g0217 | 2 | HG01175.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1587+815T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857846 | ||||||
chr2:38857961
|
T | C | 8 | a0001c0001t0002g0260a0003c0005t0002g0186a0003c0005t0002g0187others(5): Show | 8 | HG02280.hp2 HG02486.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.1587+700A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857961 | ||||||
chr2:38857984
|
C | T | 7 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(4): Show | 7 | NA18952.hp1 NA18956.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.1587+677G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38857984 | ||||||
chr2:38858093
|
G | A | 5 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(2): Show | 5 | NA18943.hp2 NA18961.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.1587+568C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38858093 | ||||||
chr2:38858129
|
A | G | 134 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(131): Show | 134 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.1587+532T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38858129 | ||||||
chr2:38858208
|
C | T | 1 | a0001c0003t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1587+453G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38858208 | ||||||
chr2:38858431
|
CTG | C | 129 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(126): Show | 129 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(126): Show |
intron_variant | MODIFIER | c.1587+228_1587+229d others(4): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38858431 | ||||||
chr2:38858499
|
G | T | 1 | a0002c0002t0001g0079 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1587+162C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38858499 | ||||||
chr2:38858539
|
A | T | 2 | a0005c0007t0002g0198a0005c0007t0002g0199 | 2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1587+122T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38858539 | ||||||
chr2:38858633
|
C | T | 1 | a0002c0002t0001g0062 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1587+28G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 6/23 | chr2 | 38858633 | ||||||
chr2:38858854
|
A | G | 2 | a0001c0001t0002g0200a0001c0001t0002g0201 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.1412-18T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38858854 | ||||||
chr2:38858981
|
AG | A | 6 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(3): Show | 6 | NA18943.hp2 NA18961.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412-146delC | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38858981 | ||||||
chr2:38859036
|
CACAA | C | 6 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(3): Show | 6 | NA18943.hp2 NA18961.hp1 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.1412-204_1412-201d others(6): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38859036 | ||||||
chr2:38859113
|
C | T | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1412-277G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38859113 | ||||||
chr2:38859284
|
G | C | 131 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(128): Show | 131 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.1412-448C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38859284 | ||||||
chr2:38859654
|
G | A | 1 | a0002c0002t0001g0034 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1412-818C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38859654 | ||||||
chr2:38859692
|
C | T | 1 | a0001c0001t0002g0215 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1412-856G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38859692 | ||||||
chr2:38859710
|
G | A | 1 | a0002c0002t0001g0126 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1412-874C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38859710 | ||||||
chr2:38859817
|
C | CT | 130 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(127): Show | 130 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.1412-982dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38859817 | ||||||
chr2:38859906
|
G | T | 7 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(4): Show | 7 | NA18952.hp1 NA18956.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.1412-1070C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38859906 | ||||||
chr2:38860213
|
G | A | 1 | a0001c0001t0003g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1411+786C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38860213 | ||||||
chr2:38860310
|
G | T | 1 | a0002c0002t0001g0008 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1411+689C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38860310 | ||||||
chr2:38860320
|
G | A | 125 | a0002c0002t0001g0007a0002c0002t0001g0008a0002c0002t0001g0010others(122): Show | 125 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1411+679C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38860320 | ||||||
chr2:38860473
|
T | C | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1411+526A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38860473 | ||||||
chr2:38860627
|
A | C | 1 | a0001c0001t0002g0225 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1411+372T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38860627 | ||||||
chr2:38860748
|
A | G | 233 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(230): Show | 235 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(232): Show |
intron_variant | MODIFIER | c.1411+251T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38860748 | ||||||
chr2:38860764
|
G | C | 1 | a0003c0005t0002g0188 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1411+235C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 5/23 | chr2 | 38860764 | ||||||
chr2:38861941
|
A | G | 1 | a0002c0002t0001g0050 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.573-104T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 4/23 | chr2 | 38861941 | ||||||
chr2:38862054
|
T | A | 2 | a0005c0007t0002g0198a0005c0007t0002g0199 | 2 | HG03669.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.572+91A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 4/23 | chr2 | 38862054 | ||||||
chr2:38862597
|
CT | C | 7 | a0001c0001t0003g0152a0001c0001t0003g0165a0001c0004t0003g0002others(4): Show | 8 | HG01256.hp1 HG02818.hp2 HG02895.hp1 others(5): Show |
intron_variant | MODIFIER | c.384-265delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 3/23 | chr2 | 38862597 | ||||||
chr2:38862688
|
G | T | 1 | a0002c0022t0001g0078 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.384-355C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 3/23 | chr2 | 38862688 | ||||||
chr2:38862769
|
C | T | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.384-436G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 3/23 | chr2 | 38862769 | ||||||
chr2:38862789
|
C | T | 18 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(15): Show | 18 | HG01106.hp2 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.384-456G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 3/23 | chr2 | 38862789 | ||||||
chr2:38862819
|
T | C | 1 | a0002c0002t0001g0077 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.384-486A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 3/23 | chr2 | 38862819 | ||||||
chr2:38862855
|
C | A | 3 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.383+506G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 3/23 | chr2 | 38862855 | ||||||
chr2:38862958
|
A | C | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.383+403T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 3/23 | chr2 | 38862958 | ||||||
chr2:38863047
|
A | C | 208 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0132others(205): Show | 210 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(207): Show |
intron_variant | MODIFIER | c.383+314T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 3/23 | chr2 | 38863047 | ||||||
chr2:38863053
|
C | T | 6 | a0001c0001t0003g0001a0001c0001t0003g0156a0001c0001t0003g0177others(3): Show | 7 | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.383+308G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 3/23 | chr2 | 38863053 | ||||||
chr2:38863173
|
T | A | 1 | a0002c0002t0001g0085 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.383+188A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 3/23 | chr2 | 38863173 | ||||||
chr2:38863260
|
A | G | 4 | a0003c0005t0002g0186a0003c0005t0002g0187a0003c0005t0002g0188others(1): Show | 4 | HG02280.hp2 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.383+101T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 3/23 | chr2 | 38863260 | ||||||
chr2:38863554
|
T | C | 277 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(274): Show | 280 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(277): Show |
intron_variant | MODIFIER | c.225-35A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38863554 | ||||||
chr2:38863600
|
C | T | 6 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.225-81G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38863600 | ||||||
chr2:38863632
|
A | G | 1 | a0004c0006t0003g0268 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.225-113T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38863632 | ||||||
chr2:38863686
|
C | G | 76 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(73): Show | 77 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(74): Show |
intron_variant | MODIFIER | c.225-167G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38863686 | ||||||
chr2:38863750
|
C | T | 7 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01192.hp1 others(4): Show |
intron_variant | MODIFIER | c.225-231G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38863750 | ||||||
chr2:38863788
|
G | A | 1 | a0001c0001t0002g0240 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.225-269C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38863788 | ||||||
chr2:38863795
|
C | T | 1 | a0001c0001t0002g0157 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.225-276G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38863795 | ||||||
chr2:38863873
|
C | T | 7 | a0001c0001t0007g0273a0001c0001t0007g0274a0001c0001t0009g0275others(4): Show | 8 | HG01361.hp2 HG02818.hp2 HG02886.hp1 others(5): Show |
intron_variant | MODIFIER | c.225-354G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38863873 | ||||||
chr2:38864006
|
C | T | 1 | a0001c0001t0003g0176 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.225-487G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864006 | ||||||
chr2:38864007
|
G | A | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.225-488C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864007 | ||||||
chr2:38864022
|
A | C | 80 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(77): Show | 81 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(78): Show |
intron_variant | MODIFIER | c.225-503T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864022 | ||||||
chr2:38864142
|
A | T | 3 | a0002c0002t0001g0034a0002c0002t0001g0092a0002c0009t0002g0093 | 3 | NA18952.hp2 NA18981.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.225-623T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864142 | ||||||
chr2:38864245
|
TA | T | 131 | a0001c0001t0002g0224a0002c0002t0001g0004a0002c0002t0001g0005others(128): Show | 131 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(128): Show |
intron_variant | MODIFIER | c.225-727delT | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864245 | ||||||
chr2:38864294
|
C | T | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.225-775G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864294 | ||||||
chr2:38864302
|
T | C | 26 | a0001c0001t0002g0202a0001c0001t0002g0203a0001c0001t0002g0205others(23): Show | 26 | HG00639.hp1 HG00741.hp2 HG01081.hp2 others(23): Show |
intron_variant | MODIFIER | c.225-783A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864302 | ||||||
chr2:38864432
|
A | G | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.225-913T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864432 | ||||||
chr2:38864474
|
G | A | 4 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.225-955C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864474 | ||||||
chr2:38864530
|
C | G | 1 | a0002c0002t0001g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.225-1011G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864530 | ||||||
chr2:38864552
|
C | A | 1 | a0001c0003t0001g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.225-1033G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864552 | ||||||
chr2:38864760
|
C | A | 2 | a0007c0013t0003g0193a0007c0013t0003g0194 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.225-1241G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864760 | ||||||
chr2:38864764
|
T | G | 130 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(127): Show | 130 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.225-1245A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864764 | ||||||
chr2:38864877
|
C | T | 1 | a0002c0002t0001g0091 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.225-1358G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864877 | ||||||
chr2:38864880
|
G | A | 130 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(127): Show | 130 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.225-1361C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864880 | ||||||
chr2:38864888
|
A | G | 1 | a0002c0002t0001g0261 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.225-1369T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864888 | ||||||
chr2:38864909
|
G | C | 139 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(136): Show | 139 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.225-1390C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864909 | ||||||
chr2:38864942
|
A | G | 130 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(127): Show | 130 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(127): Show |
intron_variant | MODIFIER | c.225-1423T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864942 | ||||||
chr2:38864986
|
A | G | 1 | a0001c0024t0003g0181 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.225-1467T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38864986 | ||||||
chr2:38865007
|
T | C | 1 | a0002c0002t0001g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.225-1488A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38865007 | ||||||
chr2:38865153
|
C | T | 197 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0132others(194): Show | 198 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(195): Show |
intron_variant | MODIFIER | c.225-1634G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38865153 | ||||||
chr2:38865216
|
T | C | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.225-1697A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38865216 | ||||||
chr2:38865220
|
A | G | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.225-1701T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38865220 | ||||||
chr2:38865334
|
A | T | 1 | a0002c0002t0001g0090 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.225-1815T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38865334 | ||||||
chr2:38865336
|
C | T | 7 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(4): Show | 7 | NA18952.hp1 NA18956.hp1 NA18961.hp2 others(4): Show |
intron_variant | MODIFIER | c.225-1817G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38865336 | ||||||
chr2:38865538
|
G | A | 3 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.225-2019C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38865538 | ||||||
chr2:38866003
|
G | A | 128 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(125): Show | 128 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.224+2179C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866003 | ||||||
chr2:38866068
|
G | T | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.224+2114C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866068 | ||||||
chr2:38866083
|
AG | A | 128 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(125): Show | 128 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(125): Show |
intron_variant | MODIFIER | c.224+2098delC | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866083 | ||||||
chr2:38866163
|
A | C | 1 | a0001c0001t0002g0248 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.224+2019T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866163 | ||||||
chr2:38866219
|
A | G | 2 | a0007c0013t0003g0193a0007c0013t0003g0194 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.224+1963T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866219 | ||||||
chr2:38866259
|
T | C | 253 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(250): Show | 256 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(253): Show |
intron_variant | MODIFIER | c.224+1923A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866259 | ||||||
chr2:38866360
|
A | G | 1 | a0002c0002t0001g0049 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.224+1822T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866360 | ||||||
chr2:38866402
|
T | C | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.224+1780A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866402 | ||||||
chr2:38866415
|
C | G | 8 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(5): Show | 8 | HG02280.hp2 HG02615.hp1 HG02622.hp1 others(5): Show |
intron_variant | MODIFIER | c.224+1767G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866415 | ||||||
chr2:38866539
|
C | T | 1 | a0001c0001t0002g0250 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.224+1643G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866539 | ||||||
chr2:38866564
|
G | C | 2 | a0007c0013t0003g0193a0007c0013t0003g0194 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.224+1618C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866564 | ||||||
chr2:38866598
|
C | G | 2 | a0002c0002t0001g0048a0002c0009t0003g0047 | 2 | HG02630.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.224+1584G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866598 | ||||||
chr2:38866627
|
T | A | 1 | a0001c0024t0003g0181 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.224+1555A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866627 | ||||||
chr2:38866685
|
A | G | 1 | a0001c0001t0002g0249 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.224+1497T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866685 | ||||||
chr2:38866705
|
C | T | 18 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(15): Show | 18 | HG01106.hp2 HG01109.hp1 HG01167.hp2 others(15): Show |
intron_variant | MODIFIER | c.224+1477G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866705 | ||||||
chr2:38866756
|
G | C | 3 | a0001c0001t0002g0264a0001c0001t0002g0265a0001c0001t0002g0266 | 3 | NA19006.hp2 NA19010.hp2 NA19091.hp2 |
intron_variant | MODIFIER | c.224+1426C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866756 | ||||||
chr2:38866765
|
G | C | 1 | a0002c0002t0001g0027 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.224+1417C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866765 | ||||||
chr2:38866794
|
C | A | 1 | a0002c0002t0001g0117 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.224+1388G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866794 | ||||||
chr2:38866840
|
C | T | 1 | a0002c0002t0001g0126 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.224+1342G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866840 | ||||||
chr2:38866954
|
C | T | 1 | a0002c0002t0001g0017 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.224+1228G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38866954 | ||||||
chr2:38867152
|
T | C | 1 | a0002c0002t0001g0126 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.224+1030A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38867152 | ||||||
chr2:38867205
|
T | C | 1 | a0002c0002t0001g0118 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.224+977A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38867205 | ||||||
chr2:38867288
|
A | G | 6 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(3): Show | 6 | NA18943.hp2 NA19002.hp2 NA19006.hp2 others(3): Show |
intron_variant | MODIFIER | c.224+894T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38867288 | ||||||
chr2:38867305
|
C | T | 1 | a0002c0002t0001g0089 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.224+877G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38867305 | ||||||
chr2:38867316
|
C | G | 21 | a0001c0001t0003g0001a0001c0001t0003g0153a0001c0001t0003g0156others(18): Show | 22 | HG01106.hp1 HG01884.hp2 HG01993.hp2 others(19): Show |
intron_variant | MODIFIER | c.224+866G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38867316 | ||||||
chr2:38867371
|
T | C | 2 | a0007c0013t0003g0193a0007c0013t0003g0194 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.224+811A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38867371 | ||||||
chr2:38867564
|
A | T | 4 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(1): Show | 4 | HG02615.hp1 HG02622.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.224+618T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38867564 | ||||||
chr2:38867596
|
T | C | 1 | a0002c0002t0001g0119 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.224+586A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38867596 | ||||||
chr2:38867690
|
C | G | 15 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0200others(12): Show | 16 | HG00735.hp2 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.224+492G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38867690 | ||||||
chr2:38868092
|
G | A | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.224+90C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38868092 | ||||||
chr2:38868104
|
A | C | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.224+78T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38868104 | ||||||
chr2:38868105
|
T | A | 1 | a0002c0002t0001g0028 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.224+77A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 2/23 | chr2 | 38868105 | ||||||
chr2:38868783
|
G | C | 1 | a0002c0002t0001g0028 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-6-372C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38868783 | ||||||
chr2:38868802
|
T | TTTTA | 22 | a0001c0001t0003g0001a0001c0001t0003g0153a0001c0001t0003g0156others(19): Show | 23 | HG01106.hp1 HG01884.hp2 HG01993.hp2 others(20): Show |
intron_variant | MODIFIER | c.-6-395_-6-392dupTA others(2): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38868802 | ||||||
chr2:38868802
|
TTTTA | T | 136 | a0001c0001t0007g0273a0001c0001t0007g0274a0001c0001t0009g0275others(133): Show | 137 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(134): Show |
intron_variant | MODIFIER | c.-6-395_-6-392delTA others(2): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38868802 | ||||||
chr2:38868864
|
T | C | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-6-453A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38868864 | ||||||
chr2:38868867
|
T | A | 133 | a0001c0001t0007g0273a0001c0001t0007g0274a0001c0001t0009g0275others(130): Show | 134 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(131): Show |
intron_variant | MODIFIER | c.-6-456A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38868867 | ||||||
chr2:38868946
|
C | T | 11 | a0001c0001t0003g0153a0001c0001t0003g0168a0001c0001t0003g0169others(8): Show | 11 | HG01106.hp1 HG01993.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6-535G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38868946 | ||||||
chr2:38868994
|
A | G | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-6-583T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38868994 | ||||||
chr2:38869235
|
G | A | 1 | a0002c0002t0001g0120 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.-6-824C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38869235 | ||||||
chr2:38869297
|
G | A | 2 | a0002c0002t0001g0062a0002c0002t0001g0063 | 2 | HG01257.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.-6-886C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38869297 | ||||||
chr2:38869399
|
A | G | 2 | a0002c0002t0001g0038a0002c0002t0001g0039 | 2 | HG02698.hp2 HG03654.hp1 |
intron_variant | MODIFIER | c.-6-988T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38869399 | ||||||
chr2:38869462
|
T | C | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-6-1051A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38869462 | ||||||
chr2:38869510
|
C | T | 3 | a0001c0001t0002g0209a0001c0001t0005g0208a0001c0017t0002g0207 | 3 | HG03654.hp2 HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-6-1099G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38869510 | ||||||
chr2:38869591
|
T | C | 276 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(273): Show | 279 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(276): Show |
intron_variant | MODIFIER | c.-6-1180A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38869591 | ||||||
chr2:38869731
|
T | A | 69 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0132others(66): Show | 70 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.-6-1320A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38869731 | ||||||
chr2:38869913
|
G | A | 2 | a0007c0013t0003g0193a0007c0013t0003g0194 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-6-1502C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38869913 | ||||||
chr2:38869915
|
T | C | 69 | a0001c0001t0002g0003a0001c0001t0002g0122a0001c0001t0002g0132others(66): Show | 70 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.-6-1504A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38869915 | ||||||
chr2:38870041
|
T | G | 1 | a0002c0002t0001g0261 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-6-1630A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38870041 | ||||||
chr2:38870213
|
A | C | 4 | a0001c0001t0003g0141a0001c0001t0003g0142a0001c0001t0003g0143others(1): Show | 4 | HG01496.hp2 HG02896.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.-6-1802T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38870213 | ||||||
chr2:38870282
|
G | C | 2 | a0006c0014t0004g0280a0006c0014t0004g0281 | 2 | HG00323.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-6-1871C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38870282 | ||||||
chr2:38870595
|
T | C | 33 | a0002c0002t0001g0004a0002c0002t0001g0005a0002c0002t0001g0006others(30): Show | 33 | HG01071.hp1 HG01123.hp1 HG01346.hp1 others(30): Show |
intron_variant | MODIFIER | c.-6-2184A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38870595 | ||||||
chr2:38870608
|
G | A | 1 | a0002c0002t0001g0130 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-6-2197C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38870608 | ||||||
chr2:38870617
|
T | C | 256 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(253): Show | 259 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.-6-2206A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38870617 | ||||||
chr2:38870651
|
G | A | 1 | a0002c0002t0001g0037 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-6-2240C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38870651 | ||||||
chr2:38870661
|
C | T | 12 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0252others(9): Show | 12 | HG01106.hp2 HG01109.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-6-2250G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38870661 | ||||||
chr2:38871015
|
T | C | 18 | a0001c0001t0002g0205a0001c0001t0002g0206a0001c0001t0002g0249others(15): Show | 18 | HG01106.hp2 HG01109.hp1 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.-6-2604A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871015 | ||||||
chr2:38871110
|
A | G | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-6-2699T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871110 | ||||||
chr2:38871183
|
C | T | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-6-2772G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871183 | ||||||
chr2:38871216
|
T | C | 64 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0196others(61): Show | 65 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(62): Show |
intron_variant | MODIFIER | c.-6-2805A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871216 | ||||||
chr2:38871314
|
G | A | 2 | a0002c0002t0001g0036a0002c0002t0001g0037 | 2 | NA18956.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.-6-2903C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871314 | ||||||
chr2:38871419
|
G | A | 1 | a0002c0022t0001g0078 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-6-3008C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871419 | ||||||
chr2:38871595
|
A | G | 1 | a0002c0002t0001g0167 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-6-3184T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871595 | ||||||
chr2:38871617
|
G | A | 1 | a0001c0001t0002g0003 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.-6-3206C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871617 | ||||||
chr2:38871621
|
T | C | 1 | a0002c0002t0001g0079 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.-6-3210A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871621 | ||||||
chr2:38871622
|
G | A | 67 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0196others(64): Show | 68 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.-6-3211C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871622 | ||||||
chr2:38871640
|
A | T | 1 | a0001c0001t0003g0204 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.-6-3229T>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871640 | ||||||
chr2:38871710
|
C | CT | 63 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0196others(60): Show | 64 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(61): Show |
intron_variant | MODIFIER | c.-6-3300dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871710 | ||||||
chr2:38871710
|
C | CTT | 13 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0252others(10): Show | 13 | HG01106.hp2 HG01109.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-6-3301_-6-3300dup others(2): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871710 | ||||||
chr2:38871715
|
T | C | 1 | a0002c0002t0001g0080 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.-6-3304A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871715 | ||||||
chr2:38871768
|
G | A | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-6-3357C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871768 | ||||||
chr2:38871839
|
C | T | 1 | a0007c0013t0003g0194 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-6-3428G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871839 | ||||||
chr2:38871850
|
G | A | 2 | a0002c0002t0001g0124a0009c0016t0001g0123 | 2 | NA18964.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.-6-3439C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871850 | ||||||
chr2:38871861
|
C | T | 21 | a0001c0001t0003g0001a0001c0001t0003g0153a0001c0001t0003g0156others(18): Show | 22 | HG01106.hp1 HG01884.hp2 HG01993.hp2 others(19): Show |
intron_variant | MODIFIER | c.-6-3450G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871861 | ||||||
chr2:38871862
|
G | A | 3 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-6-3451C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871862 | ||||||
chr2:38871868
|
G | T | 11 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(8): Show | 11 | HG02572.hp1 HG03225.hp1 NA18906.hp1 others(8): Show |
intron_variant | MODIFIER | c.-6-3457C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871868 | ||||||
chr2:38871991
|
A | C | 1 | a0001c0001t0002g0203 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.-6-3580T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38871991 | ||||||
chr2:38872068
|
A | G | 1 | a0010c0025t0001g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-6-3657T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38872068 | ||||||
chr2:38872160
|
T | C | 4 | a0002c0002t0001g0125a0002c0002t0001g0126a0002c0008t0002g0136others(1): Show | 4 | HG02080.hp2 NA19002.hp2 NA19066.hp1 others(1): Show |
intron_variant | MODIFIER | c.-7+3627A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38872160 | ||||||
chr2:38872342
|
C | T | 12 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0252others(9): Show | 12 | HG01106.hp2 HG01109.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.-7+3445G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38872342 | ||||||
chr2:38872493
|
C | A | 1 | a0002c0002t0001g0127 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-7+3294G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38872493 | ||||||
chr2:38872695
|
T | C | 1 | a0001c0001t0003g0166 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-7+3092A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38872695 | ||||||
chr2:38872776
|
A | G | 71 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0196others(68): Show | 72 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(69): Show |
intron_variant | MODIFIER | c.-7+3011T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38872776 | ||||||
chr2:38872882
|
G | C | 1 | a0001c0001t0002g0262 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-7+2905C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38872882 | ||||||
chr2:38872911
|
G | A | 232 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(229): Show | 234 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(231): Show |
intron_variant | MODIFIER | c.-7+2876C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38872911 | ||||||
chr2:38872931
|
G | A | 1 | a0002c0002t0001g0029 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.-7+2856C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38872931 | ||||||
chr2:38872987
|
A | C | 5 | a0002c0002t0001g0007a0002c0002t0001g0034a0002c0002t0001g0035others(2): Show | 5 | HG02135.hp2 NA18956.hp2 NA18973.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+2800T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38872987 | ||||||
chr2:38872992
|
A | AT | 13 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0252others(10): Show | 13 | HG01106.hp2 HG01109.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7+2794dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38872992 | ||||||
chr2:38873026
|
C | T | 13 | a0001c0001t0002g0249a0001c0001t0002g0250a0001c0001t0002g0252others(10): Show | 13 | HG01106.hp2 HG01109.hp1 HG02055.hp2 others(10): Show |
intron_variant | MODIFIER | c.-7+2761G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873026 | ||||||
chr2:38873027
|
G | A | 2 | a0007c0013t0003g0193a0007c0013t0003g0194 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-7+2760C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873027 | ||||||
chr2:38873037
|
G | C | 1 | a0001c0001t0002g0245 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-7+2750C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873037 | ||||||
chr2:38873090
|
C | T | 1 | a0002c0002t0001g0088 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.-7+2697G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873090 | ||||||
chr2:38873137
|
G | A | 5 | a0002c0002t0001g0082a0002c0002t0001g0083a0002c0002t0001g0085others(2): Show | 5 | NA18943.hp1 NA18979.hp2 NA19054.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+2650C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873137 | ||||||
chr2:38873235
|
T | A | 3 | a0002c0002t0001g0086a0002c0002t0001g0087a0002c0002t0008g0272 | 3 | HG02280.hp1 HG03041.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-7+2552A>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873235 | ||||||
chr2:38873270
|
C | T | 2 | a0001c0001t0002g0252a0001c0001t0002g0253 | 2 | HG03209.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-7+2517G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873270 | ||||||
chr2:38873305
|
A | G | 1 | a0002c0002t0001g0033 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-7+2482T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873305 | ||||||
chr2:38873500
|
A | G | 1 | a0010c0025t0001g0271 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.-7+2287T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873500 | ||||||
chr2:38873618
|
G | A | 66 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0196others(63): Show | 67 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(64): Show |
intron_variant | MODIFIER | c.-7+2169C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873618 | ||||||
chr2:38873636
|
T | C | 2 | a0002c0002t0001g0128a0002c0002t0001g0129 | 2 | NA18970.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.-7+2151A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873636 | ||||||
chr2:38873751
|
G | T | 2 | a0002c0002t0001g0032a0002c0002t0003g0031 | 2 | HG02965.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.-7+2036C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873751 | ||||||
chr2:38873836
|
C | T | 256 | a0001c0001t0002g0003a0001c0001t0002g0040a0001c0001t0002g0041others(253): Show | 259 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(256): Show |
intron_variant | MODIFIER | c.-7+1951G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873836 | ||||||
chr2:38873856
|
G | C | 1 | a0001c0001t0002g0246 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.-7+1931C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873856 | ||||||
chr2:38873954
|
T | G | 2 | a0007c0013t0003g0193a0007c0013t0003g0194 | 2 | HG02723.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.-7+1833A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873954 | ||||||
chr2:38873963
|
G | C | 72 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0196others(69): Show | 73 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(70): Show |
intron_variant | MODIFIER | c.-7+1824C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38873963 | ||||||
chr2:38874007
|
G | T | 59 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0196others(56): Show | 60 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(57): Show |
intron_variant | MODIFIER | c.-7+1780C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874007 | ||||||
chr2:38874030
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.-7+1757C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874030 | ||||||
chr2:38874067
|
C | A | 56 | a0001c0001t0002g0122a0001c0001t0002g0248a0001c0001t0005g0121others(53): Show | 56 | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(53): Show |
intron_variant | MODIFIER | c.-7+1720G>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874067 | ||||||
chr2:38874100
|
C | CT | 79 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0196others(76): Show | 80 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(77): Show |
intron_variant | MODIFIER | c.-7+1686dupA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874100 | ||||||
chr2:38874134
|
C | G | 3 | a0004c0006t0003g0268a0004c0006t0003g0269a0004c0006t0003g0270 | 3 | HG02572.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.-7+1653G>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874134 | ||||||
chr2:38874228
|
A | G | 1 | a0002c0002t0001g0030 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-7+1559T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874228 | ||||||
chr2:38874368
|
G | A | 1 | a0002c0002t0001g0130 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-7+1419C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874368 | ||||||
chr2:38874400
|
T | C | 5 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(2): Show | 5 | NA18943.hp2 NA18961.hp1 NA19006.hp2 others(2): Show |
intron_variant | MODIFIER | c.-7+1387A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874400 | ||||||
chr2:38874401
|
AT | A | 17 | a0001c0001t0002g0157a0001c0001t0002g0158a0001c0001t0002g0159others(14): Show | 17 | HG01106.hp2 HG01891.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.-7+1385delA | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874401 | ||||||
chr2:38874401
|
ATT | A | 27 | a0001c0001t0002g0252a0001c0001t0002g0253a0001c0001t0002g0254others(24): Show | 28 | HG01106.hp1 HG01109.hp1 HG01243.hp1 others(25): Show |
intron_variant | MODIFIER | c.-7+1384_-7+1385del others(2): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874401 | ||||||
chr2:38874401
|
ATTT | A | 21 | a0001c0001t0002g0200a0001c0001t0002g0201a0001c0001t0002g0202others(18): Show | 21 | HG01928.hp1 HG02280.hp2 HG02486.hp1 others(18): Show |
intron_variant | MODIFIER | c.-7+1383_-7+1385del others(3): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874401 | ||||||
chr2:38874401
|
ATTTT | A | 58 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0196others(55): Show | 59 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(56): Show |
intron_variant | MODIFIER | c.-7+1382_-7+1385del others(4): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874401 | ||||||
chr2:38874401
|
ATTTTT | A | 29 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(26): Show | 29 | HG00423.hp1 HG00423.hp2 HG00621.hp2 others(26): Show |
intron_variant | MODIFIER | c.-7+1381_-7+1385del others(5): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874401 | ||||||
chr2:38874401
|
ATTTTTT | A | 114 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(111): Show | 115 | HG00323.hp1 HG00323.hp2 HG00558.hp1 others(112): Show |
intron_variant | MODIFIER | c.-7+1380_-7+1385del others(6): Show |
DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874401 | ||||||
chr2:38874566
|
T | G | 4 | a0001c0004t0003g0002a0001c0004t0003g0190a0001c0004t0003g0191others(1): Show | 5 | HG02818.hp2 HG02895.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-7+1221A>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874566 | ||||||
chr2:38874608
|
A | G | 138 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(135): Show | 139 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.-7+1179T>C | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874608 | ||||||
chr2:38874622
|
G | A | 2 | a0006c0014t0004g0280a0006c0014t0004g0281 | 2 | HG00323.hp1 HG01433.hp2 |
intron_variant | MODIFIER | c.-7+1165C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874622 | ||||||
chr2:38874685
|
A | C | 67 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0196others(64): Show | 68 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(65): Show |
intron_variant | MODIFIER | c.-7+1102T>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874685 | ||||||
chr2:38874743
|
G | A | 138 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(135): Show | 139 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(136): Show |
intron_variant | MODIFIER | c.-7+1044C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874743 | ||||||
chr2:38874765
|
G | T | 1 | a0007c0013t0003g0193 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.-7+1022C>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874765 | ||||||
chr2:38874804
|
T | C | 6 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135others(3): Show | 6 | HG02615.hp1 HG02622.hp1 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.-7+983A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38874804 | ||||||
chr2:38875051
|
C | T | 1 | a0001c0001t0002g0196 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.-7+736G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38875051 | ||||||
chr2:38875085
|
G | A | 1 | a0002c0002t0001g0131 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.-7+702C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38875085 | ||||||
chr2:38875100
|
C | T | 3 | a0001c0001t0002g0133a0001c0001t0003g0134a0001c0001t0003g0135 | 3 | HG02615.hp1 HG02622.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-7+687G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38875100 | ||||||
chr2:38875386
|
T | C | 69 | a0001c0001t0002g0003a0001c0001t0002g0132a0001c0001t0002g0196others(66): Show | 70 | HG00609.hp2 HG00639.hp1 HG00673.hp2 others(67): Show |
intron_variant | MODIFIER | c.-7+401A>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38875386 | ||||||
chr2:38875459
|
G | A | 1 | a0001c0001t0002g0262 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-7+328C>T | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38875459 | ||||||
chr2:38875523
|
C | T | 1 | a0001c0001t0002g0132 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.-7+264G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38875523 | ||||||
chr2:38875529
|
C | T | 135 | a0001c0001t0002g0040a0001c0001t0002g0041a0001c0001t0002g0042others(132): Show | 135 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(132): Show |
intron_variant | MODIFIER | c.-7+258G>A | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38875529 | ||||||
chr2:38875674
|
G | C | 9 | a0001c0001t0002g0263a0001c0001t0002g0264a0001c0001t0002g0265others(6): Show | 9 | HG02572.hp1 HG03225.hp1 NA18906.hp1 others(6): Show |
intron_variant | MODIFIER | c.-7+113C>G | DHX57 | ENSG00000163214.21 | transcript | ENST00000457308.6 | protein_coding | 1/23 | chr2 | 38875674 |