geneid | 1954 |
---|---|
ensemblid | ENSG00000105429.13 |
hgncid | 3233 |
symbol | MEGF8 |
name | multiple EGF like domains 8 |
refseq_nuc | NM_001271938.2 |
refseq_prot | NP_001258867.1 |
ensembl_nuc | ENST00000251268.11 |
ensembl_prot | ENSP00000251268.5 |
mane_status | MANE Select |
chr | chr19 |
start | 42325635 |
end | 42378765 |
strand | + |
ver | v1.2 |
region | chr19:42325635-42378765 |
region5000 | chr19:42320635-42383765 |
regionname0 | MEGF8_chr19_42325635_42378765 |
regionname5000 | MEGF8_chr19_42320635_42383765 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 2845 | 122 | 46 | 34 | 20 | 6 | 14 | 7 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002 | 0/0 | 2845 | 31 | 10 | 6 | 8 | 1 | 6 | 4 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0003 | 0/0 | 2845 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0004 | 0/0 | 2845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0005 | 0/0 | 2845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0006 | 0/0 | 2845 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0007 | 0/0 | 2845 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0008 | 0/0 | 2845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0009 | 0/0 | 2845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0010 | 0/0 | 2845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0011 | 0/0 | 2845 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0012 | 0/0 | 2845 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0013 | 0/0 | 2845 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0014 | 0/0 | 2845 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0015 | 0/0 | 2845 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0016 | 0/0 | 2845 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0017 | 0/0 | 2845 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0018 | 0/0 | 2845 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0019 | 0/0 | 2845 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0020 | 0/0 | 2845 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 8538 | 88 | 20 | 32 | 15 | 6 | 13 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0002 | 0/0 | 8538 | 18 | 0 | 5 | 8 | 1 | 4 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0003 | 0/0 | 8538 | 14 | 14 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0004 | 0/0 | 8538 | 7 | 6 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0005 | 0/0 | 8538 | 5 | 4 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0006 | 0/0 | 8538 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0007 | 0/0 | 8538 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0008 | 0/0 | 8538 | 2 | 0 | 0 | 0 | 0 | 2 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0009 | 0/0 | 8538 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0010 | 0/0 | 8538 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0011 | 0/0 | 8538 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0012 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0013 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0014 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0015 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0016 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0017 | 0/0 | 8538 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0018 | 0/0 | 8538 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0019 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0020 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0021 | 0/0 | 8538 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0022 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0023 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0024 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0025 | 0/0 | 8538 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0026 | 0/0 | 8538 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0027 | 0/0 | 8538 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0028 | 0/0 | 8538 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0029 | 0/0 | 8538 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0030 | 0/0 | 8538 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0031 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0032 | 0/0 | 8538 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0033 | 0/0 | 8538 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0034 | 0/0 | 8538 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0035 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0036 | 0/0 | 8538 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
c0037 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2600 | 98 | 42 | 26 | 19 | 2 | 8 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0002 | 0/1 | 2599 | 20 | 1 | 8 | 2 | 4 | 4 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0003 | 0/0 | 2599 | 19 | 1 | 6 | 6 | 1 | 5 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0004 | 0/0 | 2599 | 6 | 5 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0005 | 0/0 | 2600 | 4 | 4 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0006 | 0/0 | 2600 | 3 | 0 | 0 | 3 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0007 | 0/0 | 2600 | 2 | 0 | 0 | 0 | 0 | 2 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0008 | 0/0 | 2599 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0009 | 0/0 | 2599 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0010 | 0/0 | 2599 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0011 | 0/0 | 2600 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0012 | 0/0 | 2599 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0013 | 0/0 | 2600 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0014 | 0/0 | 2599 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0015 | 0/0 | 2600 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0016 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0017 | 0/0 | 2600 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0018 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0019 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0020 | 0/0 | 2599 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0021 | 0/0 | 2599 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0022 | 0/0 | 2600 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0023 | 0/0 | 2599 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
t0024 | 0/0 | 2600 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 8538 | 88 | 20 | 32 | 15 | 6 | 13 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0003 | 0/0 | 8538 | 14 | 14 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0005 | 0/0 | 8538 | 5 | 4 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0007 | 0/0 | 8538 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0009 | 0/0 | 8538 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0010 | 0/0 | 8538 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0011 | 0/0 | 8538 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0022 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0030 | 0/0 | 8538 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0031 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0035 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0036 | 0/0 | 8538 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0037 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0002 | 0/0 | 8538 | 18 | 0 | 5 | 8 | 1 | 4 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0004 | 0/0 | 8538 | 7 | 6 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0006 | 0/0 | 8538 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0008 | 0/0 | 8538 | 2 | 0 | 0 | 0 | 0 | 2 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0015 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0003c0012 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0003c0019 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0004c0013 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0005c0016 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0006c0018 | 0/0 | 8538 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0007c0017 | 0/0 | 8538 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0008c0014 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0009c0023 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0010c0024 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0011c0026 | 0/0 | 8538 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0012c0028 | 0/0 | 8538 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0013c0027 | 0/0 | 8538 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0014c0025 | 0/0 | 8538 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0015c0020 | 0/0 | 8538 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0016c0029 | 0/0 | 8538 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0017c0032 | 0/0 | 8538 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0018c0033 | 0/0 | 8538 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0019c0021 | 0/0 | 8538 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0020c0034 | 0/0 | 8538 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 11137 | 55 | 14 | 24 | 10 | 1 | 5 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0001t0002 | 0/1 | 11136 | 19 | 1 | 7 | 2 | 4 | 4 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0001t0005 | 0/0 | 11137 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0001t0006 | 0/0 | 11137 | 3 | 0 | 0 | 3 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0001t0007 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0001t0011 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0001t0013 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0001t0015 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0001t0017 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0001t0018 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0001t0019 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0001t0024 | 0/0 | 11137 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0003t0001 | 0/0 | 11137 | 14 | 14 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0005t0003 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0005t0004 | 0/0 | 11136 | 4 | 3 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0007t0001 | 0/0 | 11137 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0009t0001 | 0/0 | 11137 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0010t0001 | 0/0 | 11137 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0011t0001 | 0/0 | 11137 | 2 | 0 | 0 | 2 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0022t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0030t0001 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0031t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0035t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0036t0001 | 0/0 | 11137 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0001c0037t0005 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0002t0001 | 0/0 | 11137 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0002t0003 | 0/0 | 11136 | 14 | 0 | 5 | 5 | 1 | 3 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0002t0007 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0002t0020 | 0/0 | 11136 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0002t0021 | 0/0 | 11136 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0004t0008 | 0/0 | 11136 | 2 | 1 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0004t0009 | 0/0 | 11136 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0004t0010 | 0/0 | 11136 | 2 | 2 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0004t0023 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0006t0001 | 0/0 | 11137 | 3 | 3 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0008t0003 | 0/0 | 11136 | 2 | 0 | 0 | 0 | 0 | 2 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0002c0015t0016 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0003c0012t0004 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0003c0019t0004 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0004c0013t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0005c0016t0022 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0006c0018t0003 | 0/0 | 11136 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0007c0017t0003 | 0/0 | 11136 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0008c0014t0012 | 0/0 | 11136 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0009c0023t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0010c0024t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0011c0026t0001 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0012c0028t0002 | 0/0 | 11136 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0013c0027t0001 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0014c0025t0001 | 0/0 | 11137 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0015c0020t0001 | 0/0 | 11137 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0016c0029t0001 | 0/0 | 11137 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0017c0032t0001 | 0/0 | 11137 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0018c0033t0001 | 0/0 | 11137 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0019c0021t0014 | 0/0 | 11136 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
a0020c0034t0001 | 0/0 | 11137 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | copy fasta | chr19 | 42320635 | 42383765 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0157 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0056 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0002g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0005g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0005g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0005g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0006g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0006g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0006g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0007g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0011g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0013g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0015g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0017g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0018g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0019g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0001t0024g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0001 | 0/0 | 4 | 4 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0003t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0005t0003g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0005t0004g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0005t0004g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0005t0004g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0005t0004g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0007t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0007t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0007t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0009t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0009t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0010t0001g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0010t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0011t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0011t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0022t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0030t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0031t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0035t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0036t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0001c0037t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0028 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0036 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0003g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0007g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0020g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0002t0021g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0008g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0008g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0010g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0010g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0004t0023g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0006t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0006t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0006t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0008t0003g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0008t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0002c0015t0016g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0003c0012t0004g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0003c0019t0004g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0004c0013t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0005c0016t0022g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0006c0018t0003g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0007c0017t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0008c0014t0012g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0009c0023t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0010c0024t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0011c0026t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0012c0028t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0013c0027t0001g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0014c0025t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0015c0020t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0016c0029t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0017c0032t0001g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0018c0033t0001g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0019c0021t0014g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
a0020c0034t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0011 | c0026 | t0001 | g0106 | EUR | GBR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00140 | hp2 | a0001 | c0001 | t0002 | g0048 | EUR | GBR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00597 | hp1 | a0001 | c0001 | t0006 | g0150 | EAS | CHS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00597 | hp2 | a0002 | c0002 | t0001 | g0034 | EAS | CHS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00609 | hp1 | a0017 | c0032 | t0001 | g0005 | EAS | CHS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00609 | hp2 | a0001 | c0001 | t0006 | g0149 | EAS | CHS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00621 | hp1 | a0001 | c0009 | t0001 | g0132 | EAS | CHS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00621 | hp2 | a0001 | c0001 | t0006 | g0137 | EAS | CHS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0151 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00639 | hp2 | a0002 | c0002 | t0003 | g0032 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00738 | hp1 | a0001 | c0010 | t0001 | g0085 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01069 | hp1 | a0002 | c0002 | t0003 | g0012 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01071 | hp2 | a0002 | c0002 | t0003 | g0030 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01074 | hp1 | a0012 | c0028 | t0002 | g0089 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0142 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01175 | hp2 | a0006 | c0018 | t0003 | g0040 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0138 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0136 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01243 | hp1 | a0002 | c0004 | t0008 | g0026 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PUR | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0074 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01346 | hp2 | a0001 | c0001 | t0024 | g0154 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0140 | EUR | IBS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0072 | EUR | IBS | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01884 | hp1 | a0001 | c0003 | t0001 | g0117 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01884 | hp2 | a0001 | c0001 | t0005 | g0087 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01891 | hp1 | a0001 | c0005 | t0004 | g0130 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01891 | hp2 | a0001 | c0003 | t0001 | g0115 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0010 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0109 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01975 | hp2 | a0020 | c0034 | t0001 | g0104 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0053 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01993 | hp1 | a0002 | c0002 | t0003 | g0029 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01993 | hp2 | a0001 | c0001 | t0002 | g0015 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0055 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0144 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02074 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02074 | hp2 | a0002 | c0002 | t0021 | g0102 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02080 | hp1 | a0001 | c0009 | t0001 | g0005 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02132 | hp2 | a0018 | c0033 | t0001 | g0006 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02135 | hp1 | a0002 | c0002 | t0003 | g0039 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02145 | hp2 | a0001 | c0003 | t0001 | g0121 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02155 | hp1 | a0007 | c0017 | t0003 | g0035 | EAS | CDX | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | CDX | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02165 | hp2 | a0002 | c0002 | t0003 | g0033 | EAS | CDX | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02257 | hp1 | a0001 | c0001 | t0019 | g0110 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02273 | hp1 | a0002 | c0002 | t0003 | g0031 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02280 | hp1 | a0001 | c0003 | t0001 | g0113 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02280 | hp2 | a0002 | c0015 | t0016 | g0123 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02300 | hp2 | a0019 | c0021 | t0014 | g0052 | AMR | PEL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0076 | EAS | KHV | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02615 | hp1 | a0002 | c0004 | t0009 | g0021 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02615 | hp2 | a0001 | c0003 | t0001 | g0017 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02630 | hp1 | a0002 | c0004 | t0023 | g0066 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02630 | hp2 | a0002 | c0006 | t0001 | g0020 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02647 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02647 | hp2 | a0001 | c0001 | t0005 | g0098 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02683 | hp1 | a0001 | c0001 | t0017 | g0077 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02683 | hp2 | a0002 | c0002 | t0003 | g0042 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02717 | hp1 | a0001 | c0003 | t0001 | g0116 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0061 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02723 | hp1 | a0001 | c0037 | t0005 | g0054 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02723 | hp2 | a0002 | c0004 | t0008 | g0025 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02735 | hp1 | a0002 | c0002 | t0007 | g0038 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02735 | hp2 | a0001 | c0001 | t0015 | g0153 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02809 | hp2 | a0015 | c0020 | t0001 | g0120 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02818 | hp1 | a0008 | c0014 | t0012 | g0101 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02818 | hp2 | a0001 | c0001 | t0005 | g0081 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02886 | hp1 | a0002 | c0006 | t0001 | g0019 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02886 | hp2 | a0001 | c0001 | t0018 | g0094 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02897 | hp2 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02922 | hp2 | a0001 | c0005 | t0004 | g0129 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02970 | hp1 | a0009 | c0023 | t0001 | g0124 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02976 | hp1 | a0001 | c0007 | t0001 | g0068 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02976 | hp2 | a0005 | c0016 | t0022 | g0100 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03041 | hp2 | a0004 | c0013 | t0001 | g0084 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0090 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03098 | hp2 | a0001 | c0010 | t0001 | g0080 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03139 | hp1 | a0001 | c0035 | t0001 | g0099 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03139 | hp2 | a0002 | c0004 | t0010 | g0024 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0118 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03225 | hp2 | a0001 | c0031 | t0001 | g0091 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03453 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03453 | hp2 | a0002 | c0006 | t0001 | g0018 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03490 | hp1 | a0001 | c0001 | t0007 | g0134 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0013 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03516 | hp1 | a0001 | c0003 | t0001 | g0112 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0161 | AFR | ESN | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03540 | hp1 | a0001 | c0003 | t0001 | g0001 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03540 | hp2 | a0001 | c0022 | t0001 | g0063 | AFR | GWD | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03669 | hp2 | a0014 | c0025 | t0001 | g0111 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03688 | hp1 | a0001 | c0001 | t0011 | g0097 | SAS | STU | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03688 | hp2 | a0002 | c0002 | t0003 | g0028 | SAS | STU | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03704 | hp1 | a0013 | c0027 | t0001 | g0050 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03704 | hp2 | a0001 | c0030 | t0001 | g0071 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03710 | hp1 | a0002 | c0008 | t0003 | g0041 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03710 | hp2 | a0001 | c0001 | t0002 | g0014 | SAS | PJL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03834 | hp1 | a0001 | c0001 | t0002 | g0070 | SAS | BEB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0075 | SAS | BEB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0082 | SAS | BEB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03927 | hp2 | a0002 | c0002 | t0003 | g0027 | SAS | BEB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0083 | SAS | STU | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG04228 | hp2 | a0002 | c0008 | t0003 | g0037 | SAS | STU | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18906 | hp1 | a0001 | c0007 | t0001 | g0047 | AFR | YRI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18906 | hp2 | a0001 | c0005 | t0003 | g0125 | AFR | YRI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18966 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18966 | hp2 | a0001 | c0036 | t0001 | g0079 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18981 | hp1 | a0002 | c0002 | t0003 | g0163 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18981 | hp2 | a0001 | c0011 | t0001 | g0065 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA18983 | hp2 | a0001 | c0011 | t0001 | g0064 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0105 | AFR | LWK | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19043 | hp2 | a0001 | c0003 | t0001 | g0119 | AFR | LWK | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19057 | hp1 | a0016 | c0029 | t0001 | g0133 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19057 | hp2 | a0002 | c0002 | t0020 | g0103 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19066 | hp1 | a0002 | c0002 | t0003 | g0164 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19088 | hp1 | a0002 | c0002 | t0003 | g0165 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19240 | hp1 | a0010 | c0024 | t0001 | g0095 | AFR | YRI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA19240 | hp2 | a0002 | c0004 | t0010 | g0023 | AFR | YRI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0139 | AFR | ASW | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA20129 | hp2 | a0001 | c0005 | t0004 | g0128 | AFR | ASW | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0152 | EUR | TSI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0059 | EUR | TSI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA20805 | hp1 | a0001 | c0001 | t0013 | g0060 | EUR | TSI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
NA20805 | hp2 | a0002 | c0002 | t0003 | g0036 | EUR | TSI | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01123 | hp1 | a0001 | c0005 | t0004 | g0126 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0147 | AMR | CLM | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02109 | hp1 | a0003 | c0012 | t0004 | g0127 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02109 | hp2 | a0002 | c0004 | t0009 | g0022 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02559 | hp1 | a0003 | c0019 | t0004 | g0122 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0160 | AFR | ACB | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03471 | hp1 | a0001 | c0007 | t0001 | g0067 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
HG03471 | hp2 | a0001 | c0003 | t0001 | g0114 | AFR | MSL | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0056 | REF | REF | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0157 | REF | REF | MEGF8_chr19_42320635_42383765 | MEGF8 | chr19 | 42320635 | 42383765 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42336021
|
G | A | 1 | a0004 | 1 | HG03041.hp2 | missense_variant | MODERATE | c.919G>A | p.Val307Met | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 6/42 | 1528/11137 | 919/8538 | 307/2845 | chr19 | 42336021 | ||
chr19:42349650
|
A | G | 1 | a0020 | 1 | HG01975.hp2 | missense_variant | MODERATE | c.2450A>G | p.His817Arg | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 14/42 | 3059/11137 | 2450/8538 | 817/2845 | chr19 | 42349650 | ||
chr19:42351538
|
G | A | 1 | a0019 | 1 | HG02300.hp2 | missense_variant | MODERATE | c.2965G>A | p.Gly989Ser | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 17/42 | 3574/11137 | 2965/8538 | 989/2845 | chr19 | 42351538 | ||
chr19:42353032
|
C | T | 1 | a0005 | 1 | HG02976.hp2 | missense_variant | MODERATE | c.3455C>T | p.Pro1152Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 20/42 | 4064/11137 | 3455/8538 | 1152/2845 | chr19 | 42353032 | ||
chr19:42353539
|
C | T | 1 | a0018 | 1 | HG02132.hp2 | missense_variant | MODERATE | c.3625C>T | p.Arg1209Trp | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 21/42 | 4234/11137 | 3625/8538 | 1209/2845 | chr19 | 42353539 | ||
chr19:42353674
|
C | T | 1 | a0017 | 1 | HG00609.hp1 | missense_variant&splice_region_variant | MODERATE | c.3760C>T | p.Arg1254Trp | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 21/42 | 4369/11137 | 3760/8538 | 1254/2845 | chr19 | 42353674 | ||
chr19:42356890
|
C | T | 1 | a0016 | 1 | NA19057.hp1 | missense_variant | MODERATE | c.4739C>T | p.Ala1580Val | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 27/42 | 5348/11137 | 4739/8538 | 1580/2845 | chr19 | 42356890 | ||
chr19:42358820
|
C | T | 1 | a0015 | 1 | HG02809.hp2 | missense_variant | MODERATE | c.5209C>T | p.Arg1737Trp | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 30/42 | 5818/11137 | 5209/8538 | 1737/2845 | chr19 | 42358820 | ||
chr19:42358883
|
A | G | 5 | a0002a0005a0006others(2): Show | 35 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(32): Show |
missense_variant | MODERATE | c.5272A>G | p.Lys1758Glu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 30/42 | 5881/11137 | 5272/8538 | 1758/2845 | chr19 | 42358883 | ||
chr19:42358931
|
G | C | 1 | a0008 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.5320G>C | p.Glu1774Gln | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 30/42 | 5929/11137 | 5320/8538 | 1774/2845 | chr19 | 42358931 | ||
chr19:42362149
|
G | A | 1 | a0009 | 1 | HG02970.hp1 | missense_variant | MODERATE | c.5780G>A | p.Arg1927His | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 33/42 | 6389/11137 | 5780/8538 | 1927/2845 | chr19 | 42362149 | ||
chr19:42368650
|
G | A | 1 | a0007 | 1 | HG02155.hp1 | missense_variant | MODERATE | c.6469G>A | p.Gly2157Ser | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 36/42 | 7078/11137 | 6469/8538 | 2157/2845 | chr19 | 42368650 | ||
chr19:42369710
|
G | A | 1 | a0010 | 1 | NA19240.hp1 | missense_variant | MODERATE | c.6821G>A | p.Arg2274His | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/42 | 7430/11137 | 6821/8538 | 2274/2845 | chr19 | 42369710 | ||
chr19:42370265
|
C | A | 1 | a0014 | 1 | HG03669.hp2 | missense_variant | MODERATE | c.6911C>A | p.Ala2304Asp | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 39/42 | 7520/11137 | 6911/8538 | 2304/2845 | chr19 | 42370265 | ||
chr19:42370749
|
G | A | 1 | a0011 | 1 | HG00140.hp1 | missense_variant | MODERATE | c.7054G>A | p.Val2352Met | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/42 | 7663/11137 | 7054/8538 | 2352/2845 | chr19 | 42370749 | ||
chr19:42375910
|
C | T | 2 | a0006a0012 | 2 | HG01074.hp1 HG01175.hp2 |
missense_variant | MODERATE | c.7673C>T | p.Pro2558Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 8282/11137 | 7673/8538 | 2558/2845 | chr19 | 42375910 | ||
chr19:42375999
|
G | A | 1 | a0008 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.7762G>A | p.Val2588Met | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 8371/11137 | 7762/8538 | 2588/2845 | chr19 | 42375999 | ||
chr19:42376377
|
G | A | 1 | a0013 | 1 | HG03704.hp1 | missense_variant | MODERATE | c.8140G>A | p.Ala2714Thr | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 8749/11137 | 8140/8538 | 2714/2845 | chr19 | 42376377 | ||
chr19:42376663
|
G | A | 1 | a0003 | 2 | HG02109.hp1 HG02559.hp1 |
missense_variant | MODERATE | c.8426G>A | p.Arg2809Lys | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 9035/11137 | 8426/8538 | 2809/2845 | chr19 | 42376663 | ||
chr19:42376704
|
A | G | 1 | a0008 | 1 | HG02818.hp1 | missense_variant | MODERATE | c.8467A>G | p.Ser2823Gly | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 9076/11137 | 8467/8538 | 2823/2845 | chr19 | 42376704 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42326250
|
C | T | 1 | a0001c0037 | 1 | HG02723.hp1 | synonymous_variant | LOW | c.7C>T | p.Leu3Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/42 | 616/11137 | 7/8538 | 3/2845 | chr19 | 42326250 | ||
chr19:42334012
|
G | A | 1 | a0003c0012 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.357G>A | p.Leu119Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 3/42 | 966/11137 | 357/8538 | 119/2845 | chr19 | 42334012 | ||
chr19:42334057
|
C | T | 1 | a0001c0036 | 1 | NA18966.hp2 | synonymous_variant | LOW | c.402C>T | p.Asn134Asn | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 3/42 | 1011/11137 | 402/8538 | 134/2845 | chr19 | 42334057 | ||
chr19:42336020
|
C | T | 1 | a0001c0035 | 1 | HG03139.hp1 | synonymous_variant | LOW | c.918C>T | p.Asp306Asp | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 6/42 | 1527/11137 | 918/8538 | 306/2845 | chr19 | 42336020 | ||
chr19:42348328
|
G | A | 9 | a0002c0002a0002c0004a0002c0006others(6): Show | 35 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(32): Show |
synonymous_variant | LOW | c.2154G>A | p.Val718Val | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 13/42 | 2763/11137 | 2154/8538 | 718/2845 | chr19 | 42348328 | ||
chr19:42348397
|
C | T | 4 | a0002c0002a0002c0008a0006c0018others(1): Show | 22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
synonymous_variant | LOW | c.2223C>T | p.Asp741Asp | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 13/42 | 2832/11137 | 2223/8538 | 741/2845 | chr19 | 42348397 | ||
chr19:42349630
|
T | C | 14 | a0001c0003a0001c0005a0002c0002others(11): Show | 57 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(54): Show |
synonymous_variant | LOW | c.2430T>C | p.Asn810Asn | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 14/42 | 3039/11137 | 2430/8538 | 810/2845 | chr19 | 42349630 | ||
chr19:42351717
|
C | T | 1 | a0001c0011 | 2 | NA18981.hp2 NA18983.hp2 |
synonymous_variant | LOW | c.3057C>T | p.His1019His | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 18/42 | 3666/11137 | 3057/8538 | 1019/2845 | chr19 | 42351717 | ||
chr19:42353010
|
C | T | 1 | a0001c0007 | 3 | HG02976.hp1 HG03471.hp1 NA18906.hp1 |
synonymous_variant | LOW | c.3433C>T | p.Leu1145Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 20/42 | 4042/11137 | 3433/8538 | 1145/2845 | chr19 | 42353010 | ||
chr19:42353027
|
C | T | 4 | a0002c0002a0002c0008a0006c0018others(1): Show | 22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
synonymous_variant | LOW | c.3450C>T | p.Pro1150Pro | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 20/42 | 4059/11137 | 3450/8538 | 1150/2845 | chr19 | 42353027 | ||
chr19:42354596
|
C | T | 3 | a0001c0003a0003c0019a0015c0020 | 16 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
synonymous_variant | LOW | c.4020C>T | p.Tyr1340Tyr | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 23/42 | 4629/11137 | 4020/8538 | 1340/2845 | chr19 | 42354596 | ||
chr19:42354617
|
C | T | 1 | a0001c0031 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.4041C>T | p.Phe1347Phe | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 23/42 | 4650/11137 | 4041/8538 | 1347/2845 | chr19 | 42354617 | ||
chr19:42354641
|
T | C | 4 | a0002c0002a0002c0008a0006c0018others(1): Show | 22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
synonymous_variant | LOW | c.4065T>C | p.Val1355Val | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 23/42 | 4674/11137 | 4065/8538 | 1355/2845 | chr19 | 42354641 | ||
chr19:42355972
|
C | T | 1 | a0001c0030 | 1 | HG03704.hp2 | synonymous_variant | LOW | c.4359C>T | p.Cys1453Cys | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 24/42 | 4968/11137 | 4359/8538 | 1453/2845 | chr19 | 42355972 | ||
chr19:42356864
|
C | T | 1 | a0002c0008 | 2 | HG03710.hp1 HG04228.hp2 |
synonymous_variant | LOW | c.4713C>T | p.Ala1571Ala | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 27/42 | 5322/11137 | 4713/8538 | 1571/2845 | chr19 | 42356864 | ||
chr19:42357415
|
C | T | 1 | a0001c0010 | 2 | HG00738.hp1 HG03098.hp2 |
synonymous_variant | LOW | c.4842C>T | p.Thr1614Thr | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 28/42 | 5451/11137 | 4842/8538 | 1614/2845 | chr19 | 42357415 | ||
chr19:42358927
|
G | A | 1 | a0003c0012 | 1 | HG02109.hp1 | synonymous_variant | LOW | c.5316G>A | p.Leu1772Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 30/42 | 5925/11137 | 5316/8538 | 1772/2845 | chr19 | 42358927 | ||
chr19:42359166
|
G | A | 1 | a0001c0022 | 1 | HG03540.hp2 | synonymous_variant | LOW | c.5412G>A | p.Ser1804Ser | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/42 | 6021/11137 | 5412/8538 | 1804/2845 | chr19 | 42359166 | ||
chr19:42359229
|
G | A | 3 | a0001c0003a0003c0019a0015c0020 | 16 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
synonymous_variant | LOW | c.5475G>A | p.Leu1825Leu | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/42 | 6084/11137 | 5475/8538 | 1825/2845 | chr19 | 42359229 | ||
chr19:42368937
|
G | A | 2 | a0002c0004a0002c0015 | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
synonymous_variant | LOW | c.6576G>A | p.Thr2192Thr | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 37/42 | 7185/11137 | 6576/8538 | 2192/2845 | chr19 | 42368937 | ||
chr19:42370748
|
C | T | 1 | a0002c0004 | 7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
synonymous_variant | LOW | c.7053C>T | p.Cys2351Cys | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/42 | 7662/11137 | 7053/8538 | 2351/2845 | chr19 | 42370748 | ||
chr19:42375968
|
C | T | 1 | a0001c0009 | 2 | HG00621.hp1 HG02080.hp1 |
synonymous_variant | LOW | c.7731C>T | p.Tyr2577Tyr | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 8340/11137 | 7731/8538 | 2577/2845 | chr19 | 42375968 | ||
chr19:42375974
|
G | A | 3 | a0002c0015a0005c0016a0008c0014 | 3 | HG02280.hp2 HG02818.hp1 HG02976.hp2 |
synonymous_variant | LOW | c.7737G>A | p.Thr2579Thr | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 8346/11137 | 7737/8538 | 2579/2845 | chr19 | 42375974 | ||
chr19:42376703
|
C | A | 1 | a0008c0014 | 1 | HG02818.hp1 | synonymous_variant | LOW | c.8466C>A | p.Gly2822Gly | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 9075/11137 | 8466/8538 | 2822/2845 | chr19 | 42376703 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42326085
|
A | T | 3 | a0002c0004t0008a0002c0004t0009a0002c0004t0010 | 6 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-159A>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/42 | 159 | chr19 | 42326085 | |||||
chr19:42326117
|
C | T | 1 | a0001c0001t0024 | 1 | HG01346.hp2 | 5_prime_UTR_variant | MODIFIER | c.-127C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/42 | 127 | chr19 | 42326117 | |||||
chr19:42376987
|
C | T | 1 | a0001c0001t0006 | 3 | HG00597.hp1 HG00609.hp2 HG00621.hp2 |
3_prime_UTR_variant | MODIFIER | c.*212C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 212 | chr19 | 42376987 | |||||
chr19:42377079
|
C | T | 3 | a0002c0004t0009a0002c0004t0010a0002c0004t0023 | 5 | HG02109.hp2 HG02615.hp1 HG02630.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*304C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 304 | chr19 | 42377079 | |||||
chr19:42377181
|
G | A | 1 | a0001c0001t0011 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*406G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 406 | chr19 | 42377181 | |||||
chr19:42377680
|
G | A | 1 | a0008c0014t0012 | 1 | HG02818.hp1 | 3_prime_UTR_variant | MODIFIER | c.*905G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 905 | chr19 | 42377680 | |||||
chr19:42377753
|
C | T | 1 | a0005c0016t0022 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*978C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 978 | chr19 | 42377753 | |||||
chr19:42377803
|
T | A | 2 | a0001c0001t0005a0001c0037t0005 | 4 | HG01884.hp2 HG02647.hp2 HG02723.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1028T>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1028 | chr19 | 42377803 | |||||
chr19:42377840
|
C | T | 2 | a0002c0002t0020a0002c0002t0021 | 2 | HG02074.hp2 NA19057.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1065C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1065 | chr19 | 42377840 | |||||
chr19:42377940
|
G | A | 1 | a0001c0001t0013 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1165G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1165 | chr19 | 42377940 | |||||
chr19:42377943
|
G | A | 7 | a0001c0005t0003a0002c0002t0003a0002c0002t0020others(4): Show | 21 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1168G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1168 | chr19 | 42377943 | |||||
chr19:42378052
|
C | A | 1 | a0019c0021t0014 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1277C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1277 | chr19 | 42378052 | |||||
chr19:42378221
|
C | T | 3 | a0001c0001t0019a0002c0004t0008a0002c0004t0010 | 5 | HG01243.hp1 HG02257.hp1 HG02723.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1446C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1446 | chr19 | 42378221 | |||||
chr19:42378393
|
A | G | 1 | a0002c0002t0021 | 1 | HG02074.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1618A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1618 | chr19 | 42378393 | |||||
chr19:42378397
|
G | A | 2 | a0001c0001t0015a0001c0001t0024 | 2 | HG01346.hp2 HG02735.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1622G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1622 | chr19 | 42378397 | |||||
chr19:42378424
|
C | T | 5 | a0001c0001t0018a0002c0004t0008a0002c0004t0009others(2): Show | 8 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1649C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1649 | chr19 | 42378424 | |||||
chr19:42378493
|
G | A | 2 | a0001c0001t0007a0002c0002t0007 | 2 | HG02735.hp1 HG03490.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1718G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1718 | chr19 | 42378493 | |||||
chr19:42378514
|
C | T | 1 | a0001c0001t0017 | 1 | HG02683.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1739C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1739 | chr19 | 42378514 | |||||
chr19:42378627
|
G | C | 3 | a0002c0004t0009a0002c0004t0023a0008c0014t0012 | 4 | HG02109.hp2 HG02615.hp1 HG02630.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1852G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1852 | chr19 | 42378627 | |||||
chr19:42378677
|
TA | T | 18 | a0001c0001t0002a0001c0005t0003a0001c0005t0004others(15): Show | 56 | HG00140.hp2 HG00639.hp2 HG00741.hp2 others(53): Show |
3_prime_UTR_variant | MODIFIER | c.*1903delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1903 | chr19 | 42378677 | |||||
chr19:42378701
|
T | C | 14 | a0001c0005t0003a0001c0005t0004a0002c0002t0003others(11): Show | 33 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1926T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 42/42 | 1926 | chr19 | 42378701 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr19:42326739
|
CT | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0043a0001c0001t0001g0044others(113): Show | 121 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(118): Show |
intron_variant | MODIFIER | c.187+329delT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42326739 | |||||
chr19:42326739
|
CTT | C | 6 | a0001c0001t0001g0016a0001c0001t0002g0013a0001c0001t0002g0014others(3): Show | 6 | HG01069.hp1 HG01993.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+328_187+329del others(2): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42326739 | |||||
chr19:42326751
|
T | C | 6 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(3): Show | 6 | HG01069.hp2 HG01934.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.187+321T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42326751 | ||||||
chr19:42326909
|
C | T | 6 | a0001c0005t0003g0125a0001c0005t0004g0126a0001c0005t0004g0128others(3): Show | 6 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+479C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42326909 | ||||||
chr19:42326931
|
T | C | 26 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(23): Show | 26 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.187+501T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42326931 | ||||||
chr19:42327033
|
A | G | 23 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0108others(20): Show | 26 | HG00140.hp1 HG01243.hp2 HG01884.hp1 others(23): Show |
intron_variant | MODIFIER | c.187+603A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42327033 | ||||||
chr19:42327044
|
T | C | 3 | a0002c0006t0001g0018a0002c0006t0001g0019a0002c0006t0001g0020 | 3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.187+614T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42327044 | ||||||
chr19:42327562
|
C | G | 5 | a0001c0005t0004g0126a0001c0005t0004g0128a0001c0005t0004g0129others(2): Show | 5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+1132C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42327562 | ||||||
chr19:42327664
|
G | A | 6 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(3): Show | 6 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+1234G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42327664 | ||||||
chr19:42327670
|
C | T | 2 | a0002c0015t0016g0123a0009c0023t0001g0124 | 2 | HG02280.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.187+1240C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42327670 | ||||||
chr19:42328209
|
A | G | 28 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(25): Show | 28 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.187+1779A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42328209 | ||||||
chr19:42328405
|
T | A | 22 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(19): Show | 22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.187+1975T>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42328405 | ||||||
chr19:42328567
|
A | AGT | 47 | a0001c0001t0001g0016a0001c0001t0001g0073a0001c0001t0001g0074others(44): Show | 51 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(48): Show |
intron_variant | MODIFIER | c.187+2159_187+2160d others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | |||||
chr19:42328567
|
A | AGTGT | 2 | a0001c0001t0005g0098a0001c0035t0001g0099 | 2 | HG02647.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.187+2157_187+2160d others(6): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | |||||
chr19:42328567
|
A | AGTGTGTG others(11): Show |
2 | a0001c0005t0004g0126a0002c0004t0009g0021 | 2 | HG01123.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.187+2143_187+2160d others(20): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | |||||
chr19:42328567
|
A | AGTGTGTG others(13): Show |
1 | a0002c0004t0009g0022 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.187+2141_187+2160d others(22): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | |||||
chr19:42328567
|
A | AGTGTGTG others(15): Show |
5 | a0002c0002t0003g0027a0002c0004t0008g0025a0002c0004t0008g0026others(2): Show | 5 | HG01243.hp1 HG02723.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.187+2139_187+2160d others(24): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | |||||
chr19:42328567
|
A | AGTGTGTG others(17): Show |
3 | a0002c0002t0003g0028a0002c0002t0003g0029a0002c0006t0001g0018 | 3 | HG01993.hp1 HG03453.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.187+2160_187+2161i others(26): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | |||||
chr19:42328567
|
A | AGTGTGTG others(19): Show |
12 | a0001c0005t0003g0125a0002c0002t0001g0034a0002c0002t0003g0012others(9): Show | 12 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.187+2160_187+2161i others(28): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | |||||
chr19:42328567
|
A | AGTGTGTG others(21): Show |
1 | a0002c0002t0003g0036 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.187+2160_187+2161i others(30): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | |||||
chr19:42328567
|
A | AGTGTGTG others(23): Show |
7 | a0001c0005t0004g0128a0002c0002t0003g0039a0002c0002t0007g0038others(4): Show | 7 | HG01175.hp2 HG02135.hp1 HG02735.hp1 others(4): Show |
intron_variant | MODIFIER | c.187+2160_187+2161i others(32): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | |||||
chr19:42328567
|
A | AGTGTGTG others(25): Show |
5 | a0001c0005t0004g0129a0001c0005t0004g0130a0002c0002t0003g0042others(2): Show | 5 | HG01891.hp1 HG02683.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.187+2160_187+2161i others(34): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | INFO_REALIGN_3_PRIME | chr19 | 42328567 | |||||
chr19:42328674
|
G | A | 1 | a0001c0001t0001g0131 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.187+2244G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42328674 | ||||||
chr19:42329015
|
G | C | 1 | a0001c0030t0001g0071 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.187+2585G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329015 | ||||||
chr19:42329127
|
C | T | 1 | a0006c0018t0003g0040 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.187+2697C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329127 | ||||||
chr19:42329198
|
G | A | 3 | a0001c0001t0001g0073a0001c0001t0001g0074a0001c0001t0002g0072 | 3 | HG01258.hp1 HG01516.hp2 HG03491.hp1 |
intron_variant | MODIFIER | c.187+2768G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329198 | ||||||
chr19:42329389
|
T | C | 1 | a0002c0002t0003g0028 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.187+2959T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329389 | ||||||
chr19:42329452
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.187+3022G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329452 | ||||||
chr19:42329498
|
G | A | 6 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(3): Show | 6 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+3068G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329498 | ||||||
chr19:42329763
|
C | T | 6 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(3): Show | 6 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.187+3333C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329763 | ||||||
chr19:42329828
|
C | T | 1 | a0001c0001t0002g0070 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.187+3398C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329828 | ||||||
chr19:42329854
|
A | G | 1 | a0001c0001t0002g0160 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.187+3424A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329854 | ||||||
chr19:42329948
|
A | C | 1 | a0003c0019t0004g0122 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.187+3518A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329948 | ||||||
chr19:42329982
|
G | C | 1 | a0002c0008t0003g0041 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.187+3552G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329982 | ||||||
chr19:42329991
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.187+3561G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42329991 | ||||||
chr19:42330178
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.188-3427A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42330178 | ||||||
chr19:42330556
|
T | C | 6 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(3): Show | 6 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.188-3049T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42330556 | ||||||
chr19:42330570
|
G | C | 1 | a0001c0001t0002g0075 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.188-3035G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42330570 | ||||||
chr19:42330599
|
A | G | 62 | a0001c0001t0001g0105a0001c0001t0001g0107a0001c0001t0001g0108others(59): Show | 65 | HG00140.hp1 HG00597.hp2 HG00639.hp2 others(62): Show |
intron_variant | MODIFIER | c.188-3006A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42330599 | ||||||
chr19:42330790
|
T | C | 1 | a0002c0008t0003g0037 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.188-2815T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42330790 | ||||||
chr19:42330937
|
C | T | 1 | a0001c0001t0002g0003 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.188-2668C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42330937 | ||||||
chr19:42331540
|
T | A | 157 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(154): Show | 163 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(160): Show |
intron_variant | MODIFIER | c.188-2065T>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42331540 | ||||||
chr19:42331545
|
G | A | 3 | a0002c0006t0001g0018a0002c0006t0001g0019a0002c0006t0001g0020 | 3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.188-2060G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42331545 | ||||||
chr19:42331849
|
C | T | 3 | a0001c0001t0011g0097a0005c0016t0022g0100a0008c0014t0012g0101 | 3 | HG02818.hp1 HG02976.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.188-1756C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42331849 | ||||||
chr19:42331939
|
A | C | 4 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0010g0023others(1): Show | 4 | HG01243.hp1 HG02723.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.188-1666A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42331939 | ||||||
chr19:42332164
|
C | T | 2 | a0005c0016t0022g0100a0008c0014t0012g0101 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.188-1441C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42332164 | ||||||
chr19:42332398
|
G | A | 13 | a0001c0003t0001g0001a0001c0003t0001g0017a0001c0003t0001g0112others(10): Show | 16 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.188-1207G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42332398 | ||||||
chr19:42332494
|
A | G | 2 | a0005c0016t0022g0100a0008c0014t0012g0101 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.188-1111A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42332494 | ||||||
chr19:42333112
|
G | A | 1 | a0001c0001t0001g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.188-493G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42333112 | ||||||
chr19:42333253
|
G | A | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG02055.hp1 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.188-352G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42333253 | ||||||
chr19:42333494
|
A | G | 2 | a0001c0007t0001g0067a0001c0007t0001g0068 | 2 | HG02976.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.188-111A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42333494 | ||||||
chr19:42333504
|
A | G | 7 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.188-101A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 1/41 | chr19 | 42333504 | ||||||
chr19:42333769
|
G | T | 1 | a0002c0002t0003g0042 | 1 | HG02683.hp2 | splice_donor_variant&intron_variant | HIGH | c.351+1G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 2/41 | chr19 | 42333769 | ||||||
chr19:42334003
|
G | A | 4 | a0002c0002t0003g0012a0002c0002t0003g0029a0002c0002t0003g0030others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01993.hp1 others(1): Show |
splice_region_variant&intron_variant | LOW | c.352-4G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 2/41 | chr19 | 42334003 | ||||||
chr19:42334265
|
G | C | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.558+52G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 3/41 | chr19 | 42334265 | ||||||
chr19:42334359
|
C | G | 2 | a0001c0011t0001g0064a0001c0011t0001g0065 | 2 | NA18981.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.558+146C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 3/41 | chr19 | 42334359 | ||||||
chr19:42334733
|
C | T | 1 | a0001c0022t0001g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.559-302C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 3/41 | chr19 | 42334733 | ||||||
chr19:42335254
|
G | A | 2 | a0005c0016t0022g0100a0008c0014t0012g0101 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.739+39G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 4/41 | chr19 | 42335254 | ||||||
chr19:42335445
|
C | A | 1 | a0001c0001t0001g0076 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.828+60C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 5/41 | chr19 | 42335445 | ||||||
chr19:42335755
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.829-176C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 5/41 | chr19 | 42335755 | ||||||
chr19:42335867
|
G | A | 1 | a0020c0034t0001g0104 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.829-64G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 5/41 | chr19 | 42335867 | ||||||
chr19:42336546
|
C | T | 1 | a0001c0001t0001g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1244+200C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 6/41 | chr19 | 42336546 | ||||||
chr19:42336734
|
G | A | 3 | a0002c0006t0001g0018a0002c0006t0001g0019a0002c0006t0001g0020 | 3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1245-73G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 6/41 | chr19 | 42336734 | ||||||
chr19:42337405
|
T | C | 22 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(19): Show | 22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.1513+199T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42337405 | ||||||
chr19:42337501
|
C | G | 7 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1513+295C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42337501 | ||||||
chr19:42337506
|
C | CT | 7 | a0001c0001t0001g0016a0001c0001t0018g0094a0002c0002t0003g0027others(4): Show | 7 | HG01175.hp2 HG02280.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.1513+319dupT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42337506 | |||||
chr19:42337631
|
T | C | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1513+425T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42337631 | ||||||
chr19:42337660
|
C | T | 1 | a0002c0015t0016g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1513+454C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42337660 | ||||||
chr19:42337802
|
G | A | 1 | a0001c0009t0001g0132 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1513+596G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42337802 | ||||||
chr19:42337811
|
T | C | 1 | a0002c0015t0016g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1513+605T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42337811 | ||||||
chr19:42338256
|
T | G | 2 | a0001c0003t0001g0112a0001c0003t0001g0113 | 2 | HG02280.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1513+1050T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338256 | ||||||
chr19:42338328
|
C | T | 1 | a0002c0002t0003g0029 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1513+1122C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338328 | ||||||
chr19:42338450
|
A | C | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1513+1244A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338450 | ||||||
chr19:42338642
|
T | G | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1513+1436T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338642 | ||||||
chr19:42338825
|
A | AT | 12 | a0001c0001t0001g0062a0001c0001t0001g0093a0001c0001t0001g0131others(9): Show | 12 | HG00597.hp1 HG01175.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.1513+1646dupT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42338825 | |||||
chr19:42338825
|
A | T | 2 | a0005c0016t0022g0100a0008c0014t0012g0101 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1513+1619A>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338825 | ||||||
chr19:42338825
|
AT | A | 29 | a0001c0001t0001g0044a0001c0001t0001g0076a0001c0001t0002g0013others(26): Show | 29 | HG00597.hp2 HG01069.hp1 HG01071.hp2 others(26): Show |
intron_variant | MODIFIER | c.1513+1646delT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42338825 | |||||
chr19:42338825
|
ATT | A | 5 | a0001c0001t0001g0016a0002c0002t0003g0032a0002c0006t0001g0018others(2): Show | 5 | HG00639.hp2 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.1513+1645_1513+164 others(6): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42338825 | |||||
chr19:42338825
|
ATTTTTTT others(8): Show |
A | 3 | a0001c0007t0001g0047a0001c0007t0001g0067a0001c0007t0001g0068 | 3 | HG02976.hp1 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1513+1632_1513+164 others(19): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42338825 | |||||
chr19:42338858
|
G | A | 1 | a0020c0034t0001g0104 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.1513+1652G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338858 | ||||||
chr19:42338967
|
T | TA | 165 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(162): Show | 171 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(168): Show |
intron_variant | MODIFIER | c.1513+1761_1513+176 others(5): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42338967 | ||||||
chr19:42339013
|
T | C | 25 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(22): Show | 25 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1513+1807T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42339013 | ||||||
chr19:42339724
|
C | T | 1 | a0001c0003t0001g0119 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1513+2518C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42339724 | ||||||
chr19:42340139
|
T | C | 1 | a0001c0001t0005g0098 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1513+2933T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42340139 | ||||||
chr19:42340375
|
G | A | 7 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.1514-3102G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42340375 | ||||||
chr19:42340576
|
T | G | 1 | a0001c0001t0002g0135 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1514-2901T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42340576 | ||||||
chr19:42340723
|
G | A | 25 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(22): Show | 25 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.1514-2754G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42340723 | ||||||
chr19:42340852
|
G | C | 2 | a0001c0001t0001g0105a0001c0001t0019g0110 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1514-2625G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42340852 | ||||||
chr19:42340962
|
C | G | 1 | a0001c0005t0003g0125 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.1514-2515C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42340962 | ||||||
chr19:42341242
|
T | C | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.1514-2235T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341242 | ||||||
chr19:42341259
|
G | C | 1 | a0001c0001t0002g0048 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1514-2218G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341259 | ||||||
chr19:42341429
|
C | CA | 24 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0049others(21): Show | 24 | HG00621.hp2 HG01175.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.1514-2027dupA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42341429 | |||||
chr19:42341429
|
CA | C | 34 | a0001c0001t0001g0156a0001c0003t0001g0118a0001c0005t0004g0128others(31): Show | 34 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.1514-2027delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42341429 | |||||
chr19:42341450
|
A | C | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1514-2027A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341450 | ||||||
chr19:42341727
|
G | C | 2 | a0002c0015t0016g0123a0008c0014t0012g0101 | 2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1514-1750G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341727 | ||||||
chr19:42341832
|
C | T | 2 | a0002c0015t0016g0123a0008c0014t0012g0101 | 2 | HG02280.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.1514-1645C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341832 | ||||||
chr19:42341835
|
TA | T | 5 | a0001c0003t0001g0112a0001c0003t0001g0113a0001c0003t0001g0117others(2): Show | 5 | HG01884.hp1 HG02145.hp2 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1514-1639delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42341835 | |||||
chr19:42341899
|
C | T | 3 | a0002c0006t0001g0018a0002c0006t0001g0019a0002c0006t0001g0020 | 3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.1514-1578C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341899 | ||||||
chr19:42341912
|
C | T | 1 | a0001c0001t0013g0060 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1514-1565C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341912 | ||||||
chr19:42341922
|
C | T | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1514-1555C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42341922 | ||||||
chr19:42342434
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1514-1043C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42342434 | ||||||
chr19:42342567
|
A | G | 9 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(6): Show | 9 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1514-910A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42342567 | ||||||
chr19:42342599
|
G | A | 2 | a0001c0001t0001g0082a0001c0001t0001g0083 | 2 | HG03927.hp1 HG04228.hp1 |
intron_variant | MODIFIER | c.1514-878G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42342599 | ||||||
chr19:42342599
|
G | T | 34 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(31): Show | 34 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.1514-878G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42342599 | ||||||
chr19:42342636
|
C | CA | 9 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(6): Show | 9 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1514-827dupA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | INFO_REALIGN_3_PRIME | chr19 | 42342636 | |||||
chr19:42343082
|
G | A | 1 | a0001c0001t0011g0097 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1514-395G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42343082 | ||||||
chr19:42343241
|
T | C | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1514-236T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42343241 | ||||||
chr19:42343302
|
C | T | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1514-175C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 8/41 | chr19 | 42343302 | ||||||
chr19:42343714
|
G | T | 1 | a0001c0001t0001g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1668+83G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 9/41 | chr19 | 42343714 | ||||||
chr19:42343841
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0031t0001g0091 | 3 | HG02145.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1669-113C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 9/41 | chr19 | 42343841 | ||||||
chr19:42344191
|
G | C | 1 | a0001c0001t0011g0097 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1788+118G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 10/41 | chr19 | 42344191 | ||||||
chr19:42344292
|
G | A | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.1789-149G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 10/41 | chr19 | 42344292 | ||||||
chr19:42344598
|
A | G | 7 | a0002c0002t0003g0012a0002c0002t0003g0029a0002c0002t0003g0030others(4): Show | 7 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(4): Show |
intron_variant | MODIFIER | c.1933+13A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 11/41 | chr19 | 42344598 | ||||||
chr19:42344612
|
A | G | 150 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(147): Show | 156 | HG00140.hp1 HG00140.hp2 HG00597.hp1 others(153): Show |
intron_variant | MODIFIER | c.1933+27A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 11/41 | chr19 | 42344612 | ||||||
chr19:42344663
|
T | C | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
splice_region_variant&intron_variant | LOW | c.1934-7T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 11/41 | chr19 | 42344663 | ||||||
chr19:42345291
|
G | T | 3 | a0002c0004t0009g0021a0002c0004t0009g0022a0002c0004t0023g0066 | 3 | HG02109.hp2 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2097+458G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42345291 | ||||||
chr19:42345969
|
T | C | 54 | a0001c0003t0001g0001a0001c0003t0001g0017a0001c0003t0001g0112others(51): Show | 57 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2097+1136T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42345969 | ||||||
chr19:42346101
|
T | C | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.2097+1268T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42346101 | ||||||
chr19:42346398
|
C | T | 1 | a0009c0023t0001g0124 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2097+1565C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42346398 | ||||||
chr19:42346402
|
C | T | 1 | a0006c0018t0003g0040 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2097+1569C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42346402 | ||||||
chr19:42346611
|
A | C | 7 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2098-1661A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42346611 | ||||||
chr19:42346800
|
C | T | 2 | a0001c0001t0001g0109a0001c0001t0002g0059 | 2 | HG01934.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.2098-1472C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42346800 | ||||||
chr19:42346984
|
C | CA | 6 | a0001c0001t0001g0090a0001c0001t0001g0143a0001c0001t0002g0072others(3): Show | 6 | HG01516.hp2 HG01978.hp1 HG02132.hp2 others(3): Show |
intron_variant | MODIFIER | c.2098-1267dupA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | INFO_REALIGN_3_PRIME | chr19 | 42346984 | |||||
chr19:42346984
|
CA | C | 34 | a0001c0001t0001g0155a0001c0001t0002g0013a0001c0001t0006g0149others(31): Show | 34 | HG00597.hp2 HG00609.hp2 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.2098-1267delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | INFO_REALIGN_3_PRIME | chr19 | 42346984 | |||||
chr19:42346984
|
CAAAAAAA others(4): Show |
C | 1 | a0001c0001t0001g0058 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.2098-1277_2098-126 others(15): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | INFO_REALIGN_3_PRIME | chr19 | 42346984 | |||||
chr19:42346999
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2098-1273A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42346999 | ||||||
chr19:42347059
|
C | A | 9 | a0001c0001t0001g0004a0001c0001t0001g0051a0001c0001t0001g0143others(6): Show | 10 | HG00597.hp1 HG00609.hp2 HG00621.hp2 others(7): Show |
intron_variant | MODIFIER | c.2098-1213C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347059 | ||||||
chr19:42347071
|
C | A | 1 | a0016c0029t0001g0133 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2098-1201C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347071 | ||||||
chr19:42347072
|
T | C | 1 | a0016c0029t0001g0133 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2098-1200T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347072 | ||||||
chr19:42347074
|
A | T | 1 | a0016c0029t0001g0133 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2098-1198A>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347074 | ||||||
chr19:42347081
|
C | T | 1 | a0016c0029t0001g0133 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.2098-1191C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347081 | ||||||
chr19:42347218
|
T | G | 1 | a0019c0021t0014g0052 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.2098-1054T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347218 | ||||||
chr19:42347585
|
C | T | 1 | a0001c0035t0001g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2098-687C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347585 | ||||||
chr19:42347760
|
C | G | 54 | a0001c0003t0001g0001a0001c0003t0001g0017a0001c0003t0001g0112others(51): Show | 57 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(54): Show |
intron_variant | MODIFIER | c.2098-512C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347760 | ||||||
chr19:42347908
|
A | G | 3 | a0002c0004t0009g0021a0002c0004t0009g0022a0002c0004t0023g0066 | 3 | HG02109.hp2 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.2098-364A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42347908 | ||||||
chr19:42348011
|
G | A | 7 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.2098-261G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42348011 | ||||||
chr19:42348126
|
C | G | 1 | a0001c0001t0001g0046 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2098-146C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42348126 | ||||||
chr19:42348186
|
G | A | 1 | a0002c0015t0016g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2098-86G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 12/41 | chr19 | 42348186 | ||||||
chr19:42348691
|
C | T | 1 | a0002c0015t0016g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2298+219C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 13/41 | chr19 | 42348691 | ||||||
chr19:42349300
|
A | G | 1 | a0001c0001t0002g0136 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2299-199A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 13/41 | chr19 | 42349300 | ||||||
chr19:42349302
|
GA | G | 21 | a0001c0003t0001g0001a0001c0003t0001g0017a0001c0003t0001g0112others(18): Show | 24 | HG01243.hp1 HG01884.hp1 HG01891.hp2 others(21): Show |
intron_variant | MODIFIER | c.2299-179delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 13/41 | INFO_REALIGN_3_PRIME | chr19 | 42349302 | |||||
chr19:42349849
|
T | G | 26 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(23): Show | 26 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(23): Show |
intron_variant | MODIFIER | c.2499+150T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 14/41 | chr19 | 42349849 | ||||||
chr19:42349930
|
C | G | 5 | a0001c0005t0004g0126a0001c0005t0004g0128a0001c0005t0004g0129others(2): Show | 5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2500-218C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 14/41 | chr19 | 42349930 | ||||||
chr19:42350453
|
G | A | 5 | a0001c0005t0004g0126a0001c0005t0004g0128a0001c0005t0004g0129others(2): Show | 5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.2736+69G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42350453 | ||||||
chr19:42350464
|
G | T | 1 | a0002c0015t0016g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2736+80G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42350464 | ||||||
chr19:42350608
|
T | C | 1 | a0001c0003t0001g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2736+224T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42350608 | ||||||
chr19:42350839
|
A | C | 19 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0055others(16): Show | 21 | HG00738.hp2 HG00741.hp2 HG01070.hp2 others(18): Show |
intron_variant | MODIFIER | c.2737-377A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42350839 | ||||||
chr19:42350943
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2737-273C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42350943 | ||||||
chr19:42350988
|
G | A | 2 | a0005c0016t0022g0100a0008c0014t0012g0101 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.2737-228G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42350988 | ||||||
chr19:42351015
|
T | C | 35 | a0001c0001t0001g0078a0002c0002t0001g0034a0002c0002t0003g0012others(32): Show | 35 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(32): Show |
intron_variant | MODIFIER | c.2737-201T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42351015 | ||||||
chr19:42351038
|
C | T | 2 | a0001c0001t0001g0073a0001c0001t0001g0074 | 2 | HG01258.hp1 HG03491.hp1 |
intron_variant | MODIFIER | c.2737-178C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 15/41 | chr19 | 42351038 | ||||||
chr19:42352146
|
G | A | 1 | a0014c0025t0001g0111 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.3102-62G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 18/41 | chr19 | 42352146 | ||||||
chr19:42352925
|
C | T | 7 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
splice_region_variant&intron_variant | LOW | c.3351-3C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 19/41 | chr19 | 42352925 | ||||||
chr19:42353245
|
C | T | 22 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(19): Show | 22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.3550+118C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 20/41 | chr19 | 42353245 | ||||||
chr19:42353293
|
A | G | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.3550+166A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 20/41 | chr19 | 42353293 | ||||||
chr19:42353360
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0045a0001c0001t0001g0046 | 3 | HG02055.hp1 HG02257.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3551-105C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 20/41 | chr19 | 42353360 | ||||||
chr19:42354118
|
GT | G | 36 | a0001c0001t0019g0110a0002c0002t0001g0034a0002c0002t0003g0012others(33): Show | 36 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(33): Show |
intron_variant | MODIFIER | c.4011+107delT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 22/41 | INFO_REALIGN_3_PRIME | chr19 | 42354118 | |||||
chr19:42354171
|
C | T | 1 | a0001c0001t0001g0148 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.4011+147C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 22/41 | chr19 | 42354171 | ||||||
chr19:42354239
|
G | A | 1 | a0001c0001t0002g0053 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4011+215G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 22/41 | chr19 | 42354239 | ||||||
chr19:42354516
|
C | G | 5 | a0001c0005t0004g0126a0001c0005t0004g0128a0001c0005t0004g0129others(2): Show | 5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.4012-72C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 22/41 | chr19 | 42354516 | ||||||
chr19:42355084
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0019g0110 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.4144+364G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 23/41 | chr19 | 42355084 | ||||||
chr19:42355255
|
CAT | C | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.4145-489_4145-488d others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 23/41 | INFO_REALIGN_3_PRIME | chr19 | 42355255 | |||||
chr19:42355375
|
G | A | 7 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.4145-383G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 23/41 | chr19 | 42355375 | ||||||
chr19:42356497
|
G | A | 1 | a0001c0001t0002g0013 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.4622+44G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 26/41 | chr19 | 42356497 | ||||||
chr19:42356712
|
G | A | 1 | a0002c0002t0003g0042 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4623-62G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 26/41 | chr19 | 42356712 | ||||||
chr19:42357068
|
C | T | 1 | a0001c0001t0001g0061 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.4830+87C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 27/41 | chr19 | 42357068 | ||||||
chr19:42357141
|
G | A | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.4830+160G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 27/41 | chr19 | 42357141 | ||||||
chr19:42357323
|
G | A | 4 | a0001c0001t0001g0069a0001c0001t0001g0151a0001c0001t0001g0155others(1): Show | 4 | HG00639.hp1 HG01074.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.4831-81G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 27/41 | chr19 | 42357323 | ||||||
chr19:42357599
|
C | T | 1 | a0002c0015t0016g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5011+15C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 28/41 | chr19 | 42357599 | ||||||
chr19:42357700
|
A | G | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.5011+116A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 28/41 | chr19 | 42357700 | ||||||
chr19:42357766
|
C | T | 3 | a0002c0006t0001g0018a0002c0006t0001g0019a0002c0006t0001g0020 | 3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5011+182C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 28/41 | chr19 | 42357766 | ||||||
chr19:42357807
|
C | T | 1 | a0001c0001t0001g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.5011+223C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 28/41 | chr19 | 42357807 | ||||||
chr19:42358749
|
G | A | 7 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.5176-38G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 29/41 | chr19 | 42358749 | ||||||
chr19:42359084
|
C | T | 1 | a0001c0035t0001g0099 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5344-14C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 30/41 | chr19 | 42359084 | ||||||
chr19:42359254
|
T | C | 1 | a0008c0014t0012g0101 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.5488+12T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42359254 | ||||||
chr19:42359380
|
T | C | 1 | a0002c0002t0020g0103 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.5488+138T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42359380 | ||||||
chr19:42359405
|
CT | C | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.5488+173delT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42359405 | |||||
chr19:42359684
|
T | C | 3 | a0002c0006t0001g0018a0002c0006t0001g0019a0002c0006t0001g0020 | 3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.5488+442T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42359684 | ||||||
chr19:42359795
|
C | G | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.5488+553C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42359795 | ||||||
chr19:42359853
|
A | AT | 31 | a0001c0001t0001g0062a0001c0001t0001g0158a0001c0001t0001g0162others(28): Show | 31 | HG00597.hp2 HG01069.hp1 HG01071.hp2 others(28): Show |
intron_variant | MODIFIER | c.5488+633dupT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42359853 | |||||
chr19:42359853
|
A | ATT | 7 | a0002c0004t0008g0026a0002c0004t0009g0021a0002c0004t0009g0022others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.5488+632_5488+633d others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42359853 | |||||
chr19:42359853
|
AT | A | 5 | a0001c0001t0002g0072a0001c0005t0004g0128a0001c0005t0004g0129others(2): Show | 5 | HG01516.hp2 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.5488+633delT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42359853 | |||||
chr19:42359900
|
G | T | 7 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.5488+658G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42359900 | ||||||
chr19:42360150
|
C | CA | 16 | a0001c0001t0002g0014a0001c0001t0002g0053a0001c0003t0001g0001others(13): Show | 19 | HG01884.hp1 HG01891.hp2 HG01978.hp2 others(16): Show |
intron_variant | MODIFIER | c.5489-608dupA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42360150 | |||||
chr19:42360150
|
CAAAA | C | 25 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(22): Show | 25 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.5489-611_5489-608d others(6): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42360150 | |||||
chr19:42360345
|
G | GT | 9 | a0001c0001t0001g0108a0001c0001t0001g0131a0001c0001t0001g0158others(6): Show | 9 | HG01175.hp1 HG01175.hp2 HG01243.hp2 others(6): Show |
intron_variant | MODIFIER | c.5489-413dupT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | INFO_REALIGN_3_PRIME | chr19 | 42360345 | |||||
chr19:42360410
|
A | G | 1 | a0001c0001t0001g0088 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.5489-365A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42360410 | ||||||
chr19:42360426
|
A | G | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.5489-349A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42360426 | ||||||
chr19:42360482
|
G | C | 2 | a0005c0016t0022g0100a0008c0014t0012g0101 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5489-293G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 31/41 | chr19 | 42360482 | ||||||
chr19:42361044
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.5720+38G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 32/41 | chr19 | 42361044 | ||||||
chr19:42361131
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0055a0001c0001t0001g0073others(14): Show | 19 | HG00140.hp2 HG00738.hp2 HG00741.hp2 others(16): Show |
intron_variant | MODIFIER | c.5720+125G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 32/41 | chr19 | 42361131 | ||||||
chr19:42361324
|
C | G | 1 | a0001c0001t0001g0148 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.5720+318C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 32/41 | chr19 | 42361324 | ||||||
chr19:42361357
|
A | G | 1 | a0002c0015t0016g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.5720+351A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 32/41 | chr19 | 42361357 | ||||||
chr19:42361901
|
G | A | 2 | a0005c0016t0022g0100a0008c0014t0012g0101 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.5721-189G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 32/41 | chr19 | 42361901 | ||||||
chr19:42362718
|
C | G | 1 | a0002c0002t0007g0038 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.6058+121C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 34/41 | chr19 | 42362718 | ||||||
chr19:42362867
|
C | T | 13 | a0001c0003t0001g0001a0001c0003t0001g0017a0001c0003t0001g0112others(10): Show | 16 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(13): Show |
intron_variant | MODIFIER | c.6059-181C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 34/41 | chr19 | 42362867 | ||||||
chr19:42362869
|
G | A | 1 | a0002c0002t0003g0033 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.6059-179G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 34/41 | chr19 | 42362869 | ||||||
chr19:42363394
|
C | T | 2 | a0005c0016t0022g0100a0008c0014t0012g0101 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6273+132C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363394 | ||||||
chr19:42363395
|
G | T | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.6273+133G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363395 | ||||||
chr19:42363601
|
G | A | 1 | a0001c0001t0001g0156 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.6273+339G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363601 | ||||||
chr19:42363736
|
C | T | 2 | a0005c0016t0022g0100a0008c0014t0012g0101 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.6273+474C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363736 | ||||||
chr19:42363845
|
C | T | 1 | a0001c0022t0001g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.6273+583C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363845 | ||||||
chr19:42363873
|
C | T | 5 | a0001c0005t0004g0126a0001c0005t0004g0128a0001c0005t0004g0129others(2): Show | 5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.6273+611C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363873 | ||||||
chr19:42363917
|
T | C | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.6273+655T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363917 | ||||||
chr19:42363929
|
T | C | 25 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(22): Show | 25 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.6273+667T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42363929 | ||||||
chr19:42364028
|
C | A | 1 | a0001c0001t0002g0075 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.6273+766C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42364028 | ||||||
chr19:42364065
|
G | A | 3 | a0002c0006t0001g0018a0002c0006t0001g0019a0002c0006t0001g0020 | 3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6273+803G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42364065 | ||||||
chr19:42364126
|
T | C | 1 | a0015c0020t0001g0120 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.6273+864T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42364126 | ||||||
chr19:42364446
|
A | G | 1 | a0001c0001t0002g0092 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.6273+1184A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42364446 | ||||||
chr19:42364598
|
C | T | 5 | a0001c0005t0004g0126a0001c0005t0004g0128a0001c0005t0004g0129others(2): Show | 5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.6273+1336C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42364598 | ||||||
chr19:42365272
|
T | C | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.6273+2010T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42365272 | ||||||
chr19:42365404
|
T | G | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.6273+2142T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42365404 | ||||||
chr19:42365772
|
T | TA | 12 | a0001c0001t0001g0007a0001c0001t0001g0058a0001c0001t0001g0090others(9): Show | 12 | HG00741.hp1 HG01123.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.6273+2536dupA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr19 | 42365772 | |||||
chr19:42365772
|
TA | T | 24 | a0001c0001t0001g0069a0001c0001t0001g0148a0001c0001t0002g0013others(21): Show | 27 | HG01074.hp2 HG01884.hp1 HG01884.hp2 others(24): Show |
intron_variant | MODIFIER | c.6273+2536delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr19 | 42365772 | |||||
chr19:42365772
|
TAAAA | T | 31 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(28): Show | 31 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(28): Show |
intron_variant | MODIFIER | c.6273+2533_6273+253 others(8): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr19 | 42365772 | |||||
chr19:42366232
|
G | A | 1 | a0002c0002t0003g0039 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.6274-2223G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42366232 | ||||||
chr19:42366721
|
A | C | 25 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(22): Show | 25 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.6274-1734A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42366721 | ||||||
chr19:42367144
|
G | A | 123 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0016others(120): Show | 128 | HG00140.hp1 HG00140.hp2 HG00597.hp2 others(125): Show |
intron_variant | MODIFIER | c.6274-1311G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367144 | ||||||
chr19:42367290
|
C | CT | 5 | a0001c0001t0001g0086a0001c0001t0001g0159a0001c0001t0001g0161others(2): Show | 5 | HG01261.hp2 HG02683.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.6274-1149dupT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr19 | 42367290 | |||||
chr19:42367290
|
CT | C | 5 | a0001c0001t0001g0073a0002c0002t0003g0012a0002c0006t0001g0018others(2): Show | 5 | HG01069.hp1 HG02630.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.6274-1149delT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr19 | 42367290 | |||||
chr19:42367294
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.6274-1161T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367294 | ||||||
chr19:42367375
|
A | G | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.6274-1080A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367375 | ||||||
chr19:42367416
|
G | A | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6274-1039G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367416 | ||||||
chr19:42367445
|
C | T | 1 | a0001c0001t0001g0008 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.6274-1010C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367445 | ||||||
chr19:42367540
|
G | A | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6274-915G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367540 | ||||||
chr19:42367560
|
T | C | 1 | a0002c0015t0016g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.6274-895T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367560 | ||||||
chr19:42367596
|
C | T | 1 | a0009c0023t0001g0124 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6274-859C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367596 | ||||||
chr19:42367854
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.6274-601G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42367854 | ||||||
chr19:42368115
|
A | G | 3 | a0002c0002t0003g0163a0002c0002t0003g0164a0002c0002t0003g0165 | 3 | NA18981.hp1 NA19066.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.6274-340A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42368115 | ||||||
chr19:42368198
|
G | A | 1 | a0001c0001t0002g0014 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.6274-257G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42368198 | ||||||
chr19:42368407
|
TC | T | 25 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(22): Show | 25 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(22): Show |
intron_variant | MODIFIER | c.6274-44delC | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | INFO_REALIGN_3_PRIME | chr19 | 42368407 | |||||
chr19:42368446
|
C | G | 1 | a0001c0001t0006g0137 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.6274-9C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 35/41 | chr19 | 42368446 | ||||||
chr19:42368673
|
T | G | 1 | a0009c0023t0001g0124 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.6481+11T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 36/41 | chr19 | 42368673 | ||||||
chr19:42368827
|
A | G | 1 | a0002c0008t0003g0041 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.6482-16A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 36/41 | chr19 | 42368827 | ||||||
chr19:42369011
|
G | A | 2 | a0001c0001t0001g0105a0001c0001t0019g0110 | 2 | HG02257.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.6641+9G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 37/41 | chr19 | 42369011 | ||||||
chr19:42369218
|
G | C | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6641+216G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 37/41 | chr19 | 42369218 | ||||||
chr19:42369245
|
C | T | 3 | a0002c0006t0001g0018a0002c0006t0001g0019a0002c0006t0001g0020 | 3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.6641+243C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 37/41 | chr19 | 42369245 | ||||||
chr19:42369487
|
G | A | 1 | a0001c0001t0002g0015 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.6642-44G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 37/41 | chr19 | 42369487 | ||||||
chr19:42369930
|
G | C | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6834+207G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/41 | chr19 | 42369930 | ||||||
chr19:42370069
|
C | G | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6835-120C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/41 | chr19 | 42370069 | ||||||
chr19:42370115
|
C | G | 2 | a0001c0011t0001g0064a0001c0011t0001g0065 | 2 | NA18981.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.6835-74C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/41 | chr19 | 42370115 | ||||||
chr19:42370130
|
C | T | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.6835-59C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/41 | chr19 | 42370130 | ||||||
chr19:42370131
|
G | A | 3 | a0001c0007t0001g0047a0001c0007t0001g0067a0001c0007t0001g0068 | 3 | HG02976.hp1 HG03471.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.6835-58G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/41 | chr19 | 42370131 | ||||||
chr19:42370150
|
C | T | 2 | a0001c0001t0005g0081a0001c0001t0005g0087 | 2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.6835-39C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 38/41 | chr19 | 42370150 | ||||||
chr19:42370587
|
A | G | 1 | a0001c0001t0001g0011 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.7006-114A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 39/41 | chr19 | 42370587 | ||||||
chr19:42370588
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.7006-113G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 39/41 | chr19 | 42370588 | ||||||
chr19:42370664
|
A | T | 1 | a0001c0001t0001g0011 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.7006-37A>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 39/41 | chr19 | 42370664 | ||||||
chr19:42370666
|
G | C | 1 | a0001c0001t0001g0011 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.7006-35G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 39/41 | chr19 | 42370666 | ||||||
chr19:42370842
|
CCGGGGG | C | 4 | a0001c0001t0001g0011a0002c0002t0020g0103a0002c0002t0021g0102others(1): Show | 4 | HG01069.hp2 HG02074.hp2 HG03710.hp1 others(1): Show |
intron_variant | MODIFIER | c.7136+12_7136+17del others(6): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370842 | ||||||
chr19:42370842
|
CCGGGGGG | C | 3 | a0002c0002t0003g0012a0002c0002t0003g0031a0002c0002t0003g0039 | 3 | HG01069.hp1 HG02135.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.7136+12_7136+18del others(7): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370842 | ||||||
chr19:42370842
|
CCGGGGGG others(1): Show |
C | 5 | a0002c0002t0003g0032a0002c0002t0003g0164a0002c0002t0003g0165others(2): Show | 5 | HG00639.hp2 HG02155.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.7136+12_7136+19del others(8): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370842 | ||||||
chr19:42370842
|
CCGGGGGG others(2): Show |
C | 7 | a0002c0002t0001g0034a0002c0002t0003g0027a0002c0002t0003g0029others(4): Show | 7 | HG00597.hp2 HG01071.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.7136+12_7136+20del others(9): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370842 | ||||||
chr19:42370842
|
CCGGGGGG others(3): Show |
C | 3 | a0002c0002t0003g0028a0002c0002t0003g0033a0002c0002t0003g0042 | 3 | HG02165.hp2 HG02683.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.7136+12_7136+21del others(10): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370842 | ||||||
chr19:42370843
|
CG | C | 19 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0045others(16): Show | 20 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(17): Show |
intron_variant | MODIFIER | c.7136+41delG | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | |||||
chr19:42370843
|
CGG | C | 15 | a0001c0001t0001g0073a0001c0001t0001g0088a0001c0001t0001g0155others(12): Show | 15 | HG00140.hp2 HG01074.hp1 HG01192.hp1 others(12): Show |
intron_variant | MODIFIER | c.7136+40_7136+41del others(2): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | |||||
chr19:42370843
|
CGGG | C | 15 | a0001c0001t0001g0055a0001c0001t0001g0062a0001c0001t0001g0107others(12): Show | 18 | HG00597.hp1 HG00741.hp1 HG01516.hp1 others(15): Show |
intron_variant | MODIFIER | c.7136+39_7136+41del others(3): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | |||||
chr19:42370843
|
CGGGG | C | 19 | a0001c0001t0001g0016a0001c0001t0001g0061a0001c0001t0001g0074others(16): Show | 19 | HG00621.hp1 HG00621.hp2 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.7136+38_7136+41del others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | |||||
chr19:42370843
|
CGGGGGGG others(6): Show |
C | 1 | a0001c0001t0001g0139 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.7136+29_7136+41del others(13): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | |||||
chr19:42370843
|
CGGGGGGG others(10): Show |
C | 1 | a0001c0001t0001g0145 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.7136+25_7136+41del others(17): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | |||||
chr19:42370843
|
CGGGGGGG others(12): Show |
C | 1 | a0001c0001t0001g0156 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.7136+23_7136+41del others(19): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | |||||
chr19:42370843
|
CGGGGGGG others(13): Show |
C | 1 | a0001c0001t0001g0144 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.7136+22_7136+41del others(20): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42370843 | |||||
chr19:42370847
|
G | T | 1 | a0002c0002t0003g0163 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.7136+16G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370847 | ||||||
chr19:42370849
|
G | A | 1 | a0001c0001t0001g0011 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.7136+18G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370849 | ||||||
chr19:42370849
|
G | T | 3 | a0002c0002t0020g0103a0002c0002t0021g0102a0002c0008t0003g0041 | 3 | HG02074.hp2 HG03710.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.7136+18G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370849 | ||||||
chr19:42370850
|
G | T | 3 | a0002c0002t0003g0012a0002c0002t0003g0031a0002c0002t0003g0039 | 3 | HG01069.hp1 HG02135.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.7136+19G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370850 | ||||||
chr19:42370851
|
G | C | 1 | a0012c0028t0002g0089 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.7136+20G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370851 | ||||||
chr19:42370851
|
G | T | 5 | a0002c0002t0003g0032a0002c0002t0003g0164a0002c0002t0003g0165others(2): Show | 5 | HG00639.hp2 HG02155.hp1 HG04228.hp2 others(2): Show |
intron_variant | MODIFIER | c.7136+20G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370851 | ||||||
chr19:42370852
|
G | T | 7 | a0002c0002t0001g0034a0002c0002t0003g0027a0002c0002t0003g0029others(4): Show | 7 | HG00597.hp2 HG01071.hp2 HG01175.hp2 others(4): Show |
intron_variant | MODIFIER | c.7136+21G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370852 | ||||||
chr19:42370853
|
G | T | 4 | a0001c0001t0005g0081a0002c0002t0003g0028a0002c0002t0003g0033others(1): Show | 4 | HG02165.hp2 HG02683.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.7136+22G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370853 | ||||||
chr19:42370854
|
G | GT | 2 | a0001c0010t0001g0080a0001c0010t0001g0085 | 2 | HG00738.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.7136+23_7136+24ins others(1): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370854 | ||||||
chr19:42370854
|
G | T | 2 | a0001c0001t0001g0108a0002c0006t0001g0020 | 2 | HG01243.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.7136+23G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370854 | ||||||
chr19:42370857
|
G | T | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.7136+26G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370857 | ||||||
chr19:42370860
|
G | C | 1 | a0001c0022t0001g0063 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.7136+29G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370860 | ||||||
chr19:42370863
|
G | GT | 2 | a0001c0001t0001g0008a0001c0001t0002g0053 | 2 | HG01978.hp2 HG02165.hp1 |
intron_variant | MODIFIER | c.7136+32_7136+33ins others(1): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370863 | ||||||
chr19:42370863
|
G | T | 6 | a0001c0001t0001g0010a0001c0001t0001g0082a0001c0001t0001g0096others(3): Show | 6 | HG01261.hp1 HG01934.hp1 HG01934.hp2 others(3): Show |
intron_variant | MODIFIER | c.7136+32G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370863 | ||||||
chr19:42370864
|
G | GT | 4 | a0001c0001t0001g0086a0001c0003t0001g0117a0001c0005t0004g0128others(1): Show | 4 | HG01884.hp1 HG02897.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.7136+33_7136+34ins others(1): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370864 | ||||||
chr19:42370864
|
G | T | 74 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0045others(71): Show | 79 | HG00140.hp1 HG00140.hp2 HG00738.hp1 others(76): Show |
intron_variant | MODIFIER | c.7136+33G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370864 | ||||||
chr19:42370865
|
G | T | 2 | a0001c0001t0001g0055a0019c0021t0014g0052 | 2 | HG02004.hp1 HG02300.hp2 |
intron_variant | MODIFIER | c.7136+34G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370865 | ||||||
chr19:42370866
|
G | T | 1 | a0001c0001t0001g0159 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.7136+35G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42370866 | ||||||
chr19:42371064
|
G | GCA | 3 | a0002c0006t0001g0018a0002c0006t0001g0019a0002c0006t0001g0020 | 3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7136+234_7136+235i others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42371064 | |||||
chr19:42371064
|
G | GCCC | 22 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(19): Show | 22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.7136+235_7136+237d others(5): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | INFO_REALIGN_3_PRIME | chr19 | 42371064 | |||||
chr19:42371068
|
C | T | 7 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(4): Show | 7 | HG01243.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.7136+237C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42371068 | ||||||
chr19:42371070
|
T | A | 1 | a0002c0002t0003g0036 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.7136+239T>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 40/41 | chr19 | 42371070 | ||||||
chr19:42371809
|
A | T | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.7269+327A>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42371809 | ||||||
chr19:42372039
|
A | AAAC | 95 | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0008others(92): Show | 98 | HG00140.hp2 HG00597.hp1 HG00609.hp1 others(95): Show |
intron_variant | MODIFIER | c.7269+590_7269+592d others(5): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372039 | |||||
chr19:42372039
|
A | AAACAAC | 5 | a0001c0001t0001g0086a0001c0001t0001g0161a0001c0001t0005g0087others(2): Show | 5 | HG01884.hp2 HG02647.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.7269+587_7269+592d others(8): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372039 | |||||
chr19:42372039
|
A | AAACAACA others(5): Show |
3 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0031t0001g0091 | 3 | HG02145.hp1 HG03098.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.7269+581_7269+592d others(14): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372039 | |||||
chr19:42372039
|
AAAC | A | 5 | a0001c0005t0004g0126a0001c0005t0004g0128a0001c0005t0004g0129others(2): Show | 5 | HG01123.hp1 HG01891.hp1 HG02109.hp1 others(2): Show |
intron_variant | MODIFIER | c.7269+590_7269+592d others(5): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372039 | |||||
chr19:42372039
|
AAACAAC | A | 22 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(19): Show | 22 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(19): Show |
intron_variant | MODIFIER | c.7269+587_7269+592d others(8): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372039 | |||||
chr19:42372067
|
AAC | A | 3 | a0002c0006t0001g0018a0002c0006t0001g0019a0002c0006t0001g0020 | 3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7269+587_7269+588d others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372067 | |||||
chr19:42372072
|
C | A | 1 | a0002c0015t0016g0123 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.7269+590C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372072 | ||||||
chr19:42372074
|
A | AAAAC | 4 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0010g0023others(1): Show | 4 | HG01243.hp1 HG02723.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.7269+593_7269+594i others(6): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372074 | |||||
chr19:42372074
|
A | ACAAAAAC | 3 | a0002c0004t0009g0021a0002c0004t0009g0022a0002c0004t0023g0066 | 3 | HG02109.hp2 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.7269+592_7269+593i others(9): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372074 | ||||||
chr19:42372074
|
A | ACAAAC | 5 | a0001c0001t0001g0010a0001c0001t0001g0107a0001c0001t0001g0108others(2): Show | 5 | HG00140.hp1 HG01243.hp2 HG01934.hp1 others(2): Show |
intron_variant | MODIFIER | c.7269+592_7269+593i others(7): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372074 | ||||||
chr19:42372074
|
A | C | 3 | a0002c0006t0001g0018a0002c0006t0001g0019a0002c0006t0001g0020 | 3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7269+592A>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372074 | ||||||
chr19:42372074
|
AAC | A | 2 | a0005c0016t0022g0100a0008c0014t0012g0101 | 2 | HG02818.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.7269+616_7269+617d others(4): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42372074 | |||||
chr19:42372142
|
T | C | 33 | a0002c0002t0001g0034a0002c0002t0003g0012a0002c0002t0003g0027others(30): Show | 33 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(30): Show |
intron_variant | MODIFIER | c.7269+660T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372142 | ||||||
chr19:42372470
|
C | A | 3 | a0002c0006t0001g0018a0002c0006t0001g0019a0002c0006t0001g0020 | 3 | HG02630.hp2 HG02886.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.7269+988C>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372470 | ||||||
chr19:42372490
|
A | G | 1 | a0001c0001t0001g0159 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.7269+1008A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372490 | ||||||
chr19:42372585
|
G | A | 1 | a0001c0001t0001g0096 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.7269+1103G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372585 | ||||||
chr19:42372836
|
C | T | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.7269+1354C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42372836 | ||||||
chr19:42373153
|
C | T | 1 | a0001c0003t0001g0112 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.7269+1671C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373153 | ||||||
chr19:42373167
|
A | G | 1 | a0001c0010t0001g0080 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.7269+1685A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373167 | ||||||
chr19:42373179
|
G | A | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.7269+1697G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373179 | ||||||
chr19:42373240
|
G | A | 37 | a0001c0003t0001g0001a0001c0003t0001g0112a0001c0003t0001g0113others(34): Show | 40 | HG00597.hp2 HG00639.hp2 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.7269+1758G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373240 | ||||||
chr19:42373255
|
G | C | 1 | a0001c0001t0005g0087 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.7269+1773G>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373255 | ||||||
chr19:42373389
|
C | G | 1 | a0001c0001t0001g0156 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.7269+1907C>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373389 | ||||||
chr19:42373477
|
T | C | 1 | a0018c0033t0001g0006 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.7269+1995T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373477 | ||||||
chr19:42373576
|
T | TG | 8 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(5): Show | 8 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(5): Show |
intron_variant | MODIFIER | c.7270-1931_7270-193 others(5): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373576 | ||||||
chr19:42373625
|
A | G | 1 | a0012c0028t0002g0089 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.7270-1882A>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373625 | ||||||
chr19:42373706
|
G | GT | 48 | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0043others(45): Show | 48 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.7270-1776dupT | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42373706 | |||||
chr19:42373706
|
G | GTT | 10 | a0002c0002t0003g0028a0002c0002t0003g0039a0002c0002t0003g0163others(7): Show | 10 | HG01175.hp2 HG02074.hp2 HG02135.hp1 others(7): Show |
intron_variant | MODIFIER | c.7270-1777_7270-177 others(6): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42373706 | |||||
chr19:42373706
|
GTTTTTTT others(6): Show |
G | 3 | a0002c0004t0009g0021a0002c0004t0009g0022a0002c0004t0023g0066 | 3 | HG02109.hp2 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.7270-1788_7270-177 others(17): Show |
MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42373706 | |||||
chr19:42373718
|
T | G | 12 | a0001c0003t0001g0001a0001c0003t0001g0112a0001c0003t0001g0113others(9): Show | 15 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.7270-1789T>G | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373718 | ||||||
chr19:42373952
|
G | T | 3 | a0002c0004t0009g0021a0002c0004t0009g0022a0002c0004t0023g0066 | 3 | HG02109.hp2 HG02615.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.7270-1555G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42373952 | ||||||
chr19:42374385
|
C | T | 9 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(6): Show | 9 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.7270-1122C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42374385 | ||||||
chr19:42374388
|
T | C | 9 | a0002c0004t0008g0025a0002c0004t0008g0026a0002c0004t0009g0021others(6): Show | 9 | HG01243.hp1 HG02109.hp2 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.7270-1119T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42374388 | ||||||
chr19:42374470
|
C | CA | 7 | a0001c0001t0001g0131a0001c0001t0002g0014a0001c0001t0002g0053others(4): Show | 7 | HG00597.hp2 HG00621.hp1 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.7270-1015dupA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42374470 | |||||
chr19:42374470
|
CA | C | 24 | a0001c0001t0001g0045a0001c0001t0001g0046a0001c0001t0001g0058others(21): Show | 24 | HG01243.hp1 HG01261.hp1 HG01261.hp2 others(21): Show |
intron_variant | MODIFIER | c.7270-1015delA | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | INFO_REALIGN_3_PRIME | chr19 | 42374470 | |||||
chr19:42374807
|
T | C | 4 | a0002c0002t0003g0012a0002c0002t0003g0029a0002c0002t0003g0030others(1): Show | 4 | HG01069.hp1 HG01071.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.7270-700T>C | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42374807 | ||||||
chr19:42375043
|
G | A | 1 | a0005c0016t0022g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.7270-464G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42375043 | ||||||
chr19:42375201
|
G | A | 11 | a0001c0003t0001g0001a0001c0003t0001g0112a0001c0003t0001g0113others(8): Show | 14 | HG01884.hp1 HG01891.hp2 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.7270-306G>A | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42375201 | ||||||
chr19:42375219
|
C | T | 1 | a0018c0033t0001g0006 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.7270-288C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42375219 | ||||||
chr19:42375230
|
C | T | 34 | a0001c0005t0003g0125a0001c0005t0004g0126a0001c0005t0004g0128others(31): Show | 34 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(31): Show |
intron_variant | MODIFIER | c.7270-277C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42375230 | ||||||
chr19:42375314
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C | T | 19 | a0002c0002t0003g0012a0002c0002t0003g0027a0002c0002t0003g0028others(16): Show | 19 | HG00639.hp2 HG01069.hp1 HG01071.hp2 others(16): Show |
intron_variant | MODIFIER | c.7270-193C>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42375314 | ||||||
chr19:42375346
|
G | T | 3 | a0001c0001t0001g0078a0001c0036t0001g0079a0002c0002t0001g0034 | 3 | HG00597.hp2 HG02523.hp1 NA18966.hp2 |
intron_variant | MODIFIER | c.7270-161G>T | MEGF8 | ENSG00000105429.13 | transcript | ENST00000251268.11 | protein_coding | 41/41 | chr19 | 42375346 |