geneid | 5394 |
---|---|
ensemblid | ENSG00000171824.14 |
hgncid | 9138 |
symbol | EXOSC10 |
name | exosome component 10 |
refseq_nuc | NM_001001998.3 |
refseq_prot | NP_001001998.1 |
ensembl_nuc | ENST00000376936.9 |
ensembl_prot | ENSP00000366135.4 |
mane_status | MANE Select |
chr | chr1 |
start | 11066618 |
end | 11099869 |
strand | - |
ver | v1.2 |
region | chr1:11066618-11099869 |
region5000 | chr1:11061618-11104869 |
regionname0 | EXOSC10_chr1_11066618_11099869 |
regionname5000 | EXOSC10_chr1_11061618_11104869 |
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 | 885 | 259 | 92 | 47 | 73 | 12 | 33 | 58 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0002 | 0/0 | 885 | 17 | 0 | 6 | 6 | 0 | 5 | 5 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0003 | 0/0 | 885 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0004 | 0/0 | 885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0005 | 0/0 | 885 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0006 | 0/0 | 885 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0007 | 0/0 | 885 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0008 | 0/0 | 885 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0009 | 0/0 | 885 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 2658 | 109 | 17 | 27 | 39 | 9 | 17 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0002 | 1/0 | 2658 | 64 | 39 | 8 | 11 | 2 | 3 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0003 | 0/0 | 2658 | 47 | 9 | 9 | 20 | 0 | 9 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0004 | 0/0 | 2658 | 16 | 0 | 5 | 6 | 0 | 5 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0005 | 0/0 | 2658 | 13 | 12 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0006 | 0/0 | 2658 | 5 | 5 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0007 | 0/0 | 2658 | 5 | 5 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0008 | 0/1 | 2658 | 4 | 0 | 1 | 0 | 0 | 2 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0009 | 0/0 | 2658 | 3 | 0 | 0 | 3 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0010 | 0/0 | 2658 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0011 | 0/0 | 2658 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0012 | 0/0 | 2658 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0013 | 0/0 | 2658 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0014 | 0/0 | 2658 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0015 | 0/0 | 2658 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0016 | 0/0 | 2658 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0017 | 0/0 | 2658 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0018 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0019 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0020 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0021 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0022 | 0/0 | 2658 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0023 | 0/0 | 2658 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0024 | 0/0 | 2658 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
c0025 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 139 | 264 | 91 | 51 | 75 | 11 | 34 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
t0002 | 0/0 | 139 | 16 | 0 | 2 | 9 | 1 | 4 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
t0003 | 0/0 | 139 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
t0004 | 0/0 | 139 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
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 | 6 | 1 | 0 | 3 | 0 | 2 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0039 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0043 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 2658 | 109 | 17 | 27 | 39 | 9 | 17 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0002 | 1/0 | 2658 | 64 | 39 | 8 | 11 | 2 | 3 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0003 | 0/0 | 2658 | 47 | 9 | 9 | 20 | 0 | 9 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0005 | 0/0 | 2658 | 13 | 12 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0006 | 0/0 | 2658 | 5 | 5 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0007 | 0/0 | 2658 | 5 | 5 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0008 | 0/1 | 2658 | 4 | 0 | 1 | 0 | 0 | 2 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0009 | 0/0 | 2658 | 3 | 0 | 0 | 3 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0010 | 0/0 | 2658 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0014 | 0/0 | 2658 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0017 | 0/0 | 2658 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0018 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0020 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0021 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0022 | 0/0 | 2658 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0023 | 0/0 | 2658 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0002c0004 | 0/0 | 2658 | 16 | 0 | 5 | 6 | 0 | 5 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0002c0013 | 0/0 | 2658 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0003c0011 | 0/0 | 2658 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0004c0025 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0005c0024 | 0/0 | 2658 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0006c0016 | 0/0 | 2658 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0007c0019 | 0/0 | 2658 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0008c0015 | 0/0 | 2658 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0009c0012 | 0/0 | 2658 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2796 | 109 | 17 | 27 | 39 | 9 | 17 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0002t0001 | 1/0 | 2796 | 63 | 39 | 7 | 11 | 2 | 3 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0002t0004 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0003t0001 | 0/0 | 2796 | 33 | 9 | 7 | 12 | 0 | 5 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0003t0002 | 0/0 | 2796 | 14 | 0 | 2 | 8 | 0 | 4 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0005t0001 | 0/0 | 2796 | 13 | 12 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0006t0001 | 0/0 | 2796 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0006t0003 | 0/0 | 2796 | 3 | 3 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0007t0001 | 0/0 | 2796 | 5 | 5 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0008t0001 | 0/1 | 2796 | 4 | 0 | 1 | 0 | 0 | 2 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0009t0001 | 0/0 | 2796 | 3 | 0 | 0 | 3 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0010t0001 | 0/0 | 2796 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0014t0001 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0017t0001 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0018t0001 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0020t0001 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0021t0001 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0022t0001 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0001c0023t0002 | 0/0 | 2796 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0002c0004t0001 | 0/0 | 2796 | 16 | 0 | 5 | 6 | 0 | 5 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0002c0013t0001 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0003c0011t0001 | 0/0 | 2796 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0004c0025t0001 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0005c0024t0002 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0006c0016t0001 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0007c0019t0001 | 0/0 | 2796 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0008c0015t0001 | 0/0 | 2796 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
a0009c0012t0001 | 0/0 | 2796 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | copy fasta | chr1 | 11061618 | 11104869 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 6 | 1 | 0 | 3 | 0 | 2 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0002 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0001t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0043 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0044 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0002t0004g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0010 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0003t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0005t0001g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0006t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0006t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0006t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0006t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0006t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0007t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0007t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0007t0001g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0007t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0007t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0008t0001g0039 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0008t0001g0045 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0008t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0008t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0009t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0009t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0009t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0010t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0010t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0014t0001g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0017t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0018t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0020t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0021t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0022t0001g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0001c0023t0002g0262 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0004t0001g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0002c0013t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0003c0011t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0003c0011t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0004c0025t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0005c0024t0002g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0006c0016t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0007c0019t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0008c0015t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
a0009c0012t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | FIN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00280 | hp2 | a0001 | c0023 | t0002 | g0262 | EUR | FIN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00323 | hp1 | a0001 | c0002 | t0001 | g0160 | EUR | FIN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0094 | EUR | FIN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00438 | hp1 | a0001 | c0003 | t0002 | g0255 | EAS | CHS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | CHS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00558 | hp1 | a0009 | c0012 | t0001 | g0194 | EAS | CHS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | CHS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00609 | hp1 | a0001 | c0009 | t0001 | g0145 | EAS | CHS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00609 | hp2 | a0001 | c0003 | t0001 | g0245 | EAS | CHS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00642 | hp1 | a0001 | c0002 | t0004 | g0012 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00673 | hp1 | a0001 | c0003 | t0001 | g0248 | EAS | CHS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00735 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG00741 | hp2 | a0001 | c0005 | t0001 | g0024 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0172 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01069 | hp2 | a0001 | c0008 | t0001 | g0173 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0155 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01081 | hp2 | a0008 | c0015 | t0001 | g0103 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01099 | hp1 | a0001 | c0003 | t0001 | g0242 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0131 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0170 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01109 | hp2 | a0001 | c0022 | t0001 | g0268 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0102 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01167 | hp2 | a0001 | c0002 | t0001 | g0070 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0027 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01175 | hp1 | a0001 | c0003 | t0002 | g0258 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0140 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01192 | hp2 | a0001 | c0002 | t0001 | g0003 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01243 | hp1 | a0001 | c0002 | t0001 | g0090 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01243 | hp2 | a0001 | c0002 | t0001 | g0056 | AMR | PUR | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01257 | hp1 | a0001 | c0003 | t0001 | g0237 | AMR | CLM | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01258 | hp2 | a0001 | c0003 | t0001 | g0238 | AMR | CLM | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01361 | hp1 | a0001 | c0003 | t0001 | g0240 | AMR | CLM | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01361 | hp2 | a0002 | c0013 | t0001 | g0207 | AMR | CLM | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01496 | hp1 | a0001 | c0002 | t0001 | g0028 | AMR | CLM | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01496 | hp2 | a0002 | c0004 | t0001 | g0198 | AMR | CLM | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0017 | EUR | IBS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0174 | EUR | IBS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | IBS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0118 | EUR | IBS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0101 | EUR | IBS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0018 | EUR | IBS | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01891 | hp1 | a0001 | c0005 | t0001 | g0067 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0212 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0117 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01943 | hp2 | a0002 | c0004 | t0001 | g0197 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01952 | hp1 | a0002 | c0004 | t0001 | g0196 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0007 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0166 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01975 | hp2 | a0001 | c0003 | t0001 | g0241 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01978 | hp2 | a0001 | c0003 | t0001 | g0239 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01993 | hp1 | a0001 | c0003 | t0001 | g0267 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02004 | hp1 | a0001 | c0003 | t0002 | g0259 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02055 | hp1 | a0001 | c0002 | t0001 | g0069 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02055 | hp2 | a0001 | c0002 | t0001 | g0038 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | KHV | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0126 | EAS | KHV | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02074 | hp2 | a0002 | c0004 | t0001 | g0204 | EAS | KHV | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0040 | EAS | KHV | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02083 | hp2 | a0006 | c0016 | t0001 | g0141 | EAS | KHV | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02135 | hp1 | a0001 | c0003 | t0002 | g0221 | EAS | KHV | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | KHV | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02145 | hp1 | a0001 | c0002 | t0001 | g0060 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02145 | hp2 | a0001 | c0007 | t0001 | g0213 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0061 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0055 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02258 | hp1 | a0001 | c0002 | t0001 | g0053 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02280 | hp2 | a0001 | c0002 | t0001 | g0079 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02300 | hp1 | a0002 | c0004 | t0001 | g0199 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02451 | hp2 | a0001 | c0020 | t0001 | g0077 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02572 | hp1 | a0001 | c0005 | t0001 | g0021 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0036 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0149 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02602 | hp2 | a0001 | c0017 | t0001 | g0190 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02615 | hp1 | a0001 | c0006 | t0003 | g0188 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02615 | hp2 | a0001 | c0002 | t0001 | g0181 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02622 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02622 | hp2 | a0001 | c0005 | t0001 | g0022 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0231 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02630 | hp2 | a0001 | c0002 | t0001 | g0075 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02647 | hp1 | a0001 | c0002 | t0001 | g0004 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02647 | hp2 | a0007 | c0019 | t0001 | g0084 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02683 | hp1 | a0001 | c0003 | t0001 | g0228 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02683 | hp2 | a0001 | c0014 | t0001 | g0097 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02717 | hp1 | a0001 | c0005 | t0001 | g0184 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02723 | hp1 | a0001 | c0002 | t0001 | g0080 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02723 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02735 | hp1 | a0001 | c0003 | t0002 | g0010 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02738 | hp1 | a0001 | c0003 | t0002 | g0222 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02738 | hp2 | a0001 | c0003 | t0001 | g0229 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02809 | hp1 | a0001 | c0018 | t0001 | g0054 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02809 | hp2 | a0001 | c0010 | t0001 | g0062 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0076 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02818 | hp2 | a0001 | c0003 | t0001 | g0260 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02886 | hp1 | a0001 | c0002 | t0001 | g0011 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02895 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02895 | hp2 | a0001 | c0005 | t0001 | g0019 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02896 | hp1 | a0001 | c0002 | t0001 | g0095 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02897 | hp1 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02897 | hp2 | a0001 | c0002 | t0001 | g0073 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02922 | hp2 | a0001 | c0007 | t0001 | g0215 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0034 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02965 | hp2 | a0001 | c0003 | t0001 | g0225 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02976 | hp1 | a0001 | c0002 | t0001 | g0037 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02976 | hp2 | a0001 | c0005 | t0001 | g0182 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03041 | hp1 | a0001 | c0003 | t0001 | g0227 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03041 | hp2 | a0001 | c0002 | t0001 | g0064 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0234 | AFR | MSL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03098 | hp2 | a0001 | c0007 | t0001 | g0214 | AFR | MSL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0180 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03130 | hp2 | a0001 | c0002 | t0001 | g0078 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03139 | hp1 | a0001 | c0002 | t0001 | g0059 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03139 | hp2 | a0001 | c0002 | t0001 | g0089 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03195 | hp2 | a0001 | c0002 | t0001 | g0071 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03209 | hp1 | a0001 | c0006 | t0003 | g0187 | AFR | MSL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03209 | hp2 | a0001 | c0002 | t0001 | g0058 | AFR | MSL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03225 | hp1 | a0001 | c0002 | t0001 | g0088 | AFR | MSL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03225 | hp2 | a0001 | c0007 | t0001 | g0216 | AFR | MSL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03453 | hp1 | a0001 | c0021 | t0001 | g0210 | AFR | MSL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03453 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | MSL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03486 | hp1 | a0001 | c0005 | t0001 | g0023 | AFR | MSL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03486 | hp2 | a0001 | c0010 | t0001 | g0063 | AFR | MSL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0122 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03490 | hp2 | a0001 | c0008 | t0001 | g0045 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03491 | hp2 | a0001 | c0003 | t0001 | g0223 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03516 | hp1 | a0001 | c0005 | t0001 | g0065 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03516 | hp2 | a0001 | c0007 | t0001 | g0217 | AFR | ESN | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0086 | AFR | GWD | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03579 | hp2 | a0001 | c0002 | t0001 | g0035 | AFR | MSL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03669 | hp1 | a0001 | c0003 | t0001 | g0232 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03669 | hp2 | a0002 | c0004 | t0001 | g0192 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03688 | hp1 | a0001 | c0003 | t0002 | g0257 | SAS | STU | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03688 | hp2 | a0001 | c0002 | t0001 | g0179 | SAS | STU | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03704 | hp2 | a0001 | c0003 | t0002 | g0010 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03710 | hp2 | a0002 | c0004 | t0001 | g0201 | SAS | PJL | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | BEB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03831 | hp2 | a0002 | c0004 | t0001 | g0202 | SAS | BEB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | BEB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG03927 | hp2 | a0002 | c0004 | t0001 | g0200 | SAS | BEB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | STU | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG04115 | hp2 | a0002 | c0004 | t0001 | g0208 | SAS | STU | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG04184 | hp1 | a0001 | c0008 | t0001 | g0052 | SAS | BEB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG04199 | hp2 | a0001 | c0002 | t0001 | g0042 | SAS | STU | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG04204 | hp1 | a0001 | c0002 | t0001 | g0031 | SAS | STU | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | STU | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | STU | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG04228 | hp2 | a0001 | c0003 | t0001 | g0233 | SAS | STU | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18522 | hp1 | a0001 | c0005 | t0001 | g0066 | AFR | YRI | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18522 | hp2 | a0001 | c0003 | t0001 | g0236 | AFR | YRI | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | CHB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18612 | hp2 | a0001 | c0002 | t0001 | g0029 | EAS | CHB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18906 | hp1 | a0001 | c0003 | t0001 | g0261 | AFR | YRI | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18906 | hp2 | a0001 | c0006 | t0001 | g0186 | AFR | YRI | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18939 | hp2 | a0001 | c0003 | t0002 | g0253 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18940 | hp2 | a0001 | c0003 | t0001 | g0226 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18941 | hp1 | a0001 | c0003 | t0001 | g0247 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18943 | hp1 | a0001 | c0003 | t0002 | g0250 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18946 | hp2 | a0001 | c0002 | t0001 | g0046 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18950 | hp1 | a0001 | c0003 | t0002 | g0252 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18954 | hp2 | a0001 | c0003 | t0001 | g0230 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18957 | hp2 | a0001 | c0002 | t0001 | g0026 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18959 | hp2 | a0001 | c0002 | t0001 | g0176 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18966 | hp1 | a0001 | c0009 | t0001 | g0144 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18966 | hp2 | a0002 | c0004 | t0001 | g0195 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18972 | hp1 | a0001 | c0003 | t0002 | g0256 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18972 | hp2 | a0002 | c0004 | t0001 | g0193 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0081 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18978 | hp2 | a0001 | c0003 | t0001 | g0224 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18981 | hp2 | a0001 | c0002 | t0001 | g0047 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18984 | hp2 | a0001 | c0003 | t0002 | g0254 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18987 | hp1 | a0001 | c0002 | t0001 | g0161 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18988 | hp1 | a0005 | c0024 | t0002 | g0263 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18988 | hp2 | a0001 | c0009 | t0001 | g0162 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18991 | hp1 | a0001 | c0003 | t0001 | g0243 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18993 | hp1 | a0001 | c0003 | t0001 | g0244 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA18994 | hp2 | a0001 | c0002 | t0001 | g0048 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19007 | hp1 | a0001 | c0003 | t0001 | g0246 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19012 | hp2 | a0002 | c0004 | t0001 | g0203 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19030 | hp1 | a0004 | c0025 | t0001 | g0269 | AFR | LWK | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19030 | hp2 | a0001 | c0002 | t0001 | g0082 | AFR | LWK | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19043 | hp1 | a0001 | c0002 | t0001 | g0074 | AFR | LWK | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19043 | hp2 | a0001 | c0002 | t0001 | g0057 | AFR | LWK | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19054 | hp2 | a0001 | c0003 | t0001 | g0264 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19055 | hp1 | a0003 | c0011 | t0001 | g0218 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19055 | hp2 | a0001 | c0003 | t0001 | g0265 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19057 | hp1 | a0002 | c0004 | t0001 | g0206 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19067 | hp2 | a0001 | c0002 | t0001 | g0050 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19070 | hp2 | a0001 | c0003 | t0001 | g0235 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19074 | hp2 | a0003 | c0011 | t0001 | g0219 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19083 | hp1 | a0001 | c0002 | t0001 | g0049 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19085 | hp1 | a0001 | c0003 | t0002 | g0251 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19088 | hp1 | a0002 | c0004 | t0001 | g0205 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19240 | hp1 | a0001 | c0002 | t0001 | g0072 | AFR | YRI | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA19240 | hp2 | a0001 | c0003 | t0001 | g0249 | AFR | YRI | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA20129 | hp1 | a0001 | c0002 | t0001 | g0025 | AFR | ASW | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0041 | AFR | ASW | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA20752 | hp2 | a0001 | c0002 | t0001 | g0044 | EUR | TSI | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01123 | hp1 | a0002 | c0004 | t0001 | g0191 | AMR | CLM | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | CLM | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02109 | hp2 | a0001 | c0005 | t0001 | g0220 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0159 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02559 | hp1 | a0001 | c0005 | t0001 | g0183 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG02559 | hp2 | a0001 | c0005 | t0001 | g0020 | AFR | ACB | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG06807 | hp1 | a0001 | c0006 | t0003 | g0189 | AFR | USA | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
HG06807 | hp2 | a0001 | c0006 | t0001 | g0185 | AFR | USA | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0014 | AFR | USA | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA20300 | hp2 | a0001 | c0002 | t0001 | g0051 | AFR | USA | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | LWK | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
NA21309 | hp2 | a0001 | c0003 | t0001 | g0266 | AFR | LWK | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
homoSapiens_chm13v2 | hp1 | a0001 | c0008 | t0001 | g0039 | REF | REF | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0001 | g0043 | REF | REF | EXOSC10_chr1_11061618_11104869 | EXOSC10 | chr1 | 11061618 | 11104869 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11070968
|
G | A | 1 | a0007 | 1 | HG02647.hp2 | missense_variant | MODERATE | c.2248C>T | p.Arg750Trp | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/25 | 2286/2796 | 2248/2658 | 750/885 | chr1 | 11070968 | ||
chr1:11073986
|
C | T | 3 | a0002a0003a0009 | 20 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(17): Show |
missense_variant | MODERATE | c.2105G>A | p.Arg702His | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/25 | 2143/2796 | 2105/2658 | 702/885 | chr1 | 11073986 | ||
chr1:11076883
|
T | A | 1 | a0006 | 1 | HG02083.hp2 | missense_variant | MODERATE | c.1945A>T | p.Thr649Ser | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/25 | 1983/2796 | 1945/2658 | 649/885 | chr1 | 11076883 | ||
chr1:11081138
|
C | T | 1 | a0009 | 1 | HG00558.hp1 | missense_variant | MODERATE | c.1381G>A | p.Gly461Arg | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 11/25 | 1419/2796 | 1381/2658 | 461/885 | chr1 | 11081138 | ||
chr1:11087575
|
C | G | 1 | a0008 | 1 | HG01081.hp2 | missense_variant | MODERATE | c.962G>C | p.Ser321Thr | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/25 | 1000/2796 | 962/2658 | 321/885 | chr1 | 11087575 | ||
chr1:11090633
|
G | A | 1 | a0005 | 1 | NA18988.hp1 | missense_variant | MODERATE | c.679C>T | p.Arg227Cys | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/25 | 717/2796 | 679/2658 | 227/885 | chr1 | 11090633 | ||
chr1:11098048
|
C | T | 3 | a0002a0003a0009 | 20 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(17): Show |
missense_variant | MODERATE | c.220G>A | p.Glu74Lys | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/25 | 258/2796 | 220/2658 | 74/885 | chr1 | 11098048 | ||
chr1:11098086
|
T | C | 1 | a0003 | 2 | NA19055.hp1 NA19074.hp2 |
missense_variant | MODERATE | c.182A>G | p.Asp61Gly | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/25 | 220/2796 | 182/2658 | 61/885 | chr1 | 11098086 | ||
chr1:11099803
|
C | A | 1 | a0004 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.29G>T | p.Arg10Met | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/25 | 67/2796 | 29/2658 | 10/885 | chr1 | 11099803 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11068052
|
C | T | 1 | a0001c0018 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.2583G>A | p.Ser861Ser | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/25 | 2621/2796 | 2583/2658 | 861/885 | chr1 | 11068052 | ||
chr1:11069599
|
C | T | 1 | a0001c0009 | 3 | HG00609.hp1 NA18966.hp1 NA18988.hp2 |
synonymous_variant | LOW | c.2448G>A | p.Thr816Thr | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/25 | 2486/2796 | 2448/2658 | 816/885 | chr1 | 11069599 | ||
chr1:11070918
|
G | A | 1 | a0001c0010 | 2 | HG02809.hp2 HG03486.hp2 |
synonymous_variant | LOW | c.2298C>T | p.Ser766Ser | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/25 | 2336/2796 | 2298/2658 | 766/885 | chr1 | 11070918 | ||
chr1:11072160
|
G | A | 12 | a0001c0001a0001c0007a0001c0009others(9): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
synonymous_variant | LOW | c.2169C>T | p.Arg723Arg | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/25 | 2207/2796 | 2169/2658 | 723/885 | chr1 | 11072160 | ||
chr1:11077369
|
G | C | 1 | a0001c0017 | 1 | HG02602.hp2 | synonymous_variant | LOW | c.1875C>G | p.Thr625Thr | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 16/25 | 1913/2796 | 1875/2658 | 625/885 | chr1 | 11077369 | ||
chr1:11077604
|
A | G | 5 | a0001c0003a0001c0006a0001c0022others(2): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
synonymous_variant | LOW | c.1797T>C | p.Ala599Ala | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 15/25 | 1835/2796 | 1797/2658 | 599/885 | chr1 | 11077604 | ||
chr1:11080766
|
G | A | 1 | a0001c0008 | 4 | HG01069.hp2 HG03490.hp2 HG04184.hp1 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.1584C>T | p.Tyr528Tyr | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/25 | 1622/2796 | 1584/2658 | 528/885 | chr1 | 11080766 | ||
chr1:11081130
|
C | G | 18 | a0001c0001a0001c0003a0001c0005others(15): Show | 210 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(207): Show |
synonymous_variant | LOW | c.1389G>C | p.Pro463Pro | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 11/25 | 1427/2796 | 1389/2658 | 463/885 | chr1 | 11081130 | ||
chr1:11082819
|
T | C | 1 | a0001c0020 | 1 | HG02451.hp2 | synonymous_variant | LOW | c.1149A>G | p.Val383Val | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/25 | 1187/2796 | 1149/2658 | 383/885 | chr1 | 11082819 | ||
chr1:11087466
|
T | C | 1 | a0001c0021 | 1 | HG03453.hp1 | synonymous_variant | LOW | c.1071A>G | p.Thr357Thr | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/25 | 1109/2796 | 1071/2658 | 357/885 | chr1 | 11087466 | ||
chr1:11087508
|
G | A | 1 | a0001c0007 | 5 | HG02145.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
synonymous_variant | LOW | c.1029C>T | p.Leu343Leu | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/25 | 1067/2796 | 1029/2658 | 343/885 | chr1 | 11087508 | ||
chr1:11087541
|
A | G | 1 | a0001c0006 | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
synonymous_variant | LOW | c.996T>C | p.Ser332Ser | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/25 | 1034/2796 | 996/2658 | 332/885 | chr1 | 11087541 | ||
chr1:11087884
|
T | C | 1 | a0001c0022 | 1 | HG01109.hp2 | synonymous_variant | LOW | c.861A>G | p.Pro287Pro | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 8/25 | 899/2796 | 861/2658 | 287/885 | chr1 | 11087884 | ||
chr1:11090610
|
G | A | 1 | a0001c0023 | 1 | HG00280.hp2 | synonymous_variant | LOW | c.702C>T | p.Pro234Pro | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/25 | 740/2796 | 702/2658 | 234/885 | chr1 | 11090610 | ||
chr1:11090625
|
C | T | 4 | a0001c0003a0001c0022a0001c0023others(1): Show | 50 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
synonymous_variant | LOW | c.687G>A | p.Glu229Glu | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/25 | 725/2796 | 687/2658 | 229/885 | chr1 | 11090625 | ||
chr1:11091075
|
G | T | 1 | a0001c0014 | 1 | HG02683.hp2 | synonymous_variant | LOW | c.582C>A | p.Ser194Ser | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 5/25 | 620/2796 | 582/2658 | 194/885 | chr1 | 11091075 | ||
chr1:11095869
|
T | C | 1 | a0002c0013 | 1 | HG01361.hp2 | synonymous_variant | LOW | c.261A>G | p.Val87Val | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/25 | 299/2796 | 261/2658 | 87/885 | chr1 | 11095869 | ||
chr1:11099766
|
T | C | 4 | a0001c0003a0001c0022a0001c0023others(1): Show | 50 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
synonymous_variant | LOW | c.66A>G | p.Gly22Gly | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/25 | 104/2796 | 66/2658 | 22/885 | chr1 | 11099766 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11066640
|
G | C | 3 | a0001c0003t0002a0001c0023t0002a0005c0024t0002 | 16 | HG00280.hp2 HG00438.hp1 HG01175.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*78C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 25/25 | 78 | chr1 | 11066640 | |||||
chr1:11066652
|
T | C | 1 | a0001c0002t0004 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*66A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 25/25 | 66 | chr1 | 11066652 | |||||
chr1:11099869
|
C | T | 1 | a0001c0006t0003 | 3 | HG02615.hp1 HG03209.hp1 HG06807.hp1 |
5_prime_UTR_variant | MODIFIER | c.-38G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/25 | 38 | chr1 | 11099869 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:11066756
|
G | A | 1 | a0001c0001t0001g0147 | 1 | HG00642.hp2 | splice_region_variant&intron_variant | LOW | c.2628-8C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11066756 | ||||||
chr1:11066791
|
T | C | 46 | a0001c0003t0001g0224a0001c0003t0001g0225a0001c0003t0001g0226others(43): Show | 47 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.2628-43A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11066791 | ||||||
chr1:11066884
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2628-136G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11066884 | ||||||
chr1:11067078
|
A | G | 1 | a0001c0001t0001g0013 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.2628-330T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067078 | ||||||
chr1:11067214
|
A | G | 1 | a0002c0004t0001g0193 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2628-466T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067214 | ||||||
chr1:11067222
|
G | A | 12 | a0001c0002t0001g0034a0001c0002t0001g0037a0001c0002t0001g0082others(9): Show | 12 | HG01109.hp2 HG02647.hp2 HG02723.hp2 others(9): Show |
intron_variant | MODIFIER | c.2628-474C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067222 | ||||||
chr1:11067227
|
C | T | 1 | a0002c0004t0001g0193 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2628-479G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067227 | ||||||
chr1:11067247
|
T | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0101a0001c0001t0001g0113others(4): Show | 9 | HG01516.hp2 HG01517.hp1 HG01928.hp1 others(6): Show |
intron_variant | MODIFIER | c.2628-499A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067247 | ||||||
chr1:11067258
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2628-510G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067258 | ||||||
chr1:11067267
|
TA | T | 6 | a0001c0005t0001g0019a0001c0005t0001g0020a0001c0005t0001g0021others(3): Show | 6 | HG00741.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2628-520delT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067267 | ||||||
chr1:11067293
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2628-545T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067293 | ||||||
chr1:11067301
|
G | A | 1 | a0001c0017t0001g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2628-553C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067301 | ||||||
chr1:11067365
|
C | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2628-617G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067365 | ||||||
chr1:11067388
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2627+620A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067388 | ||||||
chr1:11067438
|
G | GA | 93 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(90): Show | 104 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(101): Show |
intron_variant | MODIFIER | c.2627+569dupT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067438 | ||||||
chr1:11067438
|
G | GAA | 35 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0106others(32): Show | 36 | HG00558.hp1 HG01123.hp1 HG01175.hp2 others(33): Show |
intron_variant | MODIFIER | c.2627+568_2627+569d others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067438 | ||||||
chr1:11067438
|
GA | G | 47 | a0001c0003t0001g0224a0001c0003t0001g0225a0001c0003t0001g0226others(44): Show | 48 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.2627+569delT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067438 | ||||||
chr1:11067447
|
A | G | 3 | a0001c0005t0001g0065a0001c0005t0001g0066a0001c0005t0001g0067 | 3 | HG01891.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2627+561T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067447 | ||||||
chr1:11067452
|
AC | A | 3 | a0001c0005t0001g0065a0001c0005t0001g0066a0001c0005t0001g0067 | 3 | HG01891.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2627+555delG | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067452 | ||||||
chr1:11067454
|
A | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2627+554T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067454 | ||||||
chr1:11067533
|
G | A | 20 | a0002c0004t0001g0191a0002c0004t0001g0192a0002c0004t0001g0193others(17): Show | 20 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2627+475C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067533 | ||||||
chr1:11067579
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2627+429C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067579 | ||||||
chr1:11067603
|
A | G | 20 | a0002c0004t0001g0191a0002c0004t0001g0192a0002c0004t0001g0193others(17): Show | 20 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.2627+405T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067603 | ||||||
chr1:11067707
|
C | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2627+301G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067707 | ||||||
chr1:11067717
|
C | A | 8 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0175others(5): Show | 8 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2627+291G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067717 | ||||||
chr1:11067807
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.2627+201C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067807 | ||||||
chr1:11067814
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2627+194T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067814 | ||||||
chr1:11067909
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.2627+99G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067909 | ||||||
chr1:11067917
|
T | C | 3 | a0001c0005t0001g0065a0001c0005t0001g0066a0001c0005t0001g0067 | 3 | HG01891.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2627+91A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067917 | ||||||
chr1:11067944
|
A | G | 131 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(128): Show | 143 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(140): Show |
intron_variant | MODIFIER | c.2627+64T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067944 | ||||||
chr1:11067951
|
G | A | 1 | a0001c0002t0001g0087 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2627+57C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067951 | ||||||
chr1:11067957
|
C | A | 1 | a0001c0002t0001g0042 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.2627+51G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 24/24 | chr1 | 11067957 | ||||||
chr1:11068272
|
A | G | 178 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(175): Show | 191 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.2551-188T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 23/24 | chr1 | 11068272 | ||||||
chr1:11068277
|
A | C | 6 | a0001c0002t0001g0083a0001c0002t0001g0085a0001c0002t0001g0086others(3): Show | 6 | HG02647.hp2 HG02723.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2551-193T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 23/24 | chr1 | 11068277 | ||||||
chr1:11068296
|
G | A | 3 | a0001c0003t0002g0252a0001c0003t0002g0253a0001c0003t0002g0256 | 3 | NA18939.hp2 NA18950.hp1 NA18972.hp1 |
intron_variant | MODIFIER | c.2551-212C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 23/24 | chr1 | 11068296 | ||||||
chr1:11068527
|
G | C | 6 | a0001c0005t0001g0019a0001c0005t0001g0020a0001c0005t0001g0021others(3): Show | 6 | HG00741.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.2550+118C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 23/24 | chr1 | 11068527 | ||||||
chr1:11068597
|
G | A | 125 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(122): Show | 137 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.2550+48C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 23/24 | chr1 | 11068597 | ||||||
chr1:11068794
|
C | T | 1 | a0001c0003t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2489-88G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11068794 | ||||||
chr1:11068998
|
G | C | 1 | a0001c0022t0001g0268 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.2489-292C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11068998 | ||||||
chr1:11069006
|
T | C | 1 | a0001c0001t0001g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2489-300A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069006 | ||||||
chr1:11069157
|
G | A | 33 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0106others(30): Show | 34 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.2488+402C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069157 | ||||||
chr1:11069202
|
T | G | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(92): Show | 106 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.2488+357A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069202 | ||||||
chr1:11069227
|
C | CTG | 4 | a0001c0003t0001g0234a0001c0003t0001g0236a0001c0003t0001g0249others(1): Show | 4 | HG03098.hp1 NA18522.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.2488+330_2488+331d others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069227 | ||||||
chr1:11069236
|
T | C | 2 | a0001c0005t0001g0183a0001c0005t0001g0184 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.2488+323A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069236 | ||||||
chr1:11069244
|
T | TGTGTGTG others(19): Show |
7 | a0001c0001t0001g0015a0001c0001t0001g0098a0001c0001t0001g0101others(4): Show | 7 | HG01516.hp2 HG01517.hp1 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.2488+314_2488+315i others(28): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(21): Show |
7 | a0001c0001t0001g0112a0001c0001t0001g0114a0001c0001t0001g0126others(4): Show | 7 | HG00609.hp1 HG02056.hp2 HG04228.hp1 others(4): Show |
intron_variant | MODIFIER | c.2488+314_2488+315i others(30): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(23): Show |
39 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(36): Show | 49 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(46): Show |
intron_variant | MODIFIER | c.2488+314_2488+315i others(32): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(25): Show |
2 | a0001c0001t0001g0124a0001c0001t0001g0138 | 2 | NA19054.hp1 NA19067.hp1 |
intron_variant | MODIFIER | c.2488+314_2488+315i others(34): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(27): Show |
1 | a0001c0001t0001g0164 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2488+314_2488+315i others(36): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(29): Show |
3 | a0001c0001t0001g0033a0001c0001t0001g0117a0006c0016t0001g0141 | 3 | HG01928.hp2 HG02083.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.2488+314_2488+315i others(38): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(21): Show |
1 | a0001c0001t0001g0123 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2488+314_2488+315i others(30): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(23): Show |
12 | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0001g0018others(9): Show | 12 | HG00741.hp1 HG01515.hp1 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.2488+314_2488+315i others(32): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(25): Show |
9 | a0001c0001t0001g0030a0001c0001t0001g0115a0001c0001t0001g0132others(6): Show | 9 | HG00673.hp2 HG01081.hp1 HG01975.hp1 others(6): Show |
intron_variant | MODIFIER | c.2488+314_2488+315i others(34): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(27): Show |
1 | a0001c0001t0001g0128 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.2488+314_2488+315i others(36): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(29): Show |
1 | a0001c0001t0001g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2488+314_2488+315i others(38): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(19): Show |
1 | a0001c0017t0001g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2488+314_2488+315i others(28): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(25): Show |
9 | a0002c0004t0001g0192a0002c0004t0001g0193a0002c0004t0001g0195others(6): Show | 9 | HG02074.hp2 HG03669.hp2 HG03710.hp2 others(6): Show |
intron_variant | MODIFIER | c.2488+314_2488+315i others(34): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(27): Show |
1 | a0001c0001t0001g0007 | 2 | HG01952.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.2488+314_2488+315i others(36): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(23): Show |
1 | a0001c0001t0001g0129 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2488+314_2488+315i others(32): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(25): Show |
1 | a0001c0001t0001g0096 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.2488+314_2488+315i others(34): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(27): Show |
18 | a0001c0001t0001g0102a0001c0001t0001g0107a0001c0001t0001g0130others(15): Show | 18 | HG00558.hp1 HG01069.hp1 HG01074.hp2 others(15): Show |
intron_variant | MODIFIER | c.2488+314_2488+315i others(36): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(27): Show |
1 | a0001c0001t0001g0009 | 2 | HG02886.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.2488+314_2488+315i others(36): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(29): Show |
3 | a0001c0001t0001g0108a0001c0001t0001g0170a0001c0007t0001g0216 | 3 | HG01106.hp1 HG01106.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.2488+314_2488+315i others(38): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(33): Show |
4 | a0001c0007t0001g0213a0001c0007t0001g0214a0001c0007t0001g0215others(1): Show | 4 | HG02145.hp2 HG02922.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.2488+314_2488+315i others(42): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(27): Show |
1 | a0001c0021t0001g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2488+314_2488+315i others(36): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(29): Show |
1 | a0001c0001t0001g0211 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2488+314_2488+315i others(38): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(31): Show |
1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2488+314_2488+315i others(40): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(31): Show |
2 | a0001c0001t0001g0175a0001c0001t0001g0212 | 2 | HG01891.hp2 HG02451.hp1 |
intron_variant | MODIFIER | c.2488+314_2488+315i others(40): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(33): Show |
1 | a0001c0001t0001g0105 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.2488+314_2488+315i others(42): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(35): Show |
1 | a0001c0001t0001g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2488+314_2488+315i others(44): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069244
|
T | TGTGTGTG others(35): Show |
1 | a0001c0001t0001g0106 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2488+314_2488+315i others(44): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069244 | ||||||
chr1:11069260
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2488+299C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069260 | ||||||
chr1:11069368
|
T | C | 3 | a0001c0001t0001g0125a0001c0001t0001g0128a0001c0001t0001g0150 | 3 | NA18946.hp1 NA19070.hp1 NA19074.hp1 |
intron_variant | MODIFIER | c.2488+191A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069368 | ||||||
chr1:11069377
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2488+182A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069377 | ||||||
chr1:11069380
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2488+179A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069380 | ||||||
chr1:11069431
|
C | A | 1 | a0001c0005t0001g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2488+128G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069431 | ||||||
chr1:11069459
|
T | G | 1 | a0001c0001t0001g0143 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.2488+100A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 22/24 | chr1 | 11069459 | ||||||
chr1:11069791
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(181): Show | 197 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.2317-61T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11069791 | ||||||
chr1:11069981
|
A | T | 1 | a0001c0007t0001g0213 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.2317-251T>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11069981 | ||||||
chr1:11070059
|
C | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2317-329G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070059 | ||||||
chr1:11070070
|
A | C | 1 | a0001c0006t0001g0185 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.2317-340T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070070 | ||||||
chr1:11070265
|
T | TA | 49 | a0001c0001t0001g0105a0001c0001t0001g0128a0001c0001t0001g0129others(46): Show | 50 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.2317-536dupT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070265 | ||||||
chr1:11070265
|
T | TAA | 114 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(111): Show | 126 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(123): Show |
intron_variant | MODIFIER | c.2317-537_2317-536d others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070265 | ||||||
chr1:11070265
|
T | TAAA | 8 | a0001c0001t0001g0099a0001c0001t0001g0117a0001c0001t0001g0119others(5): Show | 8 | HG01928.hp2 HG02300.hp1 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.2317-538_2317-536d others(5): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070265 | ||||||
chr1:11070265
|
TA | T | 12 | a0001c0002t0001g0026a0001c0002t0001g0046a0001c0002t0001g0053others(9): Show | 12 | HG01069.hp2 HG01167.hp2 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.2317-536delT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070265 | ||||||
chr1:11070361
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2316+539T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070361 | ||||||
chr1:11070521
|
C | CA | 28 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0025others(25): Show | 29 | HG00438.hp1 HG01109.hp2 HG01167.hp2 others(26): Show |
intron_variant | MODIFIER | c.2316+378dupT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070521 | ||||||
chr1:11070521
|
CA | C | 10 | a0001c0002t0001g0028a0001c0002t0001g0057a0001c0002t0001g0176others(7): Show | 10 | HG01496.hp1 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.2316+378delT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070521 | ||||||
chr1:11070521
|
CAAAAA | C | 90 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(87): Show | 101 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(98): Show |
intron_variant | MODIFIER | c.2316+374_2316+378d others(7): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070521 | ||||||
chr1:11070521
|
CAAAAAA | C | 35 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0106others(32): Show | 36 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.2316+373_2316+378d others(8): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070521 | ||||||
chr1:11070586
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2316+314T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070586 | ||||||
chr1:11070893
|
C | T | 1 | a0001c0002t0001g0087 | 1 | HG03453.hp2 | splice_region_variant&intron_variant | LOW | c.2316+7G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 21/24 | chr1 | 11070893 | ||||||
chr1:11071046
|
C | T | 3 | a0001c0006t0003g0187a0001c0006t0003g0188a0001c0006t0003g0189 | 3 | HG02615.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2243-73G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071046 | ||||||
chr1:11071175
|
C | G | 1 | a0001c0001t0001g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2243-202G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071175 | ||||||
chr1:11071235
|
C | T | 4 | a0001c0002t0001g0003a0001c0002t0001g0040a0001c0002t0001g0041others(1): Show | 5 | HG00735.hp2 HG01192.hp2 HG02083.hp1 others(2): Show |
intron_variant | MODIFIER | c.2243-262G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071235 | ||||||
chr1:11071243
|
C | T | 1 | a0001c0006t0001g0186 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.2243-270G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071243 | ||||||
chr1:11071338
|
G | C | 1 | a0001c0001t0001g0133 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.2243-365C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071338 | ||||||
chr1:11071376
|
T | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2243-403A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071376 | ||||||
chr1:11071610
|
C | CCT | 110 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(107): Show | 122 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(119): Show |
intron_variant | MODIFIER | c.2242+476_2242+477i others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071610 | ||||||
chr1:11071627
|
C | T | 2 | a0001c0003t0001g0246a0001c0003t0001g0265 | 2 | NA19007.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2242+460G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071627 | ||||||
chr1:11071712
|
G | GC | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2242+374dupG | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071712 | ||||||
chr1:11071819
|
T | C | 8 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0175others(5): Show | 8 | HG02145.hp2 HG02280.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.2242+268A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071819 | ||||||
chr1:11071828
|
C | T | 1 | a0001c0003t0001g0225 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2242+259G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071828 | ||||||
chr1:11071837
|
C | T | 1 | a0001c0002t0001g0088 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2242+250G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071837 | ||||||
chr1:11071866
|
CCAA | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(93): Show | 107 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.2242+218_2242+220d others(5): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071866 | ||||||
chr1:11071877
|
G | A | 23 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0059others(20): Show | 24 | HG01167.hp2 HG01243.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.2242+210C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071877 | ||||||
chr1:11071883
|
G | A | 1 | a0001c0005t0001g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2242+204C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071883 | ||||||
chr1:11071988
|
G | A | 2 | a0001c0005t0001g0021a0001c0005t0001g0022 | 2 | HG02572.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.2242+99C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11071988 | ||||||
chr1:11072002
|
G | C | 1 | a0002c0004t0001g0198 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.2242+85C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11072002 | ||||||
chr1:11072005
|
G | A | 1 | a0001c0005t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.2242+82C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11072005 | ||||||
chr1:11072007
|
A | G | 3 | a0001c0002t0001g0047a0001c0002t0001g0048a0001c0002t0001g0049 | 3 | NA18981.hp2 NA18994.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2242+80T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11072007 | ||||||
chr1:11072032
|
G | C | 1 | a0001c0017t0001g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.2242+55C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 20/24 | chr1 | 11072032 | ||||||
chr1:11072249
|
C | T | 4 | a0001c0001t0001g0016a0001c0006t0003g0187a0001c0006t0003g0188others(1): Show | 4 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2158-78G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11072249 | ||||||
chr1:11072351
|
C | T | 2 | a0001c0002t0001g0034a0001c0002t0001g0037 | 2 | HG02965.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.2158-180G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11072351 | ||||||
chr1:11072368
|
G | A | 1 | a0001c0005t0001g0066 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2158-197C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11072368 | ||||||
chr1:11072463
|
G | A | 1 | a0001c0001t0001g0157 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.2158-292C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11072463 | ||||||
chr1:11072477
|
C | A | 1 | a0004c0025t0001g0269 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.2158-306G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11072477 | ||||||
chr1:11072484
|
G | C | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2158-313C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11072484 | ||||||
chr1:11072504
|
A | G | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2158-333T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11072504 | ||||||
chr1:11072581
|
G | A | 1 | a0001c0003t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2158-410C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11072581 | ||||||
chr1:11072581
|
G | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2158-410C>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11072581 | ||||||
chr1:11072744
|
G | A | 130 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(127): Show | 142 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(139): Show |
intron_variant | MODIFIER | c.2158-573C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11072744 | ||||||
chr1:11072830
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.2158-659G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11072830 | ||||||
chr1:11072908
|
G | C | 96 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(93): Show | 107 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(104): Show |
intron_variant | MODIFIER | c.2158-737C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11072908 | ||||||
chr1:11073172
|
G | A | 2 | a0001c0002t0001g0047a0001c0002t0001g0049 | 2 | NA18981.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.2157+762C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073172 | ||||||
chr1:11073183
|
A | G | 15 | a0001c0003t0002g0010a0001c0003t0002g0221a0001c0003t0002g0222others(12): Show | 16 | HG00280.hp2 HG00438.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.2157+751T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073183 | ||||||
chr1:11073185
|
C | T | 133 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(130): Show | 145 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(142): Show |
intron_variant | MODIFIER | c.2157+749G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073185 | ||||||
chr1:11073236
|
G | A | 33 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0106others(30): Show | 34 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(31): Show |
intron_variant | MODIFIER | c.2157+698C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073236 | ||||||
chr1:11073383
|
C | T | 15 | a0001c0003t0002g0010a0001c0003t0002g0221a0001c0003t0002g0222others(12): Show | 16 | HG00280.hp2 HG00438.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.2157+551G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073383 | ||||||
chr1:11073616
|
G | A | 3 | a0001c0001t0001g0009a0001c0001t0001g0211a0001c0001t0001g0212 | 4 | HG01891.hp2 HG02109.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2157+318C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073616 | ||||||
chr1:11073630
|
C | T | 24 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(21): Show | 25 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.2157+304G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073630 | ||||||
chr1:11073758
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0175 | 3 | HG02280.hp1 HG02451.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.2157+176C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073758 | ||||||
chr1:11073850
|
C | T | 1 | a0001c0002t0001g0061 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2157+84G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073850 | ||||||
chr1:11073877
|
C | CA | 21 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0037others(18): Show | 21 | HG01109.hp2 HG01243.hp2 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.2157+56dupT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073877 | ||||||
chr1:11073877
|
C | CAA | 40 | a0001c0002t0001g0011a0001c0002t0001g0036a0001c0003t0001g0225others(37): Show | 41 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.2157+55_2157+56dup others(2): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073877 | ||||||
chr1:11073899
|
A | AAAAG | 39 | a0001c0001t0001g0009a0001c0001t0001g0099a0001c0001t0001g0106others(36): Show | 40 | HG00558.hp1 HG01123.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.2157+34_2157+35ins others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073899 | ||||||
chr1:11073899
|
A | AAAG | 83 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(80): Show | 94 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.2157+34_2157+35ins others(3): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073899 | ||||||
chr1:11073899
|
A | AAG | 6 | a0001c0001t0001g0017a0001c0001t0001g0098a0001c0001t0001g0111others(3): Show | 6 | HG01515.hp1 HG02735.hp2 NA18940.hp1 others(3): Show |
intron_variant | MODIFIER | c.2157+33_2157+34dup others(2): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073899 | ||||||
chr1:11073927
|
C | T | 1 | a0001c0002t0001g0028 | 1 | HG01496.hp1 | splice_region_variant&intron_variant | LOW | c.2157+7G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 19/24 | chr1 | 11073927 | ||||||
chr1:11074046
|
A | C | 1 | a0001c0009t0001g0162 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.2083-38T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 18/24 | chr1 | 11074046 | ||||||
chr1:11074100
|
T | G | 194 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(191): Show | 207 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(204): Show |
intron_variant | MODIFIER | c.2083-92A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 18/24 | chr1 | 11074100 | ||||||
chr1:11074108
|
G | A | 2 | a0001c0002t0001g0082a0001c0002t0001g0088 | 2 | HG03225.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2083-100C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 18/24 | chr1 | 11074108 | ||||||
chr1:11074139
|
A | T | 24 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(21): Show | 25 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.2082+92T>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 18/24 | chr1 | 11074139 | ||||||
chr1:11074228
|
C | T | 3 | a0001c0005t0001g0065a0001c0005t0001g0066a0001c0005t0001g0067 | 3 | HG01891.hp1 HG03516.hp1 NA18522.hp1 |
splice_region_variant&intron_variant | LOW | c.2082+3G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 18/24 | chr1 | 11074228 | ||||||
chr1:11074355
|
A | G | 1 | a0001c0021t0001g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1987-29T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11074355 | ||||||
chr1:11074413
|
A | ATT | 45 | a0001c0003t0001g0224a0001c0003t0001g0225a0001c0003t0001g0227others(42): Show | 46 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(43): Show |
intron_variant | MODIFIER | c.1987-89_1987-88dup others(2): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11074413 | ||||||
chr1:11074437
|
G | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1987-111C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11074437 | ||||||
chr1:11074537
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1987-211A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11074537 | ||||||
chr1:11074571
|
C | A | 1 | a0002c0004t0001g0200 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1987-245G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11074571 | ||||||
chr1:11074613
|
A | G | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1987-287T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11074613 | ||||||
chr1:11074649
|
G | A | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1987-323C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11074649 | ||||||
chr1:11074692
|
T | C | 50 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(47): Show | 51 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.1987-366A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11074692 | ||||||
chr1:11074699
|
C | T | 2 | a0001c0005t0001g0183a0001c0005t0001g0184 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1987-373G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11074699 | ||||||
chr1:11074702
|
C | T | 1 | a0001c0006t0001g0186 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1987-376G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11074702 | ||||||
chr1:11074781
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1987-455A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11074781 | ||||||
chr1:11074885
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1987-559A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11074885 | ||||||
chr1:11075173
|
C | T | 1 | a0001c0009t0001g0144 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1987-847G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075173 | ||||||
chr1:11075193
|
C | T | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1987-867G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075193 | ||||||
chr1:11075617
|
A | G | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1986+1225T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075617 | ||||||
chr1:11075777
|
C | T | 1 | a0001c0003t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1986+1065G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075777 | ||||||
chr1:11075818
|
C | T | 1 | a0001c0001t0001g0119 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.1986+1024G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075818 | ||||||
chr1:11075853
|
C | CA | 87 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(84): Show | 98 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.1986+988dupT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075853 | ||||||
chr1:11075853
|
C | CAA | 64 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0015others(61): Show | 65 | HG00438.hp2 HG00642.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.1986+987_1986+988d others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075853 | ||||||
chr1:11075853
|
C | CAAA | 17 | a0001c0001t0001g0096a0001c0001t0001g0098a0001c0001t0001g0140others(14): Show | 18 | HG01192.hp1 HG01928.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1986+986_1986+988d others(5): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075853 | ||||||
chr1:11075853
|
CAAA | C | 21 | a0001c0003t0001g0224a0001c0003t0001g0226a0001c0003t0001g0228others(18): Show | 21 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(18): Show |
intron_variant | MODIFIER | c.1986+986_1986+988d others(5): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075853 | ||||||
chr1:11075853
|
CAAAA | C | 26 | a0001c0003t0001g0225a0001c0003t0001g0227a0001c0003t0001g0230others(23): Show | 27 | HG01099.hp1 HG01257.hp1 HG01258.hp2 others(24): Show |
intron_variant | MODIFIER | c.1986+985_1986+988d others(6): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075853 | ||||||
chr1:11075853
|
CAAAAAAA | C | 6 | a0001c0003t0001g0223a0001c0003t0001g0266a0001c0006t0001g0186others(3): Show | 6 | HG01109.hp2 HG02615.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.1986+982_1986+988d others(9): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075853 | ||||||
chr1:11075853
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0164 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.1986+979_1986+988d others(12): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075853 | ||||||
chr1:11075861
|
A | C | 1 | a0001c0006t0001g0186 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1986+981T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11075861 | ||||||
chr1:11076037
|
C | T | 49 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(46): Show | 50 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1986+805G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11076037 | ||||||
chr1:11076038
|
G | A | 1 | a0001c0001t0001g0152 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1986+804C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11076038 | ||||||
chr1:11076149
|
G | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1986+693C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11076149 | ||||||
chr1:11076209
|
A | G | 88 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0106others(85): Show | 90 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(87): Show |
intron_variant | MODIFIER | c.1986+633T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11076209 | ||||||
chr1:11076345
|
C | CA | 25 | a0001c0001t0001g0099a0001c0001t0001g0171a0001c0002t0001g0038others(22): Show | 25 | HG00558.hp1 HG00558.hp2 HG01123.hp1 others(22): Show |
intron_variant | MODIFIER | c.1986+496dupT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11076345 | ||||||
chr1:11076455
|
A | G | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1986+387T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11076455 | ||||||
chr1:11076489
|
C | T | 3 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0159 | 3 | HG01515.hp1 HG01517.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1986+353G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11076489 | ||||||
chr1:11076490
|
G | A | 3 | a0001c0006t0003g0187a0001c0006t0003g0188a0001c0006t0003g0189 | 3 | HG02615.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1986+352C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11076490 | ||||||
chr1:11076511
|
C | T | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1986+331G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11076511 | ||||||
chr1:11076665
|
CAG | C | 23 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0059others(20): Show | 24 | HG01167.hp2 HG01243.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1986+175_1986+176d others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11076665 | ||||||
chr1:11076758
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1986+84A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11076758 | ||||||
chr1:11076781
|
A | G | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1986+61T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 17/24 | chr1 | 11076781 | ||||||
chr1:11077080
|
C | G | 1 | a0001c0001t0001g0120 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1880-132G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 16/24 | chr1 | 11077080 | ||||||
chr1:11077136
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1880-188A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 16/24 | chr1 | 11077136 | ||||||
chr1:11077237
|
C | T | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1879+128G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 16/24 | chr1 | 11077237 | ||||||
chr1:11077562
|
T | G | 1 | a0001c0017t0001g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1800+39A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 15/24 | chr1 | 11077562 | ||||||
chr1:11077572
|
T | C | 37 | a0001c0001t0001g0009a0001c0001t0001g0105a0001c0001t0001g0106others(34): Show | 38 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(35): Show |
intron_variant | MODIFIER | c.1800+29A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 15/24 | chr1 | 11077572 | ||||||
chr1:11077721
|
C | T | 95 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(92): Show | 106 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(103): Show |
intron_variant | MODIFIER | c.1750-70G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11077721 | ||||||
chr1:11078019
|
T | C | 6 | a0001c0002t0001g0053a0001c0002t0001g0055a0001c0002t0001g0056others(3): Show | 6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1750-368A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078019 | ||||||
chr1:11078065
|
G | A | 1 | a0001c0010t0001g0063 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1750-414C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078065 | ||||||
chr1:11078141
|
G | A | 1 | a0001c0021t0001g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1750-490C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078141 | ||||||
chr1:11078144
|
G | A | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1750-493C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078144 | ||||||
chr1:11078264
|
C | CTTTTTTT others(5): Show |
4 | a0001c0006t0001g0185a0001c0006t0003g0187a0001c0006t0003g0188others(1): Show | 4 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1750-614_1750-613i others(14): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078264 | ||||||
chr1:11078264
|
C | CTTTTTTT others(6): Show |
1 | a0001c0006t0001g0186 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1750-614_1750-613i others(15): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078264 | ||||||
chr1:11078264
|
C | CTTTTTTT others(10): Show |
1 | a0001c0003t0001g0260 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1750-614_1750-613i others(19): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078264 | ||||||
chr1:11078264
|
C | CTTTTTTT others(11): Show |
24 | a0001c0003t0001g0224a0001c0003t0001g0225a0001c0003t0001g0227others(21): Show | 25 | HG00280.hp2 HG00609.hp2 HG02004.hp1 others(22): Show |
intron_variant | MODIFIER | c.1750-614_1750-613i others(20): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078264 | ||||||
chr1:11078264
|
C | CTTTTTTT others(12): Show |
18 | a0001c0003t0001g0226a0001c0003t0001g0232a0001c0003t0001g0234others(15): Show | 18 | HG00438.hp1 HG00673.hp1 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.1750-614_1750-613i others(21): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078264 | ||||||
chr1:11078264
|
C | CTTTTTTT others(13): Show |
2 | a0001c0003t0001g0239a0001c0003t0002g0221 | 2 | HG01978.hp2 HG02135.hp1 |
intron_variant | MODIFIER | c.1750-614_1750-613i others(22): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078264 | ||||||
chr1:11078289
|
G | A | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1750-638C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078289 | ||||||
chr1:11078347
|
T | A | 6 | a0001c0005t0001g0019a0001c0005t0001g0020a0001c0005t0001g0021others(3): Show | 6 | HG00741.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1750-696A>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078347 | ||||||
chr1:11078359
|
G | A | 2 | a0001c0006t0001g0185a0001c0006t0001g0186 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1750-708C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078359 | ||||||
chr1:11078403
|
G | A | 1 | a0001c0002t0001g0160 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1750-752C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078403 | ||||||
chr1:11078412
|
T | G | 98 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(95): Show | 109 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.1750-761A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078412 | ||||||
chr1:11078418
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1750-767A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078418 | ||||||
chr1:11078500
|
G | A | 2 | a0001c0006t0001g0185a0001c0006t0001g0186 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1750-849C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078500 | ||||||
chr1:11078504
|
G | A | 6 | a0001c0002t0001g0053a0001c0002t0001g0055a0001c0002t0001g0056others(3): Show | 6 | HG01243.hp2 HG02257.hp2 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.1750-853C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078504 | ||||||
chr1:11078547
|
G | A | 2 | a0001c0001t0001g0142a0001c0001t0001g0151 | 2 | NA18974.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1750-896C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078547 | ||||||
chr1:11078556
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1750-905A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078556 | ||||||
chr1:11078584
|
C | A | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1750-933G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11078584 | ||||||
chr1:11079217
|
G | A | 1 | a0001c0002t0001g0161 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.1749+494C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11079217 | ||||||
chr1:11079396
|
C | CT | 54 | a0001c0001t0001g0119a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(52): Show |
intron_variant | MODIFIER | c.1749+314dupA | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11079396 | ||||||
chr1:11079447
|
G | A | 1 | a0004c0025t0001g0269 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1749+264C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11079447 | ||||||
chr1:11079486
|
C | T | 1 | a0002c0004t0001g0202 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1749+225G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11079486 | ||||||
chr1:11079538
|
C | T | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1749+173G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11079538 | ||||||
chr1:11079550
|
G | C | 1 | a0001c0005t0001g0183 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1749+161C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11079550 | ||||||
chr1:11079674
|
G | A | 47 | a0001c0003t0001g0224a0001c0003t0001g0225a0001c0003t0001g0226others(44): Show | 48 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1749+37C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11079674 | ||||||
chr1:11079694
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1749+17C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 14/24 | chr1 | 11079694 | ||||||
chr1:11080074
|
T | C | 55 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(52): Show | 56 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1638-252A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 13/24 | chr1 | 11080074 | ||||||
chr1:11080386
|
G | A | 6 | a0001c0002t0001g0070a0001c0002t0001g0071a0001c0002t0001g0076others(3): Show | 6 | HG01167.hp2 HG02280.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1637+113C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 13/24 | chr1 | 11080386 | ||||||
chr1:11080431
|
A | G | 2 | a0001c0001t0001g0101a0001c0001t0001g0118 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.1637+68T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 13/24 | chr1 | 11080431 | ||||||
chr1:11080553
|
GAA | G | 19 | a0001c0002t0001g0025a0001c0002t0001g0083a0001c0002t0001g0085others(16): Show | 19 | HG00558.hp1 HG01123.hp1 HG01496.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.1587-6_1587-5delTT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080553 | ||||||
chr1:11080559
|
AAAAAACA others(7): Show |
A | 2 | a0001c0003t0002g0258a0001c0003t0002g0259 | 2 | HG01175.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1587-24_1587-11del others(14): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080559 | ||||||
chr1:11080561
|
A | C | 12 | a0001c0001t0001g0009a0001c0001t0001g0211a0001c0001t0001g0212others(9): Show | 13 | HG01361.hp2 HG01891.hp2 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.1587-12T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080561 | ||||||
chr1:11080561
|
AAAACACA others(3): Show |
A | 1 | a0001c0003t0002g0255 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1587-22_1587-13del others(10): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080561 | ||||||
chr1:11080561
|
AAAACACA others(5): Show |
A | 10 | a0001c0003t0001g0225a0001c0003t0001g0232a0001c0003t0001g0233others(7): Show | 10 | HG01099.hp1 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1587-24_1587-13del others(12): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080561 | ||||||
chr1:11080561
|
AAAACACA others(7): Show |
A | 34 | a0001c0003t0001g0224a0001c0003t0001g0226a0001c0003t0001g0227others(31): Show | 35 | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(32): Show |
intron_variant | MODIFIER | c.1587-26_1587-13del others(14): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080561 | ||||||
chr1:11080563
|
A | AAC | 6 | a0001c0002t0001g0034a0001c0002t0001g0042a0001c0002t0001g0072others(3): Show | 6 | HG00323.hp1 HG02965.hp1 HG03490.hp2 others(3): Show |
intron_variant | MODIFIER | c.1587-16_1587-15dup others(2): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080563 | ||||||
chr1:11080563
|
A | AACACACA others(3): Show |
1 | a0001c0005t0001g0065 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1587-24_1587-15dup others(10): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080563 | ||||||
chr1:11080563
|
A | C | 32 | a0001c0001t0001g0009a0001c0001t0001g0110a0001c0001t0001g0211others(29): Show | 33 | HG00558.hp1 HG00642.hp1 HG01123.hp1 others(30): Show |
intron_variant | MODIFIER | c.1587-14T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080563 | ||||||
chr1:11080563
|
AAC | A | 28 | a0001c0001t0001g0002a0001c0001t0001g0013a0001c0001t0001g0015others(25): Show | 30 | HG01516.hp2 HG01517.hp1 HG01943.hp1 others(27): Show |
intron_variant | MODIFIER | c.1587-16_1587-15del others(2): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080563 | ||||||
chr1:11080563
|
AACAC | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(58): Show | 70 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(67): Show |
intron_variant | MODIFIER | c.1587-18_1587-15del others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080563 | ||||||
chr1:11080563
|
AACACAC | A | 8 | a0001c0001t0001g0143a0001c0001t0001g0148a0001c0001t0001g0149others(5): Show | 8 | HG01074.hp1 HG01243.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1587-20_1587-15del others(6): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080563 | ||||||
chr1:11080564
|
ACAC | A | 5 | a0001c0001t0001g0100a0001c0001t0001g0105a0001c0001t0001g0116others(2): Show | 5 | HG01175.hp2 HG01928.hp2 HG02698.hp1 others(2): Show |
intron_variant | MODIFIER | c.1587-18_1587-16del others(3): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080564 | ||||||
chr1:11080564
|
ACACACAC | A | 3 | a0001c0007t0001g0213a0001c0007t0001g0215a0001c0007t0001g0216 | 3 | HG02145.hp2 HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1587-22_1587-16del others(7): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080564 | ||||||
chr1:11080565
|
C | A | 19 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0059others(16): Show | 20 | HG00741.hp2 HG01243.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.1587-16G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080565 | ||||||
chr1:11080567
|
C | A | 23 | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0030others(20): Show | 23 | HG01516.hp2 HG01517.hp1 HG02056.hp1 others(20): Show |
intron_variant | MODIFIER | c.1587-18G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080567 | ||||||
chr1:11080569
|
C | A | 60 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(57): Show | 69 | HG00280.hp1 HG00323.hp2 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.1587-20G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080569 | ||||||
chr1:11080571
|
C | A | 7 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0143others(4): Show | 7 | HG01074.hp1 HG01175.hp2 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.1587-22G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080571 | ||||||
chr1:11080573
|
C | A | 2 | a0001c0009t0001g0144a0001c0009t0001g0145 | 2 | HG00609.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.1587-24G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080573 | ||||||
chr1:11080592
|
ACACACAC others(7): Show |
A | 1 | a0001c0003t0002g0254 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.1587-57_1587-44del others(14): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080592 | ||||||
chr1:11080594
|
ACACACAC others(5): Show |
A | 1 | a0001c0006t0001g0186 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1587-57_1587-46del others(12): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080594 | ||||||
chr1:11080596
|
ACACACAC others(3): Show |
A | 1 | a0001c0006t0001g0185 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1587-57_1587-48del others(10): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080596 | ||||||
chr1:11080606
|
G | A | 51 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(48): Show | 52 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(49): Show |
intron_variant | MODIFIER | c.1587-57C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 12/24 | chr1 | 11080606 | ||||||
chr1:11080973
|
G | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1438-61C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 11/24 | chr1 | 11080973 | ||||||
chr1:11081045
|
A | G | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1437+37T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 11/24 | chr1 | 11081045 | ||||||
chr1:11081349
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1281-111A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11081349 | ||||||
chr1:11081376
|
A | G | 1 | a0004c0025t0001g0269 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1281-138T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11081376 | ||||||
chr1:11081697
|
G | A | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1281-459C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11081697 | ||||||
chr1:11081814
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1281-576C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11081814 | ||||||
chr1:11081853
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1281-615G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11081853 | ||||||
chr1:11081869
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1281-631C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11081869 | ||||||
chr1:11081942
|
C | T | 6 | a0001c0007t0001g0213a0001c0007t0001g0214a0001c0007t0001g0215others(3): Show | 6 | HG02145.hp2 HG02922.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1281-704G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11081942 | ||||||
chr1:11081943
|
G | A | 6 | a0001c0005t0001g0019a0001c0005t0001g0020a0001c0005t0001g0021others(3): Show | 6 | HG00741.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.1281-705C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11081943 | ||||||
chr1:11082007
|
G | A | 1 | a0001c0001t0001g0212 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1280+681C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082007 | ||||||
chr1:11082024
|
G | A | 2 | a0001c0006t0001g0185a0001c0006t0001g0186 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1280+664C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082024 | ||||||
chr1:11082063
|
C | G | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280+625G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082063 | ||||||
chr1:11082079
|
C | CA | 50 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(47): Show | 51 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.1280+608dupT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082079 | ||||||
chr1:11082134
|
A | T | 1 | a0001c0001t0001g0006 | 2 | NA18993.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.1280+554T>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082134 | ||||||
chr1:11082262
|
C | T | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280+426G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082262 | ||||||
chr1:11082319
|
G | A | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280+369C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082319 | ||||||
chr1:11082326
|
T | TAC | 3 | a0001c0006t0003g0187a0001c0006t0003g0188a0001c0006t0003g0189 | 3 | HG02615.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1280+361_1280+362i others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082326 | ||||||
chr1:11082327
|
G | A | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1280+361C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082327 | ||||||
chr1:11082327
|
G | GCA | 14 | a0001c0001t0001g0152a0001c0002t0001g0026a0001c0002t0001g0029others(11): Show | 15 | HG02735.hp1 HG02738.hp1 HG03704.hp2 others(12): Show |
intron_variant | MODIFIER | c.1280+359_1280+360d others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082327 | ||||||
chr1:11082327
|
G | GCACA | 20 | a0002c0004t0001g0191a0002c0004t0001g0192a0002c0004t0001g0193others(17): Show | 20 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1280+357_1280+360d others(6): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082327 | ||||||
chr1:11082336
|
C | T | 1 | a0001c0002t0001g0041 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1280+352G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082336 | ||||||
chr1:11082410
|
A | G | 1 | a0001c0003t0002g0255 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1280+278T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082410 | ||||||
chr1:11082592
|
C | T | 1 | a0001c0001t0001g0154 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1280+96G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 10/24 | chr1 | 11082592 | ||||||
chr1:11082929
|
C | T | 3 | a0001c0006t0003g0187a0001c0006t0003g0188a0001c0006t0003g0189 | 3 | HG02615.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1090-51G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11082929 | ||||||
chr1:11083190
|
C | T | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-312G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083190 | ||||||
chr1:11083231
|
G | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-353C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083231 | ||||||
chr1:11083302
|
C | G | 2 | a0001c0006t0001g0185a0001c0006t0001g0186 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1090-424G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083302 | ||||||
chr1:11083302
|
C | T | 1 | a0001c0005t0001g0020 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1090-424G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083302 | ||||||
chr1:11083316
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1090-438C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083316 | ||||||
chr1:11083317
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1090-439G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083317 | ||||||
chr1:11083399
|
T | C | 4 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0148others(1): Show | 4 | HG00642.hp2 HG01074.hp1 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.1090-521A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083399 | ||||||
chr1:11083422
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1090-544A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083422 | ||||||
chr1:11083510
|
C | T | 5 | a0001c0007t0001g0213a0001c0007t0001g0214a0001c0007t0001g0215others(2): Show | 5 | HG02145.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1090-632G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083510 | ||||||
chr1:11083511
|
G | A | 3 | a0001c0006t0003g0187a0001c0006t0003g0188a0001c0006t0003g0189 | 3 | HG02615.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1090-633C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083511 | ||||||
chr1:11083557
|
C | T | 1 | a0001c0001t0001g0109 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1090-679G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083557 | ||||||
chr1:11083562
|
C | CAAAAAAA others(4): Show |
1 | a0001c0003t0001g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1090-695_1090-685d others(13): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083562
|
C | CAAAAAAA others(6): Show |
20 | a0001c0003t0001g0225a0001c0003t0001g0227a0001c0003t0001g0228others(17): Show | 20 | HG00609.hp2 HG01099.hp1 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1090-697_1090-685d others(15): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083562
|
C | CAAAAAAA others(7): Show |
13 | a0001c0003t0001g0224a0001c0003t0001g0226a0001c0003t0001g0233others(10): Show | 13 | HG00558.hp1 HG01496.hp2 HG01943.hp2 others(10): Show |
intron_variant | MODIFIER | c.1090-698_1090-685d others(16): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083562
|
C | CAAAAAAA others(8): Show |
16 | a0001c0003t0001g0248a0001c0003t0001g0261a0001c0003t0002g0010others(13): Show | 17 | HG00280.hp2 HG00673.hp1 HG01123.hp1 others(14): Show |
intron_variant | MODIFIER | c.1090-699_1090-685d others(17): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083562
|
C | CAAAAAAA others(9): Show |
14 | a0001c0001t0001g0009a0001c0003t0001g0234a0001c0003t0001g0236others(11): Show | 15 | HG00438.hp1 HG02074.hp2 HG02738.hp1 others(12): Show |
intron_variant | MODIFIER | c.1090-700_1090-685d others(18): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083562
|
C | CAAAAAAA others(10): Show |
2 | a0001c0001t0001g0211a0001c0001t0001g0212 | 2 | HG01891.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.1090-701_1090-685d others(19): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083562
|
C | CAAAAAAA others(11): Show |
2 | a0001c0001t0001g0209a0001c0017t0001g0190 | 2 | HG02602.hp2 HG02717.hp2 |
intron_variant | MODIFIER | c.1090-702_1090-685d others(20): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083562
|
C | CAAAAAAA others(12): Show |
2 | a0001c0007t0001g0215a0001c0007t0001g0216 | 2 | HG02922.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1090-703_1090-685d others(21): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083562
|
C | CAAAAAAA others(13): Show |
4 | a0001c0003t0002g0258a0001c0003t0002g0259a0001c0007t0001g0213others(1): Show | 4 | HG01175.hp1 HG02004.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.1090-704_1090-685d others(22): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083562
|
C | CAAAAAAA others(14): Show |
1 | a0001c0007t0001g0214 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1090-705_1090-685d others(23): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083562
|
C | CAAAAAAA others(17): Show |
1 | a0001c0021t0001g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1090-685_1090-684i others(26): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083562
|
C | CAAAAAAA others(26): Show |
1 | a0001c0003t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1090-685_1090-684i others(35): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083562
|
CA | C | 101 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(98): Show | 112 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.1090-685delT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083562 | ||||||
chr1:11083614
|
T | TAA | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-738_1090-737d others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083614 | ||||||
chr1:11083621
|
A | T | 1 | a0001c0001t0001g0153 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1090-743T>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083621 | ||||||
chr1:11083621
|
AT | A | 5 | a0001c0001t0001g0009a0001c0001t0001g0180a0001c0001t0001g0209others(2): Show | 6 | HG01891.hp2 HG02109.hp1 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090-744delA | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083621 | ||||||
chr1:11083630
|
T | A | 1 | a0001c0002t0001g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1090-752A>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083630 | ||||||
chr1:11083631
|
A | T | 6 | a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0153others(3): Show | 6 | HG00741.hp1 HG01069.hp1 HG01074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1090-753T>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083631 | ||||||
chr1:11083789
|
C | A | 3 | a0001c0001t0001g0093a0001c0001t0001g0153a0001c0001t0001g0154 | 3 | HG00741.hp1 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1090-911G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083789 | ||||||
chr1:11083856
|
CTA | C | 3 | a0001c0005t0001g0065a0001c0005t0001g0066a0001c0005t0001g0067 | 3 | HG01891.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1090-980_1090-979d others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083856 | ||||||
chr1:11083925
|
A | G | 1 | a0001c0003t0002g0250 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1090-1047T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11083925 | ||||||
chr1:11084001
|
A | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-1123T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084001 | ||||||
chr1:11084028
|
T | G | 1 | a0001c0002t0001g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1090-1150A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084028 | ||||||
chr1:11084059
|
A | G | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1090-1181T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084059 | ||||||
chr1:11084070
|
T | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-1192A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084070 | ||||||
chr1:11084105
|
T | C | 20 | a0002c0004t0001g0191a0002c0004t0001g0192a0002c0004t0001g0193others(17): Show | 20 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.1090-1227A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084105 | ||||||
chr1:11084263
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01928.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.1090-1385T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084263 | ||||||
chr1:11084347
|
G | A | 1 | a0001c0003t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1090-1469C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084347 | ||||||
chr1:11084526
|
C | A | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1090-1648G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084526 | ||||||
chr1:11084648
|
T | G | 49 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(46): Show | 50 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1090-1770A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084648 | ||||||
chr1:11084685
|
A | G | 1 | a0001c0002t0001g0059 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.1090-1807T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084685 | ||||||
chr1:11084801
|
G | A | 1 | a0001c0001t0001g0155 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1090-1923C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084801 | ||||||
chr1:11084858
|
T | C | 15 | a0001c0003t0002g0010a0001c0003t0002g0221a0001c0003t0002g0222others(12): Show | 16 | HG00280.hp2 HG00438.hp1 HG01175.hp1 others(13): Show |
intron_variant | MODIFIER | c.1090-1980A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084858 | ||||||
chr1:11084895
|
A | G | 1 | a0001c0002t0001g0081 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1090-2017T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084895 | ||||||
chr1:11084983
|
C | T | 2 | a0001c0003t0001g0266a0001c0022t0001g0268 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1090-2105G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11084983 | ||||||
chr1:11085109
|
A | G | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1090-2231T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085109 | ||||||
chr1:11085128
|
T | C | 1 | a0001c0006t0001g0185 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1090-2250A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085128 | ||||||
chr1:11085195
|
T | C | 1 | a0001c0003t0001g0260 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1089+2253A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085195 | ||||||
chr1:11085265
|
G | C | 1 | a0001c0002t0001g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1089+2183C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085265 | ||||||
chr1:11085302
|
A | C | 3 | a0001c0001t0001g0105a0001c0001t0001g0106a0001c0001t0001g0175 | 3 | HG02280.hp1 HG02451.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1089+2146T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085302 | ||||||
chr1:11085344
|
G | A | 30 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(27): Show | 31 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.1089+2104C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085344 | ||||||
chr1:11085356
|
G | A | 3 | a0001c0005t0001g0183a0001c0005t0001g0184a0001c0005t0001g0220 | 3 | HG02109.hp2 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.1089+2092C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085356 | ||||||
chr1:11085459
|
A | T | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1089+1989T>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085459 | ||||||
chr1:11085499
|
A | G | 7 | a0001c0003t0001g0237a0001c0003t0001g0238a0001c0003t0001g0239others(4): Show | 7 | HG01099.hp1 HG01257.hp1 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.1089+1949T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085499 | ||||||
chr1:11085502
|
A | T | 1 | a0001c0003t0001g0236 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1089+1946T>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085502 | ||||||
chr1:11085530
|
T | G | 6 | a0001c0007t0001g0213a0001c0007t0001g0214a0001c0007t0001g0215others(3): Show | 6 | HG02145.hp2 HG02922.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1089+1918A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085530 | ||||||
chr1:11085569
|
G | C | 1 | a0001c0002t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1089+1879C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085569 | ||||||
chr1:11085605
|
C | T | 2 | a0001c0006t0001g0185a0001c0006t0001g0186 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1089+1843G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085605 | ||||||
chr1:11085779
|
T | C | 3 | a0001c0005t0001g0065a0001c0005t0001g0066a0001c0005t0001g0067 | 3 | HG01891.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1089+1669A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085779 | ||||||
chr1:11085791
|
T | C | 23 | a0001c0002t0001g0004a0001c0002t0001g0011a0001c0002t0001g0059others(20): Show | 24 | HG01167.hp2 HG01243.hp1 HG02055.hp1 others(21): Show |
intron_variant | MODIFIER | c.1089+1657A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085791 | ||||||
chr1:11085891
|
G | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0168 | 2 | HG01175.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.1089+1557C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085891 | ||||||
chr1:11085910
|
C | T | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089+1538G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085910 | ||||||
chr1:11085926
|
T | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089+1522A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085926 | ||||||
chr1:11085965
|
T | C | 1 | a0001c0002t0001g0027 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1089+1483A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11085965 | ||||||
chr1:11086016
|
G | A | 1 | a0001c0003t0001g0261 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1089+1432C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086016 | ||||||
chr1:11086102
|
C | A | 2 | a0001c0002t0001g0078a0001c0002t0001g0181 | 2 | HG02615.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1089+1346G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086102 | ||||||
chr1:11086217
|
T | G | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089+1231A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086217 | ||||||
chr1:11086356
|
G | A | 2 | a0001c0003t0001g0266a0001c0022t0001g0268 | 2 | HG01109.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1089+1092C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086356 | ||||||
chr1:11086421
|
A | T | 24 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(21): Show | 25 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(22): Show |
intron_variant | MODIFIER | c.1089+1027T>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086421 | ||||||
chr1:11086438
|
G | C | 1 | a0001c0002t0001g0051 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1089+1010C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086438 | ||||||
chr1:11086440
|
T | C | 1 | a0001c0003t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.1089+1008A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086440 | ||||||
chr1:11086490
|
C | T | 1 | a0001c0001t0001g0104 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1089+958G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086490 | ||||||
chr1:11086504
|
T | TTCTC | 81 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(78): Show | 82 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.1089+943_1089+944i others(6): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086504 | ||||||
chr1:11086543
|
T | C | 1 | a0001c0005t0001g0024 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1089+905A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086543 | ||||||
chr1:11086595
|
A | G | 49 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(46): Show | 50 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1089+853T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086595 | ||||||
chr1:11086855
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1089+593A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086855 | ||||||
chr1:11086958
|
A | G | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089+490T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11086958 | ||||||
chr1:11087038
|
T | G | 4 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(1): Show | 5 | HG01891.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1089+410A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11087038 | ||||||
chr1:11087106
|
T | C | 1 | a0001c0003t0002g0221 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.1089+342A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11087106 | ||||||
chr1:11087152
|
G | T | 1 | a0001c0005t0001g0019 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.1089+296C>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11087152 | ||||||
chr1:11087184
|
C | T | 85 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(82): Show | 87 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.1089+264G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11087184 | ||||||
chr1:11087199
|
T | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.1089+249A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 9/24 | chr1 | 11087199 | ||||||
chr1:11087757
|
C | T | 1 | a0001c0003t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.945+43G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 8/24 | chr1 | 11087757 | ||||||
chr1:11087995
|
A | T | 4 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(1): Show | 5 | HG01891.hp2 HG02109.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.835-85T>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 7/24 | chr1 | 11087995 | ||||||
chr1:11088028
|
T | C | 1 | a0001c0002t0004g0012 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.834+95A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 7/24 | chr1 | 11088028 | ||||||
chr1:11088029
|
C | T | 1 | a0001c0002t0004g0012 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.834+94G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 7/24 | chr1 | 11088029 | ||||||
chr1:11088230
|
C | A | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.759-32G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11088230 | ||||||
chr1:11088332
|
C | CTTCA | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.759-135_759-134ins others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11088332 | ||||||
chr1:11088375
|
T | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.759-177A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11088375 | ||||||
chr1:11088587
|
C | G | 1 | a0001c0003t0001g0235 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.759-389G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11088587 | ||||||
chr1:11088593
|
G | A | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.759-395C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11088593 | ||||||
chr1:11088594
|
T | C | 3 | a0001c0005t0001g0183a0001c0005t0001g0184a0001c0005t0001g0220 | 3 | HG02109.hp2 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.759-396A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11088594 | ||||||
chr1:11088659
|
ATCACGGT | A | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.759-468_759-462del others(7): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11088659 | ||||||
chr1:11088669
|
C | T | 1 | a0001c0003t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.759-471G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11088669 | ||||||
chr1:11088702
|
G | A | 213 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(210): Show | 226 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(223): Show |
intron_variant | MODIFIER | c.759-504C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11088702 | ||||||
chr1:11089102
|
G | C | 1 | a0001c0001t0001g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.759-904C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089102 | ||||||
chr1:11089140
|
G | C | 49 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(46): Show | 50 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.759-942C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089140 | ||||||
chr1:11089222
|
T | TA | 53 | a0001c0001t0001g0098a0001c0001t0001g0157a0001c0003t0001g0223others(50): Show | 54 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.759-1025dupT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089222 | ||||||
chr1:11089222
|
T | TAAAAAAA others(3): Show |
3 | a0001c0006t0003g0187a0001c0006t0003g0188a0001c0006t0003g0189 | 3 | HG02615.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.759-1034_759-1025d others(12): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089222 | ||||||
chr1:11089222
|
TA | T | 25 | a0001c0001t0001g0018a0001c0001t0001g0101a0001c0001t0001g0102others(22): Show | 25 | HG00558.hp2 HG01167.hp1 HG01167.hp2 others(22): Show |
intron_variant | MODIFIER | c.759-1025delT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089222 | ||||||
chr1:11089257
|
T | C | 5 | a0001c0007t0001g0213a0001c0007t0001g0214a0001c0007t0001g0215others(2): Show | 5 | HG02145.hp2 HG02922.hp2 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.759-1059A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089257 | ||||||
chr1:11089271
|
T | G | 1 | a0001c0003t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.759-1073A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089271 | ||||||
chr1:11089335
|
T | G | 1 | a0001c0002t0001g0176 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.759-1137A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089335 | ||||||
chr1:11089342
|
G | A | 1 | a0001c0002t0001g0064 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.759-1144C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089342 | ||||||
chr1:11089447
|
T | TA | 6 | a0001c0002t0001g0176a0001c0006t0001g0185a0001c0006t0001g0186others(3): Show | 6 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(3): Show |
intron_variant | MODIFIER | c.758+1106dupT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089447 | ||||||
chr1:11089608
|
C | T | 14 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0036others(11): Show | 14 | HG02055.hp2 HG02572.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.758+946G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089608 | ||||||
chr1:11089617
|
G | A | 6 | a0001c0001t0001g0158a0001c0006t0001g0185a0001c0006t0001g0186others(3): Show | 6 | HG02486.hp2 HG02615.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.758+937C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089617 | ||||||
chr1:11089619
|
C | T | 1 | a0001c0005t0001g0183 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.758+935G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089619 | ||||||
chr1:11089622
|
A | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.758+932T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089622 | ||||||
chr1:11089623
|
A | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.758+931T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089623 | ||||||
chr1:11089624
|
A | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.758+930T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089624 | ||||||
chr1:11089625
|
A | C | 2 | a0001c0006t0001g0185a0001c0006t0001g0186 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.758+929T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089625 | ||||||
chr1:11089626
|
A | C | 2 | a0001c0006t0001g0185a0001c0006t0001g0186 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.758+928T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089626 | ||||||
chr1:11089643
|
A | G | 1 | a0001c0001t0001g0100 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.758+911T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089643 | ||||||
chr1:11089726
|
A | C | 1 | a0001c0006t0001g0185 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.758+828T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089726 | ||||||
chr1:11089733
|
G | A | 1 | a0001c0021t0001g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.758+821C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089733 | ||||||
chr1:11089969
|
C | T | 85 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(82): Show | 87 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(84): Show |
intron_variant | MODIFIER | c.758+585G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089969 | ||||||
chr1:11089996
|
CT | C | 179 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(176): Show | 192 | HG00280.hp1 HG00323.hp2 HG00438.hp2 others(189): Show |
intron_variant | MODIFIER | c.758+557delA | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11089996 | ||||||
chr1:11090055
|
T | C | 14 | a0001c0002t0001g0034a0001c0002t0001g0035a0001c0002t0001g0036others(11): Show | 14 | HG02055.hp2 HG02572.hp2 HG02647.hp2 others(11): Show |
intron_variant | MODIFIER | c.758+499A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11090055 | ||||||
chr1:11090122
|
C | T | 2 | a0001c0006t0001g0185a0001c0006t0001g0186 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.758+432G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11090122 | ||||||
chr1:11090189
|
G | A | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.758+365C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11090189 | ||||||
chr1:11090240
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.758+314G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11090240 | ||||||
chr1:11090244
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.758+310C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11090244 | ||||||
chr1:11090253
|
C | T | 20 | a0002c0004t0001g0191a0002c0004t0001g0192a0002c0004t0001g0193others(17): Show | 20 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.758+301G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11090253 | ||||||
chr1:11090479
|
A | G | 3 | a0001c0005t0001g0065a0001c0005t0001g0066a0001c0005t0001g0067 | 3 | HG01891.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.758+75T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11090479 | ||||||
chr1:11090539
|
C | G | 1 | a0001c0003t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.758+15G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 6/24 | chr1 | 11090539 | ||||||
chr1:11090697
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0174 | 3 | HG00280.hp1 HG01515.hp2 HG01516.hp1 |
intron_variant | MODIFIER | c.644-29G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 5/24 | chr1 | 11090697 | ||||||
chr1:11090888
|
CTGGGCTC others(18): Show |
C | 2 | a0001c0001t0001g0017a0001c0001t0001g0159 | 2 | HG01515.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.643+101_643+125del others(25): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 5/24 | chr1 | 11090888 | ||||||
chr1:11091193
|
A | T | 1 | a0001c0002t0001g0082 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.478-14T>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 4/24 | chr1 | 11091193 | ||||||
chr1:11091257
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.478-78A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 4/24 | chr1 | 11091257 | ||||||
chr1:11091262
|
A | G | 1 | a0001c0002t0001g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.478-83T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 4/24 | chr1 | 11091262 | ||||||
chr1:11091272
|
A | G | 1 | a0002c0004t0001g0193 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.478-93T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 4/24 | chr1 | 11091272 | ||||||
chr1:11091311
|
T | C | 2 | a0001c0002t0001g0079a0001c0002t0001g0080 | 2 | HG02280.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.478-132A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 4/24 | chr1 | 11091311 | ||||||
chr1:11091423
|
T | C | 46 | a0001c0003t0001g0224a0001c0003t0001g0225a0001c0003t0001g0226others(43): Show | 47 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.477+70A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 4/24 | chr1 | 11091423 | ||||||
chr1:11091434
|
G | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.477+59C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 4/24 | chr1 | 11091434 | ||||||
chr1:11091466
|
G | C | 1 | a0001c0017t0001g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.477+27C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 4/24 | chr1 | 11091466 | ||||||
chr1:11091722
|
A | G | 211 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(208): Show | 224 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(221): Show |
intron_variant | MODIFIER | c.373-125T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11091722 | ||||||
chr1:11091729
|
C | G | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-132G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11091729 | ||||||
chr1:11091801
|
C | T | 1 | a0001c0003t0001g0264 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.373-204G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11091801 | ||||||
chr1:11091970
|
G | A | 6 | a0001c0005t0001g0019a0001c0005t0001g0020a0001c0005t0001g0021others(3): Show | 6 | HG00741.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.373-373C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11091970 | ||||||
chr1:11092014
|
T | C | 1 | a0001c0017t0001g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.373-417A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11092014 | ||||||
chr1:11092097
|
A | G | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-500T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11092097 | ||||||
chr1:11092111
|
T | C | 2 | a0001c0003t0001g0230a0001c0003t0001g0264 | 2 | NA18954.hp2 NA19054.hp2 |
intron_variant | MODIFIER | c.373-514A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11092111 | ||||||
chr1:11092292
|
T | C | 1 | a0001c0001t0001g0169 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.373-695A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11092292 | ||||||
chr1:11092308
|
G | A | 46 | a0001c0003t0001g0224a0001c0003t0001g0225a0001c0003t0001g0226others(43): Show | 47 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(44): Show |
intron_variant | MODIFIER | c.373-711C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11092308 | ||||||
chr1:11092345
|
A | G | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.373-748T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11092345 | ||||||
chr1:11092426
|
G | C | 1 | a0001c0003t0001g0223 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.373-829C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11092426 | ||||||
chr1:11092466
|
A | G | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.373-869T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11092466 | ||||||
chr1:11092492
|
C | T | 2 | a0001c0006t0001g0185a0001c0006t0001g0186 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.373-895G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11092492 | ||||||
chr1:11092521
|
CT | C | 86 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(83): Show | 88 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(85): Show |
intron_variant | MODIFIER | c.373-925delA | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11092521 | ||||||
chr1:11092675
|
G | A | 1 | a0002c0004t0001g0206 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.373-1078C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11092675 | ||||||
chr1:11092684
|
A | T | 1 | a0001c0001t0001g0098 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.373-1087T>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11092684 | ||||||
chr1:11093057
|
G | A | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-1460C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11093057 | ||||||
chr1:11093184
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.373-1587A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11093184 | ||||||
chr1:11093198
|
T | C | 2 | a0001c0001t0001g0163a0001c0001t0001g0168 | 2 | HG01175.hp2 HG03710.hp1 |
intron_variant | MODIFIER | c.373-1601A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11093198 | ||||||
chr1:11093274
|
A | G | 49 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(46): Show | 50 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.373-1677T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11093274 | ||||||
chr1:11093368
|
C | T | 1 | a0001c0003t0001g0231 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.373-1771G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11093368 | ||||||
chr1:11093602
|
C | T | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.373-2005G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11093602 | ||||||
chr1:11093682
|
A | G | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.372+2076T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11093682 | ||||||
chr1:11093708
|
G | A | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+2050C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11093708 | ||||||
chr1:11093770
|
G | A | 20 | a0002c0004t0001g0191a0002c0004t0001g0192a0002c0004t0001g0193others(17): Show | 20 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.372+1988C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11093770 | ||||||
chr1:11093808
|
A | G | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1950T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11093808 | ||||||
chr1:11093860
|
G | C | 1 | a0001c0001t0001g0164 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.372+1898C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11093860 | ||||||
chr1:11094004
|
CAGG | C | 3 | a0001c0005t0001g0065a0001c0005t0001g0066a0001c0005t0001g0067 | 3 | HG01891.hp1 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.372+1751_372+1753d others(5): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094004 | ||||||
chr1:11094016
|
G | C | 1 | a0001c0002t0001g0089 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.372+1742C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094016 | ||||||
chr1:11094027
|
T | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1731A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094027 | ||||||
chr1:11094230
|
G | A | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1528C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094230 | ||||||
chr1:11094243
|
G | A | 1 | a0001c0014t0001g0097 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.372+1515C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094243 | ||||||
chr1:11094319
|
C | T | 1 | a0001c0002t0001g0031 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.372+1439G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094319 | ||||||
chr1:11094387
|
C | T | 1 | a0001c0014t0001g0097 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.372+1371G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094387 | ||||||
chr1:11094398
|
G | A | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG01928.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.372+1360C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094398 | ||||||
chr1:11094468
|
A | G | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1290T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094468 | ||||||
chr1:11094501
|
C | G | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+1257G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094501 | ||||||
chr1:11094538
|
G | A | 15 | a0001c0002t0001g0004a0001c0002t0001g0068a0001c0002t0001g0069others(12): Show | 16 | HG01167.hp2 HG02055.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.372+1220C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094538 | ||||||
chr1:11094581
|
G | A | 1 | a0001c0017t0001g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.372+1177C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094581 | ||||||
chr1:11094603
|
C | CT | 9 | a0001c0001t0001g0030a0001c0001t0001g0096a0001c0003t0001g0223others(6): Show | 9 | HG01109.hp2 HG02615.hp1 HG03209.hp1 others(6): Show |
intron_variant | MODIFIER | c.372+1154dupA | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094603 | ||||||
chr1:11094603
|
C | CTT | 47 | a0001c0003t0001g0224a0001c0003t0001g0225a0001c0003t0001g0226others(44): Show | 48 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.372+1153_372+1154d others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094603 | ||||||
chr1:11094631
|
C | G | 1 | a0001c0021t0001g0210 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.372+1127G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094631 | ||||||
chr1:11094684
|
T | G | 1 | a0001c0001t0001g0169 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.372+1074A>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094684 | ||||||
chr1:11094694
|
G | A | 1 | a0001c0002t0001g0081 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.372+1064C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094694 | ||||||
chr1:11094704
|
G | A | 20 | a0002c0004t0001g0191a0002c0004t0001g0192a0002c0004t0001g0193others(17): Show | 20 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.372+1054C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094704 | ||||||
chr1:11094749
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.372+1009A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094749 | ||||||
chr1:11094844
|
C | T | 1 | a0001c0001t0001g0180 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.372+914G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094844 | ||||||
chr1:11094996
|
G | T | 1 | a0001c0003t0001g0266 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.372+762C>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11094996 | ||||||
chr1:11095019
|
T | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+739A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095019 | ||||||
chr1:11095082
|
G | T | 2 | a0001c0005t0001g0183a0001c0005t0001g0184 | 2 | HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.372+676C>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095082 | ||||||
chr1:11095105
|
C | T | 1 | a0001c0002t0001g0025 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.372+653G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095105 | ||||||
chr1:11095116
|
G | T | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+642C>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095116 | ||||||
chr1:11095161
|
A | G | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.372+597T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095161 | ||||||
chr1:11095207
|
G | A | 9 | a0001c0002t0001g0082a0001c0002t0001g0083a0001c0002t0001g0085others(6): Show | 9 | HG02647.hp2 HG02723.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.372+551C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095207 | ||||||
chr1:11095211
|
C | CA | 11 | a0001c0001t0001g0009a0001c0001t0001g0167a0001c0001t0001g0168others(8): Show | 12 | HG01175.hp2 HG02145.hp2 HG02602.hp2 others(9): Show |
intron_variant | MODIFIER | c.372+546dupT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095211 | ||||||
chr1:11095211
|
CA | C | 13 | a0001c0001t0001g0017a0001c0001t0001g0094a0001c0001t0001g0171others(10): Show | 13 | HG00323.hp2 HG00558.hp2 HG01069.hp1 others(10): Show |
intron_variant | MODIFIER | c.372+546delT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095211 | ||||||
chr1:11095266
|
T | A | 1 | a0001c0001t0001g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.372+492A>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095266 | ||||||
chr1:11095529
|
C | T | 3 | a0001c0005t0001g0183a0001c0005t0001g0184a0001c0005t0001g0220 | 3 | HG02109.hp2 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.372+229G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095529 | ||||||
chr1:11095606
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.372+152A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095606 | ||||||
chr1:11095638
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.372+120G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095638 | ||||||
chr1:11095639
|
G | A | 1 | a0001c0017t0001g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.372+119C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095639 | ||||||
chr1:11095700
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.372+58G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095700 | ||||||
chr1:11095708
|
C | T | 30 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(27): Show | 31 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.372+50G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 3/24 | chr1 | 11095708 | ||||||
chr1:11095988
|
C | CT | 6 | a0001c0002t0001g0025a0001c0003t0001g0224a0001c0006t0003g0187others(3): Show | 6 | HG01109.hp2 HG02615.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.249-108dupA | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11095988 | ||||||
chr1:11096114
|
G | C | 2 | a0001c0006t0001g0185a0001c0006t0001g0186 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.249-233C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096114 | ||||||
chr1:11096163
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.249-282A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096163 | ||||||
chr1:11096184
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0092 | 2 | HG00735.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.249-303T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096184 | ||||||
chr1:11096236
|
C | T | 6 | a0001c0005t0001g0019a0001c0005t0001g0020a0001c0005t0001g0021others(3): Show | 6 | HG00741.hp2 HG02559.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.249-355G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096236 | ||||||
chr1:11096459
|
C | A | 1 | a0001c0002t0001g0090 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.249-578G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096459 | ||||||
chr1:11096467
|
C | CT | 7 | a0001c0003t0001g0224a0001c0003t0001g0225a0001c0003t0001g0226others(4): Show | 7 | HG02683.hp1 HG02738.hp1 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.249-587dupA | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096467 | ||||||
chr1:11096471
|
C | T | 52 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(49): Show | 53 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.249-590G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096471 | ||||||
chr1:11096471
|
CT | C | 94 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(91): Show | 105 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.249-591delA | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096471 | ||||||
chr1:11096471
|
CTT | C | 6 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0174others(3): Show | 6 | HG00558.hp2 HG01069.hp1 HG01069.hp2 others(3): Show |
intron_variant | MODIFIER | c.249-592_249-591del others(2): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096471 | ||||||
chr1:11096475
|
T | C | 1 | a0002c0004t0001g0208 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.249-594A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096475 | ||||||
chr1:11096538
|
A | ACACC | 10 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(7): Show | 11 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.249-658_249-657ins others(4): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096538 | ||||||
chr1:11096611
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.249-730A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096611 | ||||||
chr1:11096717
|
G | A | 2 | a0001c0001t0001g0177a0001c0001t0001g0178 | 2 | HG01258.hp1 HG02004.hp2 |
intron_variant | MODIFIER | c.249-836C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096717 | ||||||
chr1:11096979
|
T | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.248+1041A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11096979 | ||||||
chr1:11097018
|
C | T | 1 | a0001c0005t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248+1002G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097018 | ||||||
chr1:11097069
|
G | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.248+951C>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097069 | ||||||
chr1:11097195
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG02135.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.248+825C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097195 | ||||||
chr1:11097196
|
C | T | 2 | a0001c0001t0001g0015a0001c0001t0001g0016 | 2 | HG02135.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.248+824G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097196 | ||||||
chr1:11097214
|
C | A | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.248+806G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097214 | ||||||
chr1:11097215
|
C | A | 1 | a0001c0005t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248+805G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097215 | ||||||
chr1:11097217
|
A | G | 1 | a0002c0004t0001g0192 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.248+803T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097217 | ||||||
chr1:11097256
|
T | C | 48 | a0001c0003t0001g0224a0001c0003t0001g0225a0001c0003t0001g0226others(45): Show | 49 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(46): Show |
intron_variant | MODIFIER | c.248+764A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097256 | ||||||
chr1:11097280
|
A | G | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.248+740T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097280 | ||||||
chr1:11097339
|
A | G | 1 | a0001c0003t0002g0222 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.248+681T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097339 | ||||||
chr1:11097372
|
C | T | 1 | a0001c0001t0001g0014 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.248+648G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097372 | ||||||
chr1:11097380
|
A | AAAAAAT | 10 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(7): Show | 11 | HG01891.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
intron_variant | MODIFIER | c.248+634_248+639dup others(6): Show |
EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097380 | ||||||
chr1:11097434
|
A | C | 1 | a0001c0001t0001g0013 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.248+586T>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097434 | ||||||
chr1:11097465
|
G | A | 1 | a0001c0022t0001g0268 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.248+555C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097465 | ||||||
chr1:11097466
|
C | T | 20 | a0002c0004t0001g0191a0002c0004t0001g0192a0002c0004t0001g0193others(17): Show | 20 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(17): Show |
intron_variant | MODIFIER | c.248+554G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097466 | ||||||
chr1:11097535
|
G | C | 1 | a0001c0002t0001g0179 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.248+485C>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097535 | ||||||
chr1:11097586
|
C | T | 1 | a0001c0003t0002g0221 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.248+434G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097586 | ||||||
chr1:11097650
|
T | C | 54 | a0001c0003t0001g0223a0001c0003t0001g0224a0001c0003t0001g0225others(51): Show | 55 | HG00280.hp2 HG00438.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.248+370A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097650 | ||||||
chr1:11097657
|
C | T | 1 | a0001c0002t0004g0012 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.248+363G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097657 | ||||||
chr1:11097725
|
C | CA | 36 | a0001c0001t0001g0009a0001c0001t0001g0180a0001c0001t0001g0209others(33): Show | 37 | HG00558.hp1 HG01361.hp2 HG01496.hp2 others(34): Show |
intron_variant | MODIFIER | c.248+294dupT | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097725 | ||||||
chr1:11097822
|
A | G | 35 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(32): Show | 36 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(33): Show |
intron_variant | MODIFIER | c.248+198T>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097822 | ||||||
chr1:11097968
|
C | G | 1 | a0001c0005t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.248+52G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 2/24 | chr1 | 11097968 | ||||||
chr1:11098232
|
C | T | 1 | a0001c0017t0001g0190 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.112-76G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/24 | chr1 | 11098232 | ||||||
chr1:11098469
|
C | T | 3 | a0001c0006t0003g0187a0001c0006t0003g0188a0001c0006t0003g0189 | 3 | HG02615.hp1 HG03209.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.112-313G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/24 | chr1 | 11098469 | ||||||
chr1:11098559
|
G | A | 1 | a0001c0005t0001g0182 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.112-403C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/24 | chr1 | 11098559 | ||||||
chr1:11098816
|
G | A | 3 | a0001c0005t0001g0183a0001c0005t0001g0184a0001c0005t0001g0220 | 3 | HG02109.hp2 HG02559.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.112-660C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/24 | chr1 | 11098816 | ||||||
chr1:11098825
|
C | T | 2 | a0001c0006t0001g0185a0001c0006t0001g0186 | 2 | HG06807.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.112-669G>A | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/24 | chr1 | 11098825 | ||||||
chr1:11098865
|
T | C | 5 | a0001c0006t0001g0185a0001c0006t0001g0186a0001c0006t0003g0187others(2): Show | 5 | HG02615.hp1 HG03209.hp1 HG06807.hp1 others(2): Show |
intron_variant | MODIFIER | c.112-709A>G | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/24 | chr1 | 11098865 | ||||||
chr1:11099061
|
C | A | 30 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(27): Show | 31 | HG00558.hp1 HG01123.hp1 HG01361.hp2 others(28): Show |
intron_variant | MODIFIER | c.111+660G>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/24 | chr1 | 11099061 | ||||||
chr1:11099421
|
C | G | 1 | a0001c0002t0001g0011 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.111+300G>C | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/24 | chr1 | 11099421 | ||||||
chr1:11099514
|
G | A | 80 | a0001c0001t0001g0009a0001c0001t0001g0209a0001c0001t0001g0211others(77): Show | 82 | HG00280.hp2 HG00438.hp1 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.111+207C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/24 | chr1 | 11099514 | ||||||
chr1:11099683
|
G | A | 1 | a0001c0005t0001g0220 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.111+38C>T | EXOSC10 | ENSG00000171824.14 | transcript | ENST00000376936.9 | protein_coding | 1/24 | chr1 | 11099683 |