geneid | 8036 |
---|---|
ensemblid | ENSG00000108061.13 |
hgncid | 15454 |
symbol | SHOC2 |
name | SHOC2 leucine rich repeat scaffold protein |
refseq_nuc | NM_007373.4 |
refseq_prot | NP_031399.2 |
ensembl_nuc | ENST00000369452.9 |
ensembl_prot | ENSP00000358464.5 |
mane_status | MANE Select |
chr | chr10 |
start | 110919604 |
end | 111013665 |
strand | + |
ver | v1.2 |
region | chr10:110919604-111013665 |
region5000 | chr10:110914604-111018665 |
regionname0 | SHOC2_chr10_110919604_111013665 |
regionname5000 | SHOC2_chr10_110914604_111018665 |
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 | 582 | 380 | 87 | 51 | 190 | 8 | 42 | 152 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0002 | 0/0 | 582 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1749 | 377 | 86 | 50 | 189 | 8 | 42 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
c0002 | 0/0 | 1749 | 6 | 5 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
c0003 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
c0004 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
c0005 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
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 | 2136 | 239 | 44 | 30 | 127 | 7 | 29 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0002 | 0/0 | 2136 | 86 | 15 | 12 | 55 | 0 | 4 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0003 | 0/0 | 2135 | 16 | 14 | 2 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0004 | 0/0 | 2135 | 13 | 10 | 2 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0005 | 0/0 | 2137 | 5 | 0 | 1 | 2 | 0 | 2 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0006 | 0/0 | 2136 | 3 | 0 | 2 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0007 | 0/0 | 2137 | 3 | 0 | 1 | 1 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0008 | 0/0 | 2136 | 3 | 2 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0009 | 0/0 | 2137 | 2 | 0 | 0 | 0 | 0 | 2 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0010 | 0/0 | 2136 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0011 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0012 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0013 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0014 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0015 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0016 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0017 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0018 | 0/0 | 2137 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0019 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0020 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0021 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0022 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0023 | 0/0 | 2136 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0024 | 0/0 | 2136 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
t0025 | 0/0 | 2136 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
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 | 4 | 0 | 0 | 4 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0003 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0023 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0332 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1749 | 377 | 86 | 50 | 189 | 8 | 42 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0003 | 0/0 | 1749 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0004 | 0/0 | 1749 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0005 | 0/0 | 1749 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0002c0002 | 0/0 | 1749 | 6 | 5 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3884 | 238 | 44 | 30 | 126 | 7 | 29 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0002 | 0/0 | 3884 | 86 | 15 | 12 | 55 | 0 | 4 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0003 | 0/0 | 3883 | 10 | 9 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0004 | 0/0 | 3883 | 12 | 10 | 1 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0005 | 0/0 | 3885 | 5 | 0 | 1 | 2 | 0 | 2 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0006 | 0/0 | 3884 | 3 | 0 | 2 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0007 | 0/0 | 3885 | 3 | 0 | 1 | 1 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0008 | 0/0 | 3884 | 3 | 2 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0009 | 0/0 | 3885 | 2 | 0 | 0 | 0 | 0 | 2 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0010 | 0/0 | 3884 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0011 | 0/0 | 3884 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0012 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0013 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0014 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0015 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0017 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0018 | 0/0 | 3885 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0019 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0020 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0021 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0022 | 0/0 | 3884 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0023 | 0/0 | 3884 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0024 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0001t0025 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0003t0001 | 0/0 | 3884 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0004t0016 | 0/0 | 3884 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0001c0005t0004 | 0/0 | 3883 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
a0002c0002t0003 | 0/0 | 3883 | 6 | 5 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | copy fasta | chr10 | 110914604 | 111018665 |
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 | 4 | 0 | 0 | 4 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0003 | 0/0 | 4 | 0 | 3 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0009 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0016 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0278 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0285 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0298 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0305 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0332 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0001g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0002 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0004 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0018 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0118 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0002g0348 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0003g0015 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0003g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0003g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0003g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0003g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0003g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0003g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0003g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0004g0027 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0004g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0004g0333 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0004g0334 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0004g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0004g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0004g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0004g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0004g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0004g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0004g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0005g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0005g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0005g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0005g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0006g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0006g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0006g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0007g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0007g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0008g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0008g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0009g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0009g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0010g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0011g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0012g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0013g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0014g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0015g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0017g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0018g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0019g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0020g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0021g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0022g0326 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0023g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0024g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0001t0025g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0003t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0004t0016g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0001c0005t0004g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0002c0002t0003g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0002c0002t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0002c0002t0003g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0002c0002t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
a0002c0002t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0053 | EUR | GBR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0275 | EUR | GBR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00140 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | GBR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | GBR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00423 | hp1 | a0001 | c0001 | t0019 | g0073 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00423 | hp2 | a0001 | c0003 | t0001 | g0302 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0239 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0020 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0205 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0287 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00609 | hp2 | a0001 | c0001 | t0002 | g0207 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0261 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0119 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | CHS | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0281 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0221 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01069 | hp2 | a0001 | c0001 | t0006 | g0247 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01071 | hp1 | a0001 | c0001 | t0006 | g0240 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01071 | hp2 | a0001 | c0001 | t0002 | g0201 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0296 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01074 | hp2 | a0001 | c0005 | t0004 | g0340 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0230 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01081 | hp2 | a0001 | c0001 | t0003 | g0284 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0315 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0242 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0303 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01168 | hp1 | a0001 | c0001 | t0004 | g0334 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01243 | hp1 | a0002 | c0002 | t0003 | g0346 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01261 | hp1 | a0001 | c0001 | t0010 | g0154 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0270 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0282 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0200 | AMR | CLM | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0280 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0341 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0276 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01943 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0004 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0192 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01978 | hp1 | a0001 | c0001 | t0007 | g0210 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02015 | hp2 | a0001 | c0001 | t0017 | g0098 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0184 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0238 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0129 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0323 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0215 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02080 | hp2 | a0001 | c0001 | t0012 | g0268 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02135 | hp1 | a0001 | c0001 | t0005 | g0288 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0305 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02145 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | CDX | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0325 | EAS | CDX | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0274 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02258 | hp1 | a0001 | c0001 | t0014 | g0146 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0127 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0241 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02273 | hp2 | a0001 | c0001 | t0002 | g0179 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0009 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0204 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0297 | AMR | PEL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02451 | hp2 | a0001 | c0001 | t0004 | g0338 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02572 | hp1 | a0002 | c0002 | t0003 | g0117 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0143 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0043 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0170 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02622 | hp1 | a0001 | c0001 | t0003 | g0126 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02622 | hp2 | a0001 | c0004 | t0016 | g0142 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0017 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0300 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0158 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0110 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02698 | hp1 | a0001 | c0001 | t0009 | g0123 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02723 | hp1 | a0001 | c0001 | t0021 | g0023 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02723 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0273 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0078 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02818 | hp2 | a0001 | c0001 | t0008 | g0321 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02896 | hp1 | a0002 | c0002 | t0003 | g0347 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0231 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0168 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02922 | hp1 | a0001 | c0001 | t0004 | g0344 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02965 | hp1 | a0001 | c0001 | t0003 | g0130 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0304 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02976 | hp1 | a0002 | c0002 | t0003 | g0345 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0166 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0263 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03017 | hp2 | a0001 | c0001 | t0022 | g0326 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0071 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03098 | hp2 | a0001 | c0001 | t0020 | g0331 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03139 | hp1 | a0001 | c0001 | t0004 | g0225 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0015 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0027 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0298 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0167 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03225 | hp1 | a0001 | c0001 | t0008 | g0224 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03453 | hp1 | a0002 | c0002 | t0003 | g0028 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0169 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0161 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03486 | hp2 | a0001 | c0001 | t0004 | g0337 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0328 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03516 | hp1 | a0002 | c0002 | t0003 | g0028 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03516 | hp2 | a0001 | c0001 | t0013 | g0226 | AFR | ESN | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03540 | hp1 | a0001 | c0001 | t0004 | g0336 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0137 | AFR | GWD | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0311 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0017 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0283 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0016 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0196 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03688 | hp1 | a0001 | c0001 | t0007 | g0211 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0278 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0118 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0005 | SAS | PJL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03831 | hp2 | a0001 | c0001 | t0005 | g0115 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03834 | hp2 | a0001 | c0001 | t0011 | g0103 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0254 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03927 | hp2 | a0001 | c0001 | t0005 | g0228 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG04115 | hp1 | a0001 | c0001 | t0002 | g0197 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0320 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0229 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG04184 | hp2 | a0001 | c0001 | t0006 | g0244 | SAS | BEB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG04199 | hp1 | a0001 | c0001 | t0009 | g0122 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0094 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG04204 | hp1 | a0001 | c0001 | t0023 | g0237 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0319 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG04228 | hp2 | a0001 | c0001 | t0002 | g0173 | SAS | STU | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18522 | hp1 | a0001 | c0001 | t0003 | g0125 | AFR | YRI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18522 | hp2 | a0001 | c0001 | t0025 | g0121 | AFR | YRI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0177 | EAS | CHB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0286 | EAS | CHB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | YRI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0128 | AFR | YRI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18949 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18954 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18959 | hp2 | a0001 | c0001 | t0024 | g0152 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18960 | hp2 | a0001 | c0001 | t0002 | g0214 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0277 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0198 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18967 | hp1 | a0001 | c0001 | t0015 | g0048 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0190 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18973 | hp1 | a0001 | c0001 | t0002 | g0348 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18974 | hp2 | a0001 | c0001 | t0007 | g0191 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18978 | hp2 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0193 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18982 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0259 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0199 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0052 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0232 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0349 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18995 | hp1 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19001 | hp1 | a0001 | c0001 | t0005 | g0050 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0308 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19002 | hp1 | a0001 | c0001 | t0002 | g0188 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19003 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0060 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19006 | hp1 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19009 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0310 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0172 | AFR | LWK | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19030 | hp2 | a0001 | c0001 | t0018 | g0162 | AFR | LWK | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19043 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | LWK | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0124 | AFR | LWK | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0235 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0175 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19058 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19065 | hp1 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0322 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19072 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19072 | hp2 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0350 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0257 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0314 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19083 | hp2 | a0001 | c0001 | t0002 | g0202 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19089 | hp1 | a0001 | c0001 | t0002 | g0234 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | YRI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | YRI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA20129 | hp1 | a0001 | c0001 | t0004 | g0339 | AFR | ASW | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0312 | AFR | ASW | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA20752 | hp1 | a0001 | c0001 | t0004 | g0333 | EUR | TSI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | TSI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0042 | EUR | TSI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | TSI | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02109 | hp1 | a0001 | c0001 | t0002 | g0171 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0335 | AFR | ACB | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | MSL | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0249 | AFR | USA | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0107 | AFR | USA | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | USA | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0132 | AFR | USA | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | LWK | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | LWK | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0285 | REF | REF | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0332 | REF | REF | SHOC2_chr10_110914604_111018665 | SHOC2 | chr10 | 110914604 | 111018665 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:111011663
|
A | G | 1 | a0002 | 6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
missense_variant | MODERATE | c.1594A>G | p.Ser532Gly | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1882/3884 | 1594/1749 | 532/582 | chr10 | 111011663 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:110964815
|
C | T | 1 | a0001c0005 | 1 | HG01074.hp2 | synonymous_variant | LOW | c.457C>T | p.Leu153Leu | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/9 | 745/3884 | 457/1749 | 153/582 | chr10 | 110964815 | ||
chr10:111004680
|
T | C | 1 | a0001c0003 | 1 | HG00423.hp2 | synonymous_variant | LOW | c.1047T>C | p.Gly349Gly | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/9 | 1335/3884 | 1047/1749 | 349/582 | chr10 | 111004680 | ||
chr10:111009265
|
C | T | 1 | a0001c0004 | 1 | HG02622.hp2 | synonymous_variant | LOW | c.1302C>T | p.Asn434Asn | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 7/9 | 1590/3884 | 1302/1749 | 434/582 | chr10 | 111009265 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:110919648
|
G | T | 1 | a0001c0001t0025 | 1 | NA18522.hp2 | 5_prime_UTR_variant | MODIFIER | c.-244G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/9 | 44711 | chr10 | 110919648 | |||||
chr10:110964157
|
A | G | 1 | a0001c0001t0024 | 1 | NA18959.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-202A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/9 | chr10 | 110964157 | ||||||
chr10:110964171
|
A | G | 1 | a0001c0001t0023 | 1 | HG04204.hp1 | 5_prime_UTR_variant | MODIFIER | c.-188A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/9 | 188 | chr10 | 110964171 | |||||
chr10:110964196
|
T | A | 1 | a0001c0001t0010 | 1 | HG01261.hp1 | 5_prime_UTR_variant | MODIFIER | c.-163T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/9 | 163 | chr10 | 110964196 | |||||
chr10:111011887
|
A | G | 1 | a0001c0001t0022 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*69A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 69 | chr10 | 111011887 | |||||
chr10:111011982
|
T | A | 1 | a0001c0001t0006 | 3 | HG01069.hp2 HG01071.hp1 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*164T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 164 | chr10 | 111011982 | |||||
chr10:111012111
|
G | A | 1 | a0001c0001t0011 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*293G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 293 | chr10 | 111012111 | |||||
chr10:111012319
|
A | G | 1 | a0001c0001t0021 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*501A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 501 | chr10 | 111012319 | |||||
chr10:111012322
|
T | C | 1 | a0001c0001t0012 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*504T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 504 | chr10 | 111012322 | |||||
chr10:111012324
|
T | C | 1 | a0001c0001t0011 | 1 | HG03834.hp2 | 3_prime_UTR_variant | MODIFIER | c.*506T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 506 | chr10 | 111012324 | |||||
chr10:111012341
|
T | C | 1 | a0001c0001t0013 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*523T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 523 | chr10 | 111012341 | |||||
chr10:111012591
|
G | A | 1 | a0001c0001t0014 | 1 | HG02258.hp1 | 3_prime_UTR_variant | MODIFIER | c.*773G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 773 | chr10 | 111012591 | |||||
chr10:111012732
|
G | A | 1 | a0001c0001t0015 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*914G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 914 | chr10 | 111012732 | |||||
chr10:111012842
|
G | T | 1 | a0001c0001t0020 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1024G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1024 | chr10 | 111012842 | |||||
chr10:111012924
|
A | C | 1 | a0001c0001t0019 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1106A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1106 | chr10 | 111012924 | |||||
chr10:111013115
|
G | A | 1 | a0001c0004t0016 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1297G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1297 | chr10 | 111013115 | |||||
chr10:111013141
|
C | T | 1 | a0001c0001t0009 | 2 | HG02698.hp1 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1323C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1323 | chr10 | 111013141 | |||||
chr10:111013303
|
G | GT | 2 | a0001c0001t0009a0001c0001t0018 | 3 | HG02698.hp1 HG04199.hp1 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1486dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1487 | INFO_REALIGN_3_PRIME | chr10 | 111013303 | ||||
chr10:111013304
|
TG | T | 2 | a0001c0001t0004a0001c0005t0004 | 13 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1487delG | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1487 | chr10 | 111013304 | |||||
chr10:111013305
|
G | GT | 2 | a0001c0001t0005a0001c0001t0007 | 8 | HG00738.hp2 HG01978.hp1 HG02135.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1500dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1501 | INFO_REALIGN_3_PRIME | chr10 | 111013305 | ||||
chr10:111013305
|
G | T | 3 | a0001c0001t0008a0001c0001t0009a0001c0001t0018 | 6 | HG01081.hp1 HG02698.hp1 HG02818.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1487G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1487 | chr10 | 111013305 | |||||
chr10:111013305
|
GT | G | 2 | a0001c0001t0003a0002c0002t0003 | 16 | HG01081.hp2 HG01243.hp1 HG02055.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1500delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1500 | INFO_REALIGN_3_PRIME | chr10 | 111013305 | ||||
chr10:111013308
|
T | G | 1 | a0001c0001t0017 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1490T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1490 | chr10 | 111013308 | |||||
chr10:111013321
|
A | G | 3 | a0001c0001t0002a0001c0001t0007a0001c0001t0013 | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1503A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1503 | chr10 | 111013321 | |||||
chr10:111013593
|
T | C | 1 | a0001c0001t0013 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1775T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 9/9 | 1775 | chr10 | 111013593 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr10:110919758
|
C | G | 2 | a0001c0001t0001g0349a0001c0001t0001g0350 | 2 | NA18990.hp1 NA19074.hp2 |
intron_variant | MODIFIER | c.-235+101C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110919758 | ||||||
chr10:110919805
|
C | G | 1 | a0001c0001t0002g0348 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-235+148C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110919805 | ||||||
chr10:110919855
|
T | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(4): Show | 8 | HG00544.hp1 HG00597.hp1 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.-235+198T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110919855 | ||||||
chr10:110919872
|
G | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 14 | HG00140.hp2 HG00639.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-235+215G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110919872 | ||||||
chr10:110919990
|
C | A | 5 | a0001c0001t0001g0008a0001c0001t0001g0047a0001c0001t0001g0049others(2): Show | 6 | HG02165.hp1 NA18966.hp1 NA18967.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+333C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110919990 | ||||||
chr10:110920101
|
G | A | 78 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(75): Show | 88 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.-235+444G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920101 | ||||||
chr10:110920110
|
G | A | 1 | a0001c0001t0001g0051 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.-235+453G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920110 | ||||||
chr10:110920148
|
T | G | 1 | a0001c0001t0001g0052 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.-235+491T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920148 | ||||||
chr10:110920192
|
C | A | 1 | a0001c0001t0001g0053 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-235+535C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920192 | ||||||
chr10:110920241
|
T | C | 1 | a0002c0002t0003g0117 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-235+584T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920241 | ||||||
chr10:110920337
|
G | C | 1 | a0001c0001t0002g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-235+680G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920337 | ||||||
chr10:110920453
|
T | C | 1 | a0001c0001t0002g0119 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-235+796T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920453 | ||||||
chr10:110920485
|
A | G | 5 | a0002c0002t0003g0028a0002c0002t0003g0117a0002c0002t0003g0345others(2): Show | 6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+828A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920485 | ||||||
chr10:110920550
|
C | A | 1 | a0001c0001t0001g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-235+893C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920550 | ||||||
chr10:110920680
|
A | T | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+1023A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920680 | ||||||
chr10:110920924
|
A | G | 1 | a0001c0001t0001g0343 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-235+1267A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920924 | ||||||
chr10:110920960
|
T | G | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-235+1303T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110920960 | ||||||
chr10:110921071
|
C | G | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-235+1414C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921071 | ||||||
chr10:110921192
|
A | G | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-235+1535A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921192 | ||||||
chr10:110921270
|
T | C | 1 | a0001c0001t0001g0054 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.-235+1613T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921270 | ||||||
chr10:110921294
|
G | A | 350 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(347): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.-235+1637G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921294 | ||||||
chr10:110921383
|
A | G | 1 | a0001c0001t0020g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-235+1726A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921383 | ||||||
chr10:110921574
|
T | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+1917T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921574 | ||||||
chr10:110921628
|
T | G | 1 | a0001c0001t0001g0055 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-235+1971T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921628 | ||||||
chr10:110921717
|
A | G | 3 | a0001c0001t0001g0026a0001c0001t0001g0329a0001c0001t0001g0330 | 4 | HG02027.hp1 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-235+2060A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921717 | ||||||
chr10:110921804
|
C | T | 1 | a0001c0001t0001g0328 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.-235+2147C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921804 | ||||||
chr10:110921809
|
T | A | 13 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(10): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-235+2152T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921809 | ||||||
chr10:110921852
|
A | G | 1 | a0001c0001t0001g0116 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.-235+2195A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921852 | ||||||
chr10:110921973
|
T | A | 1 | a0001c0001t0001g0131 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-235+2316T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110921973 | ||||||
chr10:110922002
|
A | G | 2 | a0001c0001t0001g0327a0001c0001t0022g0326 | 2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.-235+2345A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922002 | ||||||
chr10:110922129
|
T | C | 1 | a0001c0001t0003g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-235+2472T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922129 | ||||||
chr10:110922166
|
G | A | 1 | a0001c0001t0002g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.-235+2509G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922166 | ||||||
chr10:110922246
|
A | G | 4 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG02074.hp1 HG02165.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-235+2589A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922246 | ||||||
chr10:110922309
|
C | T | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+2652C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922309 | ||||||
chr10:110922343
|
G | T | 1 | a0001c0001t0001g0320 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-235+2686G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922343 | ||||||
chr10:110922452
|
C | CTG | 327 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(324): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-235+2796_-235+279 others(6): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110922452 | |||||
chr10:110922468
|
T | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+2811T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922468 | ||||||
chr10:110922499
|
T | G | 14 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-235+2842T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922499 | ||||||
chr10:110922669
|
A | T | 1 | a0001c0003t0001g0302 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-235+3012A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922669 | ||||||
chr10:110922753
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+3096G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922753 | ||||||
chr10:110922858
|
T | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0114a0001c0001t0001g0120others(19): Show | 23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-235+3201T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922858 | ||||||
chr10:110922959
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+3302G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110922959 | ||||||
chr10:110923325
|
C | A | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-235+3668C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110923325 | ||||||
chr10:110923359
|
A | G | 1 | a0001c0001t0002g0301 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.-235+3702A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110923359 | ||||||
chr10:110923404
|
T | C | 1 | a0001c0001t0001g0056 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.-235+3747T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110923404 | ||||||
chr10:110923650
|
A | G | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG02647.hp2 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-235+3993A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110923650 | ||||||
chr10:110923685
|
GAA | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-235+4030_-235+403 others(6): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110923685 | |||||
chr10:110923702
|
G | A | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-235+4045G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110923702 | ||||||
chr10:110923875
|
T | C | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-235+4218T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110923875 | ||||||
chr10:110924110
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-235+4453A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924110 | ||||||
chr10:110924150
|
A | G | 7 | a0001c0001t0003g0015a0001c0001t0003g0125a0001c0001t0003g0126others(4): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-235+4493A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924150 | ||||||
chr10:110924236
|
G | A | 3 | a0001c0001t0004g0333a0001c0001t0004g0334a0001c0001t0004g0335 | 3 | HG01168.hp1 HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-235+4579G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924236 | ||||||
chr10:110924262
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-235+4605C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924262 | ||||||
chr10:110924297
|
C | T | 1 | a0001c0001t0001g0327 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-235+4640C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924297 | ||||||
chr10:110924329
|
A | G | 13 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(10): Show | 13 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-235+4672A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924329 | ||||||
chr10:110924570
|
C | A | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+4913C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924570 | ||||||
chr10:110924585
|
T | G | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+4928T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924585 | ||||||
chr10:110924775
|
A | G | 17 | a0001c0001t0001g0025a0001c0001t0001g0120a0001c0001t0001g0306others(14): Show | 18 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.-235+5118A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924775 | ||||||
chr10:110924795
|
C | A | 1 | a0001c0001t0001g0236 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-235+5138C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924795 | ||||||
chr10:110924840
|
C | T | 7 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 8 | HG00140.hp2 HG00639.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.-235+5183C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924840 | ||||||
chr10:110924841
|
G | A | 1 | a0001c0001t0014g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-235+5184G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924841 | ||||||
chr10:110924890
|
C | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0114a0001c0001t0001g0120others(19): Show | 23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-235+5233C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924890 | ||||||
chr10:110924996
|
G | A | 5 | a0002c0002t0003g0028a0002c0002t0003g0117a0002c0002t0003g0345others(2): Show | 6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+5339G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110924996 | ||||||
chr10:110925070
|
C | CA | 141 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(138): Show | 157 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(154): Show |
intron_variant | MODIFIER | c.-235+5435dupA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110925070 | |||||
chr10:110925070
|
C | CAA | 28 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(25): Show | 29 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(26): Show |
intron_variant | MODIFIER | c.-235+5434_-235+543 others(6): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110925070 | |||||
chr10:110925070
|
CA | C | 20 | a0001c0001t0001g0145a0001c0001t0001g0319a0001c0001t0002g0231others(17): Show | 21 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.-235+5435delA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110925070 | |||||
chr10:110925087
|
A | T | 1 | a0001c0001t0001g0235 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-235+5430A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925087 | ||||||
chr10:110925089
|
AAAATT | A | 20 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0035others(17): Show | 22 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(19): Show |
intron_variant | MODIFIER | c.-235+5436_-235+544 others(9): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110925089 | |||||
chr10:110925094
|
T | A | 1 | a0001c0001t0001g0235 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-235+5437T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925094 | ||||||
chr10:110925098
|
A | T | 1 | a0001c0001t0001g0113 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-235+5441A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925098 | ||||||
chr10:110925115
|
A | G | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+5458A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925115 | ||||||
chr10:110925390
|
A | G | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-235+5733A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925390 | ||||||
chr10:110925449
|
T | G | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-235+5792T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925449 | ||||||
chr10:110925523
|
T | C | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-235+5866T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925523 | ||||||
chr10:110925526
|
G | T | 4 | a0001c0001t0001g0322a0001c0001t0001g0323a0001c0001t0001g0324others(1): Show | 4 | HG02074.hp1 HG02165.hp2 NA19007.hp2 others(1): Show |
intron_variant | MODIFIER | c.-235+5869G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925526 | ||||||
chr10:110925572
|
T | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-235+5915T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925572 | ||||||
chr10:110925573
|
T | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.-235+5916T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925573 | ||||||
chr10:110925656
|
C | T | 192 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(189): Show | 212 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(209): Show |
intron_variant | MODIFIER | c.-235+5999C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925656 | ||||||
chr10:110925942
|
G | A | 10 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0166others(7): Show | 14 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.-235+6285G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925942 | ||||||
chr10:110925960
|
T | G | 3 | a0001c0001t0004g0333a0001c0001t0004g0334a0001c0001t0004g0335 | 3 | HG01168.hp1 HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.-235+6303T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110925960 | ||||||
chr10:110926563
|
C | T | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+6906C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926563 | ||||||
chr10:110926565
|
C | T | 116 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.-235+6908C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926565 | ||||||
chr10:110926634
|
C | T | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-235+6977C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926634 | ||||||
chr10:110926676
|
A | G | 1 | a0001c0001t0005g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-235+7019A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926676 | ||||||
chr10:110926710
|
G | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+7053G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926710 | ||||||
chr10:110926763
|
C | A | 5 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(2): Show | 5 | NA18951.hp1 NA18959.hp2 NA18977.hp2 others(2): Show |
intron_variant | MODIFIER | c.-235+7106C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926763 | ||||||
chr10:110926765
|
A | G | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG01175.hp2 HG01978.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.-235+7108A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926765 | ||||||
chr10:110926955
|
A | G | 23 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(20): Show | 25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.-235+7298A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926955 | ||||||
chr10:110926976
|
G | A | 4 | a0001c0001t0001g0055a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-235+7319G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110926976 | ||||||
chr10:110927118
|
A | G | 102 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(99): Show | 110 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(107): Show |
intron_variant | MODIFIER | c.-235+7461A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927118 | ||||||
chr10:110927313
|
C | A | 13 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(10): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-235+7656C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927313 | ||||||
chr10:110927325
|
A | G | 14 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-235+7668A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927325 | ||||||
chr10:110927766
|
C | G | 1 | a0001c0001t0002g0227 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-235+8109C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927766 | ||||||
chr10:110927768
|
A | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+8111A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927768 | ||||||
chr10:110927908
|
T | C | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-235+8251T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927908 | ||||||
chr10:110927971
|
A | G | 2 | a0001c0001t0006g0247a0001c0001t0013g0226 | 2 | HG01069.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-235+8314A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110927971 | ||||||
chr10:110928087
|
C | T | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-235+8430C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928087 | ||||||
chr10:110928155
|
A | G | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-235+8498A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928155 | ||||||
chr10:110928319
|
C | T | 81 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(78): Show | 93 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(90): Show |
intron_variant | MODIFIER | c.-235+8662C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928319 | ||||||
chr10:110928578
|
A | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+8921A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928578 | ||||||
chr10:110928766
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-235+9109G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928766 | ||||||
chr10:110928825
|
G | A | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+9168G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928825 | ||||||
chr10:110928851
|
T | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+9194T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928851 | ||||||
chr10:110928911
|
A | T | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+9254A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110928911 | ||||||
chr10:110929273
|
T | A | 7 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0155others(4): Show | 9 | HG01261.hp1 HG02027.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.-235+9616T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929273 | ||||||
chr10:110929545
|
A | G | 23 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(20): Show | 25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.-235+9888A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929545 | ||||||
chr10:110929614
|
T | G | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-235+9957T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929614 | ||||||
chr10:110929864
|
A | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+10207A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929864 | ||||||
chr10:110929894
|
G | A | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-235+10237G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929894 | ||||||
chr10:110929931
|
C | T | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+10274C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929931 | ||||||
chr10:110929973
|
T | G | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-235+10316T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110929973 | ||||||
chr10:110930052
|
TATATG | T | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-235+10397_-235+10 others(11): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110930052 | |||||
chr10:110930189
|
A | G | 1 | a0001c0001t0001g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-235+10532A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930189 | ||||||
chr10:110930224
|
T | G | 5 | a0002c0002t0003g0028a0002c0002t0003g0117a0002c0002t0003g0345others(2): Show | 6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+10567T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930224 | ||||||
chr10:110930409
|
T | A | 1 | a0001c0001t0001g0066 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.-235+10752T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930409 | ||||||
chr10:110930497
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-235+10840C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930497 | ||||||
chr10:110930593
|
A | T | 1 | a0001c0001t0001g0320 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-235+10936A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930593 | ||||||
chr10:110930611
|
T | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+10954T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930611 | ||||||
chr10:110930621
|
A | C | 9 | a0001c0001t0001g0246a0001c0001t0001g0290a0001c0001t0001g0291others(6): Show | 9 | HG02071.hp1 NA18942.hp2 NA18952.hp1 others(6): Show |
intron_variant | MODIFIER | c.-235+10964A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930621 | ||||||
chr10:110930735
|
C | CTT | 13 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(10): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-235+11092_-235+11 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110930735 | |||||
chr10:110930735
|
C | CTTTTTTT others(1): Show |
6 | a0001c0001t0001g0005a0001c0001t0001g0238a0001c0001t0001g0248others(3): Show | 8 | HG00140.hp1 HG00642.hp2 HG01243.hp2 others(5): Show |
intron_variant | MODIFIER | c.-235+11086_-235+11 others(14): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110930735 | |||||
chr10:110930735
|
C | CTTTTTTT others(2): Show |
105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 117 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(114): Show |
intron_variant | MODIFIER | c.-235+11085_-235+11 others(15): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110930735 | |||||
chr10:110930735
|
C | CTTTTTTT others(3): Show |
139 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0011others(136): Show | 153 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(150): Show |
intron_variant | MODIFIER | c.-235+11084_-235+11 others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110930735 | |||||
chr10:110930735
|
C | CTTTTTTT others(4): Show |
21 | a0001c0001t0001g0054a0001c0001t0001g0062a0001c0001t0001g0064others(18): Show | 21 | HG00642.hp1 HG00673.hp1 HG01069.hp1 others(18): Show |
intron_variant | MODIFIER | c.-235+11083_-235+11 others(17): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110930735 | |||||
chr10:110930764
|
T | C | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+11107T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930764 | ||||||
chr10:110930891
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-235+11234G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110930891 | ||||||
chr10:110931127
|
C | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+11470C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931127 | ||||||
chr10:110931202
|
G | C | 1 | a0001c0001t0001g0252 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.-235+11545G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931202 | ||||||
chr10:110931252
|
G | A | 1 | a0001c0001t0008g0224 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-235+11595G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931252 | ||||||
chr10:110931290
|
A | G | 2 | a0001c0001t0004g0027a0001c0001t0004g0341 | 3 | HG01884.hp1 HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-235+11633A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931290 | ||||||
chr10:110931389
|
C | G | 286 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(283): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-235+11732C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931389 | ||||||
chr10:110931411
|
T | C | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+11754T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931411 | ||||||
chr10:110931744
|
GTTAT | G | 12 | a0001c0001t0004g0027a0001c0001t0004g0225a0001c0001t0004g0333others(9): Show | 13 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-235+12092_-235+12 others(10): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110931744 | |||||
chr10:110931830
|
G | T | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-235+12173G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931830 | ||||||
chr10:110931845
|
T | G | 1 | a0001c0001t0001g0307 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-235+12188T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931845 | ||||||
chr10:110931852
|
C | G | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-235+12195C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931852 | ||||||
chr10:110931889
|
G | A | 1 | a0001c0001t0002g0348 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-235+12232G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931889 | ||||||
chr10:110931937
|
T | C | 101 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-235+12280T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931937 | ||||||
chr10:110931995
|
A | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+12338A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110931995 | ||||||
chr10:110932051
|
C | T | 4 | a0001c0001t0001g0282a0001c0001t0001g0283a0001c0001t0001g0285others(1): Show | 4 | HG01081.hp2 HG01496.hp1 HG03654.hp1 others(1): Show |
intron_variant | MODIFIER | c.-235+12394C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932051 | ||||||
chr10:110932104
|
A | G | 105 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(102): Show | 117 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.-235+12447A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932104 | ||||||
chr10:110932307
|
T | C | 7 | a0001c0001t0003g0015a0001c0001t0003g0125a0001c0001t0003g0126others(4): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-235+12650T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932307 | ||||||
chr10:110932493
|
A | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+12836A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932493 | ||||||
chr10:110932618
|
C | A | 14 | a0001c0001t0001g0342a0001c0001t0003g0015a0001c0001t0003g0124others(11): Show | 16 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.-235+12961C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932618 | ||||||
chr10:110932622
|
T | G | 1 | a0001c0001t0001g0308 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-235+12965T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932622 | ||||||
chr10:110932689
|
A | G | 1 | a0001c0005t0004g0340 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.-235+13032A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932689 | ||||||
chr10:110932692
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-235+13035G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932692 | ||||||
chr10:110932702
|
G | T | 1 | a0001c0001t0005g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-235+13045G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932702 | ||||||
chr10:110932728
|
A | C | 24 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(21): Show | 26 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(23): Show |
intron_variant | MODIFIER | c.-235+13071A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932728 | ||||||
chr10:110932729
|
C | G | 1 | a0001c0001t0001g0235 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-235+13072C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932729 | ||||||
chr10:110932820
|
A | G | 3 | a0001c0001t0001g0014a0001c0001t0001g0024a0001c0001t0001g0106 | 5 | HG00642.hp1 HG01168.hp2 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.-235+13163A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932820 | ||||||
chr10:110932866
|
C | A | 12 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(9): Show | 12 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.-235+13209C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932866 | ||||||
chr10:110932907
|
G | T | 23 | a0001c0001t0001g0008a0001c0001t0001g0013a0001c0001t0001g0014others(20): Show | 26 | HG00408.hp2 HG00642.hp1 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.-235+13250G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932907 | ||||||
chr10:110932985
|
C | T | 1 | a0001c0001t0005g0281 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.-235+13328C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110932985 | ||||||
chr10:110933044
|
G | A | 78 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(75): Show | 88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-235+13387G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933044 | ||||||
chr10:110933135
|
G | T | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+13478G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933135 | ||||||
chr10:110933216
|
G | A | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+13559G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933216 | ||||||
chr10:110933217
|
CT | C | 5 | a0002c0002t0003g0028a0002c0002t0003g0117a0002c0002t0003g0345others(2): Show | 6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+13567delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110933217 | |||||
chr10:110933470
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.-235+13813G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933470 | ||||||
chr10:110933570
|
T | C | 1 | a0001c0001t0002g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-235+13913T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933570 | ||||||
chr10:110933822
|
A | G | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-235+14165A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933822 | ||||||
chr10:110933847
|
C | T | 13 | a0001c0001t0001g0133a0001c0001t0001g0135a0001c0001t0001g0136others(10): Show | 13 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-235+14190C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110933847 | ||||||
chr10:110933868
|
A | AT | 11 | a0001c0001t0001g0061a0001c0001t0002g0021a0001c0001t0002g0022others(8): Show | 13 | HG00408.hp2 HG02015.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-235+14221dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110933868 | |||||
chr10:110934272
|
A | G | 99 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(96): Show | 108 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.-235+14615A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934272 | ||||||
chr10:110934367
|
A | G | 2 | a0001c0001t0001g0062a0001c0001t0001g0095 | 2 | HG00544.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.-235+14710A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934367 | ||||||
chr10:110934448
|
G | T | 1 | a0001c0001t0007g0211 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-235+14791G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934448 | ||||||
chr10:110934551
|
A | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0280a0001c0001t0021g0023 | 3 | HG01884.hp2 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-235+14894A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934551 | ||||||
chr10:110934558
|
G | T | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+14901G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934558 | ||||||
chr10:110934584
|
G | A | 327 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(324): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.-235+14927G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934584 | ||||||
chr10:110934662
|
C | G | 1 | a0001c0001t0001g0104 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-235+15005C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110934662 | ||||||
chr10:110935100
|
A | G | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+15443A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110935100 | ||||||
chr10:110935267
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.-235+15610A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110935267 | ||||||
chr10:110935272
|
C | A | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+15615C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110935272 | ||||||
chr10:110935514
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-235+15857G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110935514 | ||||||
chr10:110935915
|
TG | T | 4 | a0001c0001t0001g0055a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.-235+16260delG | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110935915 | |||||
chr10:110936085
|
T | G | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+16428T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936085 | ||||||
chr10:110936095
|
A | AT | 37 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0094others(34): Show | 40 | HG01074.hp2 HG01168.hp1 HG01175.hp2 others(37): Show |
intron_variant | MODIFIER | c.-235+16456dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936095 | |||||
chr10:110936095
|
AT | A | 7 | a0001c0001t0001g0037a0001c0001t0001g0071a0001c0001t0001g0072others(4): Show | 7 | HG02922.hp1 HG03041.hp2 NA18939.hp2 others(4): Show |
intron_variant | MODIFIER | c.-235+16456delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936095 | |||||
chr10:110936135
|
C | T | 1 | a0001c0001t0007g0211 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.-235+16478C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936135 | ||||||
chr10:110936158
|
G | A | 78 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(75): Show | 88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-235+16501G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936158 | ||||||
chr10:110936172
|
C | T | 2 | a0001c0001t0002g0209a0001c0001t0007g0210 | 2 | HG01943.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.-235+16515C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936172 | ||||||
chr10:110936212
|
T | G | 2 | a0001c0001t0002g0174a0001c0001t0002g0175 | 2 | NA19055.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-235+16555T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936212 | ||||||
chr10:110936286
|
T | C | 2 | a0001c0001t0001g0011a0001c0001t0019g0073 | 3 | HG00423.hp1 NA18998.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.-235+16629T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936286 | ||||||
chr10:110936381
|
G | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-235+16724G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936381 | ||||||
chr10:110936414
|
T | C | 5 | a0002c0002t0003g0028a0002c0002t0003g0117a0002c0002t0003g0345others(2): Show | 6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+16757T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936414 | ||||||
chr10:110936423
|
A | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+16766A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936423 | ||||||
chr10:110936430
|
C | A | 1 | a0001c0001t0020g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-235+16773C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936430 | ||||||
chr10:110936458
|
A | G | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+16801A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936458 | ||||||
chr10:110936494
|
T | A | 22 | a0001c0001t0001g0025a0001c0001t0001g0114a0001c0001t0001g0120others(19): Show | 23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-235+16837T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936494 | ||||||
chr10:110936527
|
A | T | 1 | a0001c0001t0002g0208 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.-235+16870A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936527 | ||||||
chr10:110936589
|
C | CTTT | 8 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(5): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-235+16945_-235+16 others(9): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | |||||
chr10:110936589
|
C | CTTTT | 6 | a0001c0001t0001g0075a0002c0002t0003g0028a0002c0002t0003g0117others(3): Show | 7 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.-235+16944_-235+16 others(10): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | |||||
chr10:110936589
|
C | CTTTTTTT others(4): Show |
1 | a0001c0001t0001g0074 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.-235+16939_-235+16 others(17): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | |||||
chr10:110936589
|
C | CTTTTTTT others(2): Show |
6 | a0001c0001t0001g0041a0001c0001t0002g0166a0001c0001t0002g0176others(3): Show | 6 | HG01943.hp1 HG02976.hp2 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+16939_-235+16 others(15): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | |||||
chr10:110936589
|
C | CTTTTTTT others(3): Show |
86 | a0001c0001t0001g0053a0001c0001t0001g0068a0001c0001t0001g0071others(83): Show | 96 | HG00099.hp1 HG00558.hp1 HG00597.hp2 others(93): Show |
intron_variant | MODIFIER | c.-235+16938_-235+16 others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | |||||
chr10:110936589
|
C | CTTTTTTT others(4): Show |
151 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(148): Show | 168 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(165): Show |
intron_variant | MODIFIER | c.-235+16937_-235+16 others(17): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | |||||
chr10:110936589
|
C | CTTTTTTT others(5): Show |
22 | a0001c0001t0001g0008a0001c0001t0001g0060a0001c0001t0001g0064others(19): Show | 23 | HG00558.hp2 HG00738.hp2 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.-235+16936_-235+16 others(18): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | |||||
chr10:110936589
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0049 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.-235+16935_-235+16 others(19): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | |||||
chr10:110936589
|
C | CTTTTTTT others(9): Show |
1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-235+16947_-235+16 others(22): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | |||||
chr10:110936589
|
CT | C | 36 | a0001c0001t0001g0025a0001c0001t0001g0114a0001c0001t0001g0120others(33): Show | 38 | HG00438.hp2 HG00621.hp1 HG01074.hp2 others(35): Show |
intron_variant | MODIFIER | c.-235+16947delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110936589 | |||||
chr10:110936604
|
T | TTTTTTTT others(3): Show |
1 | a0001c0001t0001g0030 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-235+16947_-235+16 others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936604 | ||||||
chr10:110936604
|
T | TTTTTTTT others(4): Show |
5 | a0001c0001t0001g0006a0001c0001t0001g0031a0001c0001t0001g0032others(2): Show | 6 | HG00544.hp1 HG00597.hp1 HG02083.hp2 others(3): Show |
intron_variant | MODIFIER | c.-235+16947_-235+16 others(17): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936604 | ||||||
chr10:110936611
|
C | T | 1 | a0001c0001t0020g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-235+16954C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936611 | ||||||
chr10:110936876
|
C | G | 1 | a0001c0001t0002g0232 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-235+17219C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936876 | ||||||
chr10:110936885
|
G | T | 1 | a0001c0001t0001g0034 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.-235+17228G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936885 | ||||||
chr10:110936954
|
G | C | 8 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(5): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.-235+17297G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936954 | ||||||
chr10:110936966
|
G | A | 1 | a0001c0003t0001g0302 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.-235+17309G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936966 | ||||||
chr10:110936983
|
A | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+17326A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110936983 | ||||||
chr10:110937030
|
T | A | 1 | a0001c0001t0001g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-235+17373T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937030 | ||||||
chr10:110937036
|
A | C | 1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-235+17379A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937036 | ||||||
chr10:110937123
|
G | A | 1 | a0001c0001t0020g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-235+17466G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937123 | ||||||
chr10:110937259
|
CT | C | 5 | a0001c0001t0001g0024a0001c0001t0001g0259a0001c0001t0001g0260others(2): Show | 6 | NA18949.hp2 NA18973.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+17615delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110937259 | |||||
chr10:110937279
|
A | G | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+17622A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937279 | ||||||
chr10:110937483
|
C | T | 289 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(286): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.-235+17826C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937483 | ||||||
chr10:110937556
|
C | T | 23 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(20): Show | 25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.-235+17899C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937556 | ||||||
chr10:110937751
|
G | T | 328 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(325): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.-235+18094G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937751 | ||||||
chr10:110937831
|
A | G | 350 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(347): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.-235+18174A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937831 | ||||||
chr10:110937998
|
C | T | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-235+18341C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110937998 | ||||||
chr10:110938298
|
T | A | 1 | a0001c0001t0014g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-235+18641T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110938298 | ||||||
chr10:110938396
|
T | C | 1 | a0001c0001t0001g0289 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.-235+18739T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110938396 | ||||||
chr10:110938604
|
A | C | 1 | a0001c0001t0011g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-235+18947A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110938604 | ||||||
chr10:110938824
|
A | G | 117 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.-235+19167A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110938824 | ||||||
chr10:110938881
|
C | T | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-235+19224C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110938881 | ||||||
chr10:110939097
|
C | T | 1 | a0001c0001t0001g0280 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-235+19440C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939097 | ||||||
chr10:110939104
|
T | C | 78 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(75): Show | 88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-235+19447T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939104 | ||||||
chr10:110939216
|
A | G | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-235+19559A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939216 | ||||||
chr10:110939570
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0261 | 2 | HG00639.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.-235+19913G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939570 | ||||||
chr10:110939597
|
G | A | 2 | a0001c0001t0001g0329a0001c0001t0001g0330 | 2 | HG02027.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.-235+19940G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939597 | ||||||
chr10:110939609
|
C | T | 2 | a0001c0001t0004g0344a0001c0001t0018g0162 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-235+19952C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939609 | ||||||
chr10:110939636
|
A | G | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(285): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.-235+19979A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939636 | ||||||
chr10:110939638
|
C | T | 1 | a0001c0001t0002g0164 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-235+19981C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939638 | ||||||
chr10:110939661
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.-235+20004A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939661 | ||||||
chr10:110939827
|
A | G | 1 | a0001c0001t0001g0306 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.-235+20170A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110939827 | ||||||
chr10:110940152
|
A | T | 1 | a0001c0001t0001g0250 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-235+20495A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940152 | ||||||
chr10:110940221
|
T | G | 328 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(325): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.-235+20564T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940221 | ||||||
chr10:110940262
|
T | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+20605T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940262 | ||||||
chr10:110940289
|
C | A | 1 | a0001c0001t0001g0322 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.-235+20632C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940289 | ||||||
chr10:110940349
|
C | G | 1 | a0001c0001t0001g0261 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.-235+20692C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940349 | ||||||
chr10:110940403
|
G | T | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-235+20746G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940403 | ||||||
chr10:110940538
|
C | G | 1 | a0001c0001t0002g0206 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.-235+20881C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940538 | ||||||
chr10:110940539
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-235+20882A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940539 | ||||||
chr10:110940910
|
G | GTTTTTTT others(3): Show |
3 | a0001c0001t0001g0316a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | NA18980.hp2 NA18986.hp1 NA19066.hp2 |
intron_variant | MODIFIER | c.-235+21282_-235+21 others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
G | GTTTTTTT others(4): Show |
1 | a0001c0001t0001g0308 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-235+21281_-235+21 others(17): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
G | GTTTTTTT others(9): Show |
1 | a0001c0001t0001g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-235+21276_-235+21 others(22): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
G | GTTTTTTT others(15): Show |
1 | a0001c0001t0001g0343 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-235+21270_-235+21 others(28): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
GTTTTTTT others(4): Show |
G | 6 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0001g0161others(3): Show | 6 | HG02258.hp1 HG02683.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+21281_-235+21 others(17): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
GTTTTTTT others(5): Show |
G | 18 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(15): Show | 20 | HG01081.hp1 HG01175.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-235+21280_-235+21 others(18): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
GTTTTTTT others(6): Show |
G | 4 | a0001c0001t0001g0153a0001c0001t0004g0225a0001c0001t0008g0224others(1): Show | 4 | HG03139.hp1 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-235+21279_-235+21 others(19): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
GTTTTTTT others(7): Show |
G | 2 | a0001c0001t0004g0335a0001c0001t0025g0121 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-235+21278_-235+21 others(20): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
GTTTTTTT others(8): Show |
G | 9 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(6): Show | 10 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-235+21277_-235+21 others(21): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
GTTTTTTT others(9): Show |
G | 1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-235+21276_-235+21 others(22): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
GTTTTTTT others(10): Show |
G | 8 | a0001c0001t0002g0022a0001c0001t0002g0164a0001c0001t0002g0202others(5): Show | 9 | HG00597.hp2 HG02300.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.-235+21275_-235+21 others(23): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
GTTTTTTT others(11): Show |
G | 77 | a0001c0001t0001g0039a0001c0001t0001g0069a0001c0001t0001g0091others(74): Show | 86 | HG00558.hp1 HG00609.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.-235+21274_-235+21 others(24): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
GTTTTTTT others(12): Show |
G | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(196): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.-235+21273_-235+21 others(25): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
GTTTTTTT others(13): Show |
G | 1 | a0001c0001t0003g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-235+21272_-235+21 others(26): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940910
|
GTTTTTTT others(15): Show |
G | 1 | a0001c0001t0001g0309 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-235+21270_-235+21 others(28): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110940910 | |||||
chr10:110940919
|
T | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+21262T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940919 | ||||||
chr10:110940922
|
T | G | 6 | a0001c0001t0001g0148a0001c0001t0001g0158a0001c0001t0001g0161others(3): Show | 6 | HG02258.hp1 HG02683.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-235+21265T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940922 | ||||||
chr10:110940923
|
T | G | 18 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(15): Show | 20 | HG01081.hp1 HG01175.hp2 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.-235+21266T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940923 | ||||||
chr10:110940924
|
T | G | 4 | a0001c0001t0001g0153a0001c0001t0004g0225a0001c0001t0008g0224others(1): Show | 4 | HG03139.hp1 HG03225.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.-235+21267T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940924 | ||||||
chr10:110940925
|
T | G | 2 | a0001c0001t0004g0335a0001c0001t0025g0121 | 2 | HG02486.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-235+21268T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940925 | ||||||
chr10:110940926
|
T | G | 9 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(6): Show | 10 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.-235+21269T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940926 | ||||||
chr10:110940927
|
T | G | 1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-235+21270T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940927 | ||||||
chr10:110940928
|
T | G | 8 | a0001c0001t0002g0022a0001c0001t0002g0164a0001c0001t0002g0202others(5): Show | 9 | HG00597.hp2 HG02300.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.-235+21271T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940928 | ||||||
chr10:110940929
|
T | G | 77 | a0001c0001t0001g0039a0001c0001t0001g0069a0001c0001t0001g0091others(74): Show | 86 | HG00558.hp1 HG00609.hp2 HG00673.hp1 others(83): Show |
intron_variant | MODIFIER | c.-235+21272T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940929 | ||||||
chr10:110940930
|
T | G | 199 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(196): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.-235+21273T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940930 | ||||||
chr10:110940931
|
T | G | 1 | a0001c0001t0003g0284 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.-235+21274T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940931 | ||||||
chr10:110940934
|
T | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+21277T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940934 | ||||||
chr10:110940937
|
T | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-235+21280T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940937 | ||||||
chr10:110940947
|
T | C | 1 | a0001c0001t0001g0055 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.-235+21290T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110940947 | ||||||
chr10:110941072
|
C | A | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-235+21415C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941072 | ||||||
chr10:110941122
|
A | G | 100 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-235+21465A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941122 | ||||||
chr10:110941129
|
C | T | 100 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-235+21472C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941129 | ||||||
chr10:110941190
|
T | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-235+21533T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941190 | ||||||
chr10:110941262
|
A | C | 1 | a0001c0001t0001g0300 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-235+21605A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941262 | ||||||
chr10:110941417
|
C | T | 100 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(97): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-235+21760C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941417 | ||||||
chr10:110941472
|
C | A | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0138 | 3 | HG02809.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-235+21815C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941472 | ||||||
chr10:110941488
|
T | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-235+21831T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941488 | ||||||
chr10:110941552
|
G | A | 10 | a0001c0001t0001g0009a0001c0001t0001g0057a0001c0001t0001g0067others(7): Show | 11 | HG01346.hp1 HG02109.hp2 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.-235+21895G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941552 | ||||||
chr10:110941556
|
TC | T | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-235+21901delC | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110941556 | |||||
chr10:110941596
|
T | G | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-235+21939T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941596 | ||||||
chr10:110941608
|
C | T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.-235+21951C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941608 | ||||||
chr10:110941751
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-235+22094G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941751 | ||||||
chr10:110941824
|
T | G | 13 | a0001c0001t0004g0027a0001c0001t0004g0225a0001c0001t0004g0333others(10): Show | 14 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.-235+22167T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941824 | ||||||
chr10:110941951
|
A | G | 1 | a0001c0001t0001g0308 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.-234-22174A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110941951 | ||||||
chr10:110942086
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-234-22039G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942086 | ||||||
chr10:110942124
|
T | C | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-22001T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942124 | ||||||
chr10:110942131
|
T | TCTGGAAA others(3): Show |
289 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(286): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.-234-21990_-234-21 others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110942131 | |||||
chr10:110942615
|
T | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-21510T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942615 | ||||||
chr10:110942670
|
G | A | 1 | a0001c0001t0001g0319 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.-234-21455G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942670 | ||||||
chr10:110942680
|
A | G | 22 | a0001c0001t0001g0025a0001c0001t0001g0114a0001c0001t0001g0120others(19): Show | 23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-234-21445A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942680 | ||||||
chr10:110942689
|
T | C | 1 | a0001c0001t0001g0014 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.-234-21436T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942689 | ||||||
chr10:110942818
|
T | A | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG02647.hp2 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.-234-21307T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110942818 | ||||||
chr10:110943066
|
C | T | 1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-234-21059C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943066 | ||||||
chr10:110943179
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-234-20946G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943179 | ||||||
chr10:110943197
|
A | G | 1 | a0001c0001t0002g0118 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.-234-20928A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943197 | ||||||
chr10:110943230
|
C | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-20895C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943230 | ||||||
chr10:110943240
|
G | A | 1 | a0001c0001t0001g0254 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-234-20885G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943240 | ||||||
chr10:110943257
|
CT | C | 12 | a0001c0001t0004g0027a0001c0001t0004g0225a0001c0001t0004g0333others(9): Show | 13 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-234-20855delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110943257 | |||||
chr10:110943687
|
G | T | 1 | a0001c0001t0001g0112 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-234-20438G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943687 | ||||||
chr10:110943785
|
C | T | 117 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.-234-20340C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943785 | ||||||
chr10:110943807
|
G | A | 1 | a0001c0001t0002g0212 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.-234-20318G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943807 | ||||||
chr10:110943903
|
C | A | 1 | a0001c0001t0002g0019 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.-234-20222C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943903 | ||||||
chr10:110943981
|
C | T | 1 | a0001c0001t0001g0295 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-234-20144C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110943981 | ||||||
chr10:110944120
|
T | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-20005T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944120 | ||||||
chr10:110944173
|
C | T | 78 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(75): Show | 88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.-234-19952C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944173 | ||||||
chr10:110944293
|
T | A | 1 | a0001c0001t0001g0286 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.-234-19832T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944293 | ||||||
chr10:110944384
|
C | CA | 317 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(314): Show | 351 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(348): Show |
intron_variant | MODIFIER | c.-234-19725dupA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110944384 | |||||
chr10:110944384
|
C | CAA | 6 | a0001c0001t0001g0094a0001c0001t0001g0290a0001c0001t0002g0202others(3): Show | 6 | HG02055.hp2 HG04199.hp2 NA18959.hp1 others(3): Show |
intron_variant | MODIFIER | c.-234-19726_-234-19 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110944384 | |||||
chr10:110944420
|
A | G | 5 | a0001c0001t0002g0019a0001c0001t0002g0118a0001c0001t0002g0200others(2): Show | 6 | HG01069.hp1 HG01071.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-234-19705A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944420 | ||||||
chr10:110944576
|
G | A | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-234-19549G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944576 | ||||||
chr10:110944622
|
T | C | 286 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(283): Show | 317 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(314): Show |
intron_variant | MODIFIER | c.-234-19503T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944622 | ||||||
chr10:110944982
|
G | A | 98 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(95): Show | 106 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.-234-19143G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110944982 | ||||||
chr10:110945147
|
T | C | 40 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-234-18978T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945147 | ||||||
chr10:110945203
|
C | T | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-234-18922C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945203 | ||||||
chr10:110945204
|
G | A | 2 | a0001c0001t0004g0027a0001c0001t0004g0341 | 3 | HG01884.hp1 HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.-234-18921G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945204 | ||||||
chr10:110945238
|
T | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0114a0001c0001t0001g0120others(19): Show | 23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-234-18887T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945238 | ||||||
chr10:110945263
|
T | A | 1 | a0001c0001t0001g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.-234-18862T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945263 | ||||||
chr10:110945353
|
A | G | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-18772A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945353 | ||||||
chr10:110945430
|
A | C | 1 | a0001c0001t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-234-18695A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945430 | ||||||
chr10:110945605
|
T | G | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-234-18520T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945605 | ||||||
chr10:110945606
|
C | T | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.-234-18519C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945606 | ||||||
chr10:110945624
|
T | G | 1 | a0001c0001t0001g0235 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-234-18501T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945624 | ||||||
chr10:110945913
|
T | TG | 3 | a0001c0001t0001g0054a0001c0001t0001g0072a0001c0001t0001g0090 | 3 | NA18939.hp2 NA18956.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.-234-18211dupG | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110945913 | |||||
chr10:110945940
|
C | T | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-18185C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110945940 | ||||||
chr10:110946056
|
T | C | 1 | a0001c0001t0001g0259 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.-234-18069T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946056 | ||||||
chr10:110946128
|
A | G | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-234-17997A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946128 | ||||||
chr10:110946265
|
T | A | 1 | a0001c0001t0002g0234 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.-234-17860T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946265 | ||||||
chr10:110946291
|
T | G | 1 | a0001c0001t0001g0245 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.-234-17834T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946291 | ||||||
chr10:110946306
|
A | T | 1 | a0001c0001t0001g0131 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.-234-17819A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946306 | ||||||
chr10:110946470
|
A | C | 1 | a0001c0001t0020g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-234-17655A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946470 | ||||||
chr10:110946730
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-234-17395T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946730 | ||||||
chr10:110946741
|
G | C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-234-17384G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946741 | ||||||
chr10:110946789
|
G | A | 19 | a0001c0001t0004g0027a0001c0001t0004g0225a0001c0001t0004g0333others(16): Show | 20 | HG01074.hp2 HG01081.hp1 HG01168.hp1 others(17): Show |
intron_variant | MODIFIER | c.-234-17336G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946789 | ||||||
chr10:110946816
|
T | A | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-17309T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946816 | ||||||
chr10:110946821
|
T | G | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-17304T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946821 | ||||||
chr10:110946855
|
G | A | 12 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(9): Show | 13 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.-234-17270G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110946855 | ||||||
chr10:110947024
|
C | T | 1 | a0001c0004t0016g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.-234-17101C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947024 | ||||||
chr10:110947345
|
G | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(283): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-234-16780G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947345 | ||||||
chr10:110947388
|
G | A | 1 | a0001c0001t0020g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-234-16737G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947388 | ||||||
chr10:110947655
|
A | T | 1 | a0001c0001t0002g0177 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-234-16470A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947655 | ||||||
chr10:110947712
|
G | A | 1 | a0001c0001t0001g0298 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.-234-16413G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947712 | ||||||
chr10:110947726
|
C | T | 1 | a0001c0001t0002g0227 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.-234-16399C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947726 | ||||||
chr10:110947766
|
C | CA | 60 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(57): Show | 67 | HG00423.hp1 HG00544.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.-234-16343dupA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110947766 | |||||
chr10:110947766
|
C | CAA | 7 | a0001c0001t0001g0053a0001c0001t0001g0080a0001c0001t0001g0109others(4): Show | 7 | HG00099.hp1 HG03139.hp1 HG03516.hp2 others(4): Show |
intron_variant | MODIFIER | c.-234-16344_-234-16 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110947766 | |||||
chr10:110947766
|
CA | C | 14 | a0001c0001t0001g0305a0001c0001t0003g0015a0001c0001t0003g0124others(11): Show | 16 | HG01243.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-234-16343delA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110947766 | |||||
chr10:110947814
|
T | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-16311T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947814 | ||||||
chr10:110947827
|
G | A | 1 | a0001c0001t0002g0182 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-234-16298G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947827 | ||||||
chr10:110947834
|
C | T | 1 | a0001c0001t0001g0157 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-234-16291C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947834 | ||||||
chr10:110947949
|
C | T | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(285): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.-234-16176C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947949 | ||||||
chr10:110947956
|
T | A | 1 | a0001c0001t0014g0146 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-234-16169T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947956 | ||||||
chr10:110947964
|
T | A | 3 | a0001c0001t0004g0225a0001c0001t0008g0224a0001c0001t0025g0121 | 3 | HG03139.hp1 HG03225.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.-234-16161T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110947964 | ||||||
chr10:110948322
|
A | G | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-15803A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110948322 | ||||||
chr10:110948527
|
C | A | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-234-15598C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110948527 | ||||||
chr10:110948653
|
G | A | 1 | a0001c0001t0017g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.-234-15472G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110948653 | ||||||
chr10:110948840
|
A | G | 7 | a0001c0001t0003g0015a0001c0001t0003g0125a0001c0001t0003g0126others(4): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-234-15285A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110948840 | ||||||
chr10:110948842
|
C | T | 3 | a0001c0001t0003g0015a0001c0001t0003g0128a0001c0001t0003g0130 | 4 | HG02145.hp2 HG02965.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-234-15283C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110948842 | ||||||
chr10:110949016
|
T | C | 1 | a0001c0001t0001g0311 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-234-15109T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949016 | ||||||
chr10:110949128
|
G | C | 22 | a0001c0001t0001g0025a0001c0001t0001g0114a0001c0001t0001g0120others(19): Show | 23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-234-14997G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949128 | ||||||
chr10:110949157
|
G | A | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-14968G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949157 | ||||||
chr10:110949189
|
G | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-14936G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949189 | ||||||
chr10:110949232
|
A | G | 1 | a0001c0001t0001g0075 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.-234-14893A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949232 | ||||||
chr10:110949326
|
C | T | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-14799C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949326 | ||||||
chr10:110949664
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-14461G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949664 | ||||||
chr10:110949669
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.-234-14456C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949669 | ||||||
chr10:110949744
|
G | A | 13 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(10): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-234-14381G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949744 | ||||||
chr10:110949905
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.-234-14220A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949905 | ||||||
chr10:110949958
|
A | G | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-234-14167A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110949958 | ||||||
chr10:110950027
|
A | G | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-14098A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950027 | ||||||
chr10:110950110
|
G | T | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-14015G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950110 | ||||||
chr10:110950127
|
A | G | 14 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.-234-13998A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950127 | ||||||
chr10:110950286
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-234-13839A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950286 | ||||||
chr10:110950367
|
A | G | 1 | a0001c0001t0010g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-234-13758A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950367 | ||||||
chr10:110950448
|
C | G | 1 | a0001c0001t0020g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-234-13677C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950448 | ||||||
chr10:110950624
|
A | G | 1 | a0001c0001t0002g0233 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-234-13501A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950624 | ||||||
chr10:110950684
|
C | T | 18 | a0001c0001t0004g0027a0001c0001t0004g0225a0001c0001t0004g0333others(15): Show | 19 | HG01074.hp2 HG01081.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.-234-13441C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110950684 | ||||||
chr10:110951040
|
A | G | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-234-13085A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951040 | ||||||
chr10:110951080
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-234-13045G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951080 | ||||||
chr10:110951164
|
T | C | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-234-12961T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951164 | ||||||
chr10:110951283
|
C | T | 2 | a0001c0001t0008g0230a0001c0001t0008g0321 | 2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-234-12842C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951283 | ||||||
chr10:110951287
|
A | G | 23 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(20): Show | 25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.-234-12838A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951287 | ||||||
chr10:110951306
|
C | G | 13 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(10): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-234-12819C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951306 | ||||||
chr10:110951376
|
C | T | 1 | a0001c0001t0002g0170 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-234-12749C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951376 | ||||||
chr10:110951389
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-234-12736G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951389 | ||||||
chr10:110951448
|
C | T | 1 | a0001c0001t0002g0199 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-234-12677C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951448 | ||||||
chr10:110951488
|
A | T | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-234-12637A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951488 | ||||||
chr10:110951502
|
T | G | 3 | a0001c0001t0001g0023a0001c0001t0001g0280a0001c0001t0021g0023 | 3 | HG01884.hp2 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-234-12623T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951502 | ||||||
chr10:110951769
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0329a0001c0001t0001g0330 | 4 | HG02027.hp1 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.-234-12356G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951769 | ||||||
chr10:110951772
|
C | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0114a0001c0001t0001g0120others(19): Show | 23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-234-12353C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951772 | ||||||
chr10:110951967
|
C | T | 10 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0166others(7): Show | 14 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.-234-12158C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110951967 | ||||||
chr10:110952071
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.-234-12054G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952071 | ||||||
chr10:110952113
|
AT | A | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-234-12006delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110952113 | |||||
chr10:110952114
|
T | C | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-12011T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952114 | ||||||
chr10:110952159
|
A | G | 23 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(20): Show | 25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.-234-11966A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952159 | ||||||
chr10:110952167
|
A | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-11958A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952167 | ||||||
chr10:110952218
|
A | C | 1 | a0001c0001t0003g0127 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-234-11907A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952218 | ||||||
chr10:110952290
|
G | A | 1 | a0001c0001t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-234-11835G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952290 | ||||||
chr10:110952368
|
T | C | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-234-11757T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952368 | ||||||
chr10:110952410
|
A | G | 1 | a0001c0001t0002g0018 | 2 | NA18952.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-234-11715A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952410 | ||||||
chr10:110952613
|
G | T | 17 | a0001c0001t0001g0025a0001c0001t0001g0120a0001c0001t0001g0306others(14): Show | 18 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(15): Show |
intron_variant | MODIFIER | c.-234-11512G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952613 | ||||||
chr10:110952711
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-234-11414C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952711 | ||||||
chr10:110952719
|
C | T | 103 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-234-11406C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952719 | ||||||
chr10:110952783
|
A | G | 1 | a0001c0001t0002g0220 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.-234-11342A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952783 | ||||||
chr10:110952791
|
T | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0280a0001c0001t0021g0023 | 3 | HG01884.hp2 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.-234-11334T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952791 | ||||||
chr10:110952794
|
T | C | 1 | a0001c0001t0002g0182 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.-234-11331T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952794 | ||||||
chr10:110952845
|
A | G | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-11280A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110952845 | ||||||
chr10:110953065
|
C | A | 1 | a0001c0001t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-234-11060C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953065 | ||||||
chr10:110953124
|
T | C | 1 | a0001c0001t0001g0149 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.-234-11001T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953124 | ||||||
chr10:110953142
|
A | G | 1 | a0001c0001t0004g0334 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.-234-10983A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953142 | ||||||
chr10:110953193
|
C | T | 1 | a0001c0001t0002g0198 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.-234-10932C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953193 | ||||||
chr10:110953231
|
GT | G | 5 | a0002c0002t0003g0028a0002c0002t0003g0117a0002c0002t0003g0345others(2): Show | 6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.-234-10891delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110953231 | |||||
chr10:110953243
|
T | C | 13 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0036others(10): Show | 14 | HG00140.hp2 HG00639.hp1 HG01169.hp1 others(11): Show |
intron_variant | MODIFIER | c.-234-10882T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953243 | ||||||
chr10:110953385
|
C | T | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-10740C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953385 | ||||||
chr10:110953470
|
T | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-10655T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953470 | ||||||
chr10:110953537
|
A | G | 1 | a0001c0001t0001g0320 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-234-10588A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953537 | ||||||
chr10:110953559
|
A | T | 10 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0165others(7): Show | 12 | HG02015.hp1 HG02074.hp2 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.-234-10566A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953559 | ||||||
chr10:110953703
|
G | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-10422G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953703 | ||||||
chr10:110953713
|
T | C | 7 | a0001c0001t0003g0015a0001c0001t0003g0125a0001c0001t0003g0126others(4): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-234-10412T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953713 | ||||||
chr10:110953730
|
G | GTA | 3 | a0001c0001t0002g0183a0001c0001t0002g0198a0001c0001t0005g0115 | 3 | HG03831.hp2 NA18964.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.-234-10379_-234-10 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110953730 | |||||
chr10:110953730
|
GTA | G | 4 | a0001c0001t0004g0344a0001c0001t0009g0122a0001c0001t0009g0123others(1): Show | 4 | HG02698.hp1 HG02922.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-234-10379_-234-10 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110953730 | |||||
chr10:110953732
|
A | G | 1 | a0001c0001t0001g0343 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.-234-10393A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953732 | ||||||
chr10:110953853
|
T | G | 1 | a0001c0001t0010g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-234-10272T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110953853 | ||||||
chr10:110954057
|
G | A | 101 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(98): Show | 109 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(106): Show |
intron_variant | MODIFIER | c.-234-10068G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954057 | ||||||
chr10:110954156
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-234-9969A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954156 | ||||||
chr10:110954400
|
G | A | 1 | a0001c0001t0001g0036 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.-234-9725G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954400 | ||||||
chr10:110954420
|
A | T | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-9705A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954420 | ||||||
chr10:110954529
|
T | TAATC | 291 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(288): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-234-9594_-234-959 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110954529 | |||||
chr10:110954593
|
G | T | 5 | a0001c0001t0002g0019a0001c0001t0002g0118a0001c0001t0002g0200others(2): Show | 6 | HG01069.hp1 HG01071.hp2 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.-234-9532G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954593 | ||||||
chr10:110954611
|
G | A | 1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-234-9514G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954611 | ||||||
chr10:110954720
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-234-9405A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954720 | ||||||
chr10:110954739
|
G | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-234-9386G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954739 | ||||||
chr10:110954813
|
A | G | 328 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(325): Show | 362 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(359): Show |
intron_variant | MODIFIER | c.-234-9312A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954813 | ||||||
chr10:110954934
|
A | T | 1 | a0001c0001t0008g0224 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.-234-9191A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954934 | ||||||
chr10:110954939
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-234-9186G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954939 | ||||||
chr10:110954957
|
G | C | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.-234-9168G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110954957 | ||||||
chr10:110955175
|
G | T | 1 | a0001c0001t0001g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-234-8950G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955175 | ||||||
chr10:110955242
|
C | T | 2 | a0001c0001t0002g0167a0001c0001t0002g0171 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-234-8883C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955242 | ||||||
chr10:110955262
|
G | C | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.-234-8863G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955262 | ||||||
chr10:110955284
|
A | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-8841A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955284 | ||||||
chr10:110955290
|
A | G | 1 | a0001c0001t0002g0164 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-234-8835A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955290 | ||||||
chr10:110955293
|
A | G | 1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.-234-8832A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955293 | ||||||
chr10:110955367
|
C | G | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-234-8758C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955367 | ||||||
chr10:110955380
|
C | A | 1 | a0001c0001t0004g0337 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-234-8745C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955380 | ||||||
chr10:110955601
|
G | A | 17 | a0001c0001t0004g0027a0001c0001t0004g0225a0001c0001t0004g0333others(14): Show | 18 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(15): Show |
intron_variant | MODIFIER | c.-234-8524G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955601 | ||||||
chr10:110955732
|
C | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-8393C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955732 | ||||||
chr10:110955777
|
G | A | 1 | a0001c0001t0002g0173 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-234-8348G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955777 | ||||||
chr10:110955863
|
C | T | 12 | a0001c0001t0001g0010a0001c0001t0001g0054a0001c0001t0001g0068others(9): Show | 13 | HG00558.hp2 NA18939.hp2 NA18950.hp2 others(10): Show |
intron_variant | MODIFIER | c.-234-8262C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955863 | ||||||
chr10:110955866
|
T | G | 1 | a0002c0002t0003g0345 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.-234-8259T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955866 | ||||||
chr10:110955949
|
T | G | 1 | a0001c0001t0001g0235 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.-234-8176T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110955949 | ||||||
chr10:110956192
|
CT | C | 77 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(74): Show | 87 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(84): Show |
intron_variant | MODIFIER | c.-234-7922delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110956192 | |||||
chr10:110956209
|
G | A | 1 | a0001c0001t0003g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.-234-7916G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956209 | ||||||
chr10:110956307
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-7818G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956307 | ||||||
chr10:110956390
|
T | C | 1 | a0001c0001t0001g0262 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-234-7735T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956390 | ||||||
chr10:110956484
|
A | G | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-234-7641A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956484 | ||||||
chr10:110956518
|
T | A | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-234-7607T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956518 | ||||||
chr10:110956639
|
T | C | 23 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(20): Show | 25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.-234-7486T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956639 | ||||||
chr10:110956755
|
T | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-7370T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956755 | ||||||
chr10:110956897
|
T | A | 286 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(283): Show | 317 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(314): Show |
intron_variant | MODIFIER | c.-234-7228T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956897 | ||||||
chr10:110956898
|
G | A | 1 | a0001c0001t0002g0184 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.-234-7227G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956898 | ||||||
chr10:110956913
|
A | G | 1 | a0001c0001t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-234-7212A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110956913 | ||||||
chr10:110957042
|
T | C | 1 | a0001c0001t0001g0110 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-234-7083T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957042 | ||||||
chr10:110957101
|
A | G | 3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0138 | 3 | HG02809.hp2 HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.-234-7024A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957101 | ||||||
chr10:110957113
|
A | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-7012A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957113 | ||||||
chr10:110957201
|
G | A | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-6924G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957201 | ||||||
chr10:110957239
|
G | A | 13 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(10): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.-234-6886G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957239 | ||||||
chr10:110957416
|
C | T | 15 | a0001c0001t0001g0025a0001c0001t0001g0120a0001c0001t0001g0306others(12): Show | 16 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.-234-6709C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957416 | ||||||
chr10:110957462
|
G | A | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-6663G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957462 | ||||||
chr10:110957532
|
A | AC | 109 | a0001c0001t0001g0025a0001c0001t0001g0055a0001c0001t0001g0063others(106): Show | 121 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(118): Show |
intron_variant | MODIFIER | c.-234-6583dupC | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110957532 | |||||
chr10:110957536
|
C | A | 2 | a0001c0001t0001g0263a0001c0001t0001g0278 | 2 | HG03017.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.-234-6589C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957536 | ||||||
chr10:110957537
|
C | A | 14 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0036others(11): Show | 15 | HG00140.hp2 HG00639.hp1 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.-234-6588C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957537 | ||||||
chr10:110957771
|
C | T | 1 | a0001c0001t0001g0283 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.-234-6354C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110957771 | ||||||
chr10:110958088
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.-234-6037A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110958088 | ||||||
chr10:110958141
|
C | T | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-234-5984C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110958141 | ||||||
chr10:110958220
|
C | CT | 114 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(111): Show | 125 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.-234-5892dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr10 | 110958220 | |||||
chr10:110958365
|
C | A | 1 | a0001c0001t0001g0031 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.-234-5760C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110958365 | ||||||
chr10:110958381
|
T | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-5744T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110958381 | ||||||
chr10:110958458
|
T | C | 291 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(288): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.-234-5667T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110958458 | ||||||
chr10:110959057
|
T | C | 103 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.-234-5068T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959057 | ||||||
chr10:110959099
|
T | C | 1 | a0001c0001t0001g0264 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.-234-5026T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959099 | ||||||
chr10:110959157
|
T | G | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.-234-4968T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959157 | ||||||
chr10:110959541
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-234-4584C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959541 | ||||||
chr10:110959554
|
A | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(286): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.-234-4571A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959554 | ||||||
chr10:110959568
|
C | A | 1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-234-4557C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959568 | ||||||
chr10:110959585
|
G | A | 1 | a0001c0001t0005g0228 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-234-4540G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959585 | ||||||
chr10:110959672
|
A | C | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-4453A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959672 | ||||||
chr10:110959813
|
T | G | 1 | a0001c0001t0001g0292 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-234-4312T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959813 | ||||||
chr10:110959973
|
A | C | 1 | a0001c0001t0005g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.-234-4152A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110959973 | ||||||
chr10:110960152
|
A | G | 1 | a0001c0001t0001g0106 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-234-3973A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960152 | ||||||
chr10:110960219
|
T | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-3906T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960219 | ||||||
chr10:110960350
|
G | T | 1 | a0001c0001t0001g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-234-3775G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960350 | ||||||
chr10:110960352
|
C | T | 1 | a0001c0001t0001g0102 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.-234-3773C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960352 | ||||||
chr10:110960394
|
G | A | 16 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(13): Show | 16 | HG01175.hp2 HG01978.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.-234-3731G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960394 | ||||||
chr10:110960609
|
A | T | 1 | a0001c0001t0001g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-234-3516A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960609 | ||||||
chr10:110960726
|
A | G | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-234-3399A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960726 | ||||||
chr10:110960969
|
G | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-3156G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110960969 | ||||||
chr10:110961242
|
A | G | 289 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(286): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.-234-2883A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961242 | ||||||
chr10:110961258
|
C | T | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-234-2867C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961258 | ||||||
chr10:110961296
|
A | G | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-234-2829A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961296 | ||||||
chr10:110961398
|
T | C | 1 | a0001c0001t0001g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.-234-2727T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961398 | ||||||
chr10:110961493
|
T | C | 7 | a0001c0001t0003g0015a0001c0001t0003g0125a0001c0001t0003g0126others(4): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.-234-2632T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961493 | ||||||
chr10:110961650
|
G | T | 14 | a0001c0001t0004g0027a0001c0001t0004g0225a0001c0001t0004g0333others(11): Show | 15 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(12): Show |
intron_variant | MODIFIER | c.-234-2475G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961650 | ||||||
chr10:110961954
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-2171G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110961954 | ||||||
chr10:110962048
|
T | C | 2 | a0001c0001t0008g0230a0001c0001t0008g0321 | 2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.-234-2077T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110962048 | ||||||
chr10:110962114
|
A | G | 13 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(10): Show | 13 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.-234-2011A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110962114 | ||||||
chr10:110962254
|
G | T | 22 | a0001c0001t0001g0025a0001c0001t0001g0114a0001c0001t0001g0120others(19): Show | 23 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(20): Show |
intron_variant | MODIFIER | c.-234-1871G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110962254 | ||||||
chr10:110962682
|
C | T | 1 | a0001c0001t0001g0274 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-234-1443C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110962682 | ||||||
chr10:110962828
|
C | T | 1 | a0001c0001t0001g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.-234-1297C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110962828 | ||||||
chr10:110962830
|
A | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-1295A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110962830 | ||||||
chr10:110963095
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-234-1030G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963095 | ||||||
chr10:110963147
|
T | C | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-234-978T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963147 | ||||||
chr10:110963195
|
C | T | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-234-930C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963195 | ||||||
chr10:110963266
|
C | T | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-234-859C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963266 | ||||||
chr10:110963473
|
C | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-652C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963473 | ||||||
chr10:110963529
|
C | G | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-234-596C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963529 | ||||||
chr10:110963531
|
C | A | 1 | a0001c0001t0002g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.-234-594C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963531 | ||||||
chr10:110963564
|
T | C | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-234-561T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963564 | ||||||
chr10:110963752
|
A | G | 1 | a0001c0001t0001g0296 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-234-373A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963752 | ||||||
chr10:110963858
|
G | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.-234-267G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 1/8 | chr10 | 110963858 | ||||||
chr10:110965141
|
C | A | 1 | a0001c0001t0001g0265 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.703+80C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965141 | ||||||
chr10:110965160
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.703+99C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965160 | ||||||
chr10:110965380
|
G | GT | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.703+322dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110965380 | |||||
chr10:110965501
|
C | T | 14 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.703+440C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965501 | ||||||
chr10:110965521
|
G | C | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.703+460G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965521 | ||||||
chr10:110965530
|
A | G | 1 | a0001c0001t0002g0185 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.703+469A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965530 | ||||||
chr10:110965536
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.703+475G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965536 | ||||||
chr10:110965562
|
A | T | 1 | a0001c0001t0001g0298 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.703+501A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965562 | ||||||
chr10:110965563
|
T | A | 1 | a0001c0001t0001g0047 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.703+502T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965563 | ||||||
chr10:110965773
|
C | T | 1 | a0001c0001t0001g0011 | 2 | NA18998.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.703+712C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965773 | ||||||
chr10:110965778
|
G | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+717G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110965778 | ||||||
chr10:110966101
|
G | A | 40 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(37): Show | 46 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(43): Show |
intron_variant | MODIFIER | c.703+1040G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966101 | ||||||
chr10:110966317
|
A | T | 1 | a0001c0001t0001g0330 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.703+1256A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966317 | ||||||
chr10:110966384
|
TA | T | 3 | a0001c0001t0001g0196a0001c0001t0002g0195a0001c0001t0002g0197 | 3 | HG02602.hp2 HG03669.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.703+1324delA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966384 | ||||||
chr10:110966513
|
T | C | 2 | a0001c0001t0001g0032a0001c0001t0001g0349 | 2 | NA18990.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.703+1452T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966513 | ||||||
chr10:110966583
|
T | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+1522T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966583 | ||||||
chr10:110966623
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.703+1562A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966623 | ||||||
chr10:110966694
|
A | G | 12 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(9): Show | 12 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.703+1633A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966694 | ||||||
chr10:110966734
|
T | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.703+1673T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966734 | ||||||
chr10:110966941
|
A | T | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.703+1880A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110966941 | ||||||
chr10:110967169
|
A | G | 1 | a0001c0001t0001g0085 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.703+2108A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967169 | ||||||
chr10:110967213
|
C | T | 1 | a0001c0001t0001g0160 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.703+2152C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967213 | ||||||
chr10:110967466
|
T | C | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.703+2405T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967466 | ||||||
chr10:110967576
|
T | C | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.703+2515T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967576 | ||||||
chr10:110967643
|
C | A | 1 | a0001c0001t0001g0276 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.703+2582C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967643 | ||||||
chr10:110967663
|
A | G | 1 | a0001c0001t0002g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.703+2602A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967663 | ||||||
chr10:110967736
|
C | T | 350 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(347): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.703+2675C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110967736 | ||||||
chr10:110968068
|
T | G | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.703+3007T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968068 | ||||||
chr10:110968196
|
T | G | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.703+3135T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968196 | ||||||
chr10:110968352
|
A | G | 2 | a0001c0001t0002g0167a0001c0001t0002g0171 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.703+3291A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968352 | ||||||
chr10:110968549
|
A | C | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.703+3488A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968549 | ||||||
chr10:110968550
|
TTTATA | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0096others(1): Show | 5 | HG00408.hp2 HG02040.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+3498_703+3502d others(7): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110968550 | |||||
chr10:110968585
|
A | G | 1 | a0001c0001t0023g0237 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.703+3524A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968585 | ||||||
chr10:110968646
|
A | G | 1 | a0001c0001t0001g0318 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.703+3585A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968646 | ||||||
chr10:110968650
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+3589G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968650 | ||||||
chr10:110968740
|
G | T | 13 | a0001c0001t0001g0010a0001c0001t0001g0054a0001c0001t0001g0065others(10): Show | 14 | HG00558.hp2 NA18939.hp2 NA18950.hp2 others(11): Show |
intron_variant | MODIFIER | c.703+3679G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968740 | ||||||
chr10:110968828
|
T | C | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.703+3767T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968828 | ||||||
chr10:110968840
|
G | A | 1 | a0001c0001t0001g0077 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.703+3779G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968840 | ||||||
chr10:110968920
|
A | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+3859A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110968920 | ||||||
chr10:110969306
|
A | G | 2 | a0001c0001t0004g0344a0001c0001t0018g0162 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703+4245A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110969306 | ||||||
chr10:110969357
|
C | T | 13 | a0001c0001t0004g0027a0001c0001t0004g0225a0001c0001t0004g0333others(10): Show | 14 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(11): Show |
intron_variant | MODIFIER | c.703+4296C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110969357 | ||||||
chr10:110969540
|
C | T | 2 | a0001c0001t0004g0344a0001c0001t0018g0162 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.703+4479C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110969540 | ||||||
chr10:110969541
|
G | A | 1 | a0001c0001t0001g0099 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.703+4480G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110969541 | ||||||
chr10:110969549
|
T | C | 3 | a0001c0001t0001g0070a0001c0001t0001g0102a0001c0001t0001g0105 | 3 | NA18971.hp1 NA18995.hp2 NA19085.hp2 |
intron_variant | MODIFIER | c.703+4488T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110969549 | ||||||
chr10:110969617
|
G | A | 116 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(113): Show | 124 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.703+4556G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110969617 | ||||||
chr10:110969890
|
TATGAGAA others(6): Show |
T | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.703+4845_703+4857d others(15): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110969890 | |||||
chr10:110970001
|
C | T | 1 | a0001c0001t0024g0152 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.703+4940C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970001 | ||||||
chr10:110970149
|
A | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.703+5088A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970149 | ||||||
chr10:110970238
|
C | A | 1 | a0001c0001t0002g0206 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.703+5177C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970238 | ||||||
chr10:110970288
|
A | G | 1 | a0001c0001t0002g0207 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.703+5227A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970288 | ||||||
chr10:110970505
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+5444G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970505 | ||||||
chr10:110970639
|
A | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.703+5578A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970639 | ||||||
chr10:110970667
|
G | A | 1 | a0001c0001t0001g0282 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.703+5606G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970667 | ||||||
chr10:110970706
|
T | C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.703+5645T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970706 | ||||||
chr10:110970729
|
GT | G | 301 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(298): Show | 330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.703+5683delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110970729 | |||||
chr10:110970729
|
GTT | G | 8 | a0001c0001t0001g0086a0001c0001t0001g0114a0001c0001t0001g0304others(5): Show | 8 | HG02145.hp1 HG02965.hp2 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.703+5682_703+5683d others(4): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110970729 | |||||
chr10:110970729
|
GTTT | G | 15 | a0001c0001t0001g0025a0001c0001t0001g0120a0001c0001t0001g0306others(12): Show | 16 | HG00438.hp2 HG00621.hp1 HG01106.hp1 others(13): Show |
intron_variant | MODIFIER | c.703+5681_703+5683d others(5): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110970729 | |||||
chr10:110970734
|
T | G | 1 | a0001c0001t0020g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.703+5673T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970734 | ||||||
chr10:110970744
|
T | G | 1 | a0001c0001t0001g0303 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.703+5683T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970744 | ||||||
chr10:110970844
|
G | A | 1 | a0001c0001t0001g0256 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.703+5783G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970844 | ||||||
chr10:110970920
|
T | A | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.703+5859T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110970920 | ||||||
chr10:110971175
|
T | C | 1 | a0001c0001t0004g0336 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.703+6114T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971175 | ||||||
chr10:110971322
|
A | G | 2 | a0001c0001t0001g0084a0001c0001t0020g0331 | 2 | HG03098.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.703+6261A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971322 | ||||||
chr10:110971413
|
G | T | 3 | a0001c0001t0001g0005a0001c0001t0001g0250a0001c0001t0001g0297 | 5 | HG00140.hp1 HG00642.hp2 HG01243.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+6352G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971413 | ||||||
chr10:110971428
|
C | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+6367C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971428 | ||||||
chr10:110971564
|
A | ATTTTTTC others(3): Show |
1 | a0001c0001t0001g0068 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.703+6509_703+6510i others(12): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110971564 | |||||
chr10:110971568
|
T | C | 1 | a0001c0001t0001g0266 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.703+6507T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971568 | ||||||
chr10:110971741
|
A | G | 1 | a0001c0001t0002g0194 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.703+6680A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971741 | ||||||
chr10:110971901
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(340): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.703+6840T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971901 | ||||||
chr10:110971944
|
A | T | 4 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0157others(1): Show | 4 | HG03490.hp1 HG03492.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+6883A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110971944 | ||||||
chr10:110972089
|
C | G | 1 | a0001c0001t0001g0265 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.703+7028C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972089 | ||||||
chr10:110972217
|
C | G | 25 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0053others(22): Show | 27 | HG00099.hp1 HG01175.hp2 HG01261.hp1 others(24): Show |
intron_variant | MODIFIER | c.703+7156C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972217 | ||||||
chr10:110972629
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.703+7568G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972629 | ||||||
chr10:110972679
|
T | C | 302 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(299): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.703+7618T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972679 | ||||||
chr10:110972688
|
T | G | 1 | a0001c0001t0001g0280 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.703+7627T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972688 | ||||||
chr10:110972727
|
C | T | 14 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.703+7666C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972727 | ||||||
chr10:110972764
|
T | C | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.703+7703T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110972764 | ||||||
chr10:110973008
|
C | T | 1 | a0001c0001t0010g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703+7947C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973008 | ||||||
chr10:110973010
|
A | C | 1 | a0001c0001t0010g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.703+7949A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973010 | ||||||
chr10:110973056
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+7995G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973056 | ||||||
chr10:110973274
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.703+8213G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973274 | ||||||
chr10:110973327
|
G | A | 23 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(20): Show | 25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.703+8266G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973327 | ||||||
chr10:110973335
|
C | A | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG02647.hp2 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.703+8274C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973335 | ||||||
chr10:110973384
|
A | G | 1 | a0001c0001t0011g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.703+8323A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973384 | ||||||
chr10:110973402
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0096others(1): Show | 5 | HG00408.hp2 HG02040.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.703+8341C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973402 | ||||||
chr10:110973467
|
A | C | 1 | a0001c0001t0002g0200 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.703+8406A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973467 | ||||||
chr10:110973477
|
T | A | 1 | a0001c0001t0002g0186 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.703+8416T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973477 | ||||||
chr10:110973638
|
G | A | 1 | a0001c0001t0019g0073 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.703+8577G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973638 | ||||||
chr10:110973673
|
G | GT | 15 | a0001c0001t0001g0059a0001c0001t0001g0068a0001c0001t0001g0070others(12): Show | 16 | HG02071.hp1 HG02135.hp1 HG03654.hp1 others(13): Show |
intron_variant | MODIFIER | c.703+8620dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110973673 | |||||
chr10:110973793
|
G | A | 1 | a0001c0001t0001g0009 | 2 | HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.703+8732G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110973793 | ||||||
chr10:110973865
|
C | CAT | 5 | a0002c0002t0003g0028a0002c0002t0003g0117a0002c0002t0003g0345others(2): Show | 6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.703+8816_703+8817d others(4): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110973865 | |||||
chr10:110974009
|
G | A | 4 | a0001c0001t0004g0344a0001c0001t0009g0122a0001c0001t0009g0123others(1): Show | 4 | HG02698.hp1 HG02922.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.703+8948G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110974009 | ||||||
chr10:110974389
|
G | C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.703+9328G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110974389 | ||||||
chr10:110974473
|
G | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+9412G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110974473 | ||||||
chr10:110974649
|
G | C | 1 | a0001c0001t0001g0286 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.703+9588G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110974649 | ||||||
chr10:110974699
|
T | C | 3 | a0001c0001t0001g0026a0001c0001t0001g0329a0001c0001t0001g0330 | 4 | HG02027.hp1 NA18968.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.703+9638T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110974699 | ||||||
chr10:110974991
|
C | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+9930C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110974991 | ||||||
chr10:110975158
|
C | T | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.703+10097C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975158 | ||||||
chr10:110975158
|
CT | C | 9 | a0001c0001t0002g0187a0001c0001t0003g0015a0001c0001t0003g0124others(6): Show | 10 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.703+10112delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110975158 | |||||
chr10:110975176
|
G | A | 1 | a0001c0001t0008g0224 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.703+10115G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975176 | ||||||
chr10:110975280
|
C | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.703+10219C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975280 | ||||||
chr10:110975338
|
G | A | 23 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(20): Show | 25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.703+10277G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975338 | ||||||
chr10:110975414
|
T | A | 2 | a0001c0001t0001g0133a0001c0001t0001g0138 | 2 | HG03098.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.704-10214T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975414 | ||||||
chr10:110975443
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.704-10185A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975443 | ||||||
chr10:110975593
|
CTTTG | C | 117 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(114): Show | 126 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(123): Show |
intron_variant | MODIFIER | c.704-10031_704-1002 others(8): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110975593 | |||||
chr10:110975697
|
A | T | 1 | a0001c0001t0002g0206 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.704-9931A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975697 | ||||||
chr10:110975879
|
C | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.704-9749C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975879 | ||||||
chr10:110975903
|
T | A | 1 | a0001c0001t0001g0038 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.704-9725T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975903 | ||||||
chr10:110975908
|
T | G | 1 | a0001c0001t0015g0048 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.704-9720T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110975908 | ||||||
chr10:110975915
|
C | CT | 79 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(76): Show | 89 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.704-9703dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110975915 | |||||
chr10:110976175
|
G | T | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.704-9453G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110976175 | ||||||
chr10:110976232
|
A | G | 1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.704-9396A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110976232 | ||||||
chr10:110976316
|
C | CT | 6 | a0001c0001t0001g0051a0001c0001t0001g0114a0001c0001t0002g0180others(3): Show | 6 | HG01081.hp1 HG02572.hp1 HG04204.hp2 others(3): Show |
intron_variant | MODIFIER | c.704-9299dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110976316 | |||||
chr10:110976344
|
C | T | 1 | a0001c0001t0001g0304 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.704-9284C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110976344 | ||||||
chr10:110976396
|
C | T | 2 | a0001c0001t0001g0131a0001c0001t0001g0277 | 2 | HG01928.hp1 NA18964.hp1 |
intron_variant | MODIFIER | c.704-9232C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110976396 | ||||||
chr10:110976923
|
GCT | G | 3 | a0001c0001t0001g0312a0001c0001t0009g0122a0001c0001t0009g0123 | 3 | HG02698.hp1 HG04199.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.704-8702_704-8701d others(4): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110976923 | |||||
chr10:110977126
|
G | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.704-8502G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977126 | ||||||
chr10:110977165
|
T | C | 1 | a0001c0001t0002g0181 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.704-8463T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977165 | ||||||
chr10:110977171
|
T | C | 1 | a0001c0001t0001g0293 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.704-8457T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977171 | ||||||
chr10:110977256
|
G | T | 13 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(10): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.704-8372G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977256 | ||||||
chr10:110977397
|
C | T | 5 | a0002c0002t0003g0028a0002c0002t0003g0117a0002c0002t0003g0345others(2): Show | 6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-8231C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977397 | ||||||
chr10:110977406
|
C | T | 1 | a0001c0001t0004g0337 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.704-8222C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977406 | ||||||
chr10:110977408
|
G | A | 1 | a0002c0002t0003g0347 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.704-8220G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977408 | ||||||
chr10:110977642
|
T | C | 5 | a0001c0001t0001g0303a0001c0001t0001g0304a0001c0001t0001g0305others(2): Show | 5 | HG01109.hp1 HG02145.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-7986T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977642 | ||||||
chr10:110977696
|
G | C | 2 | a0001c0001t0001g0008a0001c0001t0005g0050 | 3 | NA18968.hp1 NA19001.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.704-7932G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977696 | ||||||
chr10:110977858
|
C | T | 2 | a0001c0001t0004g0344a0001c0001t0018g0162 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.704-7770C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977858 | ||||||
chr10:110977910
|
C | T | 4 | a0001c0001t0004g0344a0001c0001t0009g0122a0001c0001t0009g0123others(1): Show | 4 | HG02698.hp1 HG02922.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-7718C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977910 | ||||||
chr10:110977939
|
A | T | 302 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(299): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.704-7689A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977939 | ||||||
chr10:110977972
|
G | A | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.704-7656G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110977972 | ||||||
chr10:110978015
|
C | G | 2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.704-7613C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978015 | ||||||
chr10:110978166
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.704-7462T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978166 | ||||||
chr10:110978207
|
C | T | 3 | a0001c0001t0002g0169a0001c0001t0004g0027a0001c0001t0004g0341 | 4 | HG01884.hp1 HG01891.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.704-7421C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978207 | ||||||
chr10:110978212
|
G | A | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.704-7416G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978212 | ||||||
chr10:110978231
|
T | G | 1 | a0001c0001t0002g0167 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.704-7397T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978231 | ||||||
chr10:110978264
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.704-7364A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978264 | ||||||
chr10:110978413
|
C | T | 1 | a0001c0001t0001g0308 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.704-7215C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978413 | ||||||
chr10:110978583
|
C | A | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.704-7045C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978583 | ||||||
chr10:110978593
|
A | T | 6 | a0001c0001t0001g0060a0001c0001t0001g0070a0001c0001t0001g0097others(3): Show | 6 | NA18951.hp2 NA18960.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-7035A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978593 | ||||||
chr10:110978600
|
G | C | 6 | a0001c0001t0001g0060a0001c0001t0001g0070a0001c0001t0001g0097others(3): Show | 6 | NA18951.hp2 NA18960.hp1 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-7028G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978600 | ||||||
chr10:110978817
|
T | G | 1 | a0001c0001t0005g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.704-6811T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110978817 | ||||||
chr10:110979053
|
T | G | 2 | a0001c0001t0001g0327a0001c0001t0022g0326 | 2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.704-6575T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979053 | ||||||
chr10:110979210
|
A | G | 1 | a0001c0001t0002g0217 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.704-6418A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979210 | ||||||
chr10:110979309
|
A | G | 7 | a0001c0001t0003g0015a0001c0001t0003g0125a0001c0001t0003g0126others(4): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-6319A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979309 | ||||||
chr10:110979377
|
T | C | 133 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.704-6251T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979377 | ||||||
chr10:110979451
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.704-6177G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979451 | ||||||
chr10:110979469
|
G | A | 1 | a0001c0001t0002g0348 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.704-6159G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979469 | ||||||
chr10:110979488
|
A | T | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.704-6140A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979488 | ||||||
chr10:110979602
|
A | G | 133 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(130): Show | 143 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(140): Show |
intron_variant | MODIFIER | c.704-6026A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979602 | ||||||
chr10:110979610
|
T | C | 304 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(301): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
intron_variant | MODIFIER | c.704-6018T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979610 | ||||||
chr10:110979738
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.704-5890G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979738 | ||||||
chr10:110979834
|
C | T | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.704-5794C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979834 | ||||||
chr10:110979840
|
A | G | 1 | a0001c0001t0002g0018 | 2 | NA18952.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.704-5788A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110979840 | ||||||
chr10:110979884
|
T | TTTG | 343 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(340): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.704-5735_704-5733d others(5): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110979884 | |||||
chr10:110980040
|
A | G | 7 | a0001c0001t0003g0015a0001c0001t0003g0125a0001c0001t0003g0126others(4): Show | 8 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.704-5588A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980040 | ||||||
chr10:110980152
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.704-5476C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980152 | ||||||
chr10:110980158
|
C | CT | 8 | a0001c0001t0001g0319a0001c0001t0002g0205a0001c0001t0002g0219others(5): Show | 9 | HG00597.hp2 HG01081.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.704-5452dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110980158 | |||||
chr10:110980158
|
CT | C | 21 | a0001c0001t0001g0007a0001c0001t0001g0035a0001c0001t0001g0036others(18): Show | 22 | HG00140.hp2 HG00639.hp1 HG01069.hp2 others(19): Show |
intron_variant | MODIFIER | c.704-5452delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110980158 | |||||
chr10:110980238
|
G | C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.704-5390G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980238 | ||||||
chr10:110980281
|
C | T | 4 | a0001c0001t0001g0013a0001c0001t0001g0061a0001c0001t0001g0096others(1): Show | 5 | HG00408.hp2 HG02040.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.704-5347C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980281 | ||||||
chr10:110980517
|
C | T | 1 | a0001c0001t0002g0017 | 2 | HG02630.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.704-5111C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980517 | ||||||
chr10:110980626
|
A | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.704-5002A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980626 | ||||||
chr10:110980700
|
A | G | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.704-4928A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980700 | ||||||
chr10:110980757
|
C | T | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.704-4871C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980757 | ||||||
chr10:110980801
|
T | TC | 5 | a0001c0001t0001g0306a0001c0001t0001g0307a0001c0001t0001g0313others(2): Show | 5 | HG00438.hp2 HG00621.hp1 NA18954.hp1 others(2): Show |
intron_variant | MODIFIER | c.704-4826dupC | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110980801 | |||||
chr10:110980998
|
G | A | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.704-4630G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110980998 | ||||||
chr10:110981233
|
C | T | 78 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(75): Show | 88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.704-4395C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981233 | ||||||
chr10:110981234
|
G | A | 3 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0111 | 3 | HG02683.hp2 HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.704-4394G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981234 | ||||||
chr10:110981408
|
A | G | 14 | a0001c0001t0001g0342a0001c0001t0003g0015a0001c0001t0003g0124others(11): Show | 16 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.704-4220A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981408 | ||||||
chr10:110981693
|
C | T | 1 | a0001c0001t0003g0124 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.704-3935C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981693 | ||||||
chr10:110981793
|
C | T | 127 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(124): Show | 137 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(134): Show |
intron_variant | MODIFIER | c.704-3835C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981793 | ||||||
chr10:110981866
|
A | T | 9 | a0001c0001t0001g0060a0001c0001t0001g0070a0001c0001t0001g0097others(6): Show | 9 | HG02015.hp2 HG02622.hp1 HG02818.hp2 others(6): Show |
intron_variant | MODIFIER | c.704-3762A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981866 | ||||||
chr10:110981870
|
A | T | 3 | a0001c0001t0001g0151a0001c0001t0004g0225a0001c0001t0008g0224 | 3 | HG03139.hp1 HG03225.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.704-3758A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981870 | ||||||
chr10:110981873
|
T | A | 2 | a0001c0001t0003g0126a0001c0001t0008g0321 | 2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.704-3755T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981873 | ||||||
chr10:110981874
|
T | A | 205 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(202): Show | 226 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(223): Show |
intron_variant | MODIFIER | c.704-3754T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981874 | ||||||
chr10:110981876
|
T | C | 2 | a0001c0001t0003g0126a0001c0001t0008g0321 | 2 | HG02622.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.704-3752T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981876 | ||||||
chr10:110981876
|
T | TTATTATA others(3): Show |
151 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(148): Show | 166 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(163): Show |
intron_variant | MODIFIER | c.704-3750_704-3749i others(12): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110981876 | |||||
chr10:110981876
|
T | TTATTTAT others(7): Show |
34 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0163others(31): Show | 36 | HG00597.hp2 HG00609.hp2 HG00738.hp1 others(33): Show |
intron_variant | MODIFIER | c.704-3750_704-3749i others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110981876 | |||||
chr10:110981876
|
T | TTATTTAT others(11): Show |
36 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(33): Show | 44 | HG00558.hp1 HG00673.hp1 HG01257.hp1 others(41): Show |
intron_variant | MODIFIER | c.704-3750_704-3749i others(20): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110981876 | |||||
chr10:110981876
|
T | TTATTTAT others(15): Show |
2 | a0001c0001t0002g0171a0001c0001t0002g0173 | 2 | HG02109.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.704-3750_704-3749i others(24): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110981876 | |||||
chr10:110981876
|
T | TTATTTTT others(11): Show |
18 | a0001c0001t0001g0005a0001c0001t0001g0248a0001c0001t0001g0249others(15): Show | 20 | HG00099.hp2 HG00609.hp1 HG00642.hp2 others(17): Show |
intron_variant | MODIFIER | c.704-3750_704-3749i others(20): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110981876 | |||||
chr10:110981876
|
T | TTTTTTAT others(7): Show |
105 | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007others(102): Show | 113 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(110): Show |
intron_variant | MODIFIER | c.704-3751_704-3750i others(16): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110981876 | |||||
chr10:110981961
|
T | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.704-3667T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110981961 | ||||||
chr10:110982004
|
C | T | 23 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(20): Show | 25 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(22): Show |
intron_variant | MODIFIER | c.704-3624C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982004 | ||||||
chr10:110982012
|
C | G | 1 | a0001c0001t0001g0305 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.704-3616C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982012 | ||||||
chr10:110982030
|
A | G | 13 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(10): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.704-3598A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982030 | ||||||
chr10:110982038
|
A | G | 1 | a0001c0001t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.704-3590A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982038 | ||||||
chr10:110982102
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.704-3526G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982102 | ||||||
chr10:110982140
|
A | G | 36 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(33): Show | 40 | HG00408.hp2 HG00642.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.704-3488A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982140 | ||||||
chr10:110982145
|
G | A | 4 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0157others(1): Show | 4 | HG03490.hp1 HG03492.hp1 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.704-3483G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982145 | ||||||
chr10:110982319
|
T | C | 128 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.704-3309T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982319 | ||||||
chr10:110982350
|
T | G | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.704-3278T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982350 | ||||||
chr10:110982376
|
C | T | 3 | a0001c0001t0001g0258a0001c0001t0001g0276a0001c0001t0002g0216 | 3 | HG01928.hp2 HG01975.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.704-3252C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982376 | ||||||
chr10:110982409
|
T | C | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.704-3219T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982409 | ||||||
chr10:110982545
|
A | G | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.704-3083A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982545 | ||||||
chr10:110982658
|
T | G | 2 | a0001c0001t0004g0344a0001c0001t0018g0162 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.704-2970T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982658 | ||||||
chr10:110982769
|
T | C | 1 | a0001c0001t0001g0131 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.704-2859T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982769 | ||||||
chr10:110982784
|
A | C | 3 | a0001c0001t0001g0159a0001c0001t0001g0160a0001c0001t0001g0161 | 3 | HG01175.hp2 HG01978.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.704-2844A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982784 | ||||||
chr10:110982792
|
A | G | 16 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0001g0149others(13): Show | 16 | HG01175.hp2 HG01978.hp2 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.704-2836A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110982792 | ||||||
chr10:110983119
|
A | G | 14 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.704-2509A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110983119 | ||||||
chr10:110983272
|
A | G | 2 | a0001c0001t0004g0344a0001c0001t0018g0162 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.704-2356A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110983272 | ||||||
chr10:110983379
|
T | C | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.704-2249T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110983379 | ||||||
chr10:110983497
|
G | GT | 6 | a0001c0001t0001g0252a0001c0001t0001g0255a0001c0001t0001g0264others(3): Show | 6 | HG00408.hp1 HG02735.hp2 NA18939.hp1 others(3): Show |
intron_variant | MODIFIER | c.704-2124dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr10 | 110983497 | |||||
chr10:110983879
|
A | G | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-1749A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110983879 | ||||||
chr10:110984023
|
C | A | 1 | a0001c0001t0001g0049 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.704-1605C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984023 | ||||||
chr10:110984117
|
A | G | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.704-1511A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984117 | ||||||
chr10:110984131
|
A | G | 13 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(10): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.704-1497A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984131 | ||||||
chr10:110984219
|
T | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(302): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.704-1409T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984219 | ||||||
chr10:110984359
|
G | T | 3 | a0001c0001t0002g0190a0001c0001t0002g0202a0001c0001t0002g0222 | 3 | NA18969.hp1 NA19006.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.704-1269G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984359 | ||||||
chr10:110984521
|
A | G | 7 | a0001c0001t0001g0007a0001c0001t0001g0041a0001c0001t0001g0042others(4): Show | 8 | HG00140.hp2 HG00639.hp1 HG01169.hp1 others(5): Show |
intron_variant | MODIFIER | c.704-1107A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984521 | ||||||
chr10:110984567
|
C | T | 10 | a0001c0001t0001g0032a0001c0001t0001g0246a0001c0001t0001g0290others(7): Show | 11 | HG02071.hp1 NA18942.hp2 NA18952.hp1 others(8): Show |
intron_variant | MODIFIER | c.704-1061C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984567 | ||||||
chr10:110984654
|
A | G | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.704-974A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984654 | ||||||
chr10:110984749
|
A | T | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.704-879A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984749 | ||||||
chr10:110984787
|
A | G | 301 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(298): Show | 333 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(330): Show |
intron_variant | MODIFIER | c.704-841A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984787 | ||||||
chr10:110984808
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.704-820G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110984808 | ||||||
chr10:110985107
|
T | C | 10 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0166others(7): Show | 14 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.704-521T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110985107 | ||||||
chr10:110985158
|
T | C | 2 | a0001c0001t0001g0035a0001c0001t0001g0039 | 2 | NA18970.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.704-470T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110985158 | ||||||
chr10:110985200
|
C | T | 3 | a0001c0001t0001g0298a0001c0001t0001g0299a0001c0001t0001g0300 | 3 | HG02647.hp2 HG03195.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.704-428C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110985200 | ||||||
chr10:110985458
|
G | A | 1 | a0001c0001t0004g0225 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.704-170G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110985458 | ||||||
chr10:110985498
|
G | A | 1 | a0001c0001t0009g0123 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.704-130G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110985498 | ||||||
chr10:110985549
|
T | A | 2 | a0001c0001t0001g0009a0001c0001t0001g0067 | 3 | HG02109.hp2 HG02280.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.704-79T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 2/8 | chr10 | 110985549 | ||||||
chr10:110985777
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.841+12G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110985777 | ||||||
chr10:110985931
|
C | T | 22 | a0001c0001t0002g0004a0001c0001t0002g0021a0001c0001t0002g0022others(19): Show | 26 | HG01257.hp1 HG01952.hp1 HG01975.hp2 others(23): Show |
intron_variant | MODIFIER | c.841+166C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110985931 | ||||||
chr10:110986001
|
A | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.841+236A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986001 | ||||||
chr10:110986008
|
T | C | 118 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 128 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.841+243T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986008 | ||||||
chr10:110986259
|
G | T | 13 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(10): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.841+494G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986259 | ||||||
chr10:110986470
|
T | C | 1 | a0001c0001t0002g0203 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.841+705T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986470 | ||||||
chr10:110986576
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.841+811C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986576 | ||||||
chr10:110986618
|
C | T | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.841+853C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986618 | ||||||
chr10:110986619
|
G | A | 6 | a0001c0001t0001g0131a0001c0001t0001g0239a0001c0001t0001g0262others(3): Show | 6 | HG00438.hp1 HG00609.hp1 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.841+854G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986619 | ||||||
chr10:110986630
|
C | T | 1 | a0001c0001t0001g0296 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.841+865C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986630 | ||||||
chr10:110986800
|
G | C | 6 | a0001c0001t0001g0012a0001c0001t0001g0056a0001c0001t0001g0058others(3): Show | 7 | NA18953.hp1 NA18961.hp2 NA19058.hp2 others(4): Show |
intron_variant | MODIFIER | c.841+1035G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986800 | ||||||
chr10:110986977
|
A | C | 223 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(220): Show | 245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.841+1212A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110986977 | ||||||
chr10:110987042
|
A | G | 2 | a0001c0001t0008g0230a0001c0001t0008g0321 | 2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.841+1277A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987042 | ||||||
chr10:110987052
|
C | T | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.841+1287C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987052 | ||||||
chr10:110987121
|
A | G | 1 | a0001c0001t0001g0016 | 2 | HG03654.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.841+1356A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987121 | ||||||
chr10:110987163
|
TGCTTGTA others(12): Show |
T | 2 | a0001c0001t0001g0155a0001c0001t0001g0156 | 2 | HG02602.hp1 HG02735.hp1 |
intron_variant | MODIFIER | c.841+1405_841+1423d others(21): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110987163 | |||||
chr10:110987199
|
G | A | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.841+1434G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987199 | ||||||
chr10:110987417
|
C | T | 12 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(9): Show | 12 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.841+1652C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987417 | ||||||
chr10:110987460
|
C | G | 1 | a0001c0001t0001g0014 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.841+1695C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987460 | ||||||
chr10:110987484
|
A | C | 1 | a0001c0001t0008g0224 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.841+1719A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987484 | ||||||
chr10:110987497
|
T | G | 1 | a0001c0001t0001g0329 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.841+1732T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987497 | ||||||
chr10:110987706
|
A | G | 1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.841+1941A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987706 | ||||||
chr10:110987752
|
T | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.841+1987T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987752 | ||||||
chr10:110987760
|
A | T | 1 | a0001c0001t0001g0116 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.841+1995A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987760 | ||||||
chr10:110987770
|
C | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.841+2005C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987770 | ||||||
chr10:110987784
|
T | C | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.841+2019T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987784 | ||||||
chr10:110987793
|
G | A | 4 | a0001c0001t0004g0336a0001c0001t0004g0337a0001c0001t0004g0338others(1): Show | 4 | HG02451.hp2 HG03486.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.841+2028G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987793 | ||||||
chr10:110987864
|
C | G | 1 | a0001c0001t0001g0315 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.841+2099C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987864 | ||||||
chr10:110987986
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.841+2221G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987986 | ||||||
chr10:110987994
|
C | T | 1 | a0001c0001t0001g0236 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.841+2229C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110987994 | ||||||
chr10:110988070
|
G | A | 78 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(75): Show | 88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.841+2305G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110988070 | ||||||
chr10:110988448
|
A | G | 13 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(10): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.841+2683A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110988448 | ||||||
chr10:110988465
|
A | G | 2 | a0001c0001t0001g0032a0001c0001t0001g0350 | 2 | NA18990.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.841+2700A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110988465 | ||||||
chr10:110988495
|
A | G | 1 | a0001c0001t0002g0194 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.841+2730A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110988495 | ||||||
chr10:110988658
|
T | C | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.841+2893T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110988658 | ||||||
chr10:110989044
|
A | G | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.841+3279A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110989044 | ||||||
chr10:110989171
|
G | A | 7 | a0001c0001t0001g0114a0001c0001t0001g0303a0001c0001t0001g0304others(4): Show | 7 | HG01109.hp1 HG02145.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.841+3406G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110989171 | ||||||
chr10:110989351
|
T | C | 303 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(300): Show | 335 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(332): Show |
intron_variant | MODIFIER | c.841+3586T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110989351 | ||||||
chr10:110989362
|
C | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.841+3597C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110989362 | ||||||
chr10:110989391
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.841+3626T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110989391 | ||||||
chr10:110990153
|
T | C | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(184): Show | 209 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.841+4388T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990153 | ||||||
chr10:110990157
|
G | A | 1 | a0001c0001t0002g0222 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.841+4392G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990157 | ||||||
chr10:110990189
|
T | C | 321 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(318): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.841+4424T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990189 | ||||||
chr10:110990319
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.841+4554T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990319 | ||||||
chr10:110990364
|
G | C | 9 | a0001c0001t0001g0006a0001c0001t0001g0029a0001c0001t0001g0030others(6): Show | 10 | HG00544.hp1 HG00597.hp1 HG02083.hp2 others(7): Show |
intron_variant | MODIFIER | c.841+4599G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990364 | ||||||
chr10:110990385
|
A | C | 9 | a0001c0001t0002g0020a0001c0001t0002g0178a0001c0001t0002g0185others(6): Show | 10 | HG00558.hp1 HG02027.hp2 NA18956.hp1 others(7): Show |
intron_variant | MODIFIER | c.841+4620A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990385 | ||||||
chr10:110990485
|
G | C | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.841+4720G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990485 | ||||||
chr10:110990493
|
G | A | 1 | a0001c0003t0001g0302 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.841+4728G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990493 | ||||||
chr10:110990531
|
T | TG | 128 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(125): Show | 139 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(136): Show |
intron_variant | MODIFIER | c.841+4768dupG | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110990531 | |||||
chr10:110990555
|
G | A | 1 | a0001c0001t0002g0019 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.841+4790G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990555 | ||||||
chr10:110990732
|
A | C | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.841+4967A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990732 | ||||||
chr10:110990853
|
C | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(340): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.841+5088C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990853 | ||||||
chr10:110990871
|
C | T | 187 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(184): Show | 209 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(206): Show |
intron_variant | MODIFIER | c.841+5106C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110990871 | ||||||
chr10:110991046
|
G | C | 1 | a0001c0001t0002g0163 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.841+5281G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110991046 | ||||||
chr10:110991210
|
C | G | 2 | a0001c0001t0001g0303a0001c0001t0001g0305 | 2 | HG01109.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.841+5445C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110991210 | ||||||
chr10:110991405
|
A | G | 1 | a0001c0001t0002g0208 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.841+5640A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110991405 | ||||||
chr10:110991531
|
G | T | 2 | a0001c0001t0002g0167a0001c0001t0002g0171 | 2 | HG02109.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.841+5766G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110991531 | ||||||
chr10:110991673
|
G | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.841+5908G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110991673 | ||||||
chr10:110992260
|
A | C | 1 | a0001c0001t0001g0314 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.841+6495A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110992260 | ||||||
chr10:110992276
|
A | G | 1 | a0001c0001t0017g0098 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.841+6511A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110992276 | ||||||
chr10:110992376
|
A | G | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.841+6611A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110992376 | ||||||
chr10:110992619
|
A | G | 319 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(316): Show | 352 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(349): Show |
intron_variant | MODIFIER | c.841+6854A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110992619 | ||||||
chr10:110992628
|
G | A | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.841+6863G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110992628 | ||||||
chr10:110993066
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.841+7301C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993066 | ||||||
chr10:110993367
|
G | T | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.842-7048G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993367 | ||||||
chr10:110993465
|
G | T | 3 | a0001c0001t0001g0304a0001c0001t0001g0311a0001c0001t0001g0312 | 3 | HG02965.hp2 HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.842-6950G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993465 | ||||||
chr10:110993529
|
A | G | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.842-6886A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993529 | ||||||
chr10:110993777
|
T | C | 1 | a0001c0001t0002g0348 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.842-6638T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993777 | ||||||
chr10:110993887
|
G | A | 1 | a0001c0001t0001g0054 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.842-6528G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993887 | ||||||
chr10:110993963
|
C | T | 320 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(317): Show | 353 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(350): Show |
intron_variant | MODIFIER | c.842-6452C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110993963 | ||||||
chr10:110994265
|
A | T | 7 | a0001c0001t0001g0252a0001c0001t0001g0255a0001c0001t0001g0264others(4): Show | 7 | HG00408.hp1 HG02735.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.842-6150A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110994265 | ||||||
chr10:110994721
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(340): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.842-5694T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110994721 | ||||||
chr10:110994925
|
T | C | 1 | a0001c0001t0001g0141 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.842-5490T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110994925 | ||||||
chr10:110994989
|
A | G | 1 | a0001c0001t0001g0314 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.842-5426A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110994989 | ||||||
chr10:110995015
|
A | G | 1 | a0001c0001t0001g0096 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.842-5400A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995015 | ||||||
chr10:110995031
|
A | G | 1 | a0001c0001t0001g0131 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.842-5384A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995031 | ||||||
chr10:110995052
|
GAAAA | G | 2 | a0001c0001t0004g0027a0001c0001t0004g0341 | 3 | HG01884.hp1 HG01891.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.842-5362_842-5359d others(6): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995052 | ||||||
chr10:110995137
|
T | A | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.842-5278T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995137 | ||||||
chr10:110995140
|
T | C | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.842-5275T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995140 | ||||||
chr10:110995141
|
G | A | 1 | a0001c0001t0001g0082 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.842-5274G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995141 | ||||||
chr10:110995416
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.842-4999A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995416 | ||||||
chr10:110995501
|
A | T | 18 | a0001c0001t0004g0027a0001c0001t0004g0225a0001c0001t0004g0333others(15): Show | 19 | HG01074.hp2 HG01081.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.842-4914A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995501 | ||||||
chr10:110995538
|
A | C | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.842-4877A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995538 | ||||||
chr10:110995845
|
C | T | 22 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0147others(19): Show | 24 | HG01175.hp2 HG01261.hp1 HG01978.hp2 others(21): Show |
intron_variant | MODIFIER | c.842-4570C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995845 | ||||||
chr10:110995971
|
C | T | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.842-4444C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110995971 | ||||||
chr10:110996123
|
G | T | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.842-4292G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996123 | ||||||
chr10:110996333
|
G | T | 1 | a0001c0001t0001g0275 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.842-4082G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996333 | ||||||
chr10:110996368
|
A | G | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.842-4047A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996368 | ||||||
chr10:110996410
|
C | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0274 | 2 | HG02257.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.842-4005C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996410 | ||||||
chr10:110996452
|
A | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(340): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.842-3963A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996452 | ||||||
chr10:110996828
|
C | G | 1 | a0001c0001t0005g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.842-3587C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996828 | ||||||
chr10:110996889
|
A | T | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.842-3526A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110996889 | ||||||
chr10:110997427
|
A | G | 5 | a0001c0001t0001g0076a0001c0001t0001g0077a0001c0001t0001g0078others(2): Show | 5 | HG02717.hp2 HG02809.hp1 HG03041.hp1 others(2): Show |
intron_variant | MODIFIER | c.842-2988A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997427 | ||||||
chr10:110997528
|
CT | C | 153 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(150): Show | 173 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(170): Show |
intron_variant | MODIFIER | c.842-2882delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110997528 | |||||
chr10:110997532
|
T | C | 206 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(203): Show | 230 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(227): Show |
intron_variant | MODIFIER | c.842-2883T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997532 | ||||||
chr10:110997533
|
T | C | 343 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(340): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.842-2882T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997533 | ||||||
chr10:110997539
|
C | G | 3 | a0001c0001t0009g0122a0001c0001t0009g0123a0001c0001t0015g0048 | 3 | HG02698.hp1 HG04199.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.842-2876C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997539 | ||||||
chr10:110997604
|
G | A | 1 | a0001c0001t0001g0151 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.842-2811G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997604 | ||||||
chr10:110997624
|
T | A | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.842-2791T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997624 | ||||||
chr10:110997658
|
C | A | 10 | a0001c0001t0002g0021a0001c0001t0002g0022a0001c0001t0002g0165others(7): Show | 12 | HG02015.hp1 HG02074.hp2 NA18949.hp1 others(9): Show |
intron_variant | MODIFIER | c.842-2757C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997658 | ||||||
chr10:110997951
|
A | G | 1 | a0001c0001t0001g0139 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.842-2464A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110997951 | ||||||
chr10:110997998
|
CT | C | 180 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(177): Show | 202 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(199): Show |
intron_variant | MODIFIER | c.842-2402delT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110997998 | |||||
chr10:110998036
|
C | T | 350 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(347): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.842-2379C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998036 | ||||||
chr10:110998196
|
A | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.842-2219A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998196 | ||||||
chr10:110998218
|
C | T | 183 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(180): Show | 205 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(202): Show |
intron_variant | MODIFIER | c.842-2197C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998218 | ||||||
chr10:110998251
|
G | C | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.842-2164G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998251 | ||||||
chr10:110998365
|
T | G | 75 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(72): Show | 85 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(82): Show |
intron_variant | MODIFIER | c.842-2050T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998365 | ||||||
chr10:110998380
|
T | A | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.842-2035T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998380 | ||||||
chr10:110998386
|
T | G | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.842-2029T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998386 | ||||||
chr10:110998398
|
G | C | 1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.842-2017G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998398 | ||||||
chr10:110998416
|
C | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.842-1999C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998416 | ||||||
chr10:110998439
|
G | A | 1 | a0001c0001t0001g0075 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.842-1976G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998439 | ||||||
chr10:110998485
|
T | G | 2 | a0001c0001t0002g0018a0001c0001t0002g0301 | 3 | NA18952.hp2 NA18998.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.842-1930T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998485 | ||||||
chr10:110998683
|
AAGTGGTG others(2): Show |
A | 8 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(5): Show | 9 | HG02055.hp2 HG02145.hp2 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.842-1731_842-1723d others(11): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998683 | ||||||
chr10:110998724
|
T | C | 1 | a0001c0001t0002g0132 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.842-1691T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998724 | ||||||
chr10:110998951
|
T | G | 2 | a0001c0001t0001g0196a0001c0001t0002g0195 | 2 | HG02602.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.842-1464T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110998951 | ||||||
chr10:110999038
|
G | A | 4 | a0001c0001t0004g0344a0001c0001t0009g0122a0001c0001t0009g0123others(1): Show | 4 | HG02698.hp1 HG02922.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.842-1377G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999038 | ||||||
chr10:110999116
|
G | T | 2 | a0001c0001t0004g0344a0001c0001t0018g0162 | 2 | HG02922.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.842-1299G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999116 | ||||||
chr10:110999236
|
C | G | 1 | a0001c0001t0001g0051 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.842-1179C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999236 | ||||||
chr10:110999323
|
T | C | 3 | a0001c0001t0004g0337a0001c0001t0004g0338a0001c0001t0004g0339 | 3 | HG02451.hp2 HG03486.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.842-1092T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999323 | ||||||
chr10:110999330
|
C | T | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.842-1085C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999330 | ||||||
chr10:110999346
|
A | G | 1 | a0001c0001t0011g0103 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.842-1069A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999346 | ||||||
chr10:110999524
|
G | A | 1 | a0001c0001t0007g0210 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.842-891G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999524 | ||||||
chr10:110999672
|
G | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.842-743G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999672 | ||||||
chr10:110999736
|
C | CA | 11 | a0001c0001t0001g0071a0001c0001t0001g0258a0001c0001t0001g0273others(8): Show | 11 | HG01109.hp1 HG01243.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.842-656dupA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | |||||
chr10:110999736
|
C | CAA | 166 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(163): Show | 179 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(176): Show |
intron_variant | MODIFIER | c.842-657_842-656dup others(2): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | |||||
chr10:110999736
|
C | CAAA | 25 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0040others(22): Show | 28 | HG00642.hp1 HG01261.hp1 HG01928.hp1 others(25): Show |
intron_variant | MODIFIER | c.842-658_842-656dup others(3): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | |||||
chr10:110999736
|
C | CAAAA | 5 | a0001c0001t0003g0015a0001c0001t0003g0125a0001c0001t0003g0126others(2): Show | 6 | HG02145.hp2 HG02258.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.842-659_842-656dup others(4): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | |||||
chr10:110999736
|
CAAAAAA | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(30): Show | 39 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.842-661_842-656del others(6): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | |||||
chr10:110999736
|
CAAAAAAA | C | 6 | a0001c0001t0001g0072a0001c0001t0001g0108a0001c0001t0001g0109others(3): Show | 6 | HG02683.hp2 HG03491.hp1 HG03492.hp2 others(3): Show |
intron_variant | MODIFIER | c.842-662_842-656del others(7): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | |||||
chr10:110999736
|
CAAAAAAA others(4): Show |
C | 78 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(75): Show | 88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.842-666_842-656del others(11): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | |||||
chr10:110999736
|
CAAAAAAA others(7): Show |
C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.842-669_842-656del others(14): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr10 | 110999736 | |||||
chr10:110999760
|
G | A | 13 | a0001c0001t0003g0015a0001c0001t0003g0124a0001c0001t0003g0125others(10): Show | 15 | HG01243.hp1 HG02055.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.842-655G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999760 | ||||||
chr10:110999850
|
A | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0010a0001c0001t0001g0011others(36): Show | 45 | HG00099.hp1 HG00423.hp1 HG00544.hp2 others(42): Show |
intron_variant | MODIFIER | c.842-565A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999850 | ||||||
chr10:110999973
|
T | G | 134 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(131): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.842-442T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 3/8 | chr10 | 110999973 | ||||||
chr10:111000566
|
A | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.972+21A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000566 | ||||||
chr10:111000708
|
A | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.972+163A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000708 | ||||||
chr10:111000748
|
T | C | 1 | a0001c0001t0001g0010 | 2 | NA19054.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.972+203T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000748 | ||||||
chr10:111000786
|
A | G | 343 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(340): Show | 378 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(375): Show |
intron_variant | MODIFIER | c.972+241A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000786 | ||||||
chr10:111000813
|
T | C | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.972+268T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000813 | ||||||
chr10:111000822
|
G | A | 5 | a0002c0002t0003g0028a0002c0002t0003g0117a0002c0002t0003g0345others(2): Show | 6 | HG01243.hp1 HG02572.hp1 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.972+277G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000822 | ||||||
chr10:111000936
|
A | G | 1 | a0001c0001t0010g0154 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.972+391A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000936 | ||||||
chr10:111000994
|
C | T | 2 | a0001c0001t0001g0304a0001c0001t0004g0344 | 2 | HG02922.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.972+449C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111000994 | ||||||
chr10:111001060
|
C | CT | 284 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(281): Show | 315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.972+528dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 111001060 | |||||
chr10:111001157
|
C | CT | 132 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(129): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.972+629dupT | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 111001157 | |||||
chr10:111001197
|
G | T | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.972+652G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001197 | ||||||
chr10:111001220
|
C | T | 2 | a0001c0001t0001g0032a0001c0001t0001g0350 | 2 | NA18990.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.972+675C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001220 | ||||||
chr10:111001231
|
C | T | 1 | a0001c0001t0002g0203 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.972+686C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001231 | ||||||
chr10:111001243
|
C | G | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.972+698C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001243 | ||||||
chr10:111001312
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.972+767G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001312 | ||||||
chr10:111001315
|
C | T | 1 | a0001c0004t0016g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.972+770C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001315 | ||||||
chr10:111001318
|
T | C | 306 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(303): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.972+773T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001318 | ||||||
chr10:111001434
|
C | T | 1 | a0001c0001t0002g0220 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.972+889C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001434 | ||||||
chr10:111001448
|
G | A | 1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.972+903G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001448 | ||||||
chr10:111001608
|
G | T | 350 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(347): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.972+1063G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001608 | ||||||
chr10:111001760
|
G | A | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.972+1215G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001760 | ||||||
chr10:111001805
|
AGGCG | A | 18 | a0001c0001t0004g0027a0001c0001t0004g0225a0001c0001t0004g0333others(15): Show | 19 | HG01074.hp2 HG01081.hp1 HG01168.hp1 others(16): Show |
intron_variant | MODIFIER | c.972+1266_972+1269d others(6): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 111001805 | |||||
chr10:111001813
|
G | A | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 89 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.972+1268G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001813 | ||||||
chr10:111001951
|
A | G | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.972+1406A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111001951 | ||||||
chr10:111001987
|
AGTGAGCC others(3): Show |
A | 2 | a0001c0001t0008g0230a0001c0001t0008g0321 | 2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.972+1447_972+1456d others(12): Show |
SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 111001987 | |||||
chr10:111002003
|
G | A | 1 | a0001c0001t0004g0225 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.972+1458G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002003 | ||||||
chr10:111002047
|
A | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.972+1502A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002047 | ||||||
chr10:111002125
|
T | C | 1 | a0001c0001t0001g0138 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.972+1580T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002125 | ||||||
chr10:111002185
|
G | T | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.972+1640G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002185 | ||||||
chr10:111002556
|
T | A | 76 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(73): Show | 86 | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.972+2011T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002556 | ||||||
chr10:111002622
|
A | G | 3 | a0001c0001t0001g0135a0001c0001t0001g0136a0001c0001t0001g0137 | 3 | HG03225.hp2 HG03540.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.973-1984A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002622 | ||||||
chr10:111002719
|
C | T | 1 | a0001c0001t0008g0230 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.973-1887C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002719 | ||||||
chr10:111002746
|
G | A | 1 | a0001c0001t0001g0265 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.973-1860G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002746 | ||||||
chr10:111002779
|
CA | C | 288 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(285): Show | 319 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(316): Show |
intron_variant | MODIFIER | c.973-1814delA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | INFO_REALIGN_3_PRIME | chr10 | 111002779 | |||||
chr10:111002783
|
A | T | 7 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0155others(4): Show | 9 | HG01261.hp1 HG02027.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.973-1823A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111002783 | ||||||
chr10:111003107
|
T | C | 287 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(284): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.973-1499T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003107 | ||||||
chr10:111003174
|
C | T | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.973-1432C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003174 | ||||||
chr10:111003398
|
G | A | 289 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(286): Show | 320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.973-1208G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003398 | ||||||
chr10:111003520
|
G | A | 1 | a0001c0001t0006g0244 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.973-1086G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003520 | ||||||
chr10:111003552
|
T | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(347): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.973-1054T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003552 | ||||||
chr10:111003627
|
G | A | 103 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(100): Show | 112 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.973-979G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003627 | ||||||
chr10:111003677
|
C | A | 1 | a0001c0001t0007g0191 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.973-929C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003677 | ||||||
chr10:111003679
|
T | C | 1 | a0001c0001t0007g0191 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.973-927T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003679 | ||||||
chr10:111003680
|
G | T | 1 | a0001c0001t0007g0191 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.973-926G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003680 | ||||||
chr10:111003781
|
G | T | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.973-825G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003781 | ||||||
chr10:111003816
|
C | T | 287 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(284): Show | 318 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(315): Show |
intron_variant | MODIFIER | c.973-790C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003816 | ||||||
chr10:111003913
|
T | C | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 89 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(86): Show |
intron_variant | MODIFIER | c.973-693T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003913 | ||||||
chr10:111003917
|
G | A | 3 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0046 | 4 | HG00140.hp2 HG00639.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.973-689G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111003917 | ||||||
chr10:111004016
|
G | T | 1 | a0001c0001t0025g0121 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.973-590G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004016 | ||||||
chr10:111004124
|
G | T | 36 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0013others(33): Show | 40 | HG00408.hp2 HG00642.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.973-482G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004124 | ||||||
chr10:111004191
|
A | G | 1 | a0001c0001t0007g0211 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.973-415A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004191 | ||||||
chr10:111004212
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.973-394G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004212 | ||||||
chr10:111004274
|
C | G | 4 | a0001c0001t0001g0055a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | HG01109.hp2 HG02257.hp1 HG02451.hp1 others(1): Show |
intron_variant | MODIFIER | c.973-332C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004274 | ||||||
chr10:111004424
|
C | T | 1 | a0001c0001t0001g0081 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.973-182C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004424 | ||||||
chr10:111004466
|
T | G | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.973-140T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 4/8 | chr10 | 111004466 | ||||||
chr10:111004836
|
T | C | 305 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(302): Show | 337 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(334): Show |
intron_variant | MODIFIER | c.1161+42T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111004836 | ||||||
chr10:111004975
|
C | A | 3 | a0001c0001t0001g0147a0001c0001t0001g0148a0001c0001t0005g0228 | 3 | HG03490.hp1 HG03492.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1161+181C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111004975 | ||||||
chr10:111004992
|
T | C | 1 | a0001c0001t0001g0133 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1161+198T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111004992 | ||||||
chr10:111005417
|
G | A | 78 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(75): Show | 88 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(85): Show |
intron_variant | MODIFIER | c.1161+623G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005417 | ||||||
chr10:111005454
|
C | G | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1161+660C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005454 | ||||||
chr10:111005458
|
G | A | 4 | a0001c0001t0004g0344a0001c0001t0009g0122a0001c0001t0009g0123others(1): Show | 4 | HG02698.hp1 HG02922.hp1 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.1161+664G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005458 | ||||||
chr10:111005644
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1161+850C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005644 | ||||||
chr10:111005721
|
A | C | 1 | a0001c0001t0001g0342 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1161+927A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005721 | ||||||
chr10:111005856
|
T | C | 3 | a0001c0001t0001g0088a0001c0001t0001g0309a0001c0001t0001g0343 | 3 | NA18966.hp2 NA18989.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.1161+1062T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005856 | ||||||
chr10:111005922
|
G | A | 327 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(324): Show | 361 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(358): Show |
intron_variant | MODIFIER | c.1161+1128G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111005922 | ||||||
chr10:111006196
|
G | A | 1 | a0001c0004t0016g0142 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1162-1335G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006196 | ||||||
chr10:111006238
|
C | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1162-1293C>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006238 | ||||||
chr10:111006394
|
G | A | 1 | a0001c0001t0020g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1162-1137G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006394 | ||||||
chr10:111006401
|
C | T | 1 | a0001c0001t0002g0234 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1162-1130C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006401 | ||||||
chr10:111006402
|
G | A | 1 | a0001c0001t0001g0323 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1162-1129G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006402 | ||||||
chr10:111006423
|
T | G | 2 | a0001c0001t0001g0327a0001c0001t0022g0326 | 2 | HG03017.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.1162-1108T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006423 | ||||||
chr10:111006461
|
C | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1162-1070C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006461 | ||||||
chr10:111006516
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1162-1015G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006516 | ||||||
chr10:111006520
|
G | A | 1 | a0001c0001t0001g0120 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1162-1011G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006520 | ||||||
chr10:111006572
|
G | A | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1162-959G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006572 | ||||||
chr10:111006580
|
C | T | 14 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135others(11): Show | 14 | HG01891.hp1 HG02280.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1162-951C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006580 | ||||||
chr10:111006683
|
A | G | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1162-848A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006683 | ||||||
chr10:111006731
|
G | A | 1 | a0001c0001t0005g0115 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1162-800G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006731 | ||||||
chr10:111006844
|
T | C | 1 | a0001c0001t0001g0307 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1162-687T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006844 | ||||||
chr10:111006879
|
G | A | 10 | a0001c0001t0002g0002a0001c0001t0002g0017a0001c0001t0002g0166others(7): Show | 14 | HG02109.hp1 HG02615.hp2 HG02630.hp1 others(11): Show |
intron_variant | MODIFIER | c.1162-652G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006879 | ||||||
chr10:111006990
|
G | T | 3 | a0001c0001t0004g0333a0001c0001t0004g0334a0001c0001t0004g0335 | 3 | HG01168.hp1 HG02486.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1162-541G>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111006990 | ||||||
chr10:111007171
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1162-360T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111007171 | ||||||
chr10:111007254
|
C | T | 1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1162-277C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111007254 | ||||||
chr10:111007261
|
G | A | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1162-270G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111007261 | ||||||
chr10:111007278
|
G | A | 1 | a0001c0001t0001g0089 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1162-253G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111007278 | ||||||
chr10:111007291
|
C | T | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1162-240C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111007291 | ||||||
chr10:111007401
|
T | G | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1162-130T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 5/8 | chr10 | 111007401 | ||||||
chr10:111007726
|
A | G | 2 | a0001c0001t0008g0230a0001c0001t0008g0321 | 2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1284+73A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111007726 | ||||||
chr10:111007938
|
T | C | 2 | a0001c0001t0008g0230a0001c0001t0008g0321 | 2 | HG01081.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.1284+285T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111007938 | ||||||
chr10:111008405
|
A | G | 3 | a0001c0001t0001g0055a0001c0001t0001g0063a0001c0001t0001g0064 | 3 | HG01109.hp2 HG02451.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1284+752A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008405 | ||||||
chr10:111008438
|
T | A | 118 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(115): Show | 127 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1284+785T>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008438 | ||||||
chr10:111008442
|
C | G | 1 | a0001c0001t0002g0234 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1284+789C>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008442 | ||||||
chr10:111008535
|
T | G | 2 | a0001c0001t0001g0147a0001c0001t0001g0148 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1285-713T>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008535 | ||||||
chr10:111008592
|
A | G | 1 | a0001c0001t0001g0145 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1285-656A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008592 | ||||||
chr10:111008760
|
C | T | 1 | a0001c0001t0013g0226 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1285-488C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008760 | ||||||
chr10:111008845
|
T | C | 1 | a0001c0001t0020g0331 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1285-403T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008845 | ||||||
chr10:111008866
|
TA | T | 5 | a0001c0001t0001g0024a0001c0001t0001g0259a0001c0001t0001g0260others(2): Show | 6 | NA18949.hp2 NA18973.hp2 NA18983.hp1 others(3): Show |
intron_variant | MODIFIER | c.1285-379delA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | INFO_REALIGN_3_PRIME | chr10 | 111008866 | |||||
chr10:111008870
|
T | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1285-378T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111008870 | ||||||
chr10:111009058
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0044a0001c0001t0001g0046 | 4 | HG00140.hp2 HG00639.hp1 HG03669.hp2 others(1): Show |
intron_variant | MODIFIER | c.1285-190C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111009058 | ||||||
chr10:111009060
|
C | T | 1 | a0001c0001t0001g0270 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1285-188C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111009060 | ||||||
chr10:111009092
|
A | C | 104 | a0001c0001t0001g0003a0001c0001t0001g0005a0001c0001t0001g0006others(101): Show | 113 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(110): Show |
intron_variant | MODIFIER | c.1285-156A>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 6/8 | chr10 | 111009092 | ||||||
chr10:111009509
|
C | T | 1 | a0001c0001t0018g0162 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1422+124C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 7/8 | chr10 | 111009509 | ||||||
chr10:111009620
|
T | C | 2 | a0001c0001t0001g0241a0001c0001t0001g0274 | 2 | HG02257.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1423-93T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 7/8 | chr10 | 111009620 | ||||||
chr10:111009706
|
C | T | 2 | a0001c0001t0004g0225a0001c0001t0008g0224 | 2 | HG03139.hp1 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.1423-7C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 7/8 | chr10 | 111009706 | ||||||
chr10:111009860
|
A | T | 1 | a0001c0001t0004g0341 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1540+30A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111009860 | ||||||
chr10:111010286
|
T | C | 1 | a0001c0001t0004g0344 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1540+456T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111010286 | ||||||
chr10:111010541
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1540+711G>A | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111010541 | ||||||
chr10:111010546
|
G | C | 79 | a0001c0001t0001g0196a0001c0001t0002g0002a0001c0001t0002g0004others(76): Show | 90 | HG00558.hp1 HG00597.hp2 HG00609.hp2 others(87): Show |
intron_variant | MODIFIER | c.1540+716G>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111010546 | ||||||
chr10:111010681
|
TA | T | 326 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(323): Show | 360 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(357): Show |
intron_variant | MODIFIER | c.1540+860delA | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | INFO_REALIGN_3_PRIME | chr10 | 111010681 | |||||
chr10:111010893
|
T | C | 1 | a0001c0001t0008g0321 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1541-717T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111010893 | ||||||
chr10:111010957
|
C | T | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1541-653C>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111010957 | ||||||
chr10:111011020
|
T | C | 2 | a0001c0001t0009g0122a0001c0001t0009g0123 | 2 | HG02698.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.1541-590T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111011020 | ||||||
chr10:111011077
|
A | G | 5 | a0001c0001t0001g0043a0001c0001t0004g0333a0001c0001t0004g0334others(2): Show | 5 | HG01074.hp2 HG01168.hp1 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.1541-533A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111011077 | ||||||
chr10:111011105
|
T | C | 350 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0005others(347): Show | 385 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(382): Show |
intron_variant | MODIFIER | c.1541-505T>C | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111011105 | ||||||
chr10:111011134
|
A | G | 1 | a0001c0001t0001g0082 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1541-476A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111011134 | ||||||
chr10:111011223
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1541-387A>G | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111011223 | ||||||
chr10:111011581
|
A | T | 10 | a0001c0001t0004g0027a0001c0001t0004g0333a0001c0001t0004g0334others(7): Show | 11 | HG01074.hp2 HG01168.hp1 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1541-29A>T | SHOC2 | ENSG00000108061.13 | transcript | ENST00000369452.9 | protein_coding | 8/8 | chr10 | 111011581 |