geneid | 388960 |
---|---|
ensemblid | ENSG00000187833.8 |
hgncid | 34349 |
symbol | C2orf78 |
name | chromosome 2 open reading frame 78 |
refseq_nuc | NM_001080474.3 |
refseq_prot | NP_001073943.1 |
ensembl_nuc | ENST00000409561.2 |
ensembl_prot | ENSP00000387124.1 |
mane_status | MANE Select |
chr | chr2 |
start | 73784183 |
end | 73817148 |
strand | + |
ver | v1.2 |
region | chr2:73784183-73817148 |
region5000 | chr2:73779183-73822148 |
regionname0 | C2orf78_chr2_73784183_73817148 |
regionname5000 | C2orf78_chr2_73779183_73822148 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 922 | 190 | 65 | 31 | 58 | 8 | 26 | 35 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0002 | 0/0 | 922 | 7 | 6 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0003 | 0/0 | 4 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0004 | 0/0 | 922 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0005 | 0/0 | 922 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0006 | 0/0 | 922 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0007 | 0/0 | 922 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0008 | 0/0 | 922 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0009 | 0/0 | 922 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0010 | 0/0 | 922 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 2769 | 187 | 64 | 31 | 57 | 8 | 25 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0002 | 0/0 | 2672 | 6 | 5 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0003 | 0/0 | 2769 | 5 | 4 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0004 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0005 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0006 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0007 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0008 | 0/0 | 2769 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0009 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0010 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0011 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0012 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0013 | 0/0 | 2769 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
c0014 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 2769 | 187 | 64 | 31 | 57 | 8 | 25 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0001c0010 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0001c0013 | 0/0 | 2769 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0001c0014 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0002c0003 | 0/0 | 2769 | 5 | 4 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0002c0005 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0003c0002 | 0/0 | 2672 | 6 | 5 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0004c0004 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0005c0006 | 0/0 | 2769 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0006c0007 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0007c0008 | 0/0 | 2769 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0008c0011 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0009c0009 | 0/0 | 2769 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0010c0012 | 0/0 | 2769 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 3052 | 187 | 64 | 31 | 57 | 8 | 25 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0001c0010t0001 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0001c0013t0001 | 0/0 | 3052 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0001c0014t0001 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0002c0003t0001 | 0/0 | 3052 | 5 | 4 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0002c0005t0001 | 0/0 | 3052 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0003c0002t0002 | 0/0 | 2828 | 6 | 5 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0004c0004t0001 | 0/0 | 3052 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0005c0006t0001 | 0/0 | 3052 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0006c0007t0001 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0007c0008t0001 | 0/0 | 3052 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0008c0011t0001 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0009c0009t0001 | 0/0 | 3052 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
a0010c0012t0001 | 0/0 | 3052 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | copy fasta | chr2 | 73779183 | 73822148 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0019 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0142 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0010t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0013t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0001c0014t0001g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0002c0003t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0002c0003t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0002c0003t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0002c0003t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0002c0003t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0002c0005t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0002c0005t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0003c0002t0002g0001 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0003c0002t0002g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0004c0004t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0004c0004t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0005c0006t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0005c0006t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0006c0007t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0007c0008t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0008c0011t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0009c0009t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
a0010c0012t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0103 | EUR | GBR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0137 | EUR | GBR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0093 | EUR | FIN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | FIN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | CHS | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | CHS | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | CHS | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | CHS | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | CHS | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | CHS | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0176 | EAS | CHS | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | CHS | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0086 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0092 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01167 | hp1 | a0003 | c0002 | t0002 | g0001 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0067 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01243 | hp1 | a0002 | c0003 | t0001 | g0022 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | PUR | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0149 | AMR | CLM | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01346 | hp2 | a0007 | c0008 | t0001 | g0041 | AMR | CLM | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01361 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | CLM | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0019 | AMR | CLM | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PEL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PEL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0077 | AMR | PEL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | PEL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | PEL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0158 | AFR | ACB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02055 | hp2 | a0008 | c0011 | t0001 | g0048 | AFR | ACB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0152 | EAS | KHV | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | KHV | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | KHV | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | KHV | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02132 | hp1 | a0009 | c0009 | t0001 | g0089 | EAS | KHV | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02258 | hp1 | a0003 | c0002 | t0002 | g0021 | AFR | ACB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02280 | hp2 | a0003 | c0002 | t0002 | g0001 | AFR | ACB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PEL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PEL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PEL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02451 | hp1 | a0004 | c0004 | t0001 | g0035 | AFR | ACB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02451 | hp2 | a0003 | c0002 | t0002 | g0001 | AFR | ACB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | KHV | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0175 | EAS | KHV | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02622 | hp2 | a0002 | c0003 | t0001 | g0025 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0147 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0042 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0105 | SAS | PJL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0138 | SAS | PJL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0043 | SAS | PJL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0124 | SAS | PJL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02717 | hp1 | a0002 | c0005 | t0001 | g0029 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02723 | hp1 | a0005 | c0006 | t0001 | g0187 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | PJL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02738 | hp2 | a0001 | c0013 | t0001 | g0080 | SAS | PJL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02809 | hp1 | a0003 | c0002 | t0002 | g0001 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0146 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02818 | hp2 | a0001 | c0014 | t0001 | g0010 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02895 | hp2 | a0004 | c0004 | t0001 | g0185 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0051 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02896 | hp2 | a0002 | c0003 | t0001 | g0026 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0148 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0160 | SAS | PJL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0159 | SAS | PJL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03041 | hp2 | a0003 | c0002 | t0002 | g0001 | AFR | GWD | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0157 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0062 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0016 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03516 | hp1 | a0001 | c0001 | t0001 | g0133 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03516 | hp2 | a0002 | c0003 | t0001 | g0027 | AFR | ESN | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0031 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0130 | SAS | BEB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | BEB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0100 | SAS | BEB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0033 | SAS | BEB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0098 | SAS | BEB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | STU | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | STU | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0094 | SAS | BEB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | BEB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | STU | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | STU | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18522 | hp2 | a0002 | c0003 | t0001 | g0047 | AFR | YRI | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | CHB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | CHB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | CHB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18747 | hp2 | a0001 | c0010 | t0001 | g0078 | EAS | CHB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | YRI | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | YRI | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0054 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0046 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18949 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18966 | hp1 | a0006 | c0007 | t0001 | g0024 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0014 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0072 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19030 | hp1 | a0002 | c0005 | t0001 | g0028 | AFR | LWK | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | LWK | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0038 | AFR | LWK | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | LWK | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0057 | AFR | YRI | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0140 | AFR | YRI | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | ASW | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA20129 | hp2 | a0010 | c0012 | t0001 | g0169 | AFR | ASW | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0126 | EUR | TSI | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | TSI | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0102 | EUR | TSI | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0099 | EUR | TSI | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0166 | AFR | ACB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0030 | AFR | ACB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | MSL | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | USA | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | USA | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA20300 | hp1 | a0005 | c0006 | t0001 | g0186 | AFR | USA | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | USA | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0065 | AFR | LWK | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0069 | AFR | LWK | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0071 | REF | REF | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0142 | REF | REF | C2orf78_chr2_73779183_73822148 | C2orf78 | chr2 | 73779183 | 73822148 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:73815353
|
A | G | 1 | a0010 | 1 | NA20129.hp2 | missense_variant | MODERATE | c.1130A>G | p.Gln377Arg | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 3/3 | 1257/3052 | 1130/2769 | 377/922 | chr2 | 73815353 | ||
chr2:73815546
|
G | C | 1 | a0006 | 1 | NA18966.hp1 | missense_variant | MODERATE | c.1323G>C | p.Leu441Phe | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 3/3 | 1450/3052 | 1323/2769 | 441/922 | chr2 | 73815546 | ||
chr2:73815826
|
A | G | 1 | a0004 | 2 | HG02451.hp1 HG02895.hp2 |
missense_variant | MODERATE | c.1603A>G | p.Ser535Gly | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 3/3 | 1730/3052 | 1603/2769 | 535/922 | chr2 | 73815826 | ||
chr2:73815999
|
A | C | 3 | a0002a0003a0005 | 15 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(12): Show |
missense_variant | MODERATE | c.1776A>C | p.Lys592Asn | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 3/3 | 1903/3052 | 1776/2769 | 592/922 | chr2 | 73815999 | ||
chr2:73816091
|
G | A | 1 | a0007 | 1 | HG01346.hp2 | missense_variant | MODERATE | c.1868G>A | p.Arg623Gln | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 3/3 | 1995/3052 | 1868/2769 | 623/922 | chr2 | 73816091 | ||
chr2:73816106
|
T | C | 1 | a0009 | 1 | HG02132.hp1 | missense_variant | MODERATE | c.1883T>C | p.Met628Thr | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 3/3 | 2010/3052 | 1883/2769 | 628/922 | chr2 | 73816106 | ||
chr2:73816405
|
C | A | 1 | a0008 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.2182C>A | p.Gln728Lys | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 3/3 | 2309/3052 | 2182/2769 | 728/922 | chr2 | 73816405 | ||
chr2:73816829
|
C | T | 1 | a0005 | 2 | HG02723.hp1 NA20300.hp1 |
missense_variant | MODERATE | c.2606C>T | p.Thr869Met | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 3/3 | 2733/3052 | 2606/2769 | 869/922 | chr2 | 73816829 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:73814165
|
C | T | 1 | a0005c0006 | 2 | HG02723.hp1 NA20300.hp1 |
synonymous_variant | LOW | c.786C>T | p.Val262Val | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 2/3 | 913/3052 | 786/2769 | 262/922 | chr2 | 73814165 | ||
chr2:73815087
|
G | T | 1 | a0001c0014 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.864G>T | p.Leu288Leu | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 3/3 | 991/3052 | 864/2769 | 288/922 | chr2 | 73815087 | ||
chr2:73815324
|
C | T | 1 | a0001c0013 | 1 | HG02738.hp2 | synonymous_variant | LOW | c.1101C>T | p.Thr367Thr | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 3/3 | 1228/3052 | 1101/2769 | 367/922 | chr2 | 73815324 | ||
chr2:73815351
|
C | T | 1 | a0002c0005 | 2 | HG02717.hp1 NA19030.hp1 |
synonymous_variant | LOW | c.1128C>T | p.His376His | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 3/3 | 1255/3052 | 1128/2769 | 376/922 | chr2 | 73815351 | ||
chr2:73816143
|
C | A | 1 | a0001c0010 | 1 | NA18747.hp2 | synonymous_variant | LOW | c.1920C>A | p.Leu640Leu | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 3/3 | 2047/3052 | 1920/2769 | 640/922 | chr2 | 73816143 |
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 |
---|
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:73784414
|
G | A | 1 | a0002c0003t0001g0022 | 1 | HG01243.hp1 | splice_region_variant&intron_variant | LOW | c.97+8G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784414 | ||||||
chr2:73784423
|
T | C | 1 | a0002c0003t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97+17T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784423 | ||||||
chr2:73784423
|
TTTAAAAA others(4894): Show |
T | 1 | a0004c0004t0001g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.97+59_97+4959del | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73784423 | |||||
chr2:73784464
|
GATTTCTT others(19588): Show |
G | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.97+59_98-9418del | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784464 | ||||||
chr2:73784465
|
A | G | 1 | a0002c0003t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97+59A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784465 | ||||||
chr2:73784468
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.97+62T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784468 | ||||||
chr2:73784472
|
T | C | 1 | a0002c0003t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97+66T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784472 | ||||||
chr2:73784500
|
T | A | 1 | a0001c0001t0001g0004 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.97+94T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784500 | ||||||
chr2:73784508
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.97+102A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784508 | ||||||
chr2:73784511
|
G | T | 1 | a0002c0003t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97+105G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784511 | ||||||
chr2:73784530
|
G | C | 1 | a0006c0007t0001g0024 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.97+124G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784530 | ||||||
chr2:73784561
|
T | A | 5 | a0002c0003t0001g0025a0002c0003t0001g0026a0002c0003t0001g0027others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+155T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784561 | ||||||
chr2:73784586
|
T | G | 2 | a0001c0001t0001g0030a0002c0003t0001g0022 | 2 | HG01243.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.97+180T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784586 | ||||||
chr2:73784595
|
C | G | 2 | a0002c0005t0001g0028a0002c0005t0001g0029 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.97+189C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784595 | ||||||
chr2:73784599
|
C | T | 1 | a0002c0003t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97+193C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784599 | ||||||
chr2:73784636
|
G | T | 1 | a0001c0001t0001g0183 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.97+230G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784636 | ||||||
chr2:73784657
|
C | T | 14 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0173others(11): Show | 16 | HG00438.hp1 HG00621.hp1 HG01433.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+251C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784657 | ||||||
chr2:73784692
|
C | T | 4 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0001g0182others(1): Show | 4 | HG01243.hp1 HG02523.hp1 NA18950.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+286C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784692 | ||||||
chr2:73784693
|
G | A | 1 | a0002c0003t0001g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97+287G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784693 | ||||||
chr2:73784809
|
C | T | 3 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029 | 3 | HG01243.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.97+403C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784809 | ||||||
chr2:73784817
|
C | T | 2 | a0001c0001t0001g0170a0002c0003t0001g0022 | 2 | HG01243.hp1 NA18983.hp1 |
intron_variant | MODIFIER | c.97+411C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784817 | ||||||
chr2:73784835
|
C | T | 2 | a0002c0003t0001g0026a0002c0003t0001g0027 | 2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.97+429C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784835 | ||||||
chr2:73784856
|
T | C | 3 | a0001c0001t0001g0031a0001c0001t0001g0032a0002c0003t0001g0022 | 3 | HG01243.hp1 HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.97+450T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784856 | ||||||
chr2:73784862
|
G | C | 1 | a0001c0001t0001g0033 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.97+456G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784862 | ||||||
chr2:73784900
|
C | T | 1 | a0002c0003t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97+494C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73784900 | ||||||
chr2:73785037
|
G | A | 1 | a0002c0003t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97+631G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785037 | ||||||
chr2:73785037
|
GTCAATGC others(4894): Show |
G | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.97+1218_97+6118del | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73785037 | |||||
chr2:73785141
|
G | A | 5 | a0002c0003t0001g0025a0002c0003t0001g0026a0002c0003t0001g0027others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+735G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785141 | ||||||
chr2:73785157
|
G | T | 5 | a0002c0003t0001g0025a0002c0003t0001g0026a0002c0003t0001g0027others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+751G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785157 | ||||||
chr2:73785159
|
T | G | 5 | a0002c0003t0001g0025a0002c0003t0001g0026a0002c0003t0001g0027others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+753T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785159 | ||||||
chr2:73785173
|
G | T | 5 | a0002c0003t0001g0025a0002c0003t0001g0026a0002c0003t0001g0027others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+767G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785173 | ||||||
chr2:73785301
|
CAAACAAA others(8): Show |
C | 5 | a0002c0003t0001g0025a0002c0003t0001g0026a0002c0003t0001g0027others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+899_97+913delCA others(13): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73785301 | |||||
chr2:73785322
|
A | T | 5 | a0002c0003t0001g0025a0002c0003t0001g0026a0002c0003t0001g0027others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+916A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785322 | ||||||
chr2:73785364
|
G | A | 5 | a0002c0003t0001g0025a0002c0003t0001g0026a0002c0003t0001g0027others(2): Show | 5 | HG02622.hp2 HG02717.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+958G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785364 | ||||||
chr2:73785471
|
T | C | 1 | a0001c0001t0001g0034 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.97+1065T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785471 | ||||||
chr2:73785621
|
G | A | 1 | a0004c0004t0001g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.97+1215G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785621 | ||||||
chr2:73785624
|
G | A | 1 | a0002c0003t0001g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.97+1218G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785624 | ||||||
chr2:73785624
|
GAAGGAAA others(14689): Show |
G | 1 | a0001c0001t0001g0168 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.97+1363_98-13013de others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73785624 | |||||
chr2:73785663
|
G | C | 1 | a0001c0001t0001g0037 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.97+1257G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785663 | ||||||
chr2:73785675
|
T | A | 1 | a0001c0001t0001g0038 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.97+1269T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785675 | ||||||
chr2:73785719
|
A | G | 2 | a0001c0001t0001g0038a0010c0012t0001g0169 | 2 | NA19043.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.97+1313A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785719 | ||||||
chr2:73785769
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(2): Show | 10 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+1363A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785769 | ||||||
chr2:73785773
|
T | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0018others(2): Show | 10 | HG02486.hp1 HG02630.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+1367T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785773 | ||||||
chr2:73785775
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.97+1369G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785775 | ||||||
chr2:73785809
|
G | C | 1 | a0002c0003t0001g0026 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.97+1403G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785809 | ||||||
chr2:73785861
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.97+1455A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785861 | ||||||
chr2:73785877
|
C | T | 3 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | NA18612.hp2 NA18955.hp1 NA18975.hp1 |
intron_variant | MODIFIER | c.97+1471C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785877 | ||||||
chr2:73785936
|
C | T | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | NA18612.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.97+1530C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785936 | ||||||
chr2:73785956
|
C | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | NA18612.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.97+1550C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785956 | ||||||
chr2:73785961
|
A | G | 2 | a0001c0001t0001g0163a0001c0001t0001g0164 | 2 | NA18612.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.97+1555A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73785961 | ||||||
chr2:73786018
|
C | T | 3 | a0001c0001t0001g0161a0001c0001t0001g0163a0001c0001t0001g0164 | 3 | HG02074.hp1 NA18612.hp2 NA18975.hp1 |
intron_variant | MODIFIER | c.97+1612C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786018 | ||||||
chr2:73786033
|
G | C | 5 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0163others(2): Show | 5 | HG01346.hp2 NA18612.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+1627G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786033 | ||||||
chr2:73786038
|
C | T | 1 | a0002c0003t0001g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.97+1632C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786038 | ||||||
chr2:73786051
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1645A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786051 | ||||||
chr2:73786052
|
G | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1646G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786052 | ||||||
chr2:73786062
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.97+1656G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786062 | ||||||
chr2:73786064
|
AAGAG | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1662_97+1665del others(4): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73786064 | |||||
chr2:73786070
|
G | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1664G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786070 | ||||||
chr2:73786071
|
A | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1665A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786071 | ||||||
chr2:73786074
|
T | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1668T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786074 | ||||||
chr2:73786075
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.97+1669A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786075 | ||||||
chr2:73786101
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1695A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786101 | ||||||
chr2:73786118
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1712A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786118 | ||||||
chr2:73786140
|
A | G | 2 | a0001c0001t0001g0160a0007c0008t0001g0041 | 2 | HG01346.hp2 HG03017.hp1 |
intron_variant | MODIFIER | c.97+1734A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786140 | ||||||
chr2:73786148
|
C | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1742C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786148 | ||||||
chr2:73786150
|
C | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1744C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786150 | ||||||
chr2:73786151
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1745A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786151 | ||||||
chr2:73786154
|
C | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1748C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786154 | ||||||
chr2:73786155
|
G | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1749G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786155 | ||||||
chr2:73786159
|
T | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1753T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786159 | ||||||
chr2:73786160
|
G | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1754G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786160 | ||||||
chr2:73786163
|
T | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1757T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786163 | ||||||
chr2:73786172
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1766A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786172 | ||||||
chr2:73786189
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1783A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786189 | ||||||
chr2:73786191
|
G | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1785G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786191 | ||||||
chr2:73786196
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1790A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786196 | ||||||
chr2:73786201
|
G | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1795G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786201 | ||||||
chr2:73786211
|
T | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1805T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786211 | ||||||
chr2:73786215
|
C | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1809C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786215 | ||||||
chr2:73786218
|
G | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1812G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786218 | ||||||
chr2:73786220
|
A | G | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1814A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786220 | ||||||
chr2:73786225
|
T | C | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1819T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786225 | ||||||
chr2:73786228
|
G | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | HG01346.hp2 HG03017.hp1 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+1822G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786228 | ||||||
chr2:73786248
|
C | T | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG02055.hp1 HG03017.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+1842C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786248 | ||||||
chr2:73786249
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.97+1843G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786249 | ||||||
chr2:73786257
|
G | T | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG02055.hp1 HG03017.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+1851G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786257 | ||||||
chr2:73786264
|
T | TA | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG02055.hp1 HG03017.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+1858_97+1859ins others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786264 | ||||||
chr2:73786266
|
C | G | 6 | a0001c0001t0001g0156a0001c0001t0001g0157a0001c0001t0001g0158others(3): Show | 6 | HG02055.hp1 HG03017.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+1860C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786266 | ||||||
chr2:73786266
|
CTACTTGG others(19586): Show |
C | 1 | a0001c0001t0001g0115 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.97+2989_98-6490del | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73786266 | |||||
chr2:73786272
|
G | C | 1 | a0001c0001t0001g0042 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97+1866G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786272 | ||||||
chr2:73786313
|
A | T | 2 | a0002c0005t0001g0028a0002c0005t0001g0029 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.97+1907A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786313 | ||||||
chr2:73786334
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.97+1928G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786334 | ||||||
chr2:73786624
|
T | C | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.97+2218T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786624 | ||||||
chr2:73786733
|
A | G | 4 | a0001c0001t0001g0017a0001c0001t0001g0154a0001c0001t0001g0155others(1): Show | 5 | HG00438.hp2 HG02132.hp2 NA18747.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+2327A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786733 | ||||||
chr2:73786767
|
T | C | 109 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0006others(106): Show | 119 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(116): Show |
intron_variant | MODIFIER | c.97+2361T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73786767 | ||||||
chr2:73787084
|
G | A | 3 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029 | 3 | HG01243.hp1 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.97+2678G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73787084 | ||||||
chr2:73787319
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.97+2913C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73787319 | ||||||
chr2:73787395
|
G | C | 2 | a0001c0001t0001g0045a0001c0001t0001g0046 | 2 | NA18948.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.97+2989G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73787395 | ||||||
chr2:73787415
|
G | A | 2 | a0001c0001t0001g0116a0001c0001t0001g0117 | 2 | NA18906.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.97+3009G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73787415 | ||||||
chr2:73787457
|
G | A | 49 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(46): Show | 58 | HG00099.hp2 HG00280.hp2 HG01069.hp2 others(55): Show |
intron_variant | MODIFIER | c.97+3051G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73787457 | ||||||
chr2:73787586
|
C | CAAAAAAA others(4893): Show |
1 | a0001c0001t0001g0058 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.97+3325_97+3326ins others(4900): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73787586 | |||||
chr2:73787586
|
CA | C | 93 | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0008others(90): Show | 99 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(96): Show |
intron_variant | MODIFIER | c.97+3197delA | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73787586 | |||||
chr2:73787732
|
C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(175): Show | 198 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(195): Show |
intron_variant | MODIFIER | c.97+3326C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73787732 | ||||||
chr2:73787747
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.97+3341C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73787747 | ||||||
chr2:73787996
|
G | A | 1 | a0001c0001t0001g0044 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.97+3590G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73787996 | ||||||
chr2:73788187
|
AGGGAGAG others(14688): Show |
A | 5 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0181others(2): Show | 6 | HG02622.hp2 HG03098.hp2 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.97+7259_98-7118del | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73788187 | |||||
chr2:73788308
|
C | G | 9 | a0001c0001t0001g0005a0001c0001t0001g0039a0001c0001t0001g0040others(6): Show | 10 | HG02056.hp2 HG02922.hp2 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+3902C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73788308 | ||||||
chr2:73788330
|
G | A | 96 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(93): Show | 107 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.97+3924G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73788330 | ||||||
chr2:73788386
|
C | T | 1 | a0001c0001t0001g0134 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.97+3980C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73788386 | ||||||
chr2:73788517
|
G | A | 1 | a0001c0001t0001g0137 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.97+4111G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73788517 | ||||||
chr2:73788577
|
G | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+4171G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73788577 | ||||||
chr2:73788840
|
AAAATATA others(19587): Show |
A | 1 | a0001c0001t0001g0005 | 2 | HG02970.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.97+4694_98-4784del | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73788840 | |||||
chr2:73788974
|
T | C | 1 | a0002c0005t0001g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97+4568T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73788974 | ||||||
chr2:73789020
|
T | G | 2 | a0002c0003t0001g0026a0002c0003t0001g0027 | 2 | HG02896.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.97+4614T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73789020 | ||||||
chr2:73789104
|
G | A | 7 | a0001c0001t0001g0143a0001c0001t0001g0144a0002c0003t0001g0022others(4): Show | 11 | HG01074.hp1 HG01167.hp1 HG01243.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+4698G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73789104 | ||||||
chr2:73789151
|
G | A | 1 | a0001c0001t0001g0042 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.97+4745G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73789151 | ||||||
chr2:73789315
|
A | G | 1 | a0004c0004t0001g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.97+4909A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73789315 | ||||||
chr2:73789425
|
A | G | 1 | a0001c0001t0001g0031 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.97+5019A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73789425 | ||||||
chr2:73789436
|
C | A | 5 | a0001c0001t0001g0049a0001c0001t0001g0059a0001c0001t0001g0060others(2): Show | 5 | HG00558.hp1 HG02293.hp2 HG02738.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+5030C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73789436 | ||||||
chr2:73789500
|
T | C | 1 | a0001c0001t0001g0145 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.97+5094T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73789500 | ||||||
chr2:73789710
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97+5304T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73789710 | ||||||
chr2:73789718
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97+5312T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73789718 | ||||||
chr2:73789768
|
T | G | 1 | a0004c0004t0001g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.97+5362T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73789768 | ||||||
chr2:73789806
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.97+5400G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73789806 | ||||||
chr2:73789959
|
G | T | 1 | a0001c0001t0001g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.97+5553G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73789959 | ||||||
chr2:73790188
|
CACAA | C | 5 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(2): Show | 9 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.97+5808_97+5811del others(4): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73790188 | |||||
chr2:73790632
|
T | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | NA18950.hp2 NA18981.hp2 |
intron_variant | MODIFIER | c.97+6226T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790632 | ||||||
chr2:73790670
|
G | A | 4 | a0001c0001t0001g0063a0002c0003t0001g0022a0003c0002t0002g0001others(1): Show | 8 | HG01167.hp1 HG01167.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6264G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790670 | ||||||
chr2:73790674
|
A | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6268A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790674 | ||||||
chr2:73790686
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6280G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790686 | ||||||
chr2:73790694
|
A | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6288A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790694 | ||||||
chr2:73790697
|
A | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6291A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790697 | ||||||
chr2:73790704
|
T | C | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG00099.hp2 HG00280.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.97+6298T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790704 | ||||||
chr2:73790778
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6372T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790778 | ||||||
chr2:73790837
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6431T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790837 | ||||||
chr2:73790857
|
G | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6451G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790857 | ||||||
chr2:73790862
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6456G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790862 | ||||||
chr2:73790919
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6513T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790919 | ||||||
chr2:73790934
|
C | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6528C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790934 | ||||||
chr2:73790934
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.97+6528C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790934 | ||||||
chr2:73790942
|
C | T | 3 | a0001c0001t0001g0151a0002c0005t0001g0028a0002c0005t0001g0029 | 3 | HG00621.hp2 HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.97+6536C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790942 | ||||||
chr2:73790943
|
G | A | 1 | a0001c0001t0001g0111 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.97+6537G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790943 | ||||||
chr2:73790952
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6546G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790952 | ||||||
chr2:73790953
|
A | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6547A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790953 | ||||||
chr2:73790965
|
A | AAGAG | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6560_97+6561ins others(4): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73790965 | |||||
chr2:73790967
|
C | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6561C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790967 | ||||||
chr2:73790968
|
C | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6562C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790968 | ||||||
chr2:73790971
|
C | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6565C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790971 | ||||||
chr2:73790998
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6592G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73790998 | ||||||
chr2:73791015
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6609G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791015 | ||||||
chr2:73791037
|
G | A | 11 | a0001c0001t0001g0030a0001c0001t0001g0049a0001c0001t0001g0059others(8): Show | 15 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.97+6631G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791037 | ||||||
chr2:73791037
|
G | GAGGCTGA others(9787): Show |
1 | a0001c0001t0001g0164 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.97+6740_97+6741ins others(9794): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73791037 | |||||
chr2:73791037
|
G | GAGGCTGA others(4890): Show |
1 | a0001c0001t0001g0082 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.97+8820_97+8821ins others(4897): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73791037 | |||||
chr2:73791045
|
G | C | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6639G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791045 | ||||||
chr2:73791047
|
T | C | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6641T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791047 | ||||||
chr2:73791048
|
G | A | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6642G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791048 | ||||||
chr2:73791051
|
A | C | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6645A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791051 | ||||||
chr2:73791052
|
A | G | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6646A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791052 | ||||||
chr2:73791056
|
C | T | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6650C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791056 | ||||||
chr2:73791057
|
A | G | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6651A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791057 | ||||||
chr2:73791060
|
G | T | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6654G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791060 | ||||||
chr2:73791069
|
G | A | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6663G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791069 | ||||||
chr2:73791086
|
G | A | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6680G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791086 | ||||||
chr2:73791088
|
C | G | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6682C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791088 | ||||||
chr2:73791093
|
G | A | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6687G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791093 | ||||||
chr2:73791098
|
C | G | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6692C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791098 | ||||||
chr2:73791108
|
C | T | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6702C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791108 | ||||||
chr2:73791112
|
A | C | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6706A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791112 | ||||||
chr2:73791115
|
A | G | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6709A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791115 | ||||||
chr2:73791117
|
G | A | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6711G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791117 | ||||||
chr2:73791122
|
C | T | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6716C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791122 | ||||||
chr2:73791125
|
A | G | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6719A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791125 | ||||||
chr2:73791145
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6739T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791145 | ||||||
chr2:73791147
|
T | C | 12 | a0001c0001t0001g0059a0001c0001t0001g0067a0001c0001t0001g0068others(9): Show | 12 | HG01175.hp1 HG01433.hp1 HG02071.hp2 others(9): Show |
intron_variant | MODIFIER | c.97+6741T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791147 | ||||||
chr2:73791147
|
T | TGCACCTT others(19581): Show |
1 | a0001c0001t0001g0110 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.97+7224_97+7225ins others(19588): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73791147 | |||||
chr2:73791154
|
T | G | 4 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(1): Show | 8 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(5): Show |
intron_variant | MODIFIER | c.97+6748T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791154 | ||||||
chr2:73791161
|
TA | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6756delA | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791161 | ||||||
chr2:73791164
|
G | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+6758G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791164 | ||||||
chr2:73791211
|
A | T | 2 | a0002c0005t0001g0028a0002c0005t0001g0029 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.97+6805A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791211 | ||||||
chr2:73791268
|
C | T | 1 | a0002c0005t0001g0028 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.97+6862C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791268 | ||||||
chr2:73791474
|
T | C | 1 | a0001c0001t0001g0156 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.97+7068T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791474 | ||||||
chr2:73791620
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.97+7214A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791620 | ||||||
chr2:73791624
|
T | C | 1 | a0001c0001t0001g0077 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.97+7218T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791624 | ||||||
chr2:73791631
|
A | G | 9 | a0001c0001t0001g0017a0001c0001t0001g0072a0001c0001t0001g0073others(6): Show | 10 | HG00438.hp2 HG02071.hp2 HG02074.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+7225A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791631 | ||||||
chr2:73791665
|
C | T | 9 | a0002c0003t0001g0022a0002c0003t0001g0026a0002c0003t0001g0027others(6): Show | 13 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.97+7259C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791665 | ||||||
chr2:73791665
|
CGTCTTAC others(14688): Show |
C | 9 | a0001c0001t0001g0017a0001c0001t0001g0072a0001c0001t0001g0109others(6): Show | 10 | HG00438.hp2 HG01192.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+7887_98-6490del | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73791665 | |||||
chr2:73791751
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.97+7345C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791751 | ||||||
chr2:73791982
|
G | A | 5 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(2): Show | 9 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.97+7576G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73791982 | ||||||
chr2:73792090
|
G | A | 1 | a0001c0010t0001g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.97+7684G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73792090 | ||||||
chr2:73792355
|
G | A | 17 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0032others(14): Show | 23 | HG00099.hp2 HG00280.hp2 HG01167.hp1 others(20): Show |
intron_variant | MODIFIER | c.97+7949G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73792355 | ||||||
chr2:73792484
|
C | CA | 52 | a0001c0001t0001g0004a0001c0001t0001g0014a0001c0001t0001g0015others(49): Show | 56 | HG00423.hp1 HG00438.hp1 HG00621.hp1 others(53): Show |
intron_variant | MODIFIER | c.97+8094dupA | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73792484 | |||||
chr2:73792598
|
T | C | 1 | a0001c0001t0001g0018 | 2 | HG03225.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.97+8192T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73792598 | ||||||
chr2:73792786
|
C | T | 1 | a0001c0001t0001g0107 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.97+8380C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73792786 | ||||||
chr2:73793084
|
AGGGAGAG others(9791): Show |
A | 15 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(12): Show | 22 | HG01261.hp1 HG02622.hp1 HG02630.hp1 others(19): Show |
intron_variant | MODIFIER | c.97+12156_98-7118de others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73793084 | |||||
chr2:73793160
|
A | G | 1 | a0001c0001t0001g0040 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.97+8754A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73793160 | ||||||
chr2:73793205
|
C | G | 15 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0034others(12): Show | 16 | HG00597.hp1 HG01243.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.97+8799C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73793205 | ||||||
chr2:73793216
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.97+8810G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73793216 | ||||||
chr2:73793227
|
G | A | 102 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(99): Show | 112 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.97+8821G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73793227 | ||||||
chr2:73793227
|
G | GAAAGGGG others(19585): Show |
1 | a0001c0001t0001g0152 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.97+10523_97+10524i others(19594): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73793227 | |||||
chr2:73793474
|
G | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+9068G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73793474 | ||||||
chr2:73793737
|
AAAATATA others(14690): Show |
A | 3 | a0001c0001t0001g0012a0001c0001t0001g0032a0001c0001t0001g0116 | 4 | HG01243.hp2 HG02280.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.97+9591_98-4784del | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73793737 | |||||
chr2:73793917
|
T | G | 1 | a0002c0003t0001g0026 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.97+9511T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73793917 | ||||||
chr2:73793918
|
T | C | 1 | a0004c0004t0001g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.97+9512T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73793918 | ||||||
chr2:73794001
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+9595G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73794001 | ||||||
chr2:73794013
|
CATCTTGG others(14690): Show |
C | 1 | a0001c0001t0001g0106 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.97+9806_98-4569del | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73794013 | |||||
chr2:73794212
|
A | G | 1 | a0004c0004t0001g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.97+9806A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73794212 | ||||||
chr2:73794333
|
C | A | 13 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0036others(10): Show | 14 | HG00423.hp2 HG01074.hp2 HG01175.hp1 others(11): Show |
intron_variant | MODIFIER | c.97+9927C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73794333 | ||||||
chr2:73794497
|
A | G | 2 | a0001c0001t0001g0179a0001c0001t0001g0180 | 2 | NA18966.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.97+10091A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73794497 | ||||||
chr2:73794529
|
A | C | 4 | a0001c0001t0001g0019a0001c0001t0001g0178a0001c0001t0001g0179others(1): Show | 5 | HG01433.hp2 HG02293.hp1 HG02300.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+10123A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73794529 | ||||||
chr2:73794607
|
T | A | 1 | a0001c0001t0001g0162 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.97+10201T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73794607 | ||||||
chr2:73794607
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0051others(2): Show | 6 | HG02647.hp2 HG02896.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.97+10201T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73794607 | ||||||
chr2:73794615
|
T | C | 5 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0051others(2): Show | 6 | HG02647.hp2 HG02896.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.97+10209T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73794615 | ||||||
chr2:73794665
|
T | G | 2 | a0004c0004t0001g0035a0004c0004t0001g0185 | 2 | HG02451.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.97+10259T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73794665 | ||||||
chr2:73795029
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.97+10623A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795029 | ||||||
chr2:73795085
|
CACAA | C | 5 | a0001c0001t0001g0034a0001c0001t0001g0062a0002c0003t0001g0022others(2): Show | 9 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.97+10705_97+10708d others(6): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73795085 | |||||
chr2:73795567
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11161G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795567 | ||||||
chr2:73795571
|
A | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11165A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795571 | ||||||
chr2:73795583
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11177G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795583 | ||||||
chr2:73795591
|
A | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11185A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795591 | ||||||
chr2:73795594
|
A | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11188A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795594 | ||||||
chr2:73795601
|
T | C | 2 | a0001c0001t0001g0137a0001c0001t0001g0139 | 2 | HG00099.hp2 HG00280.hp2 |
intron_variant | MODIFIER | c.97+11195T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795601 | ||||||
chr2:73795675
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11269T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795675 | ||||||
chr2:73795734
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11328T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795734 | ||||||
chr2:73795754
|
G | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11348G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795754 | ||||||
chr2:73795759
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11353G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795759 | ||||||
chr2:73795816
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11410T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795816 | ||||||
chr2:73795831
|
C | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11425C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795831 | ||||||
chr2:73795849
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11443G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795849 | ||||||
chr2:73795850
|
A | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11444A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795850 | ||||||
chr2:73795862
|
A | AAGAG | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11457_97+11458i others(6): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73795862 | |||||
chr2:73795864
|
C | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11458C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795864 | ||||||
chr2:73795865
|
C | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11459C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795865 | ||||||
chr2:73795868
|
C | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11462C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795868 | ||||||
chr2:73795870
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.97+11464T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795870 | ||||||
chr2:73795894
|
C | T | 5 | a0001c0001t0001g0030a0001c0001t0001g0071a0001c0001t0001g0105others(2): Show | 5 | HG01192.hp1 HG01346.hp2 HG02486.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+11488C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795894 | ||||||
chr2:73795895
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11489G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795895 | ||||||
chr2:73795912
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11506G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795912 | ||||||
chr2:73795934
|
G | A | 15 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0036others(12): Show | 20 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.97+11528G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795934 | ||||||
chr2:73795934
|
G | GAGGCTGA others(19581): Show |
1 | a0001c0001t0001g0086 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.97+11637_97+11638i others(19590): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73795934 | |||||
chr2:73795942
|
G | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11536G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795942 | ||||||
chr2:73795944
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11538T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795944 | ||||||
chr2:73795945
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11539G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795945 | ||||||
chr2:73795948
|
A | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11542A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795948 | ||||||
chr2:73795949
|
A | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11543A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795949 | ||||||
chr2:73795953
|
C | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11547C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795953 | ||||||
chr2:73795954
|
A | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11548A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795954 | ||||||
chr2:73795957
|
G | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11551G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795957 | ||||||
chr2:73795966
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11560G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795966 | ||||||
chr2:73795983
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11577G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795983 | ||||||
chr2:73795985
|
C | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11579C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795985 | ||||||
chr2:73795990
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11584G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795990 | ||||||
chr2:73795995
|
C | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11589C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73795995 | ||||||
chr2:73796005
|
C | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11599C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796005 | ||||||
chr2:73796009
|
A | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11603A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796009 | ||||||
chr2:73796012
|
A | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11606A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796012 | ||||||
chr2:73796014
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11608G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796014 | ||||||
chr2:73796019
|
C | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11613C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796019 | ||||||
chr2:73796022
|
A | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11616A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796022 | ||||||
chr2:73796042
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11636T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796042 | ||||||
chr2:73796044
|
T | C | 18 | a0001c0001t0001g0030a0001c0001t0001g0049a0001c0001t0001g0052others(15): Show | 18 | HG01074.hp2 HG01192.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.97+11638T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796044 | ||||||
chr2:73796051
|
T | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11645T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796051 | ||||||
chr2:73796055
|
T | G | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.97+11649T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796055 | ||||||
chr2:73796058
|
TA | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11653delA | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796058 | ||||||
chr2:73796061
|
G | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+11655G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796061 | ||||||
chr2:73796430
|
T | C | 1 | a0002c0003t0001g0026 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.97+12024T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796430 | ||||||
chr2:73796497
|
C | A | 1 | a0001c0001t0001g0033 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.97+12091C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796497 | ||||||
chr2:73796528
|
A | G | 18 | a0001c0001t0001g0049a0001c0001t0001g0052a0001c0001t0001g0053others(15): Show | 18 | HG00558.hp1 HG01192.hp1 HG01346.hp2 others(15): Show |
intron_variant | MODIFIER | c.97+12122A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796528 | ||||||
chr2:73796562
|
C | T | 7 | a0001c0001t0001g0156a0002c0003t0001g0022a0002c0003t0001g0026others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.97+12156C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796562 | ||||||
chr2:73796562
|
CGTCTTAC others(9791): Show |
C | 10 | a0001c0001t0001g0034a0001c0001t0001g0045a0001c0001t0001g0046others(7): Show | 10 | HG00597.hp1 HG01261.hp2 HG02293.hp2 others(7): Show |
intron_variant | MODIFIER | c.97+12784_98-6490de others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73796562 | |||||
chr2:73796563
|
G | A | 1 | a0001c0001t0001g0119 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.97+12157G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796563 | ||||||
chr2:73796801
|
G | T | 1 | a0001c0001t0001g0004 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.97+12395G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796801 | ||||||
chr2:73796879
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+12473G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73796879 | ||||||
chr2:73797009
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.97+12603C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73797009 | ||||||
chr2:73797190
|
GGCTGACA others(9791): Show |
G | 4 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0051others(1): Show | 5 | HG02647.hp2 HG02896.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.97+12875_98-6399de others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73797190 | |||||
chr2:73797252
|
G | A | 6 | a0001c0001t0001g0038a0001c0001t0001g0137a0001c0001t0001g0139others(3): Show | 10 | HG00099.hp2 HG00280.hp2 HG01167.hp1 others(7): Show |
intron_variant | MODIFIER | c.97+12846G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73797252 | ||||||
chr2:73797260
|
G | T | 3 | a0001c0001t0001g0011a0001c0001t0001g0104a0001c0001t0001g0107 | 4 | HG01361.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+12854G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73797260 | ||||||
chr2:73797276
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0104a0001c0001t0001g0107 | 4 | HG01361.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+12870G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73797276 | ||||||
chr2:73797281
|
G | A | 3 | a0001c0001t0001g0011a0001c0001t0001g0104a0001c0001t0001g0107 | 4 | HG01361.hp1 HG02615.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.97+12875G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73797281 | ||||||
chr2:73797284
|
GAGGCACG others(9791): Show |
G | 4 | a0001c0001t0001g0011a0001c0001t0001g0104a0001c0001t0001g0107others(1): Show | 5 | HG01361.hp1 HG02615.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+12991_98-6283de others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73797284 | |||||
chr2:73797337
|
C | T | 1 | a0001c0001t0001g0103 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.97+12931C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73797337 | ||||||
chr2:73797381
|
CA | C | 120 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0008others(117): Show | 131 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(128): Show |
intron_variant | MODIFIER | c.97+12992delA | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73797381 | |||||
chr2:73797383
|
A | AAAAAAAA others(14683): Show |
1 | a0001c0001t0001g0095 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.97+13696_97+13697i others(14692): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73797383 | |||||
chr2:73797383
|
A | AAAAAAAA others(4887): Show |
2 | a0001c0001t0001g0010a0001c0014t0001g0010 | 2 | HG02818.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.97+12990_97+12991i others(4896): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73797383 | |||||
chr2:73797383
|
AAAAAAAA others(9789): Show |
A | 1 | a0001c0001t0001g0159 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.97+13121_98-6155de others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73797383 | |||||
chr2:73797425
|
T | C | 1 | a0001c0001t0001g0162 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.97+13019T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73797425 | ||||||
chr2:73797433
|
T | C | 1 | a0001c0001t0001g0128 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.97+13027T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73797433 | ||||||
chr2:73797589
|
A | G | 1 | a0001c0001t0001g0130 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.97+13183A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73797589 | ||||||
chr2:73797961
|
C | CTAAAATC others(9791): Show |
1 | a0001c0001t0001g0161 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.97+13696_97+13697i others(9800): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73797961 | |||||
chr2:73797971
|
G | A | 1 | a0004c0004t0001g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.97+13565G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73797971 | ||||||
chr2:73797971
|
G | GGGGTTAA others(4891): Show |
1 | a0004c0004t0001g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.97+13680_97+13681i others(4900): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73797971 | |||||
chr2:73797982
|
A | T | 1 | a0001c0001t0001g0084 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.97+13576A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73797982 | ||||||
chr2:73797982
|
AGGGAGAG others(4893): Show |
A | 3 | a0001c0001t0001g0146a0001c0001t0001g0147a0001c0001t0001g0166 | 3 | HG02486.hp1 HG02647.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.97+13697_98-10475d others(2): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73797982 | |||||
chr2:73798103
|
G | C | 84 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(81): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.97+13697G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73798103 | ||||||
chr2:73798125
|
A | G | 5 | a0001c0001t0001g0055a0001c0001t0001g0120a0001c0001t0001g0151others(2): Show | 5 | HG00438.hp1 HG00621.hp2 HG01943.hp2 others(2): Show |
intron_variant | MODIFIER | c.97+13719A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73798125 | ||||||
chr2:73798125
|
AAAAGGGG others(4893): Show |
A | 15 | a0001c0001t0001g0019a0001c0001t0001g0038a0001c0001t0001g0117others(12): Show | 16 | HG00099.hp2 HG00280.hp2 HG00621.hp1 others(13): Show |
intron_variant | MODIFIER | c.98-12017_98-7118de others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73798125 | |||||
chr2:73798230
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.97+13824C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73798230 | ||||||
chr2:73798372
|
G | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+13966G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73798372 | ||||||
chr2:73798607
|
C | G | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97+14201C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73798607 | ||||||
chr2:73798613
|
C | T | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97+14207C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73798613 | ||||||
chr2:73798617
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97+14211T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73798617 | ||||||
chr2:73798632
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97+14226T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73798632 | ||||||
chr2:73798635
|
A | T | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.97+14229A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73798635 | ||||||
chr2:73798635
|
AAAATATA others(9792): Show |
A | 1 | a0001c0001t0001g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.97+14489_98-4784de others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73798635 | |||||
chr2:73798899
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.97+14493G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73798899 | ||||||
chr2:73798954
|
A | ACAAGGGG others(4890): Show |
1 | a0001c0001t0001g0103 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.98-14247_98-14246i others(4899): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73798954 | |||||
chr2:73798993
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.98-14484T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73798993 | ||||||
chr2:73798994
|
C | A | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.98-14483C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73798994 | ||||||
chr2:73799046
|
T | TCGTCTCT others(4890): Show |
2 | a0001c0001t0001g0090a0001c0001t0001g0091 | 2 | HG02559.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.98-14247_98-14246i others(4899): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73799046 | |||||
chr2:73799110
|
A | G | 1 | a0004c0004t0001g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.98-14367A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73799110 | ||||||
chr2:73799231
|
C | A | 8 | a0001c0001t0001g0008a0001c0001t0001g0050a0001c0001t0001g0081others(5): Show | 9 | HG00280.hp1 HG01106.hp1 HG03654.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-14246C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73799231 | ||||||
chr2:73799427
|
A | C | 2 | a0001c0001t0001g0174a0001c0001t0001g0177 | 2 | HG02071.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.98-14050A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73799427 | ||||||
chr2:73799563
|
T | G | 2 | a0004c0004t0001g0035a0004c0004t0001g0185 | 2 | HG02451.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.98-13914T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73799563 | ||||||
chr2:73799589
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.98-13888T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73799589 | ||||||
chr2:73799611
|
C | T | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.98-13866C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73799611 | ||||||
chr2:73799821
|
T | C | 1 | a0001c0001t0001g0097 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.98-13656T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73799821 | ||||||
chr2:73799927
|
A | G | 1 | a0001c0001t0001g0033 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.98-13550A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73799927 | ||||||
chr2:73799983
|
CACAA | C | 4 | a0001c0001t0001g0143a0002c0003t0001g0022a0003c0002t0002g0001others(1): Show | 8 | HG01074.hp1 HG01167.hp1 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-13468_98-13465d others(6): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73799983 | |||||
chr2:73799983
|
CACAAACA others(4897): Show |
C | 1 | a0001c0001t0001g0004 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98-13468_98-8565de others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73799983 | |||||
chr2:73800464
|
C | T | 1 | a0001c0001t0001g0053 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.98-13013C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800464 | ||||||
chr2:73800465
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-13012G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800465 | ||||||
chr2:73800469
|
A | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-13008A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800469 | ||||||
chr2:73800481
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12996G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800481 | ||||||
chr2:73800489
|
A | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12988A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800489 | ||||||
chr2:73800492
|
A | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12985A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800492 | ||||||
chr2:73800573
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12904T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800573 | ||||||
chr2:73800632
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12845T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800632 | ||||||
chr2:73800652
|
G | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12825G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800652 | ||||||
chr2:73800657
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12820G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800657 | ||||||
chr2:73800697
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.98-12780G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800697 | ||||||
chr2:73800714
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12763T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800714 | ||||||
chr2:73800729
|
C | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12748C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800729 | ||||||
chr2:73800747
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12730G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800747 | ||||||
chr2:73800748
|
A | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12729A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800748 | ||||||
chr2:73800760
|
A | AAGAG | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12716_98-12715i others(6): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73800760 | |||||
chr2:73800762
|
C | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12715C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800762 | ||||||
chr2:73800763
|
C | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12714C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800763 | ||||||
chr2:73800766
|
C | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12711C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800766 | ||||||
chr2:73800792
|
C | CGGGGTGC others(4891): Show |
1 | a0001c0001t0001g0092 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.98-12646_98-12645i others(4900): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73800792 | |||||
chr2:73800792
|
C | T | 2 | a0001c0001t0001g0103a0007c0008t0001g0041 | 2 | HG00099.hp1 HG01346.hp2 |
intron_variant | MODIFIER | c.98-12685C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800792 | ||||||
chr2:73800793
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12684G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800793 | ||||||
chr2:73800810
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12667G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800810 | ||||||
chr2:73800832
|
G | A | 10 | a0001c0001t0001g0008a0001c0001t0001g0050a0001c0001t0001g0066others(7): Show | 15 | HG00280.hp1 HG00597.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.98-12645G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800832 | ||||||
chr2:73800840
|
G | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12637G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800840 | ||||||
chr2:73800842
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12635T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800842 | ||||||
chr2:73800843
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12634G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800843 | ||||||
chr2:73800846
|
A | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12631A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800846 | ||||||
chr2:73800847
|
A | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12630A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800847 | ||||||
chr2:73800851
|
C | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12626C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800851 | ||||||
chr2:73800852
|
A | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12625A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800852 | ||||||
chr2:73800855
|
G | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12622G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800855 | ||||||
chr2:73800864
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12613G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800864 | ||||||
chr2:73800881
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12596G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800881 | ||||||
chr2:73800883
|
C | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12594C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800883 | ||||||
chr2:73800888
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12589G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800888 | ||||||
chr2:73800893
|
C | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12584C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800893 | ||||||
chr2:73800903
|
C | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12574C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800903 | ||||||
chr2:73800907
|
A | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12570A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800907 | ||||||
chr2:73800910
|
A | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12567A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800910 | ||||||
chr2:73800912
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12565G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800912 | ||||||
chr2:73800917
|
C | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12560C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800917 | ||||||
chr2:73800920
|
A | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12557A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800920 | ||||||
chr2:73800940
|
T | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12537T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800940 | ||||||
chr2:73800942
|
T | C | 32 | a0001c0001t0001g0009a0001c0001t0001g0036a0001c0001t0001g0054others(29): Show | 33 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.98-12535T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800942 | ||||||
chr2:73800949
|
T | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12528T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800949 | ||||||
chr2:73800956
|
TA | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12520delA | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800956 | ||||||
chr2:73800959
|
G | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-12518G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73800959 | ||||||
chr2:73801415
|
A | G | 1 | a0001c0001t0001g0153 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.98-12062A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73801415 | ||||||
chr2:73801426
|
A | G | 44 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0030others(41): Show | 45 | HG00099.hp1 HG00423.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.98-12051A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73801426 | ||||||
chr2:73801460
|
C | T | 5 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(2): Show | 9 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-12017C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73801460 | ||||||
chr2:73801460
|
CGTCTTAC others(4893): Show |
C | 18 | a0001c0001t0001g0014a0001c0001t0001g0015a0001c0001t0001g0030others(15): Show | 20 | HG00423.hp1 HG01071.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.98-11389_98-6490de others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73801460 | |||||
chr2:73801777
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-11700G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73801777 | ||||||
chr2:73802088
|
G | C | 1 | a0001c0001t0001g0064 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.98-11389G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802088 | ||||||
chr2:73802088
|
GGCTGACA others(4893): Show |
G | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.98-11298_98-6399de others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802088 | |||||
chr2:73802150
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-11327G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802150 | ||||||
chr2:73802158
|
G | T | 1 | a0001c0001t0001g0064 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.98-11319G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802158 | ||||||
chr2:73802174
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.98-11303G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802174 | ||||||
chr2:73802179
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.98-11298G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802179 | ||||||
chr2:73802182
|
GAGGCACG others(4893): Show |
G | 3 | a0001c0001t0001g0064a0001c0001t0001g0112a0001c0001t0001g0141 | 3 | HG01106.hp2 HG03579.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.98-10479_98-5580de others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802182 | |||||
chr2:73802279
|
C | CA | 58 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(55): Show | 64 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.98-11183dupA | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802279 | |||||
chr2:73802279
|
C | CAA | 21 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0033others(18): Show | 22 | HG00438.hp1 HG01074.hp1 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.98-11184_98-11183d others(4): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802279 | |||||
chr2:73802279
|
C | CAAA | 8 | a0001c0001t0001g0119a0001c0001t0001g0122a0001c0001t0001g0123others(5): Show | 8 | HG01069.hp2 HG01175.hp2 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.98-11185_98-11183d others(5): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802279 | |||||
chr2:73802423
|
C | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.98-11054C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802423 | ||||||
chr2:73802557
|
GAAGA | G | 74 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0023others(71): Show | 79 | HG00099.hp1 HG00423.hp2 HG00438.hp1 others(76): Show |
intron_variant | MODIFIER | c.98-10908_98-10905d others(6): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802557 | |||||
chr2:73802561
|
A | AAAGAAAG others(4886): Show |
1 | a0001c0001t0001g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.98-10909_98-10908i others(4895): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802561 | |||||
chr2:73802561
|
A | AAAGAAAG others(14644): Show |
1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-10909_98-10908i others(14653): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802561 | |||||
chr2:73802561
|
A | AAAGAAAG others(19577): Show |
2 | a0001c0001t0001g0073a0006c0007t0001g0024 | 2 | NA18950.hp1 NA18966.hp1 |
intron_variant | MODIFIER | c.98-10909_98-10908i others(19586): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802561 | |||||
chr2:73802561
|
A | AAAGAAAG others(9783): Show |
1 | a0001c0001t0001g0009 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.98-10909_98-10908i others(9792): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802561 | |||||
chr2:73802561
|
A | AAAGAAAG others(4886): Show |
5 | a0001c0001t0001g0065a0001c0001t0001g0066a0001c0001t0001g0087others(2): Show | 5 | HG00597.hp2 HG02132.hp1 HG04228.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-10909_98-10908i others(4895): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802561 | |||||
chr2:73802561
|
A | AAAGAAAG others(4886): Show |
1 | a0001c0001t0001g0050 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.98-10909_98-10908i others(4895): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802561 | |||||
chr2:73802561
|
A | AAAGAAAG others(14680): Show |
1 | a0001c0001t0001g0101 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.98-10909_98-10908i others(14689): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802561 | |||||
chr2:73802561
|
A | AAAGAAAG others(4886): Show |
1 | a0001c0001t0001g0008 | 2 | HG03654.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.98-10909_98-10908i others(4895): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802561 | |||||
chr2:73802561
|
A | AAAGAAAG others(9787): Show |
1 | a0001c0001t0001g0126 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.98-10909_98-10908i others(9796): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802561 | |||||
chr2:73802561
|
A | AAAGAAAG others(4886): Show |
1 | a0001c0001t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.98-10909_98-10908i others(4895): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73802561 | |||||
chr2:73802578
|
T | A | 89 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.98-10899T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802578 | ||||||
chr2:73802687
|
G | A | 89 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.98-10790G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802687 | ||||||
chr2:73802742
|
C | G | 89 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.98-10735C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802742 | ||||||
chr2:73802758
|
A | C | 89 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.98-10719A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802758 | ||||||
chr2:73802764
|
A | G | 89 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.98-10713A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802764 | ||||||
chr2:73802814
|
C | T | 89 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.98-10663C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802814 | ||||||
chr2:73802882
|
T | A | 89 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(86): Show | 96 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(93): Show |
intron_variant | MODIFIER | c.98-10595T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73802882 | ||||||
chr2:73803003
|
C | G | 18 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0013others(15): Show | 25 | HG00621.hp2 HG01261.hp1 HG01943.hp2 others(22): Show |
intron_variant | MODIFIER | c.98-10474C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803003 | ||||||
chr2:73803025
|
G | A | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0006others(81): Show | 98 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(95): Show |
intron_variant | MODIFIER | c.98-10452G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803025 | ||||||
chr2:73803025
|
G | GAAAGGGG others(4890): Show |
1 | a0001c0001t0001g0057 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.98-10255_98-10254i others(4899): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73803025 | |||||
chr2:73803025
|
G | GAAAGGGG others(4891): Show |
1 | a0001c0001t0001g0153 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.98-7183_98-7182ins others(4898): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73803025 | |||||
chr2:73803025
|
G | GAAAGGGG others(4890): Show |
2 | a0001c0001t0001g0144a0001c0001t0001g0162 | 2 | HG04199.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.98-7183_98-7182ins others(4897): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73803025 | |||||
chr2:73803025
|
G | GAAAGGGG others(34267): Show |
1 | a0001c0001t0001g0143 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.98-7183_98-7182ins others(34274): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73803025 | |||||
chr2:73803025
|
G | GAAAGGGG others(19583): Show |
1 | a0001c0001t0001g0130 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.98-7118_98-7117ins others(19590): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73803025 | |||||
chr2:73803025
|
G | GAAAGGGG others(4890): Show |
6 | a0001c0001t0001g0119a0001c0001t0001g0121a0001c0001t0001g0123others(3): Show | 6 | HG01069.hp2 HG01346.hp1 HG01952.hp1 others(3): Show |
intron_variant | MODIFIER | c.98-7118_98-7117ins others(4897): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73803025 | |||||
chr2:73803025
|
G | GAAAGGGG others(4890): Show |
2 | a0001c0001t0001g0125a0001c0001t0001g0128 | 2 | HG02300.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.98-7118_98-7117ins others(4897): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73803025 | |||||
chr2:73803025
|
G | GAAAGGGG others(14686): Show |
2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | NA18955.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.98-8004_98-8003ins others(14693): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73803025 | |||||
chr2:73803125
|
G | GCGGGCGG others(4890): Show |
1 | a0001c0001t0001g0094 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.98-9347_98-9346ins others(4897): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73803125 | |||||
chr2:73803211
|
C | T | 2 | a0001c0001t0001g0006a0001c0001t0001g0023 | 3 | HG02630.hp2 HG02886.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.98-10266C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803211 | ||||||
chr2:73803222
|
G | A | 1 | a0004c0004t0001g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.98-10255G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803222 | ||||||
chr2:73803223
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.98-10254C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803223 | ||||||
chr2:73803252
|
G | C | 1 | a0002c0003t0001g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.98-10225G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803252 | ||||||
chr2:73803272
|
G | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-10205G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803272 | ||||||
chr2:73803312
|
G | A | 1 | a0002c0003t0001g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.98-10165G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803312 | ||||||
chr2:73803375
|
A | T | 1 | a0010c0012t0001g0169 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.98-10102A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803375 | ||||||
chr2:73803495
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.98-9982T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803495 | ||||||
chr2:73803669
|
T | C | 1 | a0002c0005t0001g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.98-9808T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803669 | ||||||
chr2:73803715
|
T | G | 1 | a0002c0003t0001g0027 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.98-9762T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803715 | ||||||
chr2:73803744
|
A | G | 1 | a0001c0001t0001g0133 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.98-9733A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803744 | ||||||
chr2:73803799
|
G | A | 5 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(2): Show | 9 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-9678G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73803799 | ||||||
chr2:73804061
|
G | T | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-9416G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73804061 | ||||||
chr2:73804107
|
T | TTATTGAA others(4890): Show |
1 | a0001c0001t0001g0033 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.98-8651_98-8650ins others(4897): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73804107 | |||||
chr2:73804131
|
C | CTCATTTC others(4890): Show |
1 | a0001c0001t0001g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.98-7822_98-7821ins others(4897): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73804131 | |||||
chr2:73804207
|
C | T | 1 | a0004c0004t0001g0185 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.98-9270C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73804207 | ||||||
chr2:73804288
|
T | C | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-9189T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73804288 | ||||||
chr2:73804327
|
A | ATTTCAAC others(14686): Show |
1 | a0001c0001t0001g0173 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.98-7118_98-7117ins others(14693): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73804327 | |||||
chr2:73804327
|
A | C | 9 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0175others(6): Show | 11 | HG00621.hp1 HG01433.hp2 HG02293.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-9150A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73804327 | ||||||
chr2:73804463
|
T | G | 2 | a0004c0004t0001g0035a0004c0004t0001g0185 | 2 | HG02451.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.98-9014T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73804463 | ||||||
chr2:73804489
|
T | C | 1 | a0001c0001t0001g0069 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.98-8988T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73804489 | ||||||
chr2:73804737
|
G | A | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-8740G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73804737 | ||||||
chr2:73804790
|
A | G | 1 | a0001c0001t0001g0036 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.98-8687A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73804790 | ||||||
chr2:73804819
|
G | GAGACTGC others(4890): Show |
1 | a0001c0001t0001g0122 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.98-7118_98-7117ins others(4897): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73804819 | |||||
chr2:73804883
|
CACAA | C | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-8568_98-8565del others(4): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73804883 | |||||
chr2:73805220
|
A | G | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-8257A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73805220 | ||||||
chr2:73805380
|
C | T | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-8097C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73805380 | ||||||
chr2:73805433
|
A | T | 1 | a0001c0001t0001g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.98-8044A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73805433 | ||||||
chr2:73805787
|
C | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG00099.hp2 HG00280.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.98-7690C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73805787 | ||||||
chr2:73805842
|
T | C | 2 | a0001c0001t0001g0068a0001c0001t0001g0161 | 2 | HG02074.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.98-7635T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73805842 | ||||||
chr2:73805906
|
A | T | 2 | a0002c0005t0001g0028a0002c0005t0001g0029 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98-7571A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73805906 | ||||||
chr2:73806063
|
T | C | 1 | a0001c0001t0001g0151 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.98-7414T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806063 | ||||||
chr2:73806228
|
T | C | 1 | a0002c0003t0001g0027 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.98-7249T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806228 | ||||||
chr2:73806295
|
C | A | 1 | a0001c0001t0001g0058 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.98-7182C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806295 | ||||||
chr2:73806326
|
A | G | 52 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(49): Show | 55 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(52): Show |
intron_variant | MODIFIER | c.98-7151A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806326 | ||||||
chr2:73806360
|
T | C | 62 | a0001c0001t0001g0006a0001c0001t0001g0008a0001c0001t0001g0009others(59): Show | 65 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(62): Show |
intron_variant | MODIFIER | c.98-7117T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806360 | ||||||
chr2:73806418
|
A | C | 1 | a0001c0001t0001g0161 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.98-7059A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806418 | ||||||
chr2:73806461
|
A | G | 5 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021others(2): Show | 9 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-7016A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806461 | ||||||
chr2:73806494
|
A | G | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6983A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806494 | ||||||
chr2:73806498
|
A | T | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6979A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806498 | ||||||
chr2:73806514
|
G | C | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6963G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806514 | ||||||
chr2:73806515
|
G | A | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6962G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806515 | ||||||
chr2:73806559
|
A | C | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-6918A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806559 | ||||||
chr2:73806573
|
ATTAGCCA others(2): Show |
A | 1 | a0001c0001t0001g0004 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98-6903_98-6895del others(9): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806573 | ||||||
chr2:73806580
|
A | G | 5 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(2): Show | 9 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.98-6897A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806580 | ||||||
chr2:73806581
|
G | A | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6896G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806581 | ||||||
chr2:73806583
|
G | A | 1 | a0001c0001t0001g0004 | 2 | HG02922.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.98-6894G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806583 | ||||||
chr2:73806583
|
G | T | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6894G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806583 | ||||||
chr2:73806586
|
A | G | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6891A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806586 | ||||||
chr2:73806591
|
C | CA | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6886_98-6885ins others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806591 | ||||||
chr2:73806591
|
C | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG00099.hp2 HG00280.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.98-6886C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806591 | ||||||
chr2:73806595
|
A | G | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6882A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806595 | ||||||
chr2:73806598
|
C | T | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6879C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806598 | ||||||
chr2:73806600
|
T | C | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6877T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806600 | ||||||
chr2:73806601
|
T | A | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6876T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806601 | ||||||
chr2:73806610
|
C | T | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6867C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806610 | ||||||
chr2:73806614
|
T | C | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-6863T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806614 | ||||||
chr2:73806676
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.98-6801C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806676 | ||||||
chr2:73806771
|
A | G | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-6706A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806771 | ||||||
chr2:73806782
|
A | G | 1 | a0008c0011t0001g0048 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.98-6695A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806782 | ||||||
chr2:73806858
|
C | T | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-6619C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806858 | ||||||
chr2:73806979
|
G | C | 1 | a0001c0001t0001g0002 | 3 | HG02717.hp2 HG02886.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.98-6498G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806979 | ||||||
chr2:73806984
|
T | A | 2 | a0002c0005t0001g0028a0002c0005t0001g0029 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98-6493T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806984 | ||||||
chr2:73806988
|
C | G | 17 | a0001c0001t0001g0020a0001c0001t0001g0077a0001c0001t0001g0079others(14): Show | 22 | HG01167.hp1 HG01243.hp1 HG01952.hp2 others(19): Show |
intron_variant | MODIFIER | c.98-6489C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73806988 | ||||||
chr2:73807007
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.98-6470C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807007 | ||||||
chr2:73807058
|
G | T | 78 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(75): Show | 83 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(80): Show |
intron_variant | MODIFIER | c.98-6419G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807058 | ||||||
chr2:73807074
|
G | A | 86 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 91 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.98-6403G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807074 | ||||||
chr2:73807074
|
G | GGGAGGCT others(19581): Show |
1 | a0001c0001t0001g0100 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.98-6399_98-6398ins others(19588): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73807074 | |||||
chr2:73807074
|
G | GGGAGGCT others(29375): Show |
1 | a0001c0001t0001g0170 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.98-6399_98-6398ins others(29382): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73807074 | |||||
chr2:73807074
|
G | GGGAGGCT others(19581): Show |
1 | a0001c0001t0001g0077 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.98-6399_98-6398ins others(19588): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73807074 | |||||
chr2:73807079
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-6398A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807079 | ||||||
chr2:73807082
|
A | G | 4 | a0001c0001t0001g0079a0001c0001t0001g0168a0005c0006t0001g0186others(1): Show | 4 | HG02723.hp1 HG03130.hp2 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-6395A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807082 | ||||||
chr2:73807088
|
C | T | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-6389C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807088 | ||||||
chr2:73807090
|
A | G | 1 | a0001c0001t0001g0132 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.98-6387A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807090 | ||||||
chr2:73807142
|
TGCCCTCC others(19): Show |
T | 2 | a0002c0005t0001g0028a0002c0005t0001g0029 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98-6333_98-6308del others(26): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73807142 | |||||
chr2:73807179
|
C | CA | 5 | a0001c0001t0001g0079a0001c0001t0001g0121a0001c0001t0001g0123others(2): Show | 5 | HG01952.hp1 HG03130.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-6283dupA | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73807179 | |||||
chr2:73807179
|
CA | C | 11 | a0001c0001t0001g0007a0001c0001t0001g0042a0001c0001t0001g0051others(8): Show | 16 | HG01069.hp2 HG01167.hp1 HG01243.hp1 others(13): Show |
intron_variant | MODIFIER | c.98-6283delA | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73807179 | |||||
chr2:73807225
|
T | C | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-6252T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807225 | ||||||
chr2:73807323
|
C | T | 6 | a0001c0001t0001g0079a0002c0003t0001g0022a0003c0002t0002g0001others(3): Show | 10 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(7): Show |
intron_variant | MODIFIER | c.98-6154C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807323 | ||||||
chr2:73807341
|
G | A | 1 | a0001c0001t0001g0060 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.98-6136G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807341 | ||||||
chr2:73807421
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.98-6056C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807421 | ||||||
chr2:73807455
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.98-6022G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807455 | ||||||
chr2:73807478
|
T | A | 3 | a0001c0001t0001g0079a0002c0005t0001g0028a0002c0005t0001g0029 | 3 | HG02717.hp1 HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.98-5999T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807478 | ||||||
chr2:73807587
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5890G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807587 | ||||||
chr2:73807624
|
C | G | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-5853C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807624 | ||||||
chr2:73807642
|
C | G | 3 | a0001c0001t0001g0079a0005c0006t0001g0186a0005c0006t0001g0187 | 3 | HG02723.hp1 HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.98-5835C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807642 | ||||||
chr2:73807658
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5819A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807658 | ||||||
chr2:73807664
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5813A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807664 | ||||||
chr2:73807714
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5763C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807714 | ||||||
chr2:73807757
|
A | G | 2 | a0001c0001t0001g0118a0001c0001t0001g0165 | 2 | HG01192.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.98-5720A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807757 | ||||||
chr2:73807782
|
T | A | 2 | a0001c0001t0001g0079a0002c0005t0001g0028 | 2 | HG03130.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.98-5695T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807782 | ||||||
chr2:73807812
|
C | G | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-5665C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807812 | ||||||
chr2:73807898
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5579A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807898 | ||||||
chr2:73807904
|
A | G | 96 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(93): Show | 106 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(103): Show |
intron_variant | MODIFIER | c.98-5573A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807904 | ||||||
chr2:73807930
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5547A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807930 | ||||||
chr2:73807944
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5533T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807944 | ||||||
chr2:73807951
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5526T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807951 | ||||||
chr2:73807957
|
C | A | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5520C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807957 | ||||||
chr2:73807964
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5513T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807964 | ||||||
chr2:73807972
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5505A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807972 | ||||||
chr2:73807978
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5499G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807978 | ||||||
chr2:73807981
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5496T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807981 | ||||||
chr2:73807984
|
G | A | 2 | a0002c0005t0001g0028a0002c0005t0001g0029 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98-5493G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807984 | ||||||
chr2:73807993
|
C | T | 1 | a0001c0001t0001g0093 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.98-5484C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73807993 | ||||||
chr2:73808007
|
G | T | 1 | a0004c0004t0001g0035 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.98-5470G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808007 | ||||||
chr2:73808012
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5465T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808012 | ||||||
chr2:73808021
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5456T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808021 | ||||||
chr2:73808024
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5453G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808024 | ||||||
chr2:73808028
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5449A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808028 | ||||||
chr2:73808031
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5446A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808031 | ||||||
chr2:73808036
|
A | T | 1 | a0001c0001t0001g0149 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.98-5441A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808036 | ||||||
chr2:73808038
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5439A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808038 | ||||||
chr2:73808055
|
C | G | 2 | a0001c0001t0001g0125a0001c0001t0001g0128 | 2 | HG02300.hp2 HG02735.hp1 |
intron_variant | MODIFIER | c.98-5422C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808055 | ||||||
chr2:73808061
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0001g0084 | 2 | HG00423.hp2 HG02056.hp1 |
intron_variant | MODIFIER | c.98-5416T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808061 | ||||||
chr2:73808062
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.98-5415G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808062 | ||||||
chr2:73808122
|
C | T | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-5355C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808122 | ||||||
chr2:73808123
|
A | G | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-5354A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808123 | ||||||
chr2:73808146
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5331A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808146 | ||||||
chr2:73808152
|
T | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5325T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808152 | ||||||
chr2:73808162
|
G | T | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5315G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808162 | ||||||
chr2:73808168
|
G | A | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5309G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808168 | ||||||
chr2:73808263
|
T | A | 3 | a0001c0001t0001g0079a0005c0006t0001g0186a0005c0006t0001g0187 | 3 | HG02723.hp1 HG03130.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.98-5214T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808263 | ||||||
chr2:73808266
|
A | G | 1 | a0001c0010t0001g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.98-5211A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808266 | ||||||
chr2:73808273
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5204A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808273 | ||||||
chr2:73808353
|
C | T | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-5124C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808353 | ||||||
chr2:73808406
|
G | C | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5071G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808406 | ||||||
chr2:73808412
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5065T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808412 | ||||||
chr2:73808416
|
A | T | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5061A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808416 | ||||||
chr2:73808431
|
C | T | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5046C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808431 | ||||||
chr2:73808434
|
T | A | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-5043T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808434 | ||||||
chr2:73808484
|
T | C | 1 | a0002c0003t0001g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.98-4993T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808484 | ||||||
chr2:73808681
|
C | T | 1 | a0001c0010t0001g0078 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.98-4796C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808681 | ||||||
chr2:73808693
|
C | A | 1 | a0001c0001t0001g0016 | 2 | HG03098.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.98-4784C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808693 | ||||||
chr2:73808694
|
A | G | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-4783A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808694 | ||||||
chr2:73808697
|
T | C | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-4780T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808697 | ||||||
chr2:73808710
|
A | C | 1 | a0001c0001t0001g0079 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.98-4767A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808710 | ||||||
chr2:73808753
|
A | G | 186 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(183): Show | 210 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.98-4724A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808753 | ||||||
chr2:73808799
|
G | A | 2 | a0001c0001t0001g0005a0001c0001t0001g0116 | 3 | HG02970.hp2 HG03453.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.98-4678G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808799 | ||||||
chr2:73808846
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.98-4631C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808846 | ||||||
chr2:73808860
|
T | C | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-4617T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808860 | ||||||
chr2:73808909
|
G | A | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-4568G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808909 | ||||||
chr2:73808918
|
T | C | 1 | a0010c0012t0001g0169 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.98-4559T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808918 | ||||||
chr2:73808927
|
G | T | 1 | a0001c0001t0001g0065 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.98-4550G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808927 | ||||||
chr2:73808960
|
A | G | 1 | a0001c0001t0001g0043 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.98-4517A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73808960 | ||||||
chr2:73809006
|
G | T | 2 | a0002c0005t0001g0028a0002c0005t0001g0029 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98-4471G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809006 | ||||||
chr2:73809152
|
T | C | 4 | a0001c0001t0001g0011a0001c0001t0001g0104a0001c0001t0001g0107others(1): Show | 5 | HG01361.hp1 HG02615.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-4325T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809152 | ||||||
chr2:73809191
|
T | C | 89 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(86): Show | 95 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.98-4286T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809191 | ||||||
chr2:73809250
|
C | A | 2 | a0002c0005t0001g0028a0002c0005t0001g0029 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98-4227C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809250 | ||||||
chr2:73809294
|
T | C | 1 | a0001c0001t0001g0167 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.98-4183T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809294 | ||||||
chr2:73809312
|
C | T | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-4165C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809312 | ||||||
chr2:73809351
|
T | C | 1 | a0001c0001t0001g0040 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.98-4126T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809351 | ||||||
chr2:73809487
|
G | A | 1 | a0001c0001t0001g0064 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.98-3990G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809487 | ||||||
chr2:73809532
|
G | A | 1 | a0001c0001t0001g0182 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.98-3945G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809532 | ||||||
chr2:73809586
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.98-3891G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809586 | ||||||
chr2:73809654
|
G | T | 1 | a0001c0001t0001g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.98-3823G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809654 | ||||||
chr2:73809663
|
G | C | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | NA18948.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.98-3814G>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809663 | ||||||
chr2:73809811
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.98-3666A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809811 | ||||||
chr2:73809818
|
T | C | 1 | a0001c0001t0001g0148 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.98-3659T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809818 | ||||||
chr2:73809840
|
A | T | 1 | a0001c0001t0001g0009 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.98-3637A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809840 | ||||||
chr2:73809868
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3609C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809868 | ||||||
chr2:73809869
|
T | TGGGGGGG others(59): Show |
1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3605_98-3604ins others(66): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73809869 | |||||
chr2:73809873
|
T | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3604T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809873 | ||||||
chr2:73809874
|
T | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3603T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809874 | ||||||
chr2:73809875
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3602A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809875 | ||||||
chr2:73809876
|
T | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3601T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809876 | ||||||
chr2:73809877
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3600A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809877 | ||||||
chr2:73809878
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3599A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809878 | ||||||
chr2:73809881
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3596A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809881 | ||||||
chr2:73809884
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3593C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809884 | ||||||
chr2:73809885
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3592A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73809885 | ||||||
chr2:73809887
|
GTATTCTA others(24): Show |
G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3587_98-3557del others(31): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73809887 | |||||
chr2:73810004
|
T | G | 87 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(84): Show | 93 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(90): Show |
intron_variant | MODIFIER | c.98-3473T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810004 | ||||||
chr2:73810342
|
A | G | 86 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 92 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.98-3135A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810342 | ||||||
chr2:73810414
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3063C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810414 | ||||||
chr2:73810415
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3062T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810415 | ||||||
chr2:73810421
|
G | T | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3056G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810421 | ||||||
chr2:73810422
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3055G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810422 | ||||||
chr2:73810427
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3050T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810427 | ||||||
chr2:73810437
|
G | A | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3040G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810437 | ||||||
chr2:73810439
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3038A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810439 | ||||||
chr2:73810441
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3036C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810441 | ||||||
chr2:73810450
|
C | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3027C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810450 | ||||||
chr2:73810458
|
T | A | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-3019T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810458 | ||||||
chr2:73810479
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-2998A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810479 | ||||||
chr2:73810486
|
C | A | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-2991C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810486 | ||||||
chr2:73810487
|
A | G | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-2990A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810487 | ||||||
chr2:73810496
|
C | A | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-2981C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810496 | ||||||
chr2:73810501
|
T | C | 1 | a0001c0001t0001g0127 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.98-2976T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810501 | ||||||
chr2:73810522
|
T | G | 4 | a0001c0001t0001g0006a0001c0001t0001g0023a0001c0001t0001g0079others(1): Show | 5 | HG02630.hp2 HG02886.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.98-2955T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810522 | ||||||
chr2:73810536
|
A | AAT | 6 | a0001c0001t0001g0123a0001c0001t0001g0125a0001c0001t0001g0128others(3): Show | 6 | HG00621.hp1 HG01952.hp1 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-2925_98-2924dup others(2): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810536 | |||||
chr2:73810536
|
AAT | A | 97 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(94): Show | 107 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.98-2925_98-2924del others(2): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810536 | |||||
chr2:73810550
|
T | C | 1 | a0001c0001t0001g0099 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.98-2927T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810550 | ||||||
chr2:73810568
|
G | GTATATTT others(30): Show |
1 | a0001c0001t0001g0109 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.98-2898_98-2862dup others(37): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810568 | |||||
chr2:73810589
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.98-2888T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810589 | ||||||
chr2:73810605
|
A | T | 3 | a0001c0001t0001g0137a0001c0001t0001g0138a0001c0001t0001g0139 | 3 | HG00099.hp2 HG00280.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.98-2872A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810605 | ||||||
chr2:73810609
|
A | T | 1 | a0002c0005t0001g0029 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.98-2868A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810609 | ||||||
chr2:73810626
|
AAT | A | 5 | a0001c0001t0001g0117a0001c0001t0001g0140a0001c0001t0001g0141others(2): Show | 5 | HG00621.hp2 HG01106.hp2 HG02622.hp2 others(2): Show |
intron_variant | MODIFIER | c.98-2842_98-2841del others(2): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810626 | |||||
chr2:73810648
|
GTATATAT others(15): Show |
G | 1 | a0009c0009t0001g0089 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.98-2824_98-2803del others(22): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810648 | |||||
chr2:73810654
|
ATC | A | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-2821_98-2820del others(2): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810654 | |||||
chr2:73810656
|
CTATAATA others(2): Show |
C | 2 | a0004c0004t0001g0035a0004c0004t0001g0185 | 2 | HG02451.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.98-2811_98-2803del others(9): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810656 | |||||
chr2:73810674
|
A | AC | 7 | a0002c0003t0001g0022a0002c0005t0001g0028a0002c0005t0001g0029others(4): Show | 11 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.98-2803_98-2802ins others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810674 | ||||||
chr2:73810699
|
A | G | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-2778A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810699 | ||||||
chr2:73810744
|
G | A | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-2733G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810744 | ||||||
chr2:73810769
|
T | C | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-2708T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810769 | ||||||
chr2:73810771
|
T | C | 1 | a0001c0001t0001g0053 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.98-2706T>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810771 | ||||||
chr2:73810775
|
A | AAATATAC others(36): Show |
1 | a0010c0012t0001g0169 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.98-2688_98-2646dup others(43): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810775 | |||||
chr2:73810785
|
G | A | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-2692G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810785 | ||||||
chr2:73810796
|
A | G | 3 | a0002c0003t0001g0022a0003c0002t0002g0001a0003c0002t0002g0021 | 7 | HG01167.hp1 HG01243.hp1 HG02258.hp1 others(4): Show |
intron_variant | MODIFIER | c.98-2681A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810796 | ||||||
chr2:73810817
|
T | TA | 97 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(94): Show | 107 | HG00099.hp1 HG00280.hp1 HG00423.hp2 others(104): Show |
intron_variant | MODIFIER | c.98-2660_98-2659ins others(1): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810817 | ||||||
chr2:73810821
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.98-2656T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810821 | ||||||
chr2:73810848
|
GTATAT | G | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-2623_98-2619del others(5): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810848 | |||||
chr2:73810869
|
T | A | 1 | a0001c0001t0001g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.98-2608T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810869 | ||||||
chr2:73810892
|
A | G | 2 | a0001c0001t0001g0082a0001c0001t0001g0087 | 2 | HG00558.hp2 HG00597.hp2 |
intron_variant | MODIFIER | c.98-2585A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810892 | ||||||
chr2:73810907
|
TATATA | T | 4 | a0004c0004t0001g0035a0004c0004t0001g0185a0005c0006t0001g0186others(1): Show | 4 | HG02451.hp1 HG02723.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-2564_98-2560del others(5): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810907 | |||||
chr2:73810914
|
T | G | 1 | a0001c0001t0001g0160 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.98-2563T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73810914 | ||||||
chr2:73810969
|
C | CAT | 6 | a0001c0001t0001g0074a0001c0001t0001g0091a0001c0001t0001g0137others(3): Show | 6 | HG00099.hp2 HG00280.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.98-2491_98-2490dup others(2): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810969 | |||||
chr2:73810969
|
C | CATAT | 2 | a0002c0005t0001g0028a0002c0005t0001g0029 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98-2493_98-2490dup others(4): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810969 | |||||
chr2:73810969
|
C | CATATATA others(15): Show |
1 | a0005c0006t0001g0187 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.98-2490_98-2489ins others(22): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810969 | |||||
chr2:73810969
|
C | CATATATA others(21): Show |
1 | a0005c0006t0001g0186 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.98-2490_98-2489ins others(28): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810969 | |||||
chr2:73810969
|
CAT | C | 3 | a0001c0001t0001g0016a0001c0001t0001g0044a0001c0001t0001g0101 | 4 | HG01943.hp1 HG03098.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-2491_98-2490del others(2): Show |
C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | INFO_REALIGN_3_PRIME | chr2 | 73810969 | |||||
chr2:73811094
|
C | G | 2 | a0002c0005t0001g0028a0002c0005t0001g0029 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98-2383C>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73811094 | ||||||
chr2:73811557
|
A | G | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-1920A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73811557 | ||||||
chr2:73811791
|
A | G | 9 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0042others(6): Show | 11 | HG01361.hp1 HG02615.hp1 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.98-1686A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73811791 | ||||||
chr2:73811817
|
T | A | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-1660T>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73811817 | ||||||
chr2:73811833
|
A | T | 10 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0042others(7): Show | 12 | HG01361.hp1 HG02615.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.98-1644A>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73811833 | ||||||
chr2:73811908
|
A | C | 1 | a0001c0001t0001g0076 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.98-1569A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73811908 | ||||||
chr2:73812303
|
A | G | 12 | a0001c0001t0001g0055a0001c0001t0001g0056a0001c0001t0001g0057others(9): Show | 12 | HG00621.hp2 HG01106.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.98-1174A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73812303 | ||||||
chr2:73812429
|
T | G | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.98-1048T>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73812429 | ||||||
chr2:73812468
|
C | T | 1 | a0002c0003t0001g0027 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.98-1009C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73812468 | ||||||
chr2:73812477
|
C | T | 4 | a0001c0001t0001g0063a0001c0001t0001g0066a0001c0001t0001g0070others(1): Show | 4 | HG01167.hp2 HG01433.hp1 HG04184.hp2 others(1): Show |
intron_variant | MODIFIER | c.98-1000C>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73812477 | ||||||
chr2:73812600
|
A | C | 2 | a0002c0005t0001g0028a0002c0005t0001g0029 | 2 | HG02717.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.98-877A>C | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73812600 | ||||||
chr2:73812798
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.98-679G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73812798 | ||||||
chr2:73812799
|
A | G | 1 | a0001c0001t0001g0011 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.98-678A>G | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73812799 | ||||||
chr2:73812820
|
G | T | 1 | a0001c0001t0001g0011 | 2 | HG02970.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.98-657G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 1/2 | chr2 | 73812820 | ||||||
chr2:73814307
|
G | A | 1 | a0001c0001t0001g0014 | 2 | HG00423.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.847+81G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 2/2 | chr2 | 73814307 | ||||||
chr2:73814728
|
G | A | 1 | a0002c0003t0001g0025 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.848-343G>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 2/2 | chr2 | 73814728 | ||||||
chr2:73814843
|
C | A | 2 | a0005c0006t0001g0186a0005c0006t0001g0187 | 2 | HG02723.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.848-228C>A | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 2/2 | chr2 | 73814843 | ||||||
chr2:73815011
|
G | T | 1 | a0001c0001t0001g0136 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.848-60G>T | C2orf78 | ENSG00000187833.8 | transcript | ENST00000409561.2 | protein_coding | 2/2 | chr2 | 73815011 |