geneid | 374986 |
---|---|
ensemblid | ENSG00000180488.17 |
hgncid | 24741 |
symbol | MIGA1 |
name | mitoguardin 1 |
refseq_nuc | NM_001416120.1 |
refseq_prot | NP_001403049.1 |
ensembl_nuc | ENST00000370791.9 |
ensembl_prot | ENSP00000359827.4 |
mane_status | MANE Select |
chr | chr1 |
start | 77779649 |
end | 77879540 |
strand | + |
ver | v1.2 |
region | chr1:77779649-77879540 |
region5000 | chr1:77774649-77884540 |
regionname0 | MIGA1_chr1_77779649_77879540 |
regionname5000 | MIGA1_chr1_77774649_77884540 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 600 | 280 | 74 | 44 | 112 | 10 | 38 | 84 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1803 | 276 | 72 | 44 | 111 | 10 | 37 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
c0002 | 0/0 | 1803 | 2 | 2 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
c0003 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
c0004 | 0/0 | 1803 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4585 | 78 | 10 | 7 | 47 | 4 | 10 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0002 | 0/1 | 4586 | 54 | 6 | 18 | 16 | 3 | 10 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0003 | 1/0 | 4580 | 30 | 15 | 5 | 4 | 0 | 5 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0004 | 0/0 | 4580 | 25 | 0 | 0 | 24 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0005 | 0/0 | 4579 | 14 | 1 | 3 | 7 | 1 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0006 | 0/0 | 4587 | 9 | 1 | 4 | 1 | 1 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0007 | 0/0 | 4581 | 8 | 5 | 1 | 0 | 0 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0008 | 0/0 | 4579 | 8 | 0 | 1 | 7 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0009 | 0/0 | 4579 | 6 | 6 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0010 | 0/0 | 4584 | 5 | 1 | 2 | 1 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0011 | 0/0 | 4580 | 4 | 4 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0012 | 0/0 | 4579 | 4 | 4 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0013 | 0/0 | 4581 | 4 | 4 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0014 | 0/0 | 4579 | 3 | 3 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0015 | 0/0 | 4586 | 3 | 3 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0016 | 0/0 | 4580 | 3 | 0 | 0 | 3 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0017 | 0/0 | 4580 | 3 | 0 | 1 | 0 | 0 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0018 | 0/0 | 4586 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0019 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0020 | 0/0 | 4580 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0021 | 0/0 | 4590 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0022 | 0/0 | 4585 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0023 | 0/0 | 4585 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0024 | 0/0 | 4585 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0025 | 0/0 | 4584 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0026 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0027 | 0/0 | 4586 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0028 | 0/0 | 4581 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0029 | 0/0 | 4580 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0030 | 0/0 | 4579 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0031 | 0/0 | 4585 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0032 | 0/0 | 4580 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0033 | 0/0 | 4581 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0034 | 0/0 | 4581 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0035 | 0/0 | 4580 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
t0036 | 0/0 | 4580 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1803 | 276 | 72 | 44 | 111 | 10 | 37 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0002 | 0/0 | 1803 | 2 | 2 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0003 | 0/0 | 1803 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0004 | 0/0 | 1803 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6387 | 76 | 10 | 7 | 46 | 4 | 9 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0002 | 0/1 | 6388 | 54 | 6 | 18 | 16 | 3 | 10 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0003 | 1/0 | 6382 | 29 | 14 | 5 | 4 | 0 | 5 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0004 | 0/0 | 6382 | 25 | 0 | 0 | 24 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0005 | 0/0 | 6381 | 13 | 0 | 3 | 7 | 1 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0006 | 0/0 | 6389 | 9 | 1 | 4 | 1 | 1 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0007 | 0/0 | 6383 | 8 | 5 | 1 | 0 | 0 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0008 | 0/0 | 6381 | 8 | 0 | 1 | 7 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0009 | 0/0 | 6381 | 6 | 6 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0010 | 0/0 | 6386 | 5 | 1 | 2 | 1 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0011 | 0/0 | 6382 | 4 | 4 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0012 | 0/0 | 6381 | 4 | 4 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0013 | 0/0 | 6383 | 4 | 4 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0014 | 0/0 | 6381 | 3 | 3 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0015 | 0/0 | 6388 | 3 | 3 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0016 | 0/0 | 6382 | 3 | 0 | 0 | 3 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0017 | 0/0 | 6382 | 3 | 0 | 1 | 0 | 0 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0018 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0019 | 0/0 | 6381 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0020 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0021 | 0/0 | 6392 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0022 | 0/0 | 6387 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0023 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0024 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0025 | 0/0 | 6386 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0026 | 0/0 | 6381 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0027 | 0/0 | 6388 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0028 | 0/0 | 6383 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0029 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0030 | 0/0 | 6381 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0031 | 0/0 | 6387 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0032 | 0/0 | 6382 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0033 | 0/0 | 6383 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0034 | 0/0 | 6383 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0035 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0001t0036 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0002t0003 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0002t0005 | 0/0 | 6381 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0003t0001 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
a0001c0004t0001 | 0/0 | 6387 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | copy fasta | chr1 | 77774649 | 77884540 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0014 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0058 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0108 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0001 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0186 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0009g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0009g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0009g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0009g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0009g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0010g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0010g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0010g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0010g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0010g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0011g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0011g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0011g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0011g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0012g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0012g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0012g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0012g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0013g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0013g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0013g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0014g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0014g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0014g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0015g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0015g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0015g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0016g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0016g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0016g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0017g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0017g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0017g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0018g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0019g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0020g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0021g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0022g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0023g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0024g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0025g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0026g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0027g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0028g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0029g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0030g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0031g0016 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0032g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0033g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0034g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0035g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0036g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0002t0003g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0002t0005g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0004t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0064 | EUR | GBR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | GBR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00323 | hp1 | a0001 | c0001 | t0005 | g0179 | EUR | FIN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0051 | EUR | FIN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00438 | hp1 | a0001 | c0001 | t0008 | g0192 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0161 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0060 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00597 | hp2 | a0001 | c0001 | t0008 | g0187 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0180 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0053 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0077 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00639 | hp2 | a0001 | c0001 | t0007 | g0247 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0172 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0234 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00738 | hp1 | a0001 | c0001 | t0010 | g0113 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0237 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0080 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0068 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0076 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01106 | hp2 | a0001 | c0001 | t0032 | g0034 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0259 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0232 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0256 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0039 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0127 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0040 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01255 | hp2 | a0001 | c0001 | t0010 | g0136 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0262 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0119 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0209 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01358 | hp2 | a0001 | c0001 | t0021 | g0055 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0135 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0107 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01496 | hp2 | a0001 | c0001 | t0017 | g0126 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0238 | EUR | IBS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0069 | EUR | IBS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01884 | hp2 | a0001 | c0001 | t0015 | g0006 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01891 | hp1 | a0001 | c0001 | t0014 | g0035 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01891 | hp2 | a0001 | c0001 | t0014 | g0273 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01952 | hp1 | a0001 | c0001 | t0008 | g0094 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0047 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0106 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0125 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02004 | hp2 | a0001 | c0001 | t0006 | g0075 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02055 | hp1 | a0001 | c0001 | t0011 | g0165 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0110 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0152 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0231 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0182 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0227 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0168 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02080 | hp2 | a0001 | c0001 | t0002 | g0044 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0089 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02132 | hp1 | a0001 | c0001 | t0005 | g0217 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0157 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02135 | hp2 | a0001 | c0001 | t0006 | g0220 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02145 | hp2 | a0001 | c0001 | t0009 | g0276 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | CDX | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | CDX | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0156 | EAS | CDX | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | CDX | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0048 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02257 | hp2 | a0001 | c0001 | t0012 | g0170 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0070 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0084 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02280 | hp2 | a0001 | c0001 | t0029 | g0042 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0072 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0255 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0145 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02451 | hp2 | a0001 | c0001 | t0019 | g0185 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0181 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02572 | hp1 | a0001 | c0001 | t0013 | g0216 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02572 | hp2 | a0001 | c0002 | t0003 | g0272 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0082 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0265 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02615 | hp2 | a0001 | c0001 | t0014 | g0271 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02622 | hp1 | a0001 | c0001 | t0018 | g0260 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02622 | hp2 | a0001 | c0001 | t0015 | g0199 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0257 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0266 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02647 | hp1 | a0001 | c0001 | t0030 | g0270 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02647 | hp2 | a0001 | c0002 | t0005 | g0198 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02698 | hp1 | a0001 | c0004 | t0001 | g0029 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0043 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0174 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02735 | hp2 | a0001 | c0001 | t0010 | g0235 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0261 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0031 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0171 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0009 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0214 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02886 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0176 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02895 | hp2 | a0001 | c0001 | t0010 | g0131 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0175 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02897 | hp2 | a0001 | c0001 | t0026 | g0253 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0011 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0116 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0037 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0118 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0054 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0038 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0264 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03130 | hp2 | a0001 | c0001 | t0013 | g0002 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03139 | hp1 | a0001 | c0001 | t0012 | g0162 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03139 | hp2 | a0001 | c0001 | t0023 | g0195 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0167 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0248 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0213 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03225 | hp2 | a0001 | c0001 | t0036 | g0211 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0071 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03453 | hp1 | a0001 | c0001 | t0015 | g0007 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0012 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0254 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0189 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0041 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0001 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0166 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0269 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03540 | hp1 | a0001 | c0001 | t0013 | g0002 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03540 | hp2 | a0001 | c0001 | t0009 | g0268 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03579 | hp1 | a0001 | c0001 | t0035 | g0275 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0205 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03654 | hp1 | a0001 | c0001 | t0017 | g0242 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03669 | hp1 | a0001 | c0001 | t0027 | g0079 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0239 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0241 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0015 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0229 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03831 | hp2 | a0001 | c0001 | t0022 | g0105 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0063 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0223 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0173 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0137 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0056 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0052 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04115 | hp1 | a0001 | c0001 | t0017 | g0251 | SAS | STU | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0218 | SAS | STU | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0020 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04184 | hp2 | a0001 | c0001 | t0034 | g0133 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0083 | SAS | STU | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0186 | SAS | STU | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0203 | SAS | STU | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0014 | SAS | STU | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18522 | hp1 | a0001 | c0001 | t0012 | g0163 | AFR | YRI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0128 | AFR | YRI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18612 | hp1 | a0001 | c0001 | t0005 | g0183 | EAS | CHB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0160 | EAS | CHB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18906 | hp1 | a0001 | c0001 | t0013 | g0196 | AFR | YRI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | YRI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18939 | hp1 | a0001 | c0003 | t0001 | g0114 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18939 | hp2 | a0001 | c0001 | t0016 | g0219 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18946 | hp2 | a0001 | c0001 | t0004 | g0149 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0201 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0252 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0155 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0151 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18966 | hp2 | a0001 | c0001 | t0005 | g0197 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0062 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0178 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18972 | hp2 | a0001 | c0001 | t0008 | g0112 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0143 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0169 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0098 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0018 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0103 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0057 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0226 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0086 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18993 | hp2 | a0001 | c0001 | t0008 | g0250 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18999 | hp1 | a0001 | c0001 | t0016 | g0190 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0091 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0277 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0144 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19001 | hp1 | a0001 | c0001 | t0028 | g0158 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0184 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0036 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19007 | hp1 | a0001 | c0001 | t0016 | g0202 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0215 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0139 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0236 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19043 | hp1 | a0001 | c0001 | t0020 | g0274 | AFR | LWK | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0010 | AFR | LWK | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0204 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19060 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19062 | hp1 | a0001 | c0001 | t0010 | g0019 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19066 | hp1 | a0001 | c0001 | t0004 | g0138 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19066 | hp2 | a0001 | c0001 | t0002 | g0095 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19070 | hp1 | a0001 | c0001 | t0008 | g0191 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19072 | hp2 | a0001 | c0001 | t0004 | g0150 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19074 | hp1 | a0001 | c0001 | t0008 | g0032 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19082 | hp1 | a0001 | c0001 | t0004 | g0246 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19084 | hp1 | a0001 | c0001 | t0008 | g0210 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19088 | hp1 | a0001 | c0001 | t0024 | g0222 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0132 | AFR | YRI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0099 | AFR | YRI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20752 | hp1 | a0001 | c0001 | t0031 | g0016 | EUR | TSI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0090 | EUR | TSI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20805 | hp1 | a0001 | c0001 | t0006 | g0067 | EUR | TSI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0258 | EUR | TSI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20905 | hp1 | a0001 | c0001 | t0005 | g0188 | SAS | GIH | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0081 | SAS | GIH | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0208 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0263 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02559 | hp2 | a0001 | c0001 | t0011 | g0164 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG06807 | hp1 | a0001 | c0001 | t0009 | g0003 | AFR | USA | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG06807 | hp2 | a0001 | c0001 | t0025 | g0194 | AFR | USA | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20300 | hp1 | a0001 | c0001 | t0033 | g0212 | AFR | USA | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0267 | AFR | USA | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0058 | REF | REF | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0108 | REF | REF | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
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 |
---|
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:77801375
|
A | G | 1 | a0001c0004 | 1 | HG02698.hp1 | synonymous_variant | LOW | c.144A>G | p.Ala48Ala | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 3/16 | 247/6382 | 144/1803 | 48/600 | chr1 | 77801375 | ||
chr1:77858952
|
A | G | 1 | a0001c0003 | 1 | NA18939.hp1 | synonymous_variant | LOW | c.915A>G | p.Arg305Arg | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 9/16 | 1018/6382 | 915/1803 | 305/600 | chr1 | 77858952 | ||
chr1:77874983
|
T | C | 1 | a0001c0002 | 2 | HG02572.hp2 HG02647.hp2 |
synonymous_variant | LOW | c.1722T>C | p.Asp574Asp | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 1825/6382 | 1722/1803 | 574/600 | chr1 | 77874983 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:77875120
|
T | G | 1 | a0001c0001t0018 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*56T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 56 | chr1 | 77875120 | |||||
chr1:77875341
|
A | G | 2 | a0001c0001t0013a0001c0001t0036 | 5 | HG02572.hp1 HG03130.hp2 HG03225.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*277A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 277 | chr1 | 77875341 | |||||
chr1:77876179
|
A | G | 1 | a0001c0001t0035 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1115A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 1115 | chr1 | 77876179 | |||||
chr1:77876294
|
C | T | 2 | a0001c0001t0017a0001c0001t0034 | 4 | HG01496.hp2 HG03654.hp1 HG04115.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1230C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 1230 | chr1 | 77876294 | |||||
chr1:77876303
|
A | G | 1 | a0001c0001t0009 | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1239A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 1239 | chr1 | 77876303 | |||||
chr1:77876318
|
A | G | 1 | a0001c0001t0033 | 1 | NA20300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1254A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 1254 | chr1 | 77876318 | |||||
chr1:77876541
|
T | C | 1 | a0001c0001t0019 | 1 | HG02451.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1477T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 1477 | chr1 | 77876541 | |||||
chr1:77876724
|
C | T | 2 | a0001c0001t0031a0001c0001t0032 | 2 | HG01106.hp2 NA20752.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1660C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 1660 | chr1 | 77876724 | |||||
chr1:77876837
|
A | G | 2 | a0001c0001t0008a0001c0001t0016 | 11 | HG00438.hp1 HG00597.hp2 HG01952.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1773A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 1773 | chr1 | 77876837 | |||||
chr1:77876881
|
A | G | 2 | a0001c0001t0017a0001c0001t0034 | 4 | HG01496.hp2 HG03654.hp1 HG04115.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1817A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 1817 | chr1 | 77876881 | |||||
chr1:77876973
|
G | T | 1 | a0001c0001t0030 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1909G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 1909 | chr1 | 77876973 | |||||
chr1:77877203
|
G | A | 1 | a0001c0001t0009 | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2139G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 2139 | chr1 | 77877203 | |||||
chr1:77877218
|
C | T | 1 | a0001c0001t0029 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2154C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 2154 | chr1 | 77877218 | |||||
chr1:77877302
|
A | T | 2 | a0001c0001t0004a0001c0001t0028 | 26 | HG00438.hp2 HG02056.hp1 HG02080.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2238A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 2238 | chr1 | 77877302 | |||||
chr1:77877825
|
C | T | 1 | a0001c0001t0027 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2761C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 2761 | chr1 | 77877825 | |||||
chr1:77878154
|
G | A | 4 | a0001c0001t0014a0001c0001t0019a0001c0001t0020others(1): Show | 6 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3090G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3090 | chr1 | 77878154 | |||||
chr1:77878224
|
T | C | 4 | a0001c0001t0004a0001c0001t0011a0001c0001t0012others(1): Show | 34 | HG00438.hp2 HG02055.hp1 HG02056.hp1 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*3160T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3160 | chr1 | 77878224 | |||||
chr1:77878394
|
C | CA | 6 | a0001c0001t0007a0001c0001t0013a0001c0001t0020others(3): Show | 16 | HG00639.hp2 HG02572.hp1 HG02735.hp1 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3357dupA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3358 | INFO_REALIGN_3_PRIME | chr1 | 77878394 | ||||
chr1:77878394
|
C | CAAAA | 2 | a0001c0001t0010a0001c0001t0025 | 6 | HG00738.hp1 HG01255.hp2 HG02735.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3354_*3357dupAAAA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3358 | INFO_REALIGN_3_PRIME | chr1 | 77878394 | ||||
chr1:77878394
|
C | CAAAAA | 7 | a0001c0001t0001a0001c0001t0022a0001c0001t0023others(4): Show | 82 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3353_*3357dupAAAA others(1): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3358 | INFO_REALIGN_3_PRIME | chr1 | 77878394 | ||||
chr1:77878394
|
C | CAAAAAA | 4 | a0001c0001t0002a0001c0001t0015a0001c0001t0018others(1): Show | 59 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(56): Show |
3_prime_UTR_variant | MODIFIER | c.*3352_*3357dupAAAA others(2): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3358 | INFO_REALIGN_3_PRIME | chr1 | 77878394 | ||||
chr1:77878394
|
C | CAAAAAAA | 1 | a0001c0001t0006 | 9 | HG00735.hp2 HG00741.hp2 HG01109.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3351_*3357dupAAAA others(3): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3358 | INFO_REALIGN_3_PRIME | chr1 | 77878394 | ||||
chr1:77878394
|
C | CAAAAAAA others(3): Show |
1 | a0001c0001t0021 | 1 | HG01358.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3348_*3357dupAAAA others(6): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3358 | INFO_REALIGN_3_PRIME | chr1 | 77878394 | ||||
chr1:77878394
|
CA | C | 6 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(3): Show | 33 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*3357delA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3357 | INFO_REALIGN_3_PRIME | chr1 | 77878394 | ||||
chr1:77878450
|
A | C | 1 | a0001c0001t0029 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3386A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3386 | chr1 | 77878450 | |||||
chr1:77878473
|
C | T | 1 | a0001c0001t0024 | 1 | NA19088.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3409C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3409 | chr1 | 77878473 | |||||
chr1:77878906
|
T | C | 1 | a0001c0001t0026 | 1 | HG02897.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3842T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3842 | chr1 | 77878906 | |||||
chr1:77879014
|
CA | C | 4 | a0001c0001t0014a0001c0001t0019a0001c0001t0020others(1): Show | 6 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*3953delA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 3953 | INFO_REALIGN_3_PRIME | chr1 | 77879014 | ||||
chr1:77879300
|
A | C | 3 | a0001c0001t0015a0001c0001t0023a0001c0001t0025 | 5 | HG01884.hp2 HG02622.hp2 HG03139.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*4236A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 4236 | chr1 | 77879300 | |||||
chr1:77879499
|
A | C | 1 | a0001c0001t0022 | 1 | HG03831.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4435A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 16/16 | 4435 | chr1 | 77879499 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:77779810
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.-16+74G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77779810 | ||||||
chr1:77779862
|
C | T | 1 | a0001c0001t0002g0277 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-16+126C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77779862 | ||||||
chr1:77780360
|
A | G | 1 | a0001c0001t0009g0276 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-16+624A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77780360 | ||||||
chr1:77780585
|
C | G | 25 | a0001c0001t0001g0269a0001c0001t0002g0255a0001c0001t0002g0256others(22): Show | 26 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.-16+849C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77780585 | ||||||
chr1:77780691
|
C | T | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-16+955C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77780691 | ||||||
chr1:77780726
|
A | G | 1 | a0001c0001t0001g0252 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-16+990A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77780726 | ||||||
chr1:77780732
|
A | G | 1 | a0001c0001t0017g0251 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-16+996A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77780732 | ||||||
chr1:77780799
|
A | G | 1 | a0001c0001t0008g0250 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.-16+1063A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77780799 | ||||||
chr1:77780804
|
T | TAATGATT others(3): Show |
1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-16+1069_-16+1078d others(12): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr1 | 77780804 | |||||
chr1:77780908
|
CT | C | 14 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(11): Show | 14 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(11): Show |
intron_variant | MODIFIER | c.-16+1188delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | INFO_REALIGN_3_PRIME | chr1 | 77780908 | |||||
chr1:77781047
|
C | T | 1 | a0001c0001t0001g0249 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-16+1311C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77781047 | ||||||
chr1:77781052
|
G | A | 1 | a0001c0001t0001g0008 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-16+1316G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77781052 | ||||||
chr1:77781796
|
A | C | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-15-1442A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77781796 | ||||||
chr1:77781891
|
G | C | 5 | a0001c0001t0003g0009a0001c0001t0007g0010a0001c0001t0007g0011others(2): Show | 5 | HG02818.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.-15-1347G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77781891 | ||||||
chr1:77782005
|
G | A | 1 | a0001c0001t0002g0277 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.-15-1233G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77782005 | ||||||
chr1:77782757
|
G | C | 1 | a0001c0001t0003g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-15-481G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77782757 | ||||||
chr1:77783004
|
C | A | 2 | a0001c0001t0001g0014a0001c0001t0002g0015 | 2 | HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-15-234C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 1/15 | chr1 | 77783004 | ||||||
chr1:77783908
|
C | G | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.99+557C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77783908 | ||||||
chr1:77784066
|
T | G | 7 | a0001c0001t0003g0265a0001c0001t0006g0266a0001c0001t0007g0264others(4): Show | 8 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+715T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77784066 | ||||||
chr1:77784081
|
G | A | 19 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG01106.hp2 HG02083.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+730G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77784081 | ||||||
chr1:77784307
|
C | T | 7 | a0001c0001t0003g0265a0001c0001t0006g0266a0001c0001t0007g0264others(4): Show | 8 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+956C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77784307 | ||||||
chr1:77784388
|
A | C | 1 | a0001c0001t0007g0247 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.99+1037A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77784388 | ||||||
chr1:77784705
|
A | T | 1 | a0001c0001t0004g0246 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.99+1354A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77784705 | ||||||
chr1:77784725
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.99+1374A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77784725 | ||||||
chr1:77784738
|
C | T | 1 | a0001c0001t0001g0244 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.99+1387C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77784738 | ||||||
chr1:77784766
|
C | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG01106.hp2 HG02083.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+1415C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77784766 | ||||||
chr1:77784773
|
T | G | 16 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(13): Show | 17 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+1422T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77784773 | ||||||
chr1:77784843
|
G | A | 7 | a0001c0001t0001g0269a0001c0001t0014g0035a0001c0001t0014g0271others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+1492G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77784843 | ||||||
chr1:77784911
|
CATT | C | 3 | a0001c0001t0003g0265a0001c0001t0006g0266a0001c0001t0007g0264 | 3 | HG02615.hp1 HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.99+1563_99+1565del others(3): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77784911 | |||||
chr1:77785142
|
G | A | 1 | a0001c0001t0004g0036 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.99+1791G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77785142 | ||||||
chr1:77785236
|
T | C | 16 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(13): Show | 17 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+1885T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77785236 | ||||||
chr1:77785238
|
G | A | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+1887G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77785238 | ||||||
chr1:77785269
|
C | T | 1 | a0001c0001t0032g0034 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.99+1918C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77785269 | ||||||
chr1:77785294
|
A | T | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.99+1943A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77785294 | ||||||
chr1:77785345
|
A | AT | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+2009dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77785345 | |||||
chr1:77785346
|
T | A | 1 | a0001c0001t0031g0016 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.99+1995T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77785346 | ||||||
chr1:77785638
|
C | T | 4 | a0001c0001t0002g0241a0001c0001t0003g0263a0001c0001t0017g0242others(1): Show | 4 | HG02109.hp2 HG03654.hp1 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+2287C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77785638 | ||||||
chr1:77785645
|
G | A | 2 | a0001c0001t0003g0037a0001c0001t0003g0038 | 2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.99+2294G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77785645 | ||||||
chr1:77785690
|
G | T | 1 | a0001c0001t0003g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.99+2339G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77785690 | ||||||
chr1:77785778
|
C | T | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.99+2427C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77785778 | ||||||
chr1:77785783
|
C | T | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+2432C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77785783 | ||||||
chr1:77785941
|
G | A | 2 | a0001c0001t0005g0039a0001c0001t0005g0040 | 2 | HG01169.hp2 HG01255.hp1 |
intron_variant | MODIFIER | c.99+2590G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77785941 | ||||||
chr1:77786239
|
C | T | 4 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 4 | HG00099.hp2 HG00738.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.99+2888C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77786239 | ||||||
chr1:77786426
|
G | A | 1 | a0001c0001t0002g0255 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.99+3075G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77786426 | ||||||
chr1:77786956
|
A | T | 1 | a0001c0001t0001g0236 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.99+3605A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77786956 | ||||||
chr1:77787015
|
C | T | 1 | a0001c0001t0010g0235 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.99+3664C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77787015 | ||||||
chr1:77787151
|
A | C | 22 | a0001c0001t0001g0269a0001c0001t0002g0255a0001c0001t0002g0256others(19): Show | 23 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.99+3800A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77787151 | ||||||
chr1:77787205
|
C | T | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+3854C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77787205 | ||||||
chr1:77787347
|
A | T | 3 | a0001c0001t0002g0232a0001c0001t0002g0233a0001c0001t0006g0234 | 3 | HG00735.hp2 HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.99+3996A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77787347 | ||||||
chr1:77787386
|
CT | C | 28 | a0001c0001t0001g0269a0001c0001t0002g0241a0001c0001t0002g0255others(25): Show | 29 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(26): Show |
intron_variant | MODIFIER | c.99+4050delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77787386 | |||||
chr1:77787527
|
T | A | 1 | a0001c0001t0029g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.99+4176T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77787527 | ||||||
chr1:77787546
|
A | G | 161 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(158): Show | 163 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(160): Show |
intron_variant | MODIFIER | c.99+4195A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77787546 | ||||||
chr1:77787722
|
G | A | 1 | a0001c0001t0015g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.99+4371G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77787722 | ||||||
chr1:77787856
|
C | T | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+4505C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77787856 | ||||||
chr1:77788056
|
G | A | 18 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(15): Show | 18 | HG01070.hp1 HG01099.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.99+4705G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788056 | ||||||
chr1:77788146
|
G | A | 9 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0049others(6): Show | 9 | HG01884.hp2 HG01952.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.99+4795G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788146 | ||||||
chr1:77788233
|
C | G | 1 | a0001c0001t0014g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.99+4882C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788233 | ||||||
chr1:77788427
|
G | A | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+5076G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788427 | ||||||
chr1:77788573
|
C | T | 80 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(77): Show | 81 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.99+5222C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788573 | ||||||
chr1:77788609
|
A | G | 15 | a0001c0001t0001g0221a0001c0001t0001g0223a0001c0001t0001g0224others(12): Show | 15 | HG00621.hp1 HG02056.hp2 HG02074.hp2 others(12): Show |
intron_variant | MODIFIER | c.99+5258A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788609 | ||||||
chr1:77788611
|
T | A | 1 | a0001c0001t0001g0236 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.99+5260T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788611 | ||||||
chr1:77788614
|
G | A | 1 | a0001c0001t0001g0236 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.99+5263G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788614 | ||||||
chr1:77788641
|
T | G | 37 | a0001c0001t0001g0159a0001c0001t0002g0144a0001c0001t0004g0036others(34): Show | 37 | HG00438.hp2 HG01891.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.99+5290T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788641 | ||||||
chr1:77788675
|
C | G | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.99+5324C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788675 | ||||||
chr1:77788906
|
C | T | 1 | a0001c0001t0002g0255 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.99+5555C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788906 | ||||||
chr1:77788984
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.99+5633A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788984 | ||||||
chr1:77788995
|
G | A | 1 | a0001c0001t0002g0017 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.99+5644G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77788995 | ||||||
chr1:77789095
|
A | G | 3 | a0001c0001t0002g0241a0001c0001t0017g0242a0001c0001t0017g0251 | 3 | HG03654.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.99+5744A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77789095 | ||||||
chr1:77789105
|
A | T | 1 | a0001c0001t0016g0219 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.99+5754A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77789105 | ||||||
chr1:77789201
|
C | CT | 65 | a0001c0001t0001g0033a0001c0001t0001g0159a0001c0001t0002g0120others(62): Show | 65 | HG00438.hp2 HG00639.hp2 HG00735.hp1 others(62): Show |
intron_variant | MODIFIER | c.99+5870dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77789201 | |||||
chr1:77789201
|
C | CTT | 7 | a0001c0001t0001g0269a0001c0001t0005g0218a0001c0001t0014g0271others(4): Show | 7 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.99+5869_99+5870dup others(2): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77789201 | |||||
chr1:77789201
|
CTTTTT | C | 7 | a0001c0001t0003g0265a0001c0001t0006g0266a0001c0001t0007g0264others(4): Show | 8 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.99+5866_99+5870del others(5): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77789201 | |||||
chr1:77789250
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.99+5899C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77789250 | ||||||
chr1:77789264
|
C | T | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+5913C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77789264 | ||||||
chr1:77789336
|
G | A | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.99+5985G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77789336 | ||||||
chr1:77789355
|
T | C | 1 | a0001c0001t0001g0050 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.99+6004T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77789355 | ||||||
chr1:77789383
|
T | A | 3 | a0001c0001t0001g0051a0001c0001t0002g0052a0001c0001t0002g0120 | 3 | HG00323.hp2 HG01192.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.99+6032T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77789383 | ||||||
chr1:77789544
|
A | C | 2 | a0001c0001t0001g0051a0001c0001t0002g0052 | 2 | HG00323.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.99+6193A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77789544 | ||||||
chr1:77790137
|
G | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG01106.hp2 HG02083.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+6786G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77790137 | ||||||
chr1:77790174
|
C | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG01106.hp2 HG02083.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+6823C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77790174 | ||||||
chr1:77790197
|
A | G | 16 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(13): Show | 17 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+6846A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77790197 | ||||||
chr1:77790231
|
T | C | 1 | a0001c0001t0001g0008 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.99+6880T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77790231 | ||||||
chr1:77790466
|
C | A | 8 | a0001c0001t0003g0263a0001c0001t0003g0265a0001c0001t0006g0266others(5): Show | 9 | HG02109.hp2 HG02145.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.99+7115C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77790466 | ||||||
chr1:77790553
|
A | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG01106.hp2 HG02083.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.99+7202A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77790553 | ||||||
chr1:77790561
|
C | T | 1 | a0001c0001t0015g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.99+7210C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77790561 | ||||||
chr1:77790639
|
G | A | 1 | a0001c0001t0003g0053 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.99+7288G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77790639 | ||||||
chr1:77790722
|
G | C | 16 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(13): Show | 17 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+7371G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77790722 | ||||||
chr1:77791061
|
A | C | 1 | a0001c0001t0001g0240 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.99+7710A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791061 | ||||||
chr1:77791243
|
T | TA | 44 | a0001c0001t0001g0018a0001c0001t0001g0045a0001c0001t0001g0051others(41): Show | 44 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(41): Show |
intron_variant | MODIFIER | c.99+7914dupA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77791243 | |||||
chr1:77791243
|
T | TAA | 10 | a0001c0001t0002g0120a0001c0001t0002g0144a0001c0001t0004g0137others(7): Show | 10 | HG01192.hp1 HG03927.hp2 NA18962.hp1 others(7): Show |
intron_variant | MODIFIER | c.99+7913_99+7914dup others(2): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77791243 | |||||
chr1:77791243
|
TA | T | 105 | a0001c0001t0001g0115a0001c0001t0001g0121a0001c0001t0001g0122others(102): Show | 106 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.99+7914delA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77791243 | |||||
chr1:77791248
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.99+7897A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791248 | ||||||
chr1:77791257
|
A | C | 16 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(13): Show | 17 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.99+7906A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791257 | ||||||
chr1:77791258
|
A | C | 2 | a0001c0001t0002g0119a0001c0001t0003g0248 | 2 | HG01257.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.99+7907A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791258 | ||||||
chr1:77791259
|
A | AC | 4 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0118others(1): Show | 4 | HG02257.hp2 HG02922.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+7908_99+7909ins others(1): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791259 | ||||||
chr1:77791259
|
A | C | 3 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013 | 3 | HG02886.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.99+7908A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791259 | ||||||
chr1:77791261
|
A | C | 3 | a0001c0001t0002g0241a0001c0001t0017g0242a0001c0001t0017g0251 | 3 | HG03654.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.99+7910A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791261 | ||||||
chr1:77791262
|
A | C | 80 | a0001c0001t0001g0122a0001c0001t0001g0123a0001c0001t0001g0129others(77): Show | 81 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.99+7911A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791262 | ||||||
chr1:77791265
|
AC | A | 4 | a0001c0001t0014g0271a0001c0001t0014g0273a0001c0001t0020g0274others(1): Show | 4 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.99+7915delC | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791265 | ||||||
chr1:77791266
|
C | A | 3 | a0001c0001t0001g0269a0001c0001t0002g0043a0001c0001t0030g0270 | 3 | HG02647.hp1 HG02698.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.99+7915C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791266 | ||||||
chr1:77791419
|
G | A | 132 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(129): Show | 133 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(130): Show |
intron_variant | MODIFIER | c.99+8068G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791419 | ||||||
chr1:77791442
|
A | G | 2 | a0001c0001t0003g0265a0001c0001t0006g0266 | 2 | HG02615.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.99+8091A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791442 | ||||||
chr1:77791445
|
T | C | 3 | a0001c0001t0002g0241a0001c0001t0017g0242a0001c0001t0017g0251 | 3 | HG03654.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.99+8094T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791445 | ||||||
chr1:77791505
|
T | C | 3 | a0001c0001t0001g0047a0001c0001t0002g0044a0001c0001t0002g0046 | 3 | HG01952.hp2 HG02080.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.99+8154T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791505 | ||||||
chr1:77791559
|
G | GT | 5 | a0001c0001t0002g0031a0001c0001t0002g0120a0001c0001t0008g0032others(2): Show | 5 | HG00738.hp1 HG01192.hp1 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.99+8231dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77791559 | |||||
chr1:77791559
|
GT | G | 39 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(36): Show | 39 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(36): Show |
intron_variant | MODIFIER | c.99+8231delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77791559 | |||||
chr1:77791559
|
GTT | G | 130 | a0001c0001t0001g0063a0001c0001t0001g0065a0001c0001t0001g0066others(127): Show | 131 | HG00099.hp1 HG00438.hp1 HG00438.hp2 others(128): Show |
intron_variant | MODIFIER | c.99+8230_99+8231del others(2): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77791559 | |||||
chr1:77791559
|
GTTT | G | 28 | a0001c0001t0001g0269a0001c0001t0002g0255a0001c0001t0002g0256others(25): Show | 29 | HG00323.hp1 HG01109.hp2 HG01168.hp2 others(26): Show |
intron_variant | MODIFIER | c.99+8229_99+8231del others(3): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77791559 | |||||
chr1:77791841
|
G | C | 3 | a0001c0001t0002g0241a0001c0001t0017g0242a0001c0001t0017g0251 | 3 | HG03654.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.99+8490G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791841 | ||||||
chr1:77791987
|
C | A | 1 | a0001c0001t0031g0016 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.99+8636C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77791987 | ||||||
chr1:77792104
|
C | G | 2 | a0001c0001t0001g0066a0001c0001t0009g0054 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.99+8753C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77792104 | ||||||
chr1:77792786
|
C | CT | 47 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(44): Show | 47 | HG00621.hp1 HG01070.hp1 HG01099.hp2 others(44): Show |
intron_variant | MODIFIER | c.100-8526dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77792786 | |||||
chr1:77792949
|
C | T | 19 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | HG01106.hp2 HG02083.hp1 HG02155.hp2 others(16): Show |
intron_variant | MODIFIER | c.100-8382C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77792949 | ||||||
chr1:77793378
|
T | A | 1 | a0001c0001t0003g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.100-7953T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77793378 | ||||||
chr1:77793446
|
T | G | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-7885T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77793446 | ||||||
chr1:77793626
|
A | AT | 14 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(11): Show | 14 | HG00621.hp1 HG02056.hp2 HG02074.hp2 others(11): Show |
intron_variant | MODIFIER | c.100-7690dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77793626 | |||||
chr1:77793626
|
A | T | 1 | a0001c0001t0002g0229 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.100-7705A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77793626 | ||||||
chr1:77793707
|
T | G | 3 | a0001c0001t0003g0180a0001c0001t0005g0181a0001c0001t0005g0182 | 3 | HG00609.hp1 HG02074.hp1 HG02523.hp1 |
intron_variant | MODIFIER | c.100-7624T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77793707 | ||||||
chr1:77793744
|
C | T | 5 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0175others(2): Show | 5 | HG00735.hp1 HG02735.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.100-7587C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77793744 | ||||||
chr1:77793783
|
C | CT | 28 | a0001c0001t0001g0110a0001c0001t0001g0111a0001c0001t0001g0208others(25): Show | 28 | HG00621.hp1 HG00639.hp2 HG01192.hp1 others(25): Show |
intron_variant | MODIFIER | c.100-7527dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77793783 | |||||
chr1:77793783
|
CT | C | 6 | a0001c0001t0001g0051a0001c0001t0003g0248a0001c0001t0004g0146others(3): Show | 6 | HG00323.hp2 HG00738.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-7527delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77793783 | |||||
chr1:77794007
|
T | C | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.100-7324T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77794007 | ||||||
chr1:77794031
|
T | C | 3 | a0001c0001t0002g0241a0001c0001t0017g0242a0001c0001t0017g0251 | 3 | HG03654.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.100-7300T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77794031 | ||||||
chr1:77794036
|
G | A | 80 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(77): Show | 81 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(78): Show |
intron_variant | MODIFIER | c.100-7295G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77794036 | ||||||
chr1:77794071
|
G | A | 4 | a0001c0001t0002g0069a0001c0001t0006g0067a0001c0001t0006g0068others(1): Show | 4 | HG00741.hp2 HG01358.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.100-7260G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77794071 | ||||||
chr1:77794081
|
G | A | 1 | a0001c0001t0003g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.100-7250G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77794081 | ||||||
chr1:77794112
|
T | A | 3 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013 | 3 | HG02886.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.100-7219T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77794112 | ||||||
chr1:77794160
|
G | A | 1 | a0001c0001t0019g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.100-7171G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77794160 | ||||||
chr1:77794311
|
T | G | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.100-7020T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77794311 | ||||||
chr1:77794586
|
G | T | 1 | a0001c0001t0009g0268 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.100-6745G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77794586 | ||||||
chr1:77794649
|
A | G | 3 | a0001c0001t0002g0241a0001c0001t0017g0242a0001c0001t0017g0251 | 3 | HG03654.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.100-6682A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77794649 | ||||||
chr1:77795168
|
T | G | 9 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0049others(6): Show | 9 | HG01884.hp2 HG01952.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-6163T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77795168 | ||||||
chr1:77795632
|
C | CT | 7 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0049others(4): Show | 7 | HG01952.hp2 HG02080.hp2 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.100-5683dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77795632 | |||||
chr1:77795794
|
T | C | 1 | a0001c0001t0002g0070 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.100-5537T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77795794 | ||||||
chr1:77796028
|
C | A | 1 | a0001c0001t0003g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.100-5303C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77796028 | ||||||
chr1:77796090
|
C | T | 1 | a0001c0001t0005g0217 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.100-5241C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77796090 | ||||||
chr1:77796122
|
AT | A | 10 | a0001c0001t0001g0051a0001c0001t0003g0057a0001c0001t0011g0164others(7): Show | 10 | HG00323.hp2 HG02055.hp1 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.100-5195delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77796122 | |||||
chr1:77796140
|
A | G | 98 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(95): Show | 99 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(96): Show |
intron_variant | MODIFIER | c.100-5191A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77796140 | ||||||
chr1:77796142
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100-5189G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77796142 | ||||||
chr1:77796339
|
C | T | 1 | a0001c0001t0001g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.100-4992C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77796339 | ||||||
chr1:77796422
|
AT | A | 7 | a0001c0001t0001g0051a0001c0001t0001g0122a0001c0001t0001g0249others(4): Show | 7 | HG00323.hp2 HG01168.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.100-4893delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77796422 | |||||
chr1:77796565
|
G | T | 2 | a0001c0001t0001g0135a0001c0001t0010g0136 | 2 | HG01255.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.100-4766G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77796565 | ||||||
chr1:77796582
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100-4749T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77796582 | ||||||
chr1:77796736
|
A | G | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.100-4595A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77796736 | ||||||
chr1:77796759
|
C | A | 1 | a0001c0001t0004g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.100-4572C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77796759 | ||||||
chr1:77797047
|
G | A | 16 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(13): Show | 17 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-4284G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77797047 | ||||||
chr1:77797500
|
A | C | 16 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(13): Show | 17 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.100-3831A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77797500 | ||||||
chr1:77797733
|
T | C | 1 | a0001c0001t0001g0115 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.100-3598T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77797733 | ||||||
chr1:77797795
|
T | C | 1 | a0001c0001t0001g0021 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.100-3536T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77797795 | ||||||
chr1:77797889
|
T | A | 1 | a0001c0001t0014g0271 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.100-3442T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77797889 | ||||||
chr1:77798068
|
T | A | 2 | a0001c0001t0001g0066a0001c0001t0009g0054 | 2 | HG02559.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.100-3263T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77798068 | ||||||
chr1:77798539
|
T | C | 1 | a0001c0001t0003g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.100-2792T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77798539 | ||||||
chr1:77798571
|
A | G | 1 | a0001c0001t0002g0262 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.100-2760A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77798571 | ||||||
chr1:77798574
|
A | G | 38 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(35): Show | 38 | HG00621.hp1 HG01070.hp1 HG01099.hp2 others(35): Show |
intron_variant | MODIFIER | c.100-2757A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77798574 | ||||||
chr1:77798864
|
A | G | 2 | a0001c0001t0003g0209a0001c0001t0005g0218 | 2 | HG01346.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.100-2467A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77798864 | ||||||
chr1:77799263
|
T | G | 1 | a0001c0001t0001g0022 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.100-2068T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77799263 | ||||||
chr1:77799526
|
A | C | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.100-1805A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77799526 | ||||||
chr1:77799706
|
C | A | 5 | a0001c0001t0011g0164a0001c0001t0011g0165a0001c0001t0012g0162others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.100-1625C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77799706 | ||||||
chr1:77799855
|
C | CA | 9 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0049others(6): Show | 9 | HG01884.hp2 HG01952.hp2 HG02080.hp2 others(6): Show |
intron_variant | MODIFIER | c.100-1465dupA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | INFO_REALIGN_3_PRIME | chr1 | 77799855 | |||||
chr1:77800423
|
A | T | 22 | a0001c0001t0001g0269a0001c0001t0002g0255a0001c0001t0002g0256others(19): Show | 23 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.100-908A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77800423 | ||||||
chr1:77800690
|
C | T | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.100-641C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77800690 | ||||||
chr1:77800732
|
C | T | 162 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(159): Show | 164 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(161): Show |
intron_variant | MODIFIER | c.100-599C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77800732 | ||||||
chr1:77800806
|
T | C | 1 | a0001c0001t0001g0244 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.100-525T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 2/15 | chr1 | 77800806 | ||||||
chr1:77801743
|
C | T | 4 | a0001c0001t0001g0238a0001c0001t0001g0239a0001c0001t0001g0240others(1): Show | 4 | HG00099.hp2 HG00738.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.277+235C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 3/15 | chr1 | 77801743 | ||||||
chr1:77802095
|
T | C | 16 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(13): Show | 17 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.277+587T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 3/15 | chr1 | 77802095 | ||||||
chr1:77802271
|
C | G | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.277+763C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 3/15 | chr1 | 77802271 | ||||||
chr1:77802357
|
C | G | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.277+849C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 3/15 | chr1 | 77802357 | ||||||
chr1:77802363
|
A | G | 11 | a0001c0001t0003g0009a0001c0001t0003g0172a0001c0001t0003g0173others(8): Show | 11 | HG00639.hp2 HG00735.hp1 HG02735.hp1 others(8): Show |
intron_variant | MODIFIER | c.277+855A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 3/15 | chr1 | 77802363 | ||||||
chr1:77802427
|
C | T | 1 | a0001c0001t0003g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.278-843C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 3/15 | chr1 | 77802427 | ||||||
chr1:77802446
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0006g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.278-824G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 3/15 | chr1 | 77802446 | ||||||
chr1:77802622
|
A | T | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.278-648A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 3/15 | chr1 | 77802622 | ||||||
chr1:77802730
|
A | G | 4 | a0001c0001t0011g0164a0001c0001t0011g0165a0001c0001t0012g0162others(1): Show | 4 | HG02055.hp1 HG02559.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.278-540A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 3/15 | chr1 | 77802730 | ||||||
chr1:77803077
|
A | T | 2 | a0001c0001t0001g0109a0001c0001t0002g0062 | 2 | HG02155.hp1 NA18968.hp1 |
intron_variant | MODIFIER | c.278-193A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 3/15 | chr1 | 77803077 | ||||||
chr1:77803238
|
A | G | 1 | a0001c0001t0020g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.278-32A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 3/15 | chr1 | 77803238 | ||||||
chr1:77803522
|
G | A | 56 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0050others(53): Show | 56 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(53): Show |
intron_variant | MODIFIER | c.414+116G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77803522 | ||||||
chr1:77803617
|
T | G | 3 | a0001c0001t0002g0241a0001c0001t0017g0242a0001c0001t0017g0251 | 3 | HG03654.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.414+211T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77803617 | ||||||
chr1:77803858
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.414+452G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77803858 | ||||||
chr1:77804065
|
C | A | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.414+659C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77804065 | ||||||
chr1:77804384
|
G | T | 1 | a0001c0001t0002g0048 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.414+978G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77804384 | ||||||
chr1:77804462
|
T | A | 1 | a0001c0001t0003g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.414+1056T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77804462 | ||||||
chr1:77804610
|
A | G | 1 | a0001c0001t0004g0161 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.414+1204A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77804610 | ||||||
chr1:77804622
|
AT | A | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.414+1232delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr1 | 77804622 | |||||
chr1:77804858
|
A | T | 2 | a0001c0001t0004g0143a0001c0001t0004g0160 | 2 | NA18612.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.414+1452A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77804858 | ||||||
chr1:77804908
|
T | C | 1 | a0001c0001t0004g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.414+1502T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77804908 | ||||||
chr1:77804951
|
T | C | 4 | a0001c0001t0003g0254a0001c0001t0007g0247a0001c0001t0026g0253others(1): Show | 4 | HG00639.hp2 HG02897.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.414+1545T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77804951 | ||||||
chr1:77804993
|
C | CT | 37 | a0001c0001t0001g0159a0001c0001t0001g0206a0001c0001t0002g0144others(34): Show | 37 | HG00438.hp2 HG01891.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.414+1606dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr1 | 77804993 | |||||
chr1:77804993
|
CT | C | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.414+1606delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr1 | 77804993 | |||||
chr1:77805018
|
G | A | 27 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(24): Show | 27 | HG00639.hp1 HG00741.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.414+1612G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805018 | ||||||
chr1:77805117
|
C | T | 1 | a0001c0001t0010g0019 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.414+1711C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805117 | ||||||
chr1:77805119
|
C | T | 1 | a0001c0001t0009g0003 | 2 | HG02818.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.414+1713C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805119 | ||||||
chr1:77805143
|
C | T | 8 | a0001c0001t0001g0269a0001c0001t0007g0247a0001c0001t0014g0271others(5): Show | 8 | HG00639.hp2 HG01891.hp2 HG02572.hp2 others(5): Show |
intron_variant | MODIFIER | c.414+1737C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805143 | ||||||
chr1:77805156
|
G | A | 2 | a0001c0001t0006g0067a0001c0001t0006g0068 | 2 | HG00741.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.414+1750G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805156 | ||||||
chr1:77805170
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.414+1764A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805170 | ||||||
chr1:77805171
|
T | A | 2 | a0001c0001t0003g0209a0001c0001t0005g0218 | 2 | HG01346.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.414+1765T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805171 | ||||||
chr1:77805259
|
A | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.415-1716A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805259 | ||||||
chr1:77805438
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.415-1537G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805438 | ||||||
chr1:77805461
|
C | CT | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(245): Show | 250 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.415-1496dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr1 | 77805461 | |||||
chr1:77805461
|
C | CTT | 11 | a0001c0001t0001g0109a0001c0001t0002g0062a0001c0001t0002g0104others(8): Show | 11 | HG02109.hp2 HG02155.hp1 HG02451.hp2 others(8): Show |
intron_variant | MODIFIER | c.415-1497_415-1496d others(4): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr1 | 77805461 | |||||
chr1:77805461
|
CTT | C | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.415-1497_415-1496d others(4): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr1 | 77805461 | |||||
chr1:77805593
|
G | C | 1 | a0001c0001t0014g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.415-1382G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805593 | ||||||
chr1:77805598
|
T | C | 1 | a0001c0001t0002g0120 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.415-1377T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805598 | ||||||
chr1:77805628
|
C | A | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.415-1347C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805628 | ||||||
chr1:77805825
|
G | A | 25 | a0001c0001t0001g0269a0001c0001t0002g0255a0001c0001t0002g0256others(22): Show | 26 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.415-1150G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77805825 | ||||||
chr1:77806134
|
A | C | 1 | a0001c0001t0014g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.415-841A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77806134 | ||||||
chr1:77806361
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.415-614C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77806361 | ||||||
chr1:77806394
|
A | G | 2 | a0001c0001t0002g0205a0001c0001t0019g0185 | 2 | HG02451.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.415-581A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77806394 | ||||||
chr1:77806632
|
A | G | 27 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(24): Show | 27 | HG01106.hp2 HG01884.hp2 HG01952.hp2 others(24): Show |
intron_variant | MODIFIER | c.415-343A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77806632 | ||||||
chr1:77806764
|
CTCT | C | 5 | a0001c0001t0001g0159a0001c0001t0002g0144a0001c0001t0004g0142others(2): Show | 5 | HG00438.hp2 NA18959.hp2 NA18962.hp1 others(2): Show |
intron_variant | MODIFIER | c.415-206_415-204del others(3): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | INFO_REALIGN_3_PRIME | chr1 | 77806764 | |||||
chr1:77806853
|
T | C | 2 | a0001c0001t0007g0247a0001c0001t0035g0275 | 2 | HG00639.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.415-122T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77806853 | ||||||
chr1:77806941
|
G | A | 1 | a0001c0001t0014g0273 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.415-34G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 4/15 | chr1 | 77806941 | ||||||
chr1:77807217
|
G | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 142 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.541+116G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77807217 | ||||||
chr1:77807307
|
G | A | 2 | a0001c0001t0002g0070a0001c0001t0002g0106 | 2 | HG01981.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.541+206G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77807307 | ||||||
chr1:77807307
|
G | T | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.541+206G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77807307 | ||||||
chr1:77807440
|
A | G | 1 | a0001c0001t0001g0207 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.541+339A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77807440 | ||||||
chr1:77807537
|
A | G | 1 | a0001c0001t0030g0270 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.541+436A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77807537 | ||||||
chr1:77807564
|
TGTTA | T | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.541+467_541+470del others(4): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr1 | 77807564 | |||||
chr1:77807855
|
C | T | 1 | a0001c0001t0007g0174 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.541+754C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77807855 | ||||||
chr1:77807874
|
A | T | 7 | a0001c0001t0003g0265a0001c0001t0006g0266a0001c0001t0007g0264others(4): Show | 8 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.541+773A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77807874 | ||||||
chr1:77808099
|
C | T | 3 | a0001c0001t0003g0254a0001c0001t0026g0253a0001c0001t0035g0275 | 3 | HG02897.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.541+998C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77808099 | ||||||
chr1:77808130
|
CT | C | 7 | a0001c0001t0001g0085a0001c0001t0002g0058a0001c0001t0003g0057others(4): Show | 7 | HG01891.hp1 HG02273.hp2 NA18985.hp1 others(4): Show |
intron_variant | MODIFIER | c.541+1047delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr1 | 77808130 | |||||
chr1:77808131
|
T | TC | 3 | a0001c0001t0011g0166a0001c0001t0011g0167a0001c0001t0012g0145 | 3 | HG02451.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.541+1030_541+1031i others(3): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77808131 | ||||||
chr1:77808132
|
T | C | 63 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(60): Show | 63 | HG00323.hp2 HG00438.hp2 HG01106.hp2 others(60): Show |
intron_variant | MODIFIER | c.541+1031T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77808132 | ||||||
chr1:77808133
|
T | C | 3 | a0001c0001t0011g0166a0001c0001t0011g0167a0001c0001t0012g0145 | 3 | HG02451.hp1 HG03209.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.541+1032T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77808133 | ||||||
chr1:77808905
|
G | C | 3 | a0001c0001t0003g0254a0001c0001t0026g0253a0001c0001t0035g0275 | 3 | HG02897.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.541+1804G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77808905 | ||||||
chr1:77809050
|
A | G | 1 | a0001c0001t0005g0179 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.541+1949A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77809050 | ||||||
chr1:77809107
|
A | AAAC | 31 | a0001c0001t0001g0159a0001c0001t0001g0206a0001c0001t0002g0043others(28): Show | 31 | HG00438.hp2 HG01891.hp1 HG02056.hp1 others(28): Show |
intron_variant | MODIFIER | c.541+2033_541+2035d others(5): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr1 | 77809107 | |||||
chr1:77809107
|
AAACAACA others(2): Show |
A | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.541+2027_541+2035d others(11): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr1 | 77809107 | |||||
chr1:77809617
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.541+2516T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77809617 | ||||||
chr1:77809672
|
G | T | 1 | a0001c0001t0002g0103 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.541+2571G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77809672 | ||||||
chr1:77809754
|
G | GT | 6 | a0001c0001t0002g0204a0001c0001t0002g0227a0001c0001t0003g0203others(3): Show | 6 | HG02074.hp2 HG02647.hp1 HG02738.hp1 others(3): Show |
intron_variant | MODIFIER | c.541+2669dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr1 | 77809754 | |||||
chr1:77809754
|
GT | G | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(132): Show | 136 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.541+2669delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr1 | 77809754 | |||||
chr1:77809759
|
T | G | 1 | a0001c0001t0003g0071 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.541+2658T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77809759 | ||||||
chr1:77809886
|
C | T | 7 | a0001c0001t0003g0265a0001c0001t0006g0266a0001c0001t0007g0264others(4): Show | 8 | HG02145.hp2 HG02615.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.541+2785C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77809886 | ||||||
chr1:77810522
|
G | A | 1 | a0001c0001t0032g0034 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.542-3212G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77810522 | ||||||
chr1:77810928
|
T | G | 1 | a0001c0001t0003g0041 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.542-2806T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77810928 | ||||||
chr1:77811060
|
A | G | 1 | a0001c0001t0002g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.542-2674A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811060 | ||||||
chr1:77811292
|
G | A | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0050others(50): Show | 53 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.542-2442G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811292 | ||||||
chr1:77811370
|
C | A | 1 | a0001c0001t0015g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.542-2364C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811370 | ||||||
chr1:77811466
|
T | C | 1 | a0001c0001t0001g0023 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.542-2268T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811466 | ||||||
chr1:77811564
|
C | T | 9 | a0001c0001t0001g0178a0001c0001t0002g0204a0001c0001t0008g0187others(6): Show | 9 | HG00438.hp1 HG00597.hp2 NA18939.hp2 others(6): Show |
intron_variant | MODIFIER | c.542-2170C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811564 | ||||||
chr1:77811682
|
C | T | 8 | a0001c0001t0011g0164a0001c0001t0011g0165a0001c0001t0011g0166others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.542-2052C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811682 | ||||||
chr1:77811695
|
C | T | 1 | a0001c0001t0003g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.542-2039C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811695 | ||||||
chr1:77811695
|
CA | C | 3 | a0001c0001t0002g0241a0001c0001t0017g0242a0001c0001t0017g0251 | 3 | HG03654.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.542-2038delA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811695 | ||||||
chr1:77811707
|
C | T | 1 | a0001c0001t0001g0099 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.542-2027C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811707 | ||||||
chr1:77811750
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.542-1984C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811750 | ||||||
chr1:77811751
|
G | A | 3 | a0001c0001t0002g0241a0001c0001t0017g0242a0001c0001t0017g0251 | 3 | HG03654.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.542-1983G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811751 | ||||||
chr1:77811810
|
C | T | 1 | a0001c0001t0001g0178 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.542-1924C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811810 | ||||||
chr1:77811852
|
C | T | 1 | a0001c0001t0003g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.542-1882C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811852 | ||||||
chr1:77811893
|
C | T | 2 | a0001c0001t0003g0209a0001c0001t0005g0218 | 2 | HG01346.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.542-1841C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811893 | ||||||
chr1:77811903
|
C | T | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.542-1831C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811903 | ||||||
chr1:77811910
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.542-1824T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811910 | ||||||
chr1:77812196
|
T | G | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.542-1538T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77812196 | ||||||
chr1:77812451
|
A | AAATAAAT others(9): Show |
5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0002g0086others(2): Show | 5 | NA18966.hp1 NA18975.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.542-1277_542-1262d others(18): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | INFO_REALIGN_3_PRIME | chr1 | 77812451 | |||||
chr1:77812603
|
T | G | 1 | a0001c0001t0004g0036 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.542-1131T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77812603 | ||||||
chr1:77812770
|
A | G | 1 | a0001c0001t0002g0098 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.542-964A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77812770 | ||||||
chr1:77813062
|
C | A | 2 | a0001c0001t0008g0187a0001c0001t0016g0219 | 2 | HG00597.hp2 NA18939.hp2 |
intron_variant | MODIFIER | c.542-672C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77813062 | ||||||
chr1:77813071
|
C | T | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.542-663C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77813071 | ||||||
chr1:77813271
|
C | T | 1 | a0001c0001t0001g0097 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.542-463C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77813271 | ||||||
chr1:77813326
|
A | G | 5 | a0001c0001t0001g0096a0001c0001t0001g0097a0001c0001t0001g0102others(2): Show | 5 | NA18939.hp1 NA18952.hp2 NA18985.hp1 others(2): Show |
intron_variant | MODIFIER | c.542-408A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77813326 | ||||||
chr1:77813362
|
A | G | 1 | a0001c0001t0013g0002 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.542-372A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77813362 | ||||||
chr1:77813397
|
A | G | 1 | a0001c0001t0007g0247 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.542-337A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77813397 | ||||||
chr1:77813400
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0026others(1): Show | 4 | NA18945.hp2 NA18968.hp2 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.542-334G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77813400 | ||||||
chr1:77813415
|
A | G | 1 | a0001c0001t0013g0002 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.542-319A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77813415 | ||||||
chr1:77813421
|
G | A | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.542-313G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77813421 | ||||||
chr1:77813914
|
A | G | 1 | a0001c0001t0015g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.675+47A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 6/15 | chr1 | 77813914 | ||||||
chr1:77813923
|
T | G | 1 | a0001c0001t0026g0253 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.675+56T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 6/15 | chr1 | 77813923 | ||||||
chr1:77813924
|
T | G | 1 | a0001c0001t0002g0124 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.675+57T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 6/15 | chr1 | 77813924 | ||||||
chr1:77813997
|
C | A | 2 | a0001c0001t0003g0037a0001c0001t0003g0038 | 2 | HG02976.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.675+130C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 6/15 | chr1 | 77813997 | ||||||
chr1:77814243
|
A | T | 1 | a0001c0001t0019g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.675+376A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 6/15 | chr1 | 77814243 | ||||||
chr1:77814620
|
T | G | 2 | a0001c0001t0007g0247a0001c0001t0035g0275 | 2 | HG00639.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.676-488T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 6/15 | chr1 | 77814620 | ||||||
chr1:77814628
|
C | T | 1 | a0001c0001t0001g0252 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.676-480C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 6/15 | chr1 | 77814628 | ||||||
chr1:77814688
|
A | G | 8 | a0001c0001t0011g0164a0001c0001t0011g0165a0001c0001t0011g0166others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.676-420A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 6/15 | chr1 | 77814688 | ||||||
chr1:77814763
|
C | G | 1 | a0001c0001t0009g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.676-345C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 6/15 | chr1 | 77814763 | ||||||
chr1:77815023
|
T | C | 2 | a0001c0001t0002g0072a0001c0001t0002g0083 | 2 | HG02300.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.676-85T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 6/15 | chr1 | 77815023 | ||||||
chr1:77815317
|
T | C | 144 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(141): Show | 145 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.799+86T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77815317 | ||||||
chr1:77815505
|
T | C | 1 | a0001c0001t0002g0098 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.799+274T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77815505 | ||||||
chr1:77815784
|
C | T | 3 | a0001c0001t0001g0214a0001c0001t0002g0213a0001c0001t0033g0212 | 3 | HG02886.hp1 HG03225.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.799+553C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77815784 | ||||||
chr1:77815820
|
A | C | 1 | a0001c0001t0009g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.799+589A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77815820 | ||||||
chr1:77815904
|
A | C | 1 | a0001c0001t0022g0105 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.799+673A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77815904 | ||||||
chr1:77815966
|
G | C | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.799+735G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77815966 | ||||||
chr1:77816009
|
T | A | 1 | a0001c0001t0024g0222 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.799+778T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77816009 | ||||||
chr1:77816056
|
A | G | 180 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(177): Show | 181 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.799+825A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77816056 | ||||||
chr1:77816132
|
T | C | 26 | a0001c0001t0001g0269a0001c0001t0002g0255a0001c0001t0002g0256others(23): Show | 27 | HG00639.hp2 HG01109.hp2 HG01168.hp2 others(24): Show |
intron_variant | MODIFIER | c.799+901T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77816132 | ||||||
chr1:77816308
|
A | G | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.799+1077A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77816308 | ||||||
chr1:77816453
|
T | G | 1 | a0001c0001t0004g0246 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.799+1222T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77816453 | ||||||
chr1:77816572
|
T | C | 3 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0002g0015 | 3 | HG03239.hp1 HG03704.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.799+1341T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77816572 | ||||||
chr1:77817136
|
T | G | 1 | a0001c0001t0002g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.799+1905T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77817136 | ||||||
chr1:77817298
|
G | A | 18 | a0001c0001t0001g0121a0001c0001t0001g0122a0001c0001t0001g0123others(15): Show | 18 | HG01070.hp1 HG01099.hp2 HG01109.hp1 others(15): Show |
intron_variant | MODIFIER | c.799+2067G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77817298 | ||||||
chr1:77817383
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.799+2152G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77817383 | ||||||
chr1:77817915
|
T | C | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.799+2684T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77817915 | ||||||
chr1:77817955
|
A | AT | 33 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(30): Show | 33 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(30): Show |
intron_variant | MODIFIER | c.799+2744dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77817955 | |||||
chr1:77817955
|
A | ATT | 53 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0023others(50): Show | 53 | HG00323.hp2 HG00597.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.799+2743_799+2744d others(4): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77817955 | |||||
chr1:77817955
|
A | T | 1 | a0001c0001t0001g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.799+2724A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77817955 | ||||||
chr1:77817955
|
AT | A | 64 | a0001c0001t0001g0159a0001c0001t0001g0269a0001c0001t0002g0241others(61): Show | 65 | HG00438.hp2 HG00735.hp1 HG01891.hp1 others(62): Show |
intron_variant | MODIFIER | c.799+2744delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77817955 | |||||
chr1:77817955
|
ATTTTTTT others(4): Show |
A | 1 | a0001c0001t0033g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.799+2734_799+2744d others(13): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77817955 | |||||
chr1:77818029
|
T | C | 143 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.799+2798T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77818029 | ||||||
chr1:77818036
|
G | A | 143 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(140): Show | 144 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.799+2805G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77818036 | ||||||
chr1:77818054
|
C | G | 3 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0002t0003g0272 | 3 | HG02572.hp2 HG02615.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.799+2823C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77818054 | ||||||
chr1:77818070
|
C | T | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.799+2839C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77818070 | ||||||
chr1:77818122
|
A | AT | 9 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0002g0229others(6): Show | 9 | HG02622.hp1 HG03209.hp2 HG03831.hp1 others(6): Show |
intron_variant | MODIFIER | c.799+2909dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77818122 | |||||
chr1:77818122
|
AT | A | 5 | a0001c0001t0001g0100a0001c0001t0002g0232a0001c0001t0003g0038others(2): Show | 5 | HG01168.hp1 HG02280.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.799+2909delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77818122 | |||||
chr1:77818344
|
A | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.799+3113A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77818344 | ||||||
chr1:77818526
|
A | G | 142 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.799+3295A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77818526 | ||||||
chr1:77818862
|
C | G | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.799+3631C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77818862 | ||||||
chr1:77819048
|
C | A | 1 | a0001c0002t0003g0272 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.799+3817C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77819048 | ||||||
chr1:77819080
|
C | CA | 24 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0091others(21): Show | 24 | HG00438.hp2 HG00609.hp1 HG01192.hp1 others(21): Show |
intron_variant | MODIFIER | c.799+3866dupA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77819080 | |||||
chr1:77819161
|
A | G | 5 | a0001c0001t0003g0009a0001c0001t0007g0010a0001c0001t0007g0011others(2): Show | 5 | HG02818.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.799+3930A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77819161 | ||||||
chr1:77819170
|
A | G | 1 | a0001c0001t0009g0268 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.799+3939A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77819170 | ||||||
chr1:77819388
|
A | G | 1 | a0001c0002t0003g0272 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.799+4157A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77819388 | ||||||
chr1:77819576
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.799+4345G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77819576 | ||||||
chr1:77819620
|
G | C | 1 | a0001c0001t0011g0167 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.799+4389G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77819620 | ||||||
chr1:77819791
|
A | C | 1 | a0001c0001t0002g0262 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.799+4560A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77819791 | ||||||
chr1:77819849
|
C | T | 277 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(274): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.799+4618C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77819849 | ||||||
chr1:77820106
|
CT | C | 18 | a0001c0001t0001g0024a0001c0001t0001g0051a0001c0001t0001g0085others(15): Show | 18 | HG00323.hp2 HG01099.hp1 HG01168.hp1 others(15): Show |
intron_variant | MODIFIER | c.799+4893delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77820106 | |||||
chr1:77820243
|
A | G | 1 | a0001c0001t0011g0166 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.799+5012A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77820243 | ||||||
chr1:77820320
|
T | C | 1 | a0001c0001t0001g0063 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.799+5089T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77820320 | ||||||
chr1:77820468
|
C | G | 3 | a0001c0001t0009g0003a0001c0001t0009g0268a0001c0001t0009g0276 | 4 | HG02145.hp2 HG02818.hp1 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.799+5237C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77820468 | ||||||
chr1:77820650
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.799+5419C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77820650 | ||||||
chr1:77820978
|
A | G | 1 | a0001c0001t0015g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.799+5747A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77820978 | ||||||
chr1:77820989
|
C | G | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.799+5758C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77820989 | ||||||
chr1:77821128
|
C | T | 3 | a0001c0001t0001g0135a0001c0001t0010g0136a0001c0001t0010g0235 | 3 | HG01255.hp2 HG01433.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.799+5897C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77821128 | ||||||
chr1:77821133
|
TA | T | 117 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(114): Show |
intron_variant | MODIFIER | c.799+5916delA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77821133 | |||||
chr1:77821390
|
A | AT | 14 | a0001c0001t0001g0024a0001c0001t0001g0178a0001c0001t0001g0228others(11): Show | 14 | HG00621.hp1 HG01891.hp2 HG01981.hp2 others(11): Show |
intron_variant | MODIFIER | c.799+6176dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77821390 | |||||
chr1:77821420
|
C | T | 1 | a0001c0001t0015g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.799+6189C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77821420 | ||||||
chr1:77821683
|
C | T | 1 | a0001c0001t0002g0227 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.799+6452C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77821683 | ||||||
chr1:77821766
|
T | G | 1 | a0001c0001t0002g0107 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.799+6535T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77821766 | ||||||
chr1:77821831
|
G | A | 1 | a0001c0001t0023g0195 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.799+6600G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77821831 | ||||||
chr1:77821908
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.799+6677T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77821908 | ||||||
chr1:77822087
|
A | G | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.799+6856A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77822087 | ||||||
chr1:77822123
|
C | T | 142 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(139): Show | 143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.799+6892C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77822123 | ||||||
chr1:77822131
|
TA | T | 30 | a0001c0001t0001g0177a0001c0001t0001g0178a0001c0001t0001g0193others(27): Show | 30 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(27): Show |
intron_variant | MODIFIER | c.799+6909delA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77822131 | |||||
chr1:77822196
|
T | TA | 116 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(113): Show | 116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): Show |
intron_variant | MODIFIER | c.799+6972dupA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77822196 | |||||
chr1:77822630
|
C | T | 29 | a0001c0001t0001g0018a0001c0001t0001g0021a0001c0001t0001g0022others(26): Show | 29 | HG01106.hp2 HG01884.hp2 HG01952.hp2 others(26): Show |
intron_variant | MODIFIER | c.799+7399C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77822630 | ||||||
chr1:77822835
|
G | GT | 20 | a0001c0001t0001g0030a0001c0001t0001g0033a0001c0001t0001g0045others(17): Show | 20 | HG01358.hp1 HG01358.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.799+7627dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77822835 | |||||
chr1:77822835
|
GT | G | 37 | a0001c0001t0001g0177a0001c0001t0001g0193a0001c0001t0001g0200others(34): Show | 38 | HG00323.hp1 HG00597.hp2 HG00609.hp1 others(35): Show |
intron_variant | MODIFIER | c.799+7627delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77822835 | |||||
chr1:77822840
|
T | G | 1 | a0001c0001t0002g0277 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.799+7609T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77822840 | ||||||
chr1:77822842
|
T | G | 2 | a0001c0001t0001g0244a0001c0001t0005g0181 | 2 | HG02523.hp1 HG02523.hp2 |
intron_variant | MODIFIER | c.799+7611T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77822842 | ||||||
chr1:77822858
|
T | C | 1 | a0001c0001t0002g0017 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.799+7627T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77822858 | ||||||
chr1:77822930
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0002g0098 | 2 | NA18977.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.799+7699C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77822930 | ||||||
chr1:77822967
|
C | T | 1 | a0001c0001t0007g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.799+7736C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77822967 | ||||||
chr1:77823024
|
G | T | 1 | a0001c0001t0003g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.799+7793G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823024 | ||||||
chr1:77823088
|
G | T | 1 | a0001c0001t0002g0015 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.799+7857G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823088 | ||||||
chr1:77823092
|
C | T | 2 | a0001c0001t0002g0056a0001c0001t0002g0081 | 2 | HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.799+7861C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823092 | ||||||
chr1:77823120
|
C | T | 1 | a0001c0001t0003g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.799+7889C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823120 | ||||||
chr1:77823136
|
C | T | 1 | a0001c0001t0003g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.799+7905C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823136 | ||||||
chr1:77823200
|
G | C | 5 | a0001c0001t0003g0009a0001c0001t0007g0010a0001c0001t0007g0011others(2): Show | 5 | HG02818.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.799+7969G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823200 | ||||||
chr1:77823252
|
T | C | 1 | a0001c0001t0003g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.799+8021T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823252 | ||||||
chr1:77823277
|
G | A | 6 | a0001c0001t0001g0269a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp2 HG02572.hp2 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.799+8046G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823277 | ||||||
chr1:77823278
|
T | C | 1 | a0001c0001t0014g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.799+8047T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823278 | ||||||
chr1:77823322
|
T | C | 3 | a0001c0001t0002g0241a0001c0001t0017g0242a0001c0001t0017g0251 | 3 | HG03654.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.799+8091T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823322 | ||||||
chr1:77823360
|
G | A | 25 | a0001c0001t0001g0269a0001c0001t0002g0255a0001c0001t0002g0256others(22): Show | 26 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(23): Show |
intron_variant | MODIFIER | c.799+8129G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823360 | ||||||
chr1:77823930
|
A | G | 1 | a0001c0001t0004g0160 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.799+8699A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823930 | ||||||
chr1:77823969
|
A | G | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.799+8738A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77823969 | ||||||
chr1:77824000
|
T | C | 1 | a0001c0001t0031g0016 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.799+8769T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77824000 | ||||||
chr1:77824556
|
T | C | 1 | a0001c0001t0004g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.799+9325T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77824556 | ||||||
chr1:77824680
|
G | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.799+9449G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77824680 | ||||||
chr1:77824844
|
A | G | 3 | a0001c0001t0003g0254a0001c0001t0026g0253a0001c0001t0035g0275 | 3 | HG02897.hp2 HG03486.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.799+9613A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77824844 | ||||||
chr1:77824983
|
C | CT | 99 | a0001c0001t0001g0008a0001c0001t0001g0014a0001c0001t0001g0018others(96): Show | 99 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(96): Show |
intron_variant | MODIFIER | c.799+9775dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77824983 | |||||
chr1:77824983
|
C | CTT | 12 | a0001c0001t0001g0001a0001c0001t0001g0047a0001c0001t0002g0044others(9): Show | 12 | HG01099.hp1 HG01257.hp2 HG01952.hp2 others(9): Show |
intron_variant | MODIFIER | c.799+9774_799+9775d others(4): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77824983 | |||||
chr1:77824983
|
CT | C | 7 | a0001c0001t0001g0244a0001c0001t0001g0249a0001c0001t0004g0036others(4): Show | 7 | HG02451.hp1 HG02451.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.799+9775delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77824983 | |||||
chr1:77824983
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0001t0001g0051a0001c0001t0002g0052 | 2 | HG00323.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.799+9766_799+9775d others(12): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77824983 | |||||
chr1:77824983
|
CTTTTTTT others(4): Show |
C | 16 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(13): Show | 17 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(14): Show |
intron_variant | MODIFIER | c.799+9765_799+9775d others(13): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77824983 | |||||
chr1:77825074
|
C | T | 1 | a0001c0001t0003g0071 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.799+9843C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77825074 | ||||||
chr1:77825475
|
A | G | 1 | a0001c0001t0002g0015 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.799+10244A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77825475 | ||||||
chr1:77825476
|
T | C | 1 | a0001c0001t0036g0211 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.799+10245T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77825476 | ||||||
chr1:77825719
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.799+10488A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77825719 | ||||||
chr1:77825752
|
C | CT | 8 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0099others(5): Show | 8 | HG01884.hp1 HG02055.hp2 HG02145.hp1 others(5): Show |
intron_variant | MODIFIER | c.799+10530dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77825752 | |||||
chr1:77826440
|
G | A | 2 | a0001c0001t0001g0099a0001c0001t0001g0110 | 2 | HG02055.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.799+11209G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77826440 | ||||||
chr1:77826637
|
A | T | 5 | a0001c0001t0001g0045a0001c0001t0001g0047a0001c0001t0001g0049others(2): Show | 5 | HG01952.hp2 HG02080.hp2 HG02132.hp2 others(2): Show |
intron_variant | MODIFIER | c.799+11406A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77826637 | ||||||
chr1:77826828
|
G | A | 37 | a0001c0001t0001g0159a0001c0001t0002g0144a0001c0001t0004g0036others(34): Show | 37 | HG00438.hp2 HG01891.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.799+11597G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77826828 | ||||||
chr1:77826949
|
C | T | 1 | a0001c0001t0003g0180 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.799+11718C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77826949 | ||||||
chr1:77826950
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.799+11719G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77826950 | ||||||
chr1:77827038
|
C | G | 1 | a0001c0001t0001g0236 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.799+11807C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827038 | ||||||
chr1:77827043
|
G | A | 1 | a0001c0001t0001g0207 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.799+11812G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827043 | ||||||
chr1:77827047
|
T | C | 3 | a0001c0001t0002g0241a0001c0001t0017g0242a0001c0001t0017g0251 | 3 | HG03654.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.799+11816T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827047 | ||||||
chr1:77827085
|
G | A | 1 | a0001c0001t0002g0119 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.799+11854G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827085 | ||||||
chr1:77827140
|
G | A | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.799+11909G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827140 | ||||||
chr1:77827232
|
C | T | 1 | a0001c0001t0002g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.799+12001C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827232 | ||||||
chr1:77827233
|
G | A | 22 | a0001c0001t0001g0269a0001c0001t0002g0255a0001c0001t0002g0256others(19): Show | 23 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(20): Show |
intron_variant | MODIFIER | c.799+12002G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827233 | ||||||
chr1:77827380
|
G | T | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.799+12149G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827380 | ||||||
chr1:77827437
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.799+12206G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827437 | ||||||
chr1:77827595
|
A | T | 3 | a0001c0001t0007g0011a0001c0001t0007g0012a0001c0001t0007g0013 | 3 | HG02886.hp2 HG02922.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.799+12364A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827595 | ||||||
chr1:77827599
|
T | C | 1 | a0001c0001t0009g0276 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.799+12368T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827599 | ||||||
chr1:77827604
|
A | G | 1 | a0001c0001t0003g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.799+12373A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827604 | ||||||
chr1:77827615
|
A | T | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.799+12384A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827615 | ||||||
chr1:77827633
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.799+12402A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827633 | ||||||
chr1:77827733
|
T | C | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.799+12502T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827733 | ||||||
chr1:77827757
|
T | G | 1 | a0001c0001t0025g0194 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.799+12526T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827757 | ||||||
chr1:77827816
|
G | A | 1 | a0001c0001t0002g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.799+12585G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77827816 | ||||||
chr1:77828057
|
T | TATAA | 3 | a0001c0001t0001g0207a0001c0001t0007g0247a0001c0001t0035g0275 | 3 | HG00639.hp2 HG03490.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.799+12848_799+1285 others(8): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77828057 | |||||
chr1:77828196
|
G | A | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.799+12965G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77828196 | ||||||
chr1:77828301
|
C | T | 37 | a0001c0001t0001g0159a0001c0001t0002g0144a0001c0001t0004g0036others(34): Show | 37 | HG00438.hp2 HG01891.hp1 HG02055.hp1 others(34): Show |
intron_variant | MODIFIER | c.799+13070C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77828301 | ||||||
chr1:77828459
|
C | T | 1 | a0001c0001t0002g0058 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.799+13228C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77828459 | ||||||
chr1:77828502
|
A | G | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.799+13271A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77828502 | ||||||
chr1:77828599
|
G | A | 1 | a0001c0001t0007g0011 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.799+13368G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77828599 | ||||||
chr1:77829089
|
G | T | 1 | a0001c0001t0003g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.799+13858G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77829089 | ||||||
chr1:77829161
|
T | G | 1 | a0001c0001t0001g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.799+13930T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77829161 | ||||||
chr1:77829190
|
T | C | 1 | a0001c0001t0026g0253 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.799+13959T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77829190 | ||||||
chr1:77829198
|
T | A | 9 | a0001c0001t0001g0159a0001c0001t0002g0144a0001c0001t0004g0139others(6): Show | 9 | HG00438.hp2 HG02056.hp1 HG02080.hp1 others(6): Show |
intron_variant | MODIFIER | c.799+13967T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77829198 | ||||||
chr1:77829524
|
C | T | 2 | a0001c0001t0003g0254a0001c0001t0026g0253 | 2 | HG02897.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.800-13783C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77829524 | ||||||
chr1:77829631
|
G | A | 1 | a0001c0001t0025g0194 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.800-13676G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77829631 | ||||||
chr1:77829635
|
A | AT | 36 | a0001c0001t0001g0023a0001c0001t0001g0049a0001c0001t0001g0091others(33): Show | 36 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(33): Show |
intron_variant | MODIFIER | c.800-13665dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77829635 | |||||
chr1:77829791
|
A | G | 2 | a0001c0001t0001g0225a0001c0001t0002g0226 | 2 | NA18989.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.800-13516A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77829791 | ||||||
chr1:77829805
|
T | TTTTTAAT others(24): Show |
1 | a0001c0001t0002g0031 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.800-13487_800-1348 others(35): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77829805 | |||||
chr1:77829821
|
G | A | 29 | a0001c0001t0001g0060a0001c0001t0001g0207a0001c0001t0001g0208others(26): Show | 29 | HG00099.hp1 HG00597.hp1 HG00609.hp1 others(26): Show |
intron_variant | MODIFIER | c.800-13486G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77829821 | ||||||
chr1:77829881
|
C | G | 1 | a0001c0001t0003g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.800-13426C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77829881 | ||||||
chr1:77829943
|
T | G | 1 | a0001c0001t0001g0101 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.800-13364T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77829943 | ||||||
chr1:77830252
|
A | C | 10 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0002g0046others(7): Show | 10 | HG01884.hp2 HG02132.hp2 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.800-13055A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77830252 | ||||||
chr1:77830339
|
A | T | 1 | a0001c0001t0002g0069 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.800-12968A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77830339 | ||||||
chr1:77830407
|
G | A | 1 | a0001c0001t0024g0222 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.800-12900G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77830407 | ||||||
chr1:77830593
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.800-12714C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77830593 | ||||||
chr1:77830597
|
A | C | 269 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(266): Show | 271 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.800-12710A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77830597 | ||||||
chr1:77830712
|
A | G | 1 | a0001c0001t0006g0261 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.800-12595A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77830712 | ||||||
chr1:77830818
|
A | G | 1 | a0001c0001t0002g0081 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.800-12489A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77830818 | ||||||
chr1:77830965
|
T | C | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.800-12342T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77830965 | ||||||
chr1:77831009
|
C | T | 1 | a0001c0001t0005g0237 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.800-12298C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77831009 | ||||||
chr1:77831262
|
G | C | 1 | a0001c0001t0001g0050 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.800-12045G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77831262 | ||||||
chr1:77831417
|
A | G | 1 | a0001c0001t0004g0143 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.800-11890A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77831417 | ||||||
chr1:77831599
|
G | T | 1 | a0001c0001t0001g0100 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.800-11708G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77831599 | ||||||
chr1:77831676
|
T | G | 3 | a0001c0001t0001g0092a0001c0001t0001g0101a0001c0001t0001g0243 | 3 | HG02165.hp2 NA18945.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.800-11631T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77831676 | ||||||
chr1:77832096
|
A | G | 1 | a0001c0001t0002g0241 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.800-11211A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77832096 | ||||||
chr1:77832113
|
T | C | 1 | a0001c0001t0001g0018 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.800-11194T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77832113 | ||||||
chr1:77832515
|
C | G | 34 | a0001c0001t0004g0036a0001c0001t0004g0137a0001c0001t0004g0138others(31): Show | 34 | HG00438.hp2 HG02055.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.800-10792C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77832515 | ||||||
chr1:77832772
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.800-10535G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77832772 | ||||||
chr1:77833143
|
G | A | 8 | a0001c0001t0011g0164a0001c0001t0011g0165a0001c0001t0011g0166others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.800-10164G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77833143 | ||||||
chr1:77833635
|
C | G | 1 | a0001c0001t0010g0019 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.800-9672C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77833635 | ||||||
chr1:77833802
|
T | C | 1 | a0001c0001t0001g0207 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.800-9505T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77833802 | ||||||
chr1:77834001
|
A | G | 20 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(17): Show | 20 | HG00639.hp2 HG00735.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.800-9306A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77834001 | ||||||
chr1:77834042
|
G | A | 1 | a0001c0001t0005g0237 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.800-9265G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77834042 | ||||||
chr1:77834236
|
C | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.800-9071C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77834236 | ||||||
chr1:77834372
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.800-8935C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77834372 | ||||||
chr1:77834648
|
G | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.800-8659G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77834648 | ||||||
chr1:77834667
|
C | A | 19 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(16): Show | 19 | HG00735.hp1 HG01496.hp2 HG02735.hp1 others(16): Show |
intron_variant | MODIFIER | c.800-8640C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77834667 | ||||||
chr1:77834730
|
G | A | 6 | a0001c0001t0014g0035a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.800-8577G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77834730 | ||||||
chr1:77834760
|
C | T | 1 | a0001c0001t0005g0197 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.800-8547C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77834760 | ||||||
chr1:77834775
|
T | G | 1 | a0001c0001t0004g0141 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.800-8532T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77834775 | ||||||
chr1:77834930
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.800-8377G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77834930 | ||||||
chr1:77835350
|
G | A | 1 | a0001c0001t0003g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.800-7957G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77835350 | ||||||
chr1:77836037
|
A | G | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.800-7270A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77836037 | ||||||
chr1:77836245
|
A | G | 2 | a0001c0001t0004g0138a0001c0001t0004g0151 | 2 | NA18960.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.800-7062A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77836245 | ||||||
chr1:77836376
|
A | G | 1 | a0001c0001t0001g0239 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.800-6931A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77836376 | ||||||
chr1:77836380
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.800-6927A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77836380 | ||||||
chr1:77836548
|
T | C | 12 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(9): Show | 12 | HG00639.hp2 HG01109.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.800-6759T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77836548 | ||||||
chr1:77836664
|
A | G | 1 | a0001c0001t0008g0112 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.800-6643A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77836664 | ||||||
chr1:77836812
|
T | A | 1 | a0001c0001t0015g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.800-6495T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77836812 | ||||||
chr1:77836813
|
A | T | 13 | a0001c0001t0001g0049a0001c0001t0002g0255a0001c0001t0002g0256others(10): Show | 13 | HG00639.hp2 HG01109.hp2 HG01168.hp2 others(10): Show |
intron_variant | MODIFIER | c.800-6494A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77836813 | ||||||
chr1:77836917
|
T | TC | 4 | a0001c0001t0009g0003a0001c0001t0009g0267a0001c0001t0009g0268others(1): Show | 5 | HG02145.hp2 HG02818.hp1 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.800-6387dupC | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77836917 | |||||
chr1:77837016
|
G | C | 2 | a0001c0001t0002g0056a0001c0001t0002g0081 | 2 | HG03942.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.800-6291G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77837016 | ||||||
chr1:77837143
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.800-6164A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77837143 | ||||||
chr1:77837370
|
G | T | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.800-5937G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77837370 | ||||||
chr1:77837557
|
T | C | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.800-5750T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77837557 | ||||||
chr1:77837672
|
G | T | 1 | a0001c0001t0003g0201 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.800-5635G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77837672 | ||||||
chr1:77837990
|
C | T | 12 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(9): Show | 12 | HG00639.hp2 HG01109.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.800-5317C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77837990 | ||||||
chr1:77838008
|
T | G | 1 | a0001c0001t0004g0036 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.800-5299T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77838008 | ||||||
chr1:77838089
|
A | G | 12 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(9): Show | 12 | HG00639.hp2 HG01109.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.800-5218A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77838089 | ||||||
chr1:77838216
|
C | G | 1 | a0001c0001t0005g0215 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.800-5091C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77838216 | ||||||
chr1:77838249
|
T | C | 1 | a0001c0001t0005g0215 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.800-5058T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77838249 | ||||||
chr1:77838325
|
C | CTTAT | 2 | a0001c0001t0008g0191a0001c0001t0008g0210 | 2 | NA19070.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.800-4960_800-4957d others(6): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77838325 | |||||
chr1:77838325
|
CTTAT | C | 9 | a0001c0001t0003g0116a0001c0001t0007g0011a0001c0001t0007g0012others(6): Show | 9 | HG01496.hp2 HG02886.hp2 HG02922.hp1 others(6): Show |
intron_variant | MODIFIER | c.800-4960_800-4957d others(6): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77838325 | |||||
chr1:77838348
|
A | ATTTATTA others(1): Show |
6 | a0001c0001t0014g0035a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.800-4957_800-4956i others(10): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77838348 | |||||
chr1:77838682
|
A | G | 1 | a0001c0001t0001g0224 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.800-4625A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77838682 | ||||||
chr1:77838875
|
A | T | 2 | a0001c0001t0003g0175a0001c0001t0003g0176 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.800-4432A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77838875 | ||||||
chr1:77839087
|
G | A | 1 | a0001c0001t0026g0253 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.800-4220G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77839087 | ||||||
chr1:77839195
|
C | A | 6 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.800-4112C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77839195 | ||||||
chr1:77839196
|
A | G | 11 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(8): Show | 12 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.800-4111A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77839196 | ||||||
chr1:77839212
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.800-4095C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77839212 | ||||||
chr1:77839242
|
C | G | 1 | a0001c0001t0002g0241 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.800-4065C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77839242 | ||||||
chr1:77839668
|
C | T | 4 | a0001c0001t0003g0265a0001c0001t0006g0266a0001c0001t0007g0247others(1): Show | 4 | HG00639.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.800-3639C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77839668 | ||||||
chr1:77839686
|
C | A | 232 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(229): Show | 234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): Show |
intron_variant | MODIFIER | c.800-3621C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77839686 | ||||||
chr1:77839694
|
A | G | 1 | a0001c0001t0017g0126 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.800-3613A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77839694 | ||||||
chr1:77839720
|
A | C | 11 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(8): Show | 12 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.800-3587A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77839720 | ||||||
chr1:77839807
|
A | G | 25 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0063others(22): Show | 25 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.800-3500A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77839807 | ||||||
chr1:77839932
|
C | A | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.800-3375C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77839932 | ||||||
chr1:77840013
|
G | T | 1 | a0001c0001t0002g0031 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.800-3294G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840013 | ||||||
chr1:77840098
|
T | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.800-3209T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840098 | ||||||
chr1:77840174
|
G | T | 69 | a0001c0001t0003g0009a0001c0001t0003g0037a0001c0001t0003g0038others(66): Show | 71 | HG00438.hp2 HG00735.hp1 HG01496.hp2 others(68): Show |
intron_variant | MODIFIER | c.800-3133G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840174 | ||||||
chr1:77840522
|
C | T | 1 | a0001c0001t0002g0089 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.800-2785C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840522 | ||||||
chr1:77840527
|
G | A | 1 | a0001c0001t0001g0244 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.800-2780G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840527 | ||||||
chr1:77840547
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.800-2760C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840547 | ||||||
chr1:77840632
|
C | G | 12 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(9): Show | 12 | HG00639.hp2 HG01109.hp2 HG01168.hp2 others(9): Show |
intron_variant | MODIFIER | c.800-2675C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840632 | ||||||
chr1:77840695
|
T | C | 1 | a0001c0001t0019g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.800-2612T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840695 | ||||||
chr1:77840696
|
C | T | 1 | a0001c0001t0019g0185 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.800-2611C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840696 | ||||||
chr1:77840767
|
G | A | 1 | a0001c0001t0002g0044 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.800-2540G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840767 | ||||||
chr1:77840823
|
TAATAA | T | 11 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(8): Show | 12 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.800-2470_800-2466d others(7): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77840823 | |||||
chr1:77840856
|
A | G | 11 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(8): Show | 12 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.800-2451A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840856 | ||||||
chr1:77840962
|
A | G | 1 | a0001c0001t0017g0251 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.800-2345A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840962 | ||||||
chr1:77841219
|
T | C | 2 | a0001c0001t0002g0144a0001c0003t0001g0114 | 2 | NA18939.hp1 NA19000.hp2 |
intron_variant | MODIFIER | c.800-2088T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77841219 | ||||||
chr1:77841544
|
A | G | 1 | a0001c0001t0001g0177 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.800-1763A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77841544 | ||||||
chr1:77841737
|
C | CTTTCT | 233 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(230): Show | 235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.800-1557_800-1553d others(7): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77841737 | |||||
chr1:77841772
|
C | A | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.800-1535C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77841772 | ||||||
chr1:77841948
|
A | AT | 7 | a0001c0001t0001g0088a0001c0001t0001g0193a0001c0001t0001g0269others(4): Show | 7 | HG02738.hp1 HG03516.hp2 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.800-1341dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | INFO_REALIGN_3_PRIME | chr1 | 77841948 | |||||
chr1:77841974
|
G | T | 1 | a0001c0001t0001g0122 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.800-1333G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77841974 | ||||||
chr1:77842022
|
A | G | 4 | a0001c0001t0017g0126a0001c0001t0017g0242a0001c0001t0017g0251others(1): Show | 4 | HG01496.hp2 HG03654.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.800-1285A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77842022 | ||||||
chr1:77842549
|
T | G | 151 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): Show |
intron_variant | MODIFIER | c.800-758T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77842549 | ||||||
chr1:77842975
|
A | G | 1 | a0001c0001t0015g0006 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.800-332A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77842975 | ||||||
chr1:77843022
|
A | G | 1 | a0001c0001t0008g0032 | 1 | NA19074.hp1 | intron_variant | MODIFIER | c.800-285A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77843022 | ||||||
chr1:77843175
|
C | A | 1 | a0001c0001t0005g0215 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.800-132C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77843175 | ||||||
chr1:77843583
|
A | G | 1 | a0001c0001t0001g0066 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.900+176A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77843583 | ||||||
chr1:77843637
|
A | T | 2 | a0001c0001t0003g0009a0001c0001t0007g0010 | 2 | HG02818.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.900+230A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77843637 | ||||||
chr1:77843857
|
A | G | 2 | a0001c0001t0001g0023a0001c0001t0001g0200 | 2 | NA18952.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.900+450A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77843857 | ||||||
chr1:77844100
|
T | A | 1 | a0001c0001t0001g0236 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.900+693T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844100 | ||||||
chr1:77844100
|
T | TAA | 7 | a0001c0001t0004g0141a0001c0001t0004g0147a0001c0001t0004g0153others(4): Show | 7 | NA18957.hp2 NA18982.hp1 NA18993.hp1 others(4): Show |
intron_variant | MODIFIER | c.900+706_900+707dup others(2): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844100 | |||||
chr1:77844100
|
TA | T | 6 | a0001c0001t0001g0060a0001c0001t0001g0090a0001c0001t0001g0243others(3): Show | 6 | HG00597.hp1 HG00738.hp1 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+707delA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844100 | |||||
chr1:77844100
|
TAA | T | 12 | a0001c0001t0001g0111a0001c0001t0001g0200a0001c0001t0003g0071others(9): Show | 12 | HG00597.hp2 HG01106.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.900+706_900+707del others(2): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844100 | |||||
chr1:77844109
|
AAAAAATA others(7): Show |
A | 2 | a0001c0001t0003g0038a0001c0001t0003g0171 | 2 | HG02809.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.900+704_900+717del others(14): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844109 | |||||
chr1:77844111
|
A | T | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.900+704A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844111 | ||||||
chr1:77844111
|
AAAATAT | A | 17 | a0001c0001t0003g0180a0001c0001t0003g0203a0001c0001t0003g0209others(14): Show | 17 | HG00323.hp1 HG00438.hp1 HG00609.hp1 others(14): Show |
intron_variant | MODIFIER | c.900+706_900+711del others(6): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844111 | |||||
chr1:77844112
|
AAAT | A | 28 | a0001c0001t0001g0021a0001c0001t0001g0050a0001c0001t0001g0061others(25): Show | 28 | HG00099.hp2 HG00609.hp2 HG01516.hp1 others(25): Show |
intron_variant | MODIFIER | c.900+707_900+709del others(3): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844112 | |||||
chr1:77844112
|
AAATATAT others(6): Show |
A | 4 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0268others(1): Show | 5 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+707_900+719del others(13): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844112 | |||||
chr1:77844113
|
A | AAAAAATA others(5): Show |
3 | a0001c0001t0004g0152a0001c0001t0004g0157a0001c0001t0004g0168 | 3 | HG02056.hp1 HG02080.hp1 HG02135.hp1 |
intron_variant | MODIFIER | c.900+707_900+708ins others(12): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844113 | |||||
chr1:77844113
|
A | AAAT | 6 | a0001c0001t0001g0214a0001c0001t0002g0052a0001c0001t0003g0009others(3): Show | 6 | HG02698.hp1 HG02818.hp2 HG02886.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+707_900+708ins others(3): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844113 | |||||
chr1:77844113
|
A | AAATATAT | 6 | a0001c0001t0001g0230a0001c0001t0001g0249a0001c0001t0003g0116others(3): Show | 6 | HG02886.hp2 HG02922.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+707_900+708ins others(7): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844113 | |||||
chr1:77844113
|
A | AAATATAT others(8): Show |
2 | a0001c0001t0003g0117a0001c0001t0003g0118 | 2 | HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.900+707_900+708ins others(15): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844113 | |||||
chr1:77844113
|
A | AATATATA others(3): Show |
2 | a0001c0001t0003g0173a0001c0001t0007g0264 | 2 | HG03130.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.900+722_900+731dup others(10): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844113 | |||||
chr1:77844113
|
A | T | 18 | a0001c0001t0001g0005a0001c0001t0001g0099a0001c0001t0001g0110others(15): Show | 19 | HG00741.hp1 HG01891.hp1 HG02055.hp2 others(16): Show |
intron_variant | MODIFIER | c.900+706A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844113 | ||||||
chr1:77844114
|
AT | A | 22 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0130others(19): Show | 22 | HG00621.hp1 HG00621.hp2 HG00735.hp2 others(19): Show |
intron_variant | MODIFIER | c.900+708delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844114 | ||||||
chr1:77844114
|
ATAT | A | 26 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0026others(23): Show | 26 | HG01106.hp2 HG02080.hp2 HG02083.hp1 others(23): Show |
intron_variant | MODIFIER | c.900+708_900+710del others(3): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844114 | ||||||
chr1:77844114
|
ATATAT | A | 34 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(31): Show | 34 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.900+708_900+712del others(5): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844114 | ||||||
chr1:77844115
|
T | A | 32 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0001g0047others(29): Show | 32 | HG01168.hp2 HG01257.hp1 HG01358.hp2 others(29): Show |
intron_variant | MODIFIER | c.900+708T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844115 | ||||||
chr1:77844117
|
T | A | 19 | a0001c0001t0001g0047a0001c0001t0001g0122a0001c0001t0001g0225others(16): Show | 19 | HG01169.hp2 HG01952.hp2 HG02055.hp1 others(16): Show |
intron_variant | MODIFIER | c.900+710T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844117 | ||||||
chr1:77844119
|
T | A | 20 | a0001c0001t0001g0018a0001c0001t0001g0024a0001c0001t0001g0026others(17): Show | 20 | HG02055.hp1 HG02083.hp1 HG02257.hp2 others(17): Show |
intron_variant | MODIFIER | c.900+712T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844119 | ||||||
chr1:77844121
|
T | A | 6 | a0001c0001t0001g0026a0001c0001t0001g0049a0001c0001t0001g0063others(3): Show | 6 | HG01346.hp2 HG02132.hp2 HG03453.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+714T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844121 | ||||||
chr1:77844121
|
TATATATA others(15): Show |
T | 1 | a0001c0001t0003g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.900+718_900+739del others(22): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844121 | |||||
chr1:77844123
|
T | G | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.900+716T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844123 | ||||||
chr1:77844123
|
TATATATA others(13): Show |
T | 8 | a0001c0001t0003g0037a0001c0001t0003g0248a0001c0001t0003g0263others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.900+720_900+739del others(20): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844123 | |||||
chr1:77844125
|
TATATATA others(11): Show |
T | 1 | a0001c0001t0009g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.900+722_900+739del others(18): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844125 | |||||
chr1:77844127
|
T | G | 5 | a0001c0001t0017g0126a0001c0001t0017g0242a0001c0001t0017g0251others(2): Show | 5 | HG01496.hp2 HG03579.hp1 HG03654.hp1 others(2): Show |
intron_variant | MODIFIER | c.900+720T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844127 | ||||||
chr1:77844131
|
T | G | 6 | a0001c0001t0017g0126a0001c0001t0017g0242a0001c0001t0017g0251others(3): Show | 6 | HG01496.hp2 HG02897.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+724T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844131 | ||||||
chr1:77844133
|
TATATAG | T | 8 | a0001c0001t0001g0177a0001c0001t0003g0084a0001c0001t0003g0201others(5): Show | 8 | HG01358.hp2 HG02273.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.900+730_900+735del others(6): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844133 | |||||
chr1:77844133
|
TATATAGA others(3): Show |
T | 1 | a0001c0001t0005g0197 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.900+730_900+739del others(10): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844133 | |||||
chr1:77844135
|
T | G | 8 | a0001c0001t0007g0247a0001c0001t0017g0126a0001c0001t0017g0242others(5): Show | 8 | HG00639.hp2 HG01496.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.900+728T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844135 | ||||||
chr1:77844135
|
TATAG | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0033a0001c0001t0005g0184 | 3 | HG02155.hp2 NA18959.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.900+756_900+759del others(4): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844135 | |||||
chr1:77844137
|
T | G | 1 | a0001c0001t0014g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.900+730T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844137 | ||||||
chr1:77844137
|
TAG | T | 12 | a0001c0001t0001g0023a0001c0001t0001g0047a0001c0001t0001g0122others(9): Show | 12 | HG01109.hp1 HG01192.hp1 HG01192.hp2 others(9): Show |
intron_variant | MODIFIER | c.900+732_900+733del others(2): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844137 | |||||
chr1:77844137
|
TAGATAG | T | 19 | a0001c0001t0001g0228a0001c0001t0002g0046a0001c0001t0003g0038others(16): Show | 20 | HG00621.hp1 HG00621.hp2 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.900+732_900+737del others(6): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77844137 | |||||
chr1:77844139
|
G | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(190): Show | 193 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(190): Show |
intron_variant | MODIFIER | c.900+732G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844139 | ||||||
chr1:77844143
|
G | T | 155 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(152): Show | 155 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(152): Show |
intron_variant | MODIFIER | c.900+736G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844143 | ||||||
chr1:77844147
|
G | T | 36 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0099others(33): Show | 36 | HG00621.hp1 HG00621.hp2 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.900+740G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844147 | ||||||
chr1:77844297
|
CAT | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.900+891_900+892del others(2): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844297 | ||||||
chr1:77844307
|
A | G | 1 | a0001c0001t0014g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.900+900A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844307 | ||||||
chr1:77844376
|
A | G | 2 | a0001c0001t0001g0051a0001c0001t0002g0052 | 2 | HG00323.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.900+969A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844376 | ||||||
chr1:77844390
|
A | T | 1 | a0001c0001t0004g0155 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.900+983A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844390 | ||||||
chr1:77844486
|
G | A | 1 | a0001c0001t0004g0157 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.900+1079G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844486 | ||||||
chr1:77844530
|
G | A | 1 | a0001c0001t0004g0146 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.900+1123G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844530 | ||||||
chr1:77844897
|
G | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.900+1490G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844897 | ||||||
chr1:77844990
|
A | G | 1 | a0001c0001t0003g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.900+1583A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844990 | ||||||
chr1:77845360
|
C | T | 14 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(11): Show | 14 | HG00735.hp1 HG02735.hp1 HG02818.hp2 others(11): Show |
intron_variant | MODIFIER | c.900+1953C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77845360 | ||||||
chr1:77845905
|
A | G | 1 | a0001c0001t0002g0262 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.900+2498A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77845905 | ||||||
chr1:77845937
|
G | T | 1 | a0001c0001t0017g0251 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.900+2530G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77845937 | ||||||
chr1:77845947
|
C | CT | 19 | a0001c0001t0001g0236a0001c0001t0003g0009a0001c0001t0003g0116others(16): Show | 19 | HG00735.hp1 HG01496.hp2 HG02735.hp1 others(16): Show |
intron_variant | MODIFIER | c.900+2557dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77845947 | |||||
chr1:77845991
|
A | T | 1 | a0001c0001t0003g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.900+2584A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77845991 | ||||||
chr1:77846039
|
A | G | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.900+2632A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77846039 | ||||||
chr1:77846234
|
G | A | 8 | a0001c0001t0011g0164a0001c0001t0011g0165a0001c0001t0011g0166others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.900+2827G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77846234 | ||||||
chr1:77846505
|
A | T | 2 | a0001c0001t0002g0031a0001c0001t0005g0237 | 2 | HG00738.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.900+3098A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77846505 | ||||||
chr1:77846582
|
C | T | 1 | a0001c0001t0001g0028 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.900+3175C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77846582 | ||||||
chr1:77846587
|
G | A | 1 | a0001c0001t0003g0057 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.900+3180G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77846587 | ||||||
chr1:77846673
|
A | C | 235 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(232): Show | 237 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.900+3266A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77846673 | ||||||
chr1:77846864
|
G | A | 1 | a0001c0001t0007g0247 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.900+3457G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77846864 | ||||||
chr1:77846889
|
A | G | 2 | a0001c0001t0014g0035a0001c0001t0035g0275 | 2 | HG01891.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.900+3482A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77846889 | ||||||
chr1:77847052
|
A | G | 1 | a0001c0001t0003g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.900+3645A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77847052 | ||||||
chr1:77847103
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.900+3696A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77847103 | ||||||
chr1:77847298
|
G | T | 1 | a0001c0001t0005g0237 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.900+3891G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77847298 | ||||||
chr1:77847479
|
AAAATACA others(23): Show |
A | 1 | a0001c0002t0003g0272 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.900+4087_900+4116d others(32): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77847479 | |||||
chr1:77847486
|
A | G | 6 | a0001c0001t0014g0035a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.900+4079A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77847486 | ||||||
chr1:77847495
|
G | A | 1 | a0001c0001t0009g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.900+4088G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77847495 | ||||||
chr1:77847809
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.900+4402G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77847809 | ||||||
chr1:77847927
|
G | A | 1 | a0001c0004t0001g0029 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.900+4520G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77847927 | ||||||
chr1:77847949
|
G | A | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.900+4542G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77847949 | ||||||
chr1:77848060
|
A | G | 1 | a0001c0001t0013g0216 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.900+4653A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77848060 | ||||||
chr1:77848080
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.900+4673G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77848080 | ||||||
chr1:77848115
|
G | A | 1 | a0001c0001t0014g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.900+4708G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77848115 | ||||||
chr1:77848395
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.900+4988A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77848395 | ||||||
chr1:77848410
|
G | T | 1 | a0001c0001t0002g0059 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.900+5003G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77848410 | ||||||
chr1:77848578
|
G | A | 277 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(274): Show | 279 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(276): Show |
intron_variant | MODIFIER | c.900+5171G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77848578 | ||||||
chr1:77848613
|
A | G | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.900+5206A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77848613 | ||||||
chr1:77848793
|
A | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0063others(24): Show | 27 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(24): Show |
intron_variant | MODIFIER | c.900+5386A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77848793 | ||||||
chr1:77848973
|
A | ATGTGGAT others(7): Show |
1 | a0001c0001t0013g0002 | 2 | HG03130.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.900+5569_900+5582d others(16): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77848973 | |||||
chr1:77848998
|
T | C | 3 | a0001c0001t0001g0225a0001c0001t0002g0226a0001c0001t0002g0277 | 3 | NA18989.hp1 NA18990.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.900+5591T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77848998 | ||||||
chr1:77849165
|
C | T | 1 | a0001c0001t0003g0082 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.900+5758C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77849165 | ||||||
chr1:77849220
|
C | T | 234 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.900+5813C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77849220 | ||||||
chr1:77849480
|
G | A | 26 | a0001c0001t0004g0036a0001c0001t0004g0137a0001c0001t0004g0138others(23): Show | 26 | HG00438.hp2 HG02056.hp1 HG02080.hp1 others(23): Show |
intron_variant | MODIFIER | c.900+6073G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77849480 | ||||||
chr1:77849526
|
C | T | 2 | a0001c0001t0004g0148a0001c0001t0004g0149 | 2 | NA18946.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.900+6119C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77849526 | ||||||
chr1:77850034
|
C | CA | 10 | a0001c0001t0001g0005a0001c0001t0001g0051a0001c0001t0001g0110others(7): Show | 10 | HG00323.hp2 HG01192.hp1 HG01496.hp2 others(7): Show |
intron_variant | MODIFIER | c.900+6645dupA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77850034 | |||||
chr1:77850035
|
A | T | 2 | a0001c0002t0003g0272a0001c0002t0005g0198 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.900+6628A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77850035 | ||||||
chr1:77850036
|
A | C | 2 | a0001c0002t0003g0272a0001c0002t0005g0198 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.900+6629A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77850036 | ||||||
chr1:77850106
|
A | T | 1 | a0001c0001t0033g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.900+6699A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77850106 | ||||||
chr1:77850854
|
C | G | 1 | a0001c0001t0003g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.900+7447C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77850854 | ||||||
chr1:77850862
|
CT | C | 154 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(151): Show | 154 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(151): Show |
intron_variant | MODIFIER | c.900+7466delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77850862 | |||||
chr1:77850866
|
T | C | 2 | a0001c0001t0005g0179a0001c0001t0014g0271 | 2 | HG00323.hp1 HG02615.hp2 |
intron_variant | MODIFIER | c.900+7459T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77850866 | ||||||
chr1:77851304
|
T | A | 1 | a0001c0001t0010g0019 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.901-7634T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77851304 | ||||||
chr1:77851448
|
C | T | 1 | a0001c0001t0007g0010 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.901-7490C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77851448 | ||||||
chr1:77851649
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0005 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.901-7289A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77851649 | ||||||
chr1:77851834
|
T | C | 34 | a0001c0001t0004g0036a0001c0001t0004g0137a0001c0001t0004g0138others(31): Show | 34 | HG00438.hp2 HG02055.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.901-7104T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77851834 | ||||||
chr1:77851876
|
C | CT | 117 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0014others(114): Show | 118 | HG00099.hp1 HG00621.hp1 HG00621.hp2 others(115): Show |
intron_variant | MODIFIER | c.901-7044dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77851876 | |||||
chr1:77851879
|
T | TC | 60 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0021others(57): Show | 60 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(57): Show |
intron_variant | MODIFIER | c.901-7059_901-7058i others(3): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77851879 | ||||||
chr1:77851931
|
T | C | 1 | a0001c0001t0001g0224 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.901-7007T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77851931 | ||||||
chr1:77852032
|
G | C | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.901-6906G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77852032 | ||||||
chr1:77852253
|
C | T | 1 | a0001c0001t0029g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.901-6685C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77852253 | ||||||
chr1:77852495
|
G | A | 241 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.901-6443G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77852495 | ||||||
chr1:77852934
|
G | A | 16 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG02735.hp1 others(13): Show |
intron_variant | MODIFIER | c.901-6004G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77852934 | ||||||
chr1:77852943
|
G | A | 11 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(8): Show | 12 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.901-5995G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77852943 | ||||||
chr1:77853195
|
A | G | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.901-5743A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77853195 | ||||||
chr1:77853222
|
C | T | 1 | a0001c0001t0009g0054 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.901-5716C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77853222 | ||||||
chr1:77853578
|
A | G | 1 | a0001c0001t0016g0190 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.901-5360A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77853578 | ||||||
chr1:77853701
|
A | G | 1 | a0001c0001t0026g0253 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.901-5237A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77853701 | ||||||
chr1:77853727
|
G | A | 11 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(8): Show | 12 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.901-5211G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77853727 | ||||||
chr1:77853765
|
G | A | 1 | a0001c0002t0005g0198 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.901-5173G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77853765 | ||||||
chr1:77853769
|
G | A | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.901-5169G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77853769 | ||||||
chr1:77853826
|
C | A | 11 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(8): Show | 12 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.901-5112C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77853826 | ||||||
chr1:77854095
|
C | T | 1 | a0001c0001t0017g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.901-4843C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77854095 | ||||||
chr1:77854096
|
G | A | 1 | a0001c0001t0007g0186 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.901-4842G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77854096 | ||||||
chr1:77854135
|
T | C | 1 | a0001c0001t0001g0214 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.901-4803T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77854135 | ||||||
chr1:77854257
|
A | T | 1 | a0001c0001t0003g0076 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.901-4681A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77854257 | ||||||
chr1:77854382
|
C | T | 26 | a0001c0001t0004g0036a0001c0001t0004g0137a0001c0001t0004g0138others(23): Show | 26 | HG00438.hp2 HG02056.hp1 HG02080.hp1 others(23): Show |
intron_variant | MODIFIER | c.901-4556C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77854382 | ||||||
chr1:77854409
|
A | AGATACCC others(4): Show |
1 | a0001c0001t0028g0158 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.901-4527_901-4517d others(13): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77854409 | |||||
chr1:77854544
|
T | C | 1 | a0001c0001t0029g0042 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.901-4394T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77854544 | ||||||
chr1:77854584
|
T | G | 4 | a0001c0001t0002g0073a0001c0001t0002g0077a0001c0001t0002g0078others(1): Show | 4 | HG00639.hp1 HG01070.hp2 HG01433.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-4354T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77854584 | ||||||
chr1:77854890
|
C | G | 2 | a0001c0001t0007g0247a0001c0001t0033g0212 | 2 | HG00639.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.901-4048C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77854890 | ||||||
chr1:77854954
|
C | T | 20 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(17): Show | 20 | HG00639.hp2 HG00735.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.901-3984C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77854954 | ||||||
chr1:77854984
|
A | G | 2 | a0001c0001t0003g0201a0001c0001t0005g0184 | 2 | NA18948.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.901-3954A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77854984 | ||||||
chr1:77855105
|
C | G | 1 | a0001c0001t0002g0098 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.901-3833C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77855105 | ||||||
chr1:77855455
|
G | A | 34 | a0001c0001t0004g0036a0001c0001t0004g0137a0001c0001t0004g0138others(31): Show | 34 | HG00438.hp2 HG02055.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.901-3483G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77855455 | ||||||
chr1:77855491
|
C | A | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.901-3447C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77855491 | ||||||
chr1:77855553
|
G | A | 1 | a0001c0001t0003g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.901-3385G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77855553 | ||||||
chr1:77855597
|
G | A | 34 | a0001c0001t0004g0036a0001c0001t0004g0137a0001c0001t0004g0138others(31): Show | 34 | HG00438.hp2 HG02055.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.901-3341G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77855597 | ||||||
chr1:77855701
|
G | A | 1 | a0001c0001t0001g0245 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.901-3237G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77855701 | ||||||
chr1:77855712
|
A | G | 1 | a0001c0001t0015g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.901-3226A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77855712 | ||||||
chr1:77855778
|
C | G | 4 | a0001c0001t0017g0126a0001c0001t0017g0242a0001c0001t0017g0251others(1): Show | 4 | HG01496.hp2 HG03654.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-3160C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77855778 | ||||||
chr1:77855834
|
G | A | 1 | a0001c0001t0002g0127 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.901-3104G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77855834 | ||||||
chr1:77855866
|
G | A | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.901-3072G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77855866 | ||||||
chr1:77856018
|
T | C | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.901-2920T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77856018 | ||||||
chr1:77856284
|
A | T | 20 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(17): Show | 20 | HG00639.hp2 HG00735.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.901-2654A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77856284 | ||||||
chr1:77856325
|
G | A | 6 | a0001c0001t0014g0035a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.901-2613G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77856325 | ||||||
chr1:77856417
|
T | C | 1 | a0001c0001t0028g0158 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.901-2521T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77856417 | ||||||
chr1:77856522
|
G | A | 1 | a0001c0001t0004g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.901-2416G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77856522 | ||||||
chr1:77856801
|
T | C | 1 | a0001c0001t0001g0177 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.901-2137T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77856801 | ||||||
chr1:77857095
|
C | A | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.901-1843C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77857095 | ||||||
chr1:77857140
|
G | A | 1 | a0001c0001t0024g0222 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.901-1798G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77857140 | ||||||
chr1:77857178
|
A | G | 1 | a0001c0001t0005g0218 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.901-1760A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77857178 | ||||||
chr1:77857221
|
C | T | 1 | a0001c0001t0002g0204 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.901-1717C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77857221 | ||||||
chr1:77857322
|
G | GT | 7 | a0001c0001t0007g0186a0001c0001t0014g0035a0001c0001t0014g0271others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.901-1603dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77857322 | |||||
chr1:77857322
|
GT | G | 163 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(160): Show | 163 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.901-1603delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77857322 | |||||
chr1:77857333
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.901-1605T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77857333 | ||||||
chr1:77857335
|
T | G | 1 | a0001c0001t0028g0158 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.901-1603T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77857335 | ||||||
chr1:77857336
|
G | T | 1 | a0001c0001t0028g0158 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.901-1602G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77857336 | ||||||
chr1:77857491
|
G | A | 3 | a0001c0001t0003g0265a0001c0001t0006g0266a0001c0001t0007g0264 | 3 | HG02615.hp1 HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.901-1447G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77857491 | ||||||
chr1:77857692
|
CTCTAGAA others(4): Show |
C | 16 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG02735.hp1 others(13): Show |
intron_variant | MODIFIER | c.901-1231_901-1221d others(13): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77857692 | |||||
chr1:77857705
|
C | T | 4 | a0001c0001t0017g0126a0001c0001t0017g0242a0001c0001t0017g0251others(1): Show | 4 | HG01496.hp2 HG03654.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-1233C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77857705 | ||||||
chr1:77857723
|
G | C | 1 | a0001c0001t0003g0172 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.901-1215G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77857723 | ||||||
chr1:77857726
|
G | GT | 42 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0063others(39): Show | 42 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(39): Show |
intron_variant | MODIFIER | c.901-1195dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77857726 | |||||
chr1:77857726
|
G | GTT | 16 | a0001c0001t0002g0083a0001c0001t0002g0106a0001c0001t0002g0255others(13): Show | 16 | HG01109.hp2 HG01257.hp1 HG01981.hp1 others(13): Show |
intron_variant | MODIFIER | c.901-1196_901-1195d others(4): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77857726 | |||||
chr1:77857726
|
G | T | 3 | a0001c0001t0003g0116a0001c0001t0003g0117a0001c0001t0003g0118 | 3 | HG02922.hp2 HG02976.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.901-1212G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77857726 | ||||||
chr1:77857897
|
T | A | 1 | a0001c0001t0028g0158 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.901-1041T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77857897 | ||||||
chr1:77858014
|
T | A | 1 | a0001c0001t0028g0158 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.901-924T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77858014 | ||||||
chr1:77858070
|
G | C | 16 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG02735.hp1 others(13): Show |
intron_variant | MODIFIER | c.901-868G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77858070 | ||||||
chr1:77858098
|
C | T | 20 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(17): Show | 20 | HG00639.hp2 HG00735.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.901-840C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77858098 | ||||||
chr1:77858261
|
C | T | 1 | a0001c0001t0002g0226 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.901-677C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77858261 | ||||||
chr1:77858262
|
G | A | 4 | a0001c0001t0017g0126a0001c0001t0017g0242a0001c0001t0017g0251others(1): Show | 4 | HG01496.hp2 HG03654.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.901-676G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77858262 | ||||||
chr1:77858344
|
C | CA | 17 | a0001c0001t0001g0177a0001c0001t0003g0009a0001c0001t0003g0116others(14): Show | 17 | HG00639.hp2 HG00735.hp1 HG02735.hp1 others(14): Show |
intron_variant | MODIFIER | c.901-581dupA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | INFO_REALIGN_3_PRIME | chr1 | 77858344 | |||||
chr1:77858708
|
T | C | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.901-230T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77858708 | ||||||
chr1:77858804
|
G | A | 5 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0002g0086others(2): Show | 5 | NA18966.hp1 NA18975.hp2 NA18982.hp2 others(2): Show |
intron_variant | MODIFIER | c.901-134G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77858804 | ||||||
chr1:77858834
|
G | A | 1 | a0001c0001t0005g0197 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.901-104G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77858834 | ||||||
chr1:77859103
|
T | C | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1019+47T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 9/15 | chr1 | 77859103 | ||||||
chr1:77859875
|
G | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1093-165G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 10/15 | chr1 | 77859875 | ||||||
chr1:77859937
|
T | A | 11 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(8): Show | 11 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1093-103T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 10/15 | chr1 | 77859937 | ||||||
chr1:77860730
|
A | AT | 4 | a0001c0001t0017g0126a0001c0001t0017g0242a0001c0001t0017g0251others(1): Show | 4 | HG01496.hp2 HG03654.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180-492dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 11/15 | INFO_REALIGN_3_PRIME | chr1 | 77860730 | |||||
chr1:77860757
|
C | T | 1 | a0001c0001t0005g0197 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1180-467C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 11/15 | chr1 | 77860757 | ||||||
chr1:77860873
|
A | G | 11 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(8): Show | 11 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1180-351A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 11/15 | chr1 | 77860873 | ||||||
chr1:77861427
|
G | T | 1 | a0001c0001t0002g0031 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1278+105G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77861427 | ||||||
chr1:77861529
|
G | C | 1 | a0001c0001t0002g0119 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1278+207G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77861529 | ||||||
chr1:77861605
|
G | A | 1 | a0001c0001t0020g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1278+283G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77861605 | ||||||
chr1:77861621
|
A | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(272): Show | 277 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.1278+299A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77861621 | ||||||
chr1:77861630
|
G | C | 16 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(13): Show | 18 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.1278+308G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77861630 | ||||||
chr1:77861698
|
T | G | 29 | a0001c0001t0004g0036a0001c0001t0004g0137a0001c0001t0004g0138others(26): Show | 29 | HG00438.hp2 HG02056.hp1 HG02080.hp1 others(26): Show |
intron_variant | MODIFIER | c.1278+376T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77861698 | ||||||
chr1:77861861
|
CCAGGCAT others(299): Show |
C | 9 | a0001c0001t0004g0036a0001c0001t0011g0164a0001c0001t0011g0165others(6): Show | 9 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1278+616_1278+921d others(2): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr1 | 77861861 | |||||
chr1:77861878
|
C | T | 1 | a0001c0001t0026g0253 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1278+556C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77861878 | ||||||
chr1:77862013
|
C | T | 4 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0268others(1): Show | 5 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.1278+691C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77862013 | ||||||
chr1:77862095
|
C | G | 11 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(8): Show | 12 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1278+773C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77862095 | ||||||
chr1:77862221
|
C | T | 1 | a0001c0001t0004g0137 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1278+899C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77862221 | ||||||
chr1:77862244
|
C | T | 1 | a0001c0001t0009g0267 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1278+922C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77862244 | ||||||
chr1:77862390
|
A | T | 240 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.1278+1068A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77862390 | ||||||
chr1:77862563
|
C | T | 1 | a0001c0001t0002g0119 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1278+1241C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77862563 | ||||||
chr1:77862567
|
A | T | 11 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(8): Show | 12 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1278+1245A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77862567 | ||||||
chr1:77862810
|
G | T | 4 | a0001c0001t0001g0087a0001c0001t0001g0088a0001c0001t0002g0086others(1): Show | 4 | NA18966.hp1 NA18975.hp2 NA18992.hp1 others(1): Show |
intron_variant | MODIFIER | c.1279-1084G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77862810 | ||||||
chr1:77862946
|
C | CA | 11 | a0001c0001t0001g0228a0001c0001t0001g0245a0001c0001t0002g0048others(8): Show | 11 | HG00621.hp1 HG01109.hp2 HG01168.hp2 others(8): Show |
intron_variant | MODIFIER | c.1279-933dupA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | INFO_REALIGN_3_PRIME | chr1 | 77862946 | |||||
chr1:77863118
|
T | G | 5 | a0001c0001t0014g0271a0001c0001t0014g0273a0001c0001t0019g0185others(2): Show | 5 | HG01891.hp2 HG02451.hp2 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.1279-776T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77863118 | ||||||
chr1:77863280
|
T | C | 11 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(8): Show | 12 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1279-614T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77863280 | ||||||
chr1:77863643
|
G | T | 1 | a0001c0001t0001g0130 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.1279-251G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77863643 | ||||||
chr1:77863665
|
A | T | 23 | a0001c0001t0001g0018a0001c0001t0001g0022a0001c0001t0001g0024others(20): Show | 23 | HG00621.hp1 HG01106.hp2 HG01952.hp2 others(20): Show |
intron_variant | MODIFIER | c.1279-229A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77863665 | ||||||
chr1:77863801
|
C | A | 1 | a0001c0001t0007g0247 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1279-93C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 12/15 | chr1 | 77863801 | ||||||
chr1:77864206
|
C | CA | 6 | a0001c0001t0002g0227a0001c0001t0002g0231a0001c0001t0005g0217others(3): Show | 6 | HG01109.hp2 HG02056.hp2 HG02074.hp2 others(3): Show |
intron_variant | MODIFIER | c.1413+192dupA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr1 | 77864206 | |||||
chr1:77864254
|
C | T | 1 | a0001c0001t0003g0080 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1413+226C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | chr1 | 77864254 | ||||||
chr1:77864400
|
G | A | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1413+372G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | chr1 | 77864400 | ||||||
chr1:77864403
|
C | T | 2 | a0001c0001t0002g0231a0001c0001t0003g0053 | 2 | HG00621.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1413+375C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | chr1 | 77864403 | ||||||
chr1:77864832
|
C | T | 6 | a0001c0001t0014g0035a0001c0001t0014g0271a0001c0001t0014g0273others(3): Show | 6 | HG01891.hp1 HG01891.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.1413+804C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | chr1 | 77864832 | ||||||
chr1:77865119
|
G | A | 234 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(231): Show | 236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): Show |
intron_variant | MODIFIER | c.1413+1091G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | chr1 | 77865119 | ||||||
chr1:77865192
|
T | A | 1 | a0001c0001t0014g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1414-1146T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | chr1 | 77865192 | ||||||
chr1:77865541
|
C | T | 43 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0025others(40): Show | 43 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1414-797C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | chr1 | 77865541 | ||||||
chr1:77865593
|
C | CA | 8 | a0001c0001t0011g0164a0001c0001t0011g0165a0001c0001t0011g0166others(5): Show | 8 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.1414-736dupA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr1 | 77865593 | |||||
chr1:77865794
|
CT | C | 12 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(9): Show | 12 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1414-532delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr1 | 77865794 | |||||
chr1:77865911
|
TTTTG | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1414-411_1414-408d others(6): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | INFO_REALIGN_3_PRIME | chr1 | 77865911 | |||||
chr1:77866037
|
C | T | 1 | a0001c0001t0020g0274 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1414-301C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | chr1 | 77866037 | ||||||
chr1:77866166
|
C | T | 1 | a0001c0001t0003g0254 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1414-172C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | chr1 | 77866166 | ||||||
chr1:77866263
|
A | G | 3 | a0001c0001t0011g0164a0001c0001t0011g0165a0001c0001t0012g0163 | 3 | HG02055.hp1 HG02559.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1414-75A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 13/15 | chr1 | 77866263 | ||||||
chr1:77866685
|
AT | A | 98 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0063others(95): Show | 100 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.1467+312delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77866685 | |||||
chr1:77866685
|
ATT | A | 8 | a0001c0001t0002g0262a0001c0001t0004g0036a0001c0001t0004g0150others(5): Show | 8 | HG01257.hp1 HG01496.hp2 HG03654.hp1 others(5): Show |
intron_variant | MODIFIER | c.1467+311_1467+312d others(4): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77866685 | |||||
chr1:77866747
|
G | A | 2 | a0001c0001t0001g0001a0001c0001t0006g0001 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.1467+356G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77866747 | ||||||
chr1:77866890
|
G | A | 1 | a0001c0001t0010g0113 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1467+499G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77866890 | ||||||
chr1:77867239
|
A | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1467+848A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77867239 | ||||||
chr1:77867370
|
G | A | 1 | a0001c0001t0026g0253 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1467+979G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77867370 | ||||||
chr1:77867380
|
C | T | 3 | a0001c0001t0003g0265a0001c0001t0006g0266a0001c0001t0007g0264 | 3 | HG02615.hp1 HG02630.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1467+989C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77867380 | ||||||
chr1:77867587
|
C | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1467+1196C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77867587 | ||||||
chr1:77867628
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1467+1237C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77867628 | ||||||
chr1:77867794
|
T | G | 1 | a0001c0001t0007g0264 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1467+1403T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77867794 | ||||||
chr1:77867924
|
TTAA | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1467+1535_1467+153 others(7): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77867924 | |||||
chr1:77867947
|
C | T | 4 | a0001c0001t0017g0126a0001c0001t0017g0242a0001c0001t0017g0251others(1): Show | 4 | HG01496.hp2 HG03654.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+1556C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77867947 | ||||||
chr1:77868236
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1467+1845T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77868236 | ||||||
chr1:77868375
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1467+1984T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77868375 | ||||||
chr1:77868532
|
C | T | 2 | a0001c0001t0003g0175a0001c0001t0003g0176 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1467+2141C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77868532 | ||||||
chr1:77868570
|
A | G | 241 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(238): Show | 243 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(240): Show |
intron_variant | MODIFIER | c.1467+2179A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77868570 | ||||||
chr1:77868919
|
C | CT | 6 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1467+2539dupT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77868919 | |||||
chr1:77868930
|
T | A | 4 | a0001c0001t0001g0252a0001c0001t0013g0216a0001c0001t0014g0273others(1): Show | 4 | HG01891.hp2 HG02572.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+2539T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77868930 | ||||||
chr1:77868935
|
T | A | 4 | a0001c0001t0003g0265a0001c0001t0005g0215a0001c0001t0006g0266others(1): Show | 4 | HG02615.hp1 HG02630.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+2544T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77868935 | ||||||
chr1:77868940
|
A | T | 1 | a0001c0001t0027g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1467+2549A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77868940 | ||||||
chr1:77868940
|
ATTTT | A | 16 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG02735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1467+2558_1467+256 others(8): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77868940 | |||||
chr1:77868943
|
T | A | 1 | a0001c0001t0003g0263 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1467+2552T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77868943 | ||||||
chr1:77868944
|
T | A | 70 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0025others(67): Show | 71 | HG00099.hp2 HG00438.hp1 HG00597.hp1 others(68): Show |
intron_variant | MODIFIER | c.1467+2553T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77868944 | ||||||
chr1:77868958
|
T | A | 1 | a0001c0001t0005g0183 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1467+2567T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77868958 | ||||||
chr1:77868985
|
G | A | 4 | a0001c0001t0002g0046a0001c0001t0002g0231a0001c0001t0003g0053others(1): Show | 4 | HG00621.hp2 HG02056.hp2 HG02135.hp2 others(1): Show |
intron_variant | MODIFIER | c.1467+2594G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77868985 | ||||||
chr1:77869121
|
A | G | 1 | a0001c0001t0014g0035 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1467+2730A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869121 | ||||||
chr1:77869189
|
C | T | 1 | a0001c0001t0003g0209 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1467+2798C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869189 | ||||||
chr1:77869314
|
C | T | 1 | a0001c0001t0001g0243 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1467+2923C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869314 | ||||||
chr1:77869368
|
C | T | 8 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(5): Show | 8 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(5): Show |
intron_variant | MODIFIER | c.1467+2977C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869368 | ||||||
chr1:77869391
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1467+3000T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869391 | ||||||
chr1:77869397
|
T | C | 1 | a0001c0001t0002g0128 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1467+3006T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869397 | ||||||
chr1:77869451
|
C | T | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1467+3060C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869451 | ||||||
chr1:77869484
|
G | A | 1 | a0001c0001t0002g0043 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1467+3093G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869484 | ||||||
chr1:77869579
|
C | T | 3 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0007g0174 | 3 | HG00735.hp1 HG02735.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.1467+3188C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869579 | ||||||
chr1:77869580
|
C | G | 3 | a0001c0001t0015g0199a0001c0001t0023g0195a0001c0001t0025g0194 | 3 | HG02622.hp2 HG03139.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1467+3189C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869580 | ||||||
chr1:77869593
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1467+3202C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869593 | ||||||
chr1:77869594
|
G | A | 4 | a0001c0001t0017g0126a0001c0001t0017g0242a0001c0001t0017g0251others(1): Show | 4 | HG01496.hp2 HG03654.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1467+3203G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869594 | ||||||
chr1:77869603
|
G | T | 1 | a0001c0001t0027g0079 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1467+3212G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869603 | ||||||
chr1:77869637
|
A | AG | 26 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0063others(23): Show | 26 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1467+3250dupG | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77869637 | |||||
chr1:77869643
|
G | A | 1 | a0001c0001t0005g0218 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1467+3252G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869643 | ||||||
chr1:77869646
|
C | T | 1 | a0001c0001t0026g0253 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1467+3255C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869646 | ||||||
chr1:77869670
|
C | T | 5 | a0001c0001t0003g0009a0001c0001t0007g0010a0001c0001t0007g0011others(2): Show | 5 | HG02818.hp2 HG02886.hp2 HG02922.hp1 others(2): Show |
intron_variant | MODIFIER | c.1467+3279C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869670 | ||||||
chr1:77869683
|
C | T | 1 | a0001c0001t0004g0140 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.1467+3292C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869683 | ||||||
chr1:77869687
|
T | C | 240 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(237): Show | 242 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.1467+3296T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869687 | ||||||
chr1:77869691
|
C | T | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1467+3300C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869691 | ||||||
chr1:77869729
|
G | A | 4 | a0001c0001t0013g0002a0001c0001t0013g0196a0001c0001t0013g0216others(1): Show | 5 | HG02572.hp1 HG03130.hp2 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1468-3275G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869729 | ||||||
chr1:77869738
|
A | AC | 125 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0008others(122): Show | 125 | HG00099.hp2 HG00323.hp1 HG00438.hp1 others(122): Show |
intron_variant | MODIFIER | c.1468-3256dupC | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77869738 | |||||
chr1:77869738
|
A | ACC | 48 | a0001c0001t0001g0123a0001c0001t0001g0135a0001c0001t0002g0048others(45): Show | 48 | HG00597.hp2 HG00609.hp1 HG00738.hp2 others(45): Show |
intron_variant | MODIFIER | c.1468-3257_1468-325 others(6): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77869738 | |||||
chr1:77869738
|
A | ACCC | 26 | a0001c0001t0001g0252a0001c0001t0004g0036a0001c0001t0004g0138others(23): Show | 26 | HG00438.hp2 HG01255.hp1 HG02055.hp1 others(23): Show |
intron_variant | MODIFIER | c.1468-3258_1468-325 others(7): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77869738 | |||||
chr1:77869744
|
C | CG | 8 | a0001c0001t0003g0037a0001c0001t0003g0248a0001c0001t0003g0254others(5): Show | 9 | HG02109.hp2 HG02280.hp2 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1468-3260_1468-325 others(5): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869744 | ||||||
chr1:77869744
|
C | G | 1 | a0001c0001t0015g0007 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1468-3260C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869744 | ||||||
chr1:77869746
|
C | A | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1468-3258C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869746 | ||||||
chr1:77869748
|
C | T | 1 | a0001c0001t0015g0199 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1468-3256C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869748 | ||||||
chr1:77869770
|
GCTGGCCG others(219): Show |
G | 1 | a0001c0001t0005g0183 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.1468-3162_1468-293 others(4): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77869770 | |||||
chr1:77869872
|
CCCCACCT others(43): Show |
C | 3 | a0001c0001t0001g0208a0001c0001t0009g0054a0001c0001t0009g0268 | 3 | HG02109.hp1 HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1468-3082_1468-303 others(54): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77869872 | |||||
chr1:77869897
|
G | C | 3 | a0001c0001t0001g0091a0001c0001t0001g0093a0001c0001t0002g0095 | 3 | HG00609.hp2 NA18999.hp2 NA19066.hp2 |
intron_variant | MODIFIER | c.1468-3107G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77869897 | ||||||
chr1:77869989
|
TGGGGCGA others(120): Show |
T | 1 | a0001c0001t0001g0090 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1468-2955_1468-282 others(4): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77869989 | |||||
chr1:77870002
|
C | T | 5 | a0001c0001t0003g0071a0001c0001t0003g0076a0001c0001t0003g0080others(2): Show | 5 | HG00741.hp1 HG01106.hp1 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1468-3002C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870002 | ||||||
chr1:77870028
|
G | A | 3 | a0001c0001t0001g0051a0001c0001t0002g0048a0001c0001t0002g0052 | 3 | HG00323.hp2 HG02257.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1468-2976G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870028 | ||||||
chr1:77870048
|
G | A | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1468-2956G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870048 | ||||||
chr1:77870084
|
C | CGGGGGGC others(349): Show |
1 | a0001c0001t0003g0248 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1468-2797_1468-279 others(360): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77870084 | |||||
chr1:77870129
|
C | G | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1468-2875C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870129 | ||||||
chr1:77870139
|
GGCTCCTC others(123): Show |
G | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1468-2848_1468-271 others(4): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77870139 | |||||
chr1:77870167
|
G | A | 1 | a0001c0001t0003g0189 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1468-2837G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870167 | ||||||
chr1:77870195
|
G | A | 1 | a0001c0001t0026g0253 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1468-2809G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870195 | ||||||
chr1:77870208
|
G | A | 11 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0171others(8): Show | 12 | HG02109.hp2 HG02280.hp2 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.1468-2796G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870208 | ||||||
chr1:77870221
|
A | AC | 22 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0003g0071others(19): Show | 22 | HG00609.hp1 HG00738.hp2 HG01109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1468-2772dupC | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77870221 | |||||
chr1:77870221
|
AC | A | 162 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(160): Show |
intron_variant | MODIFIER | c.1468-2772delC | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77870221 | |||||
chr1:77870276
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0109 | 2 | HG02155.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.1468-2728C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870276 | ||||||
chr1:77870299
|
C | T | 11 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(8): Show | 11 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1468-2705C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870299 | ||||||
chr1:77870348
|
G | A | 11 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(8): Show | 11 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1468-2656G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870348 | ||||||
chr1:77870435
|
C | T | 9 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(6): Show | 9 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1468-2569C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870435 | ||||||
chr1:77870450
|
G | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(1): Show | 4 | NA18945.hp2 NA18968.hp1 NA18990.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-2554G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870450 | ||||||
chr1:77870488
|
C | T | 34 | a0001c0001t0004g0036a0001c0001t0004g0137a0001c0001t0004g0138others(31): Show | 34 | HG00438.hp2 HG02055.hp1 HG02056.hp1 others(31): Show |
intron_variant | MODIFIER | c.1468-2516C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870488 | ||||||
chr1:77870490
|
GCCGGGCA others(8): Show |
G | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1468-2511_1468-249 others(19): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77870490 | |||||
chr1:77870541
|
GCGCTCCT others(33): Show |
G | 1 | a0001c0001t0003g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1468-2454_1468-241 others(44): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77870541 | |||||
chr1:77870549
|
C | T | 1 | a0001c0001t0001g0230 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.1468-2455C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870549 | ||||||
chr1:77870572
|
C | T | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1468-2432C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870572 | ||||||
chr1:77870577
|
A | G | 16 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG02735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1468-2427A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870577 | ||||||
chr1:77870616
|
A | G | 1 | a0001c0001t0033g0212 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1468-2388A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870616 | ||||||
chr1:77870639
|
A | G | 1 | a0001c0001t0007g0264 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1468-2365A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870639 | ||||||
chr1:77870660
|
C | G | 20 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(17): Show | 20 | HG00639.hp2 HG00735.hp1 HG01496.hp2 others(17): Show |
intron_variant | MODIFIER | c.1468-2344C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870660 | ||||||
chr1:77870676
|
C | CG | 16 | a0001c0001t0001g0008a0001c0001t0001g0028a0001c0001t0001g0135others(13): Show | 16 | HG00735.hp1 HG00741.hp1 HG01109.hp2 others(13): Show |
intron_variant | MODIFIER | c.1468-2324dupG | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77870676 | |||||
chr1:77870742
|
G | A | 4 | a0001c0001t0017g0126a0001c0001t0017g0242a0001c0001t0017g0251others(1): Show | 4 | HG01496.hp2 HG03654.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-2262G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870742 | ||||||
chr1:77870839
|
C | G | 1 | a0001c0001t0003g0171 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1468-2165C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870839 | ||||||
chr1:77870843
|
A | C | 1 | a0001c0001t0026g0253 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1468-2161A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870843 | ||||||
chr1:77870919
|
CA | C | 207 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(204): Show | 209 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(206): Show |
intron_variant | MODIFIER | c.1468-2074delA | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77870919 | |||||
chr1:77870921
|
A | C | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1468-2083A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870921 | ||||||
chr1:77870946
|
C | T | 1 | a0001c0001t0006g0266 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1468-2058C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870946 | ||||||
chr1:77870952
|
G | A | 7 | a0001c0001t0001g0123a0001c0001t0001g0129a0001c0001t0001g0130others(4): Show | 7 | HG01070.hp1 HG01099.hp2 HG01255.hp2 others(4): Show |
intron_variant | MODIFIER | c.1468-2052G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870952 | ||||||
chr1:77870969
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1468-2035G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870969 | ||||||
chr1:77870970
|
C | G | 1 | a0001c0001t0001g0087 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.1468-2034C>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77870970 | ||||||
chr1:77871047
|
C | A | 4 | a0001c0001t0017g0126a0001c0001t0017g0242a0001c0001t0017g0251others(1): Show | 4 | HG01496.hp2 HG03654.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-1957C>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77871047 | ||||||
chr1:77871055
|
C | T | 1 | a0001c0001t0012g0170 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1468-1949C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77871055 | ||||||
chr1:77871085
|
C | T | 4 | a0001c0001t0017g0126a0001c0001t0017g0242a0001c0001t0017g0251others(1): Show | 4 | HG01496.hp2 HG03654.hp1 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.1468-1919C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77871085 | ||||||
chr1:77871091
|
A | G | 1 | a0001c0001t0002g0020 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1468-1913A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77871091 | ||||||
chr1:77871094
|
G | A | 1 | a0001c0001t0002g0020 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1468-1910G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77871094 | ||||||
chr1:77871094
|
G | GGGAGAGG others(4): Show |
1 | a0001c0001t0001g0085 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1468-1908_1468-190 others(15): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871094 | |||||
chr1:77871094
|
G | GGGGAGA | 5 | a0001c0001t0009g0003a0001c0001t0009g0054a0001c0001t0009g0267others(2): Show | 6 | HG02145.hp2 HG02818.hp1 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1468-1883_1468-187 others(10): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871094 | |||||
chr1:77871116
|
AGAGGGAG others(2): Show |
A | 5 | a0001c0001t0001g0066a0001c0001t0001g0206a0001c0001t0002g0241others(2): Show | 5 | HG02080.hp1 HG02559.hp1 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.1468-1877_1468-186 others(13): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871116 | |||||
chr1:77871122
|
A | G | 3 | a0001c0001t0017g0126a0001c0001t0017g0251a0001c0001t0034g0133 | 3 | HG01496.hp2 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1468-1882A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77871122 | ||||||
chr1:77871122
|
AGAG | A | 26 | a0001c0001t0001g0049a0001c0001t0001g0060a0001c0001t0001g0088others(23): Show | 26 | HG00597.hp1 HG00735.hp2 HG01070.hp1 others(23): Show |
intron_variant | MODIFIER | c.1468-1877_1468-187 others(7): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871122 | |||||
chr1:77871125
|
G | GGAGGGA | 38 | a0001c0001t0003g0009a0001c0001t0003g0071a0001c0001t0003g0076others(35): Show | 38 | HG00323.hp1 HG00438.hp1 HG00597.hp2 others(35): Show |
intron_variant | MODIFIER | c.1468-1867_1468-186 others(10): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGA | 49 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0014others(46): Show | 49 | HG00323.hp2 HG00609.hp2 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.1468-1878_1468-187 others(7): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGACG others(38): Show |
1 | a0001c0001t0003g0265 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1468-1878_1468-187 others(49): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGACG others(44): Show |
1 | a0001c0001t0007g0264 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1468-1878_1468-187 others(55): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(5): Show |
1 | a0001c0001t0004g0141 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1468-1878_1468-187 others(16): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(5): Show |
28 | a0001c0001t0003g0037a0001c0001t0003g0038a0001c0001t0003g0116others(25): Show | 29 | HG00639.hp2 HG00735.hp1 HG01891.hp2 others(26): Show |
intron_variant | MODIFIER | c.1468-1878_1468-187 others(16): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(2): Show |
40 | a0001c0001t0001g0001a0001c0001t0001g0018a0001c0001t0001g0021others(37): Show | 40 | HG00099.hp2 HG00738.hp1 HG01070.hp2 others(37): Show |
intron_variant | MODIFIER | c.1468-1878_1468-187 others(13): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(11): Show |
32 | a0001c0001t0004g0036a0001c0001t0004g0137a0001c0001t0004g0138others(29): Show | 32 | HG00438.hp2 HG02055.hp1 HG02056.hp1 others(29): Show |
intron_variant | MODIFIER | c.1468-1878_1468-187 others(22): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(11): Show |
4 | a0001c0001t0003g0171a0001c0001t0003g0248a0001c0001t0003g0263others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.1468-1878_1468-187 others(22): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(8): Show |
22 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(19): Show | 22 | HG00099.hp1 HG01106.hp2 HG01496.hp1 others(19): Show |
intron_variant | MODIFIER | c.1468-1878_1468-187 others(19): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(14): Show |
6 | a0001c0001t0001g0109a0001c0001t0001g0228a0001c0001t0001g0245others(3): Show | 6 | HG00621.hp1 HG00741.hp2 HG02004.hp2 others(3): Show |
intron_variant | MODIFIER | c.1468-1878_1468-187 others(25): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(20): Show |
5 | a0001c0001t0001g0025a0001c0001t0002g0069a0001c0001t0002g0073others(2): Show | 5 | HG00639.hp1 HG01358.hp2 HG01433.hp1 others(2): Show |
intron_variant | MODIFIER | c.1468-1878_1468-187 others(31): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(68): Show |
1 | a0001c0001t0002g0257 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1468-1878_1468-187 others(79): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(92): Show |
1 | a0001c0001t0006g0266 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1468-1878_1468-187 others(103): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(146): Show |
2 | a0001c0001t0002g0262a0001c0001t0006g0259 | 2 | HG01109.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1468-1878_1468-187 others(157): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(152): Show |
3 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0018g0260 | 3 | HG01168.hp2 HG02300.hp2 HG02622.hp1 |
intron_variant | MODIFIER | c.1468-1878_1468-187 others(163): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(164): Show |
1 | a0001c0001t0001g0008 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1468-1878_1468-187 others(175): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGAGAGG others(176): Show |
1 | a0001c0001t0002g0258 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1468-1878_1468-187 others(187): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGGGAGA others(88): Show |
1 | a0001c0001t0017g0251 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1468-1878_1468-187 others(99): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGGGAGG others(58): Show |
1 | a0001c0001t0017g0126 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1468-1878_1468-187 others(69): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGGGAGG others(64): Show |
1 | a0001c0001t0034g0133 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1468-1878_1468-187 others(75): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871125
|
G | GGGGGAGG others(76): Show |
1 | a0001c0001t0017g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1468-1878_1468-187 others(87): Show |
MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871125 | |||||
chr1:77871139
|
A | G | 1 | a0001c0001t0017g0242 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1468-1865A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77871139 | ||||||
chr1:77871225
|
G | A | 1 | a0001c0001t0003g0009 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1468-1779G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77871225 | ||||||
chr1:77871375
|
G | A | 2 | a0001c0001t0003g0201a0001c0001t0005g0184 | 2 | NA18948.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.1468-1629G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77871375 | ||||||
chr1:77871913
|
T | C | 2 | a0001c0001t0003g0265a0001c0001t0007g0264 | 2 | HG02615.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1468-1091T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77871913 | ||||||
chr1:77871975
|
CT | C | 35 | a0001c0001t0001g0045a0001c0001t0004g0036a0001c0001t0004g0137others(32): Show | 35 | HG00438.hp2 HG02055.hp1 HG02056.hp1 others(32): Show |
intron_variant | MODIFIER | c.1468-1019delT | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | INFO_REALIGN_3_PRIME | chr1 | 77871975 | |||||
chr1:77872118
|
C | T | 11 | a0001c0001t0001g0021a0001c0001t0001g0050a0001c0001t0001g0085others(8): Show | 11 | NA18939.hp1 NA18948.hp1 NA18952.hp2 others(8): Show |
intron_variant | MODIFIER | c.1468-886C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77872118 | ||||||
chr1:77872790
|
T | C | 3 | a0001c0001t0001g0238a0001c0001t0001g0240a0001c0001t0010g0113 | 3 | HG00099.hp2 HG00738.hp1 HG01516.hp1 |
intron_variant | MODIFIER | c.1468-214T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77872790 | ||||||
chr1:77872904
|
C | T | 3 | a0001c0001t0001g0177a0001c0001t0001g0206a0001c0001t0001g0224 | 3 | NA18941.hp1 NA18960.hp1 NA19001.hp2 |
intron_variant | MODIFIER | c.1468-100C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 14/15 | chr1 | 77872904 | ||||||
chr1:77873231
|
A | G | 1 | a0001c0001t0004g0160 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1584+111A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77873231 | ||||||
chr1:77873382
|
A | G | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1584+262A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77873382 | ||||||
chr1:77873570
|
G | A | 1 | a0001c0001t0006g0220 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1584+450G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77873570 | ||||||
chr1:77873687
|
G | A | 1 | a0001c0001t0002g0120 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1584+567G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77873687 | ||||||
chr1:77873796
|
A | T | 26 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0063others(23): Show | 26 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.1584+676A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77873796 | ||||||
chr1:77873969
|
G | T | 16 | a0001c0001t0003g0009a0001c0001t0003g0116a0001c0001t0003g0117others(13): Show | 16 | HG00639.hp2 HG00735.hp1 HG02735.hp1 others(13): Show |
intron_variant | MODIFIER | c.1584+849G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77873969 | ||||||
chr1:77874149
|
T | G | 1 | a0001c0001t0002g0229 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1585-697T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77874149 | ||||||
chr1:77874214
|
T | A | 1 | a0001c0001t0009g0276 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1585-632T>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77874214 | ||||||
chr1:77874214
|
T | C | 2 | a0001c0001t0004g0143a0001c0001t0004g0160 | 2 | NA18612.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1585-632T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77874214 | ||||||
chr1:77874354
|
A | T | 152 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 152 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(149): Show |
intron_variant | MODIFIER | c.1585-492A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77874354 | ||||||
chr1:77874446
|
A | G | 11 | a0001c0001t0002g0255a0001c0001t0002g0256a0001c0001t0002g0257others(8): Show | 11 | HG01109.hp2 HG01168.hp2 HG01257.hp1 others(8): Show |
intron_variant | MODIFIER | c.1585-400A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77874446 | ||||||
chr1:77874594
|
T | C | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1585-252T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77874594 | ||||||
chr1:77874760
|
G | C | 1 | a0001c0001t0035g0275 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1585-86G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77874760 |