Item | Value |
---|---|
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 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1800 | 276 | 72 | 44 | 111 | 10 | 37 | MIGA1_chr1_77774649_77884540 | MIGA1 | ATGTC others(1795): Show |
chr1 | 77774649 | 77884540 | ||
a0001c0002 | 0/0 | 1800 | 2 | 2 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | ATGTC others(1795): Show |
chr1 | 77774649 | 77884540 | ||
a0001c0003 | 0/0 | 1800 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | ATGTC others(1795): Show |
chr1 | 77774649 | 77884540 | ||
a0001c0004 | 0/0 | 1800 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | ATGTC others(1795): Show |
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 | CTTCT others(6382): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0002 | 0/1 | 6388 | 54 | 6 | 18 | 16 | 3 | 10 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6383): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0003 | 1/0 | 6382 | 29 | 14 | 5 | 4 | 0 | 5 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6377): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0004 | 0/0 | 6382 | 25 | 0 | 0 | 24 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6377): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0005 | 0/0 | 6381 | 13 | 0 | 3 | 7 | 1 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6376): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0006 | 0/0 | 6389 | 9 | 1 | 4 | 1 | 1 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6384): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0007 | 0/0 | 6383 | 8 | 5 | 1 | 0 | 0 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6378): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0008 | 0/0 | 6381 | 8 | 0 | 1 | 7 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6376): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0009 | 0/0 | 6381 | 6 | 6 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6376): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0010 | 0/0 | 6386 | 5 | 1 | 2 | 1 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6381): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0011 | 0/0 | 6382 | 4 | 4 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6377): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0012 | 0/0 | 6381 | 4 | 4 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6376): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0013 | 0/0 | 6383 | 4 | 4 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6378): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0014 | 0/0 | 6381 | 3 | 3 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6376): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0015 | 0/0 | 6388 | 3 | 3 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6383): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0016 | 0/0 | 6382 | 3 | 0 | 0 | 3 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6377): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0017 | 0/0 | 6382 | 3 | 0 | 1 | 0 | 0 | 2 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6377): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0018 | 0/0 | 6388 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6383): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0019 | 0/0 | 6381 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6376): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0020 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6377): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0021 | 0/0 | 6392 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6387): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0022 | 0/0 | 6387 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6382): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0023 | 0/0 | 6387 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6382): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0024 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6382): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0025 | 0/0 | 6386 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6381): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0026 | 0/0 | 6381 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6376): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0027 | 0/0 | 6388 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6383): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0028 | 0/0 | 6383 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6378): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0029 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6377): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0030 | 0/0 | 6381 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6376): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0031 | 0/0 | 6387 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6382): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0032 | 0/0 | 6382 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6377): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0033 | 0/0 | 6383 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6378): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0034 | 0/0 | 6383 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6378): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0035 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6377): Show |
chr1 | 77774649 | 77884540 |
a0001c0001t0036 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6377): Show |
chr1 | 77774649 | 77884540 |
a0001c0002t0003 | 0/0 | 6382 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6377): Show |
chr1 | 77774649 | 77884540 |
a0001c0002t0005 | 0/0 | 6381 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6376): Show |
chr1 | 77774649 | 77884540 |
a0001c0003t0001 | 0/0 | 6387 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6382): Show |
chr1 | 77774649 | 77884540 |
a0001c0004t0001 | 0/0 | 6387 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | CTTCT others(6382): Show |
chr1 | 77774649 | 77884540 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0019 | 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 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0034 | 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 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0086 | 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 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0095 | 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 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0121 | 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 |
a0001c0001t0001g0128 | 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 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 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 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0222 | 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 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0235 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0001g0246 | 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 |
a0001c0001t0001g0270 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0032 | 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 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0059 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0071 | 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 |
a0001c0001t0002g0075 | 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 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0090 | 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 |
a0001c0001t0002g0102 | 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 |
a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0002g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0118 | 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 |
a0001c0001t0002g0122 | 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 |
a0001c0001t0002g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0238 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0012 | 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 |
a0001c0001t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0109 | 1/0 | 1 | 0 | 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 |
a0001c0001t0003g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0177 | 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 |
a0001c0001t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0003g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | 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 |
a0001c0001t0004g0145 | 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 |
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 |
a0001c0001t0004g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 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 |
a0001c0001t0005g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0176 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0005g0234 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0002 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0068 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0006g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0001 | 0/0 | 2 | 2 | 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 |
a0001c0001t0007g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0007g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0009g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0009g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0009g0264 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0009g0265 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0009g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0010g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0010g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0010g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0010g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0011g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0011g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0011g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | 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 |
a0001c0001t0012g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0012g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0012g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0012g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0013g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0013g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0013g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0014g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0014g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0014g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0015g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0015g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0015g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0016g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0016g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0016g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0017g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0017g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0017g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0018g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0019g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0020g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0021g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0022g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0023g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0024g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0025g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0026g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0027g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0028g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0029g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0030g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0031g0017 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0032g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0033g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0034g0132 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0035g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0001t0036g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0002t0003g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0002t0005g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0003t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
a0001c0004t0001g0030 | 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 | g0065 | EUR | GBR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0237 | EUR | GBR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00323 | hp1 | a0001 | c0001 | t0005 | g0176 | EUR | FIN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0052 | EUR | FIN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00438 | hp1 | a0001 | c0001 | t0008 | g0201 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00438 | hp2 | a0001 | c0001 | t0004 | g0158 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0061 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00597 | hp2 | a0001 | c0001 | t0008 | g0184 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0177 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0054 | EAS | CHS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0078 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00639 | hp2 | a0001 | c0001 | t0007 | g0244 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0169 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00735 | hp2 | a0001 | c0001 | t0006 | g0231 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00738 | hp1 | a0001 | c0001 | t0010 | g0114 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0234 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00741 | hp1 | a0001 | c0001 | t0003 | g0081 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG00741 | hp2 | a0001 | c0001 | t0006 | g0069 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0075 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0122 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01106 | hp1 | a0001 | c0001 | t0003 | g0077 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01106 | hp2 | a0001 | c0001 | t0032 | g0035 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01109 | hp2 | a0001 | c0001 | t0006 | g0255 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0229 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0230 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01169 | hp2 | a0001 | c0001 | t0005 | g0040 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0119 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01192 | hp2 | a0001 | c0001 | t0002 | g0126 | AMR | PUR | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0041 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01255 | hp2 | a0001 | c0001 | t0010 | g0135 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01257 | hp1 | a0001 | c0001 | t0002 | g0259 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0118 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01346 | hp1 | a0001 | c0001 | t0003 | g0206 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01346 | hp2 | a0001 | c0001 | t0001 | g0066 | 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 | g0056 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01433 | hp1 | a0001 | c0001 | t0002 | g0074 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0134 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0108 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01496 | hp2 | a0001 | c0001 | t0017 | g0125 | AMR | CLM | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0235 | EUR | IBS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0070 | EUR | IBS | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01884 | hp2 | a0001 | c0001 | t0015 | g0009 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01891 | hp1 | a0001 | c0001 | t0014 | g0036 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01891 | hp2 | a0001 | c0001 | t0014 | g0268 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01952 | hp1 | a0001 | c0001 | t0008 | g0097 | 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 | g0107 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0124 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02004 | hp2 | a0001 | c0001 | t0006 | g0076 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02055 | hp1 | a0001 | c0001 | t0011 | g0160 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0150 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02074 | hp1 | a0001 | c0001 | t0005 | g0179 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0224 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02080 | hp1 | a0001 | c0001 | t0004 | g0165 | 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 | g0029 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0090 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02132 | hp1 | a0001 | c0001 | t0005 | g0214 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02135 | hp1 | a0001 | c0001 | t0004 | g0149 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02135 | hp2 | a0001 | c0001 | t0006 | g0217 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02145 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02145 | hp2 | a0001 | c0001 | t0009 | g0273 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | CDX | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | CDX | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02165 | hp1 | a0001 | c0001 | t0004 | g0155 | EAS | CDX | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0095 | 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 | g0167 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0071 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02273 | hp2 | a0001 | c0001 | t0003 | g0085 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02280 | hp2 | a0001 | c0001 | t0029 | g0043 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02300 | hp1 | a0001 | c0001 | t0002 | g0073 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02300 | hp2 | a0001 | c0001 | t0002 | g0252 | AMR | PEL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02451 | hp1 | a0001 | c0001 | t0012 | g0144 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02451 | hp2 | a0001 | c0001 | t0019 | g0182 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02523 | hp1 | a0001 | c0001 | t0005 | g0178 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | KHV | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02572 | hp1 | a0001 | c0001 | t0013 | g0213 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02572 | hp2 | a0001 | c0002 | t0003 | g0267 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02602 | hp2 | a0001 | c0001 | t0003 | g0083 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02615 | hp1 | a0001 | c0001 | t0003 | g0262 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02615 | hp2 | a0001 | c0001 | t0014 | g0266 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02622 | hp1 | a0001 | c0001 | t0018 | g0258 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02622 | hp2 | a0001 | c0001 | t0015 | g0194 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02630 | hp1 | a0001 | c0001 | t0002 | g0254 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0263 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02647 | hp1 | a0001 | c0001 | t0030 | g0271 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02647 | hp2 | a0001 | c0002 | t0005 | g0192 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02698 | hp1 | a0001 | c0004 | t0001 | g0030 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0049 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0171 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02735 | hp2 | a0001 | c0001 | t0010 | g0232 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02738 | hp1 | a0001 | c0001 | t0006 | g0257 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0032 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0121 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02809 | hp2 | a0001 | c0001 | t0003 | g0168 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02818 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02818 | hp2 | a0001 | c0001 | t0003 | g0012 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0211 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02886 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0173 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02895 | hp2 | a0001 | c0001 | t0010 | g0130 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02897 | hp1 | a0001 | c0001 | t0003 | g0172 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02897 | hp2 | a0001 | c0001 | t0026 | g0250 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02922 | hp1 | a0001 | c0001 | t0007 | g0014 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02922 | hp2 | a0001 | c0001 | t0003 | g0117 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02976 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02976 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0055 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03098 | hp2 | a0001 | c0001 | t0003 | g0039 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03130 | hp1 | a0001 | c0001 | t0007 | g0261 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03130 | hp2 | a0001 | c0001 | t0013 | g0005 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03139 | hp1 | a0001 | c0001 | t0012 | g0159 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03139 | hp2 | a0001 | c0001 | t0023 | g0188 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03209 | hp1 | a0001 | c0001 | t0011 | g0164 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03209 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0210 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03225 | hp2 | a0001 | c0001 | t0036 | g0207 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03239 | hp2 | a0001 | c0001 | t0003 | g0072 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03453 | hp1 | a0001 | c0001 | t0015 | g0010 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03453 | hp2 | a0001 | c0001 | t0007 | g0001 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0251 | 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 | g0204 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03492 | hp1 | a0001 | c0001 | t0003 | g0042 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03492 | hp2 | a0001 | c0001 | t0006 | g0002 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03516 | hp1 | a0001 | c0001 | t0011 | g0163 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0270 | AFR | ESN | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03540 | hp1 | a0001 | c0001 | t0013 | g0005 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03540 | hp2 | a0001 | c0001 | t0009 | g0265 | AFR | GWD | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03579 | hp1 | a0001 | c0001 | t0035 | g0272 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03579 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | MSL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03654 | hp1 | a0001 | c0001 | t0017 | g0239 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03669 | hp1 | a0001 | c0001 | t0027 | g0080 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0238 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03704 | hp2 | a0001 | c0001 | t0002 | g0016 | SAS | PJL | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0226 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03831 | hp2 | a0001 | c0001 | t0022 | g0106 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03927 | hp1 | a0001 | c0001 | t0003 | g0170 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0136 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0057 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0053 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04115 | hp1 | a0001 | c0001 | t0017 | g0248 | SAS | STU | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04115 | hp2 | a0001 | c0001 | t0005 | g0215 | SAS | STU | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0021 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04184 | hp2 | a0001 | c0001 | t0034 | g0132 | SAS | BEB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0084 | SAS | STU | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0183 | SAS | STU | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04228 | hp1 | a0001 | c0001 | t0003 | g0193 | SAS | STU | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0015 | SAS | STU | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18522 | hp1 | a0001 | c0001 | t0012 | g0161 | AFR | YRI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0127 | AFR | YRI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18612 | hp1 | a0001 | c0001 | t0005 | g0180 | EAS | CHB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18612 | hp2 | a0001 | c0001 | t0004 | g0157 | EAS | CHB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18906 | hp1 | a0001 | c0001 | t0013 | g0190 | AFR | YRI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18906 | hp2 | a0001 | c0001 | t0003 | g0003 | AFR | YRI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18939 | hp1 | a0001 | c0003 | t0001 | g0115 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18939 | hp2 | a0001 | c0001 | t0016 | g0216 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18946 | hp2 | a0001 | c0001 | t0004 | g0004 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18948 | hp2 | a0001 | c0001 | t0003 | g0196 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18957 | hp2 | a0001 | c0001 | t0004 | g0154 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18960 | hp2 | a0001 | c0001 | t0004 | g0148 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18962 | hp1 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18966 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0063 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18972 | hp2 | a0001 | c0001 | t0008 | g0113 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0142 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18975 | hp1 | a0001 | c0001 | t0004 | g0166 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18975 | hp2 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18982 | hp1 | a0001 | c0001 | t0004 | g0153 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0104 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0058 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0027 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18990 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0087 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0152 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18993 | hp2 | a0001 | c0001 | t0008 | g0247 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18999 | hp1 | a0001 | c0001 | t0016 | g0199 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0274 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19001 | hp1 | a0001 | c0001 | t0028 | g0151 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19004 | hp1 | a0001 | c0001 | t0005 | g0181 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19007 | hp1 | a0001 | c0001 | t0016 | g0198 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0018 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19009 | hp1 | a0001 | c0001 | t0004 | g0140 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0212 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19011 | hp1 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19043 | hp1 | a0001 | c0001 | t0020 | g0269 | AFR | LWK | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0013 | AFR | LWK | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0197 | 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 | g0139 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19062 | hp1 | a0001 | c0001 | t0010 | g0020 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0099 | 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 | g0088 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19065 | hp2 | a0001 | c0001 | t0004 | g0004 | 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 | g0098 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19070 | hp1 | a0001 | c0001 | t0008 | g0200 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19070 | hp2 | a0001 | c0001 | t0004 | g0146 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19072 | hp2 | a0001 | c0001 | t0004 | g0147 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19074 | hp1 | a0001 | c0001 | t0008 | g0033 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19074 | hp2 | a0001 | c0001 | t0004 | g0145 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19082 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19084 | hp1 | a0001 | c0001 | t0008 | g0208 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19088 | hp1 | a0001 | c0001 | t0024 | g0219 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0131 | AFR | YRI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0103 | AFR | YRI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20752 | hp1 | a0001 | c0001 | t0031 | g0017 | EUR | TSI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0091 | EUR | TSI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20805 | hp1 | a0001 | c0001 | t0006 | g0068 | EUR | TSI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0256 | EUR | TSI | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20905 | hp1 | a0001 | c0001 | t0005 | g0185 | SAS | GIH | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0082 | SAS | GIH | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02109 | hp2 | a0001 | c0001 | t0003 | g0260 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG02559 | hp2 | a0001 | c0001 | t0011 | g0162 | AFR | ACB | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG06807 | hp1 | a0001 | c0001 | t0009 | g0006 | AFR | USA | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
HG06807 | hp2 | a0001 | c0001 | t0025 | g0187 | AFR | USA | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20300 | hp1 | a0001 | c0001 | t0033 | g0209 | AFR | USA | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
NA20300 | hp2 | a0001 | c0001 | t0009 | g0264 | AFR | USA | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
homoSapiens | chm13v2 | a0001 | c0001 | t0002 | g0059 | REF | REF | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
homoSapiens | grch38p0 | a0001 | c0001 | t0003 | g0109 | REF | REF | MIGA1_chr1_77774649_77884540 | MIGA1 | chr1 | 77774649 | 77884540 |
view | 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 |
---|
view | 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 |
view | 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 | a0001c0001t0013 a0001c0001t0036 |
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 | a0001c0001t0017 a0001c0001t0034 |
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 | a0001c0001t0031 a0001c0001t0032 |
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 | a0001c0001t0008 a0001c0001t0016 |
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 | a0001c0001t0017 a0001c0001t0034 |
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 | a0001c0001t0004 a0001c0001t0028 |
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 | a0001c0001t0014 a0001c0001t0019 a0001c0001t0020 others(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 | a0001c0001t0004 a0001c0001t0011 a0001c0001t0012 others(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 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0020 others(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 | a0001c0001t0010 a0001c0001t0025 |
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 | a0001c0001t0001 a0001c0001t0022 a0001c0001t0023 others(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 | a0001c0001t0002 a0001c0001t0015 a0001c0001t0018 others(1): Show |
58 | HG00099.hp1 HG00639.hp1 HG01070.hp2 others(55): 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 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0009 others(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 | a0001c0001t0014 a0001c0001t0019 a0001c0001t0020 others(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 | a0001c0001t0015 a0001c0001t0023 a0001c0001t0025 |
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 |
view | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0002g0274 | 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 | a0001c0001t0009g0273 | 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 | a0001c0001t0001g0270 a0001c0001t0002g0252 a0001c0001t0002g0253 others(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 | a0001c0001t0035g0272 | 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 | a0001c0001t0001g0249 | 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 | a0001c0001t0017g0248 | 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 | a0001c0001t0008g0247 | 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 | a0001c0001t0035g0272 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0011 | 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 | a0001c0001t0003g0245 | 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 | 4 | a0001c0001t0003g0012 a0001c0001t0007g0001 a0001c0001t0007g0013 others(1): 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 | a0001c0001t0002g0274 | 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 | a0001c0001t0003g0260 | 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 | a0001c0001t0001g0015 a0001c0001t0002g0016 |
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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0003g0262 a0001c0001t0006g0263 a0001c0001t0007g0261 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0003g0262 a0001c0001t0006g0263 a0001c0001t0007g0261 others(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 | a0001c0001t0007g0244 | 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 | a0001c0001t0004g0243 | 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0001g0270 a0001c0001t0014g0036 a0001c0001t0014g0266 others(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 | a0001c0001t0003g0262 a0001c0001t0006g0263 a0001c0001t0007g0261 |
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 | a0001c0001t0004g0037 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0032g0035 | 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0031g0017 | 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 | a0001c0001t0002g0238 a0001c0001t0003g0260 a0001c0001t0017g0239 others(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 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
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 | a0001c0001t0003g0260 | 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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0005g0040 a0001c0001t0005g0041 |
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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(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 | a0001c0001t0002g0252 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0010g0232 | 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 | a0001c0001t0001g0270 a0001c0001t0002g0252 a0001c0001t0002g0253 others(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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0002g0229 a0001c0001t0002g0230 a0001c0001t0006g0231 |
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 | a0001c0001t0001g0270 a0001c0001t0002g0238 a0001c0001t0002g0252 others(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 | a0001c0001t0029g0043 | 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 | 159 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(156): 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 | a0001c0001t0015g0009 | 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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0050 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0218 a0001c0001t0001g0220 a0001c0001t0001g0221 others(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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0233 | 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 | 36 | a0001c0001t0001g0156 a0001c0001t0002g0143 a0001c0001t0004g0004 others(33): 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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0002g0252 | 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 | a0001c0001t0003g0245 | 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 | a0001c0001t0002g0018 | 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 | a0001c0001t0002g0238 a0001c0001t0017g0239 a0001c0001t0017g0248 |
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 | a0001c0001t0016g0216 | 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 | 63 | a0001c0001t0001g0034 a0001c0001t0001g0156 a0001c0001t0002g0119 others(60): 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 | a0001c0001t0001g0270 a0001c0001t0005g0215 a0001c0001t0014g0266 others(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 | a0001c0001t0003g0262 a0001c0001t0006g0263 a0001c0001t0007g0261 others(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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0001g0051 | 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 | a0001c0001t0001g0052 a0001c0001t0002g0053 a0001c0001t0002g0119 |
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 | a0001c0001t0001g0052 a0001c0001t0002g0053 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0001g0011 | 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 | a0001c0001t0003g0260 a0001c0001t0003g0262 a0001c0001t0006g0263 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0015g0010 | 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 | a0001c0001t0003g0054 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0001g0237 | 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 | 42 | a0001c0001t0001g0019 a0001c0001t0001g0045 a0001c0001t0001g0052 others(39): Show |
43 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(40): 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 | a0001c0001t0002g0119 a0001c0001t0002g0143 a0001c0001t0004g0136 others(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 | 104 | a0001c0001t0001g0116 a0001c0001t0001g0120 a0001c0001t0001g0121 others(101): 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 | a0001c0001t0003g0245 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0002g0118 a0001c0001t0003g0245 |
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 | 3 | a0001c0001t0003g0003 a0001c0001t0003g0117 a0001c0001t0012g0167 |
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 | 2 | a0001c0001t0007g0001 a0001c0001t0007g0014 |
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 | a0001c0001t0002g0238 a0001c0001t0017g0239 a0001c0001t0017g0248 |
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 | a0001c0001t0001g0121 a0001c0001t0001g0123 a0001c0001t0001g0128 others(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 | a0001c0001t0014g0266 a0001c0001t0014g0268 a0001c0001t0020g0269 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0049 a0001c0001t0030g0271 |
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 | 130 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(127): 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 | a0001c0001t0003g0262 a0001c0001t0006g0263 |
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 | a0001c0001t0002g0238 a0001c0001t0017g0239 a0001c0001t0017g0248 |
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 | a0001c0001t0001g0047 a0001c0001t0002g0044 a0001c0001t0002g0046 |
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 | a0001c0001t0002g0032 a0001c0001t0002g0119 a0001c0001t0008g0033 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0015 others(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 | 128 | a0001c0001t0001g0064 a0001c0001t0001g0066 a0001c0001t0001g0067 others(125): 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 | a0001c0001t0001g0270 a0001c0001t0002g0252 a0001c0001t0002g0253 others(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 | a0001c0001t0002g0238 a0001c0001t0017g0239 a0001c0001t0017g0248 |
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 | a0001c0001t0031g0017 | 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 | a0001c0001t0001g0067 a0001c0001t0009g0055 |
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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0003g0206 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0001g0220 a0001c0001t0001g0221 a0001c0001t0001g0222 others(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 | a0001c0001t0002g0226 | 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 | a0001c0001t0003g0177 a0001c0001t0005g0178 a0001c0001t0005g0179 |
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 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0003g0172 others(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 | a0001c0001t0001g0111 a0001c0001t0001g0112 a0001c0001t0001g0205 others(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 | a0001c0001t0001g0052 a0001c0001t0003g0245 a0001c0001t0004g0145 others(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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0002g0238 a0001c0001t0017g0239 a0001c0001t0017g0248 |
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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(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 | a0001c0001t0002g0070 a0001c0001t0006g0068 a0001c0001t0006g0069 others(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 | a0001c0001t0003g0260 | 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 | 2 | a0001c0001t0007g0001 a0001c0001t0007g0014 |
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 | a0001c0001t0019g0182 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0009g0265 | 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 | a0001c0001t0002g0238 a0001c0001t0017g0239 a0001c0001t0017g0248 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0050 others(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 | a0001c0001t0002g0071 | 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 | a0001c0001t0003g0177 | 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 | a0001c0001t0005g0214 | 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 | a0001c0001t0001g0052 a0001c0001t0003g0058 a0001c0001t0011g0160 others(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 | 97 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(94): 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 | a0001c0001t0003g0245 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0001g0052 a0001c0001t0001g0121 a0001c0001t0001g0246 others(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 | a0001c0001t0001g0134 a0001c0001t0010g0135 |
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 | a0001c0001t0003g0245 | 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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0004g0136 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0001g0116 | 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 | a0001c0001t0001g0022 | 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 | a0001c0001t0014g0266 | 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 | a0001c0001t0001g0067 a0001c0001t0009g0055 |
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 | a0001c0001t0003g0168 | 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 | a0001c0001t0002g0259 | 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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(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 | a0001c0001t0003g0206 a0001c0001t0005g0215 |
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 | a0001c0001t0001g0023 | 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 | a0001c0001t0003g0245 | 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 | a0001c0001t0011g0160 a0001c0001t0011g0162 a0001c0001t0012g0159 others(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 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0050 others(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 | a0001c0001t0001g0270 a0001c0001t0002g0252 a0001c0001t0002g0253 others(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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | 160 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(157): 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0235 a0001c0001t0001g0236 a0001c0001t0001g0237 others(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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0001g0133 | 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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | 10 | a0001c0001t0003g0012 a0001c0001t0003g0169 a0001c0001t0003g0170 others(7): 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 | a0001c0001t0003g0206 | 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 | a0001c0001t0001g0002 a0001c0001t0006g0002 |
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 | a0001c0001t0035g0272 | 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 | a0001c0001t0011g0160 a0001c0001t0011g0162 a0001c0001t0012g0159 others(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 | a0001c0001t0001g0110 a0001c0001t0002g0063 |
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 | a0001c0001t0020g0269 | 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 | 54 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0051 others(51): Show |
55 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(52): 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 | a0001c0001t0002g0238 a0001c0001t0017g0239 a0001c0001t0017g0248 |
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 | a0001c0001t0003g0245 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0003g0168 | 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 | a0001c0001t0004g0158 | 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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0004g0142 a0001c0001t0004g0157 |
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 | a0001c0001t0004g0136 | 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 | a0001c0001t0003g0251 a0001c0001t0007g0244 a0001c0001t0026g0250 others(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 | a0001c0001t0001g0156 a0001c0001t0001g0203 a0001c0001t0002g0143 others(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 | 139 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): 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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0015 others(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 | a0001c0001t0010g0020 | 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 | a0001c0001t0009g0006 | 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 | a0001c0001t0001g0270 a0001c0001t0007g0244 a0001c0001t0014g0266 others(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 | a0001c0001t0006g0068 a0001c0001t0006g0069 |
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 | a0001c0001t0003g0245 | 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 | a0001c0001t0003g0206 a0001c0001t0005g0215 |
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 | 140 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(137): Show |
142 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(139): 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 | a0001c0001t0003g0245 | 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 | 244 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(241): Show |
249 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(246): 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 | a0001c0001t0001g0110 a0001c0001t0002g0063 a0001c0001t0002g0105 others(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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0002g0119 | 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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0001g0270 a0001c0001t0002g0252 a0001c0001t0002g0253 others(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 | a0001c0001t0014g0268 | 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 | a0001c0001t0003g0245 | 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 | a0001c0001t0002g0202 a0001c0001t0019g0182 |
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 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | a0001c0001t0001g0156 a0001c0001t0002g0143 a0001c0001t0004g0141 others(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 | a0001c0001t0007g0244 a0001c0001t0035g0272 |
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 | a0001c0001t0014g0268 | 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 | 139 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(136): Show |
141 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(138): 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 | a0001c0001t0002g0071 a0001c0001t0002g0107 |
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 | a0001c0001t0003g0245 | 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 | a0001c0001t0001g0204 | 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 | a0001c0001t0030g0271 | 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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0007g0171 | 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 | a0001c0001t0003g0262 a0001c0001t0006g0263 a0001c0001t0007g0261 others(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 | a0001c0001t0003g0251 a0001c0001t0026g0250 a0001c0001t0035g0272 |
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 | 6 | a0001c0001t0001g0086 a0001c0001t0003g0058 a0001c0001t0003g0085 others(3): Show |
6 | HG01891.hp1 HG02273.hp2 NA18985.hp1 others(3): 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 | a0001c0001t0011g0163 a0001c0001t0011g0164 a0001c0001t0012g0144 |
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 | 62 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(59): 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 | a0001c0001t0011g0163 a0001c0001t0011g0164 a0001c0001t0012g0144 |
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 | a0001c0001t0003g0251 a0001c0001t0026g0250 a0001c0001t0035g0272 |
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 | a0001c0001t0005g0176 | 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 | 30 | a0001c0001t0001g0156 a0001c0001t0001g0203 a0001c0001t0002g0049 others(27): 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | 114 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): 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 | a0001c0001t0002g0104 | 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 | a0001c0001t0002g0197 a0001c0001t0002g0224 a0001c0001t0003g0193 others(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 | 134 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(131): 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 | a0001c0001t0003g0072 | 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 | a0001c0001t0003g0262 a0001c0001t0006g0263 a0001c0001t0007g0261 others(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 | a0001c0001t0032g0035 | 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 | a0001c0001t0003g0042 | 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 | a0001c0001t0002g0202 | 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 | 51 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0051 others(48): Show |
52 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(49): 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 | a0001c0001t0015g0010 | 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 | a0001c0001t0001g0024 | 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 | a0001c0001t0001g0175 a0001c0001t0002g0197 a0001c0001t0008g0184 others(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 | a0001c0001t0011g0160 a0001c0001t0011g0162 a0001c0001t0011g0163 others(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 | a0001c0001t0003g0168 | 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 | a0001c0001t0002g0238 a0001c0001t0017g0239 a0001c0001t0017g0248 |
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 | a0001c0001t0001g0103 | 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 | a0001c0001t0001g0050 | 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 | a0001c0001t0002g0238 a0001c0001t0017g0239 a0001c0001t0017g0248 |
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 | a0001c0001t0001g0175 | 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 | a0001c0001t0003g0251 | 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 | a0001c0001t0003g0206 a0001c0001t0005g0215 |
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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.542-1824T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 5/15 | chr1 | 77811910 | |||||||
chr1:77812196 | T | G | 115 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): 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 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0002g0087 others(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 | a0001c0001t0004g0037 | 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 | a0001c0001t0002g0102 | 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 | a0001c0001t0008g0184 a0001c0001t0016g0216 |
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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0001g0101 | 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 | a0001c0001t0001g0099 a0001c0001t0001g0100 a0001c0001t0001g0101 others(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 | a0001c0001t0013g0005 | 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 | a0001c0001t0007g0244 | 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 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(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 | a0001c0001t0013g0005 | 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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0015g0009 | 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 | a0001c0001t0026g0250 | 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 | a0001c0001t0002g0122 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 |
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 | a0001c0001t0019g0182 | 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 | a0001c0001t0007g0244 a0001c0001t0035g0272 |
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 | a0001c0001t0001g0249 | 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 | a0001c0001t0011g0160 a0001c0001t0011g0162 a0001c0001t0011g0163 others(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 | a0001c0001t0009g0264 | 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 | a0001c0001t0002g0073 a0001c0001t0002g0084 |
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 | 142 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(139): Show |
144 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(141): 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 | a0001c0001t0002g0102 | 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 | a0001c0001t0001g0211 a0001c0001t0002g0210 a0001c0001t0033g0209 |
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 | a0001c0001t0009g0264 | 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 | a0001c0001t0022g0106 | 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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0024g0219 | 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 | 177 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(174): Show |
180 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(177): 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 | a0001c0001t0001g0270 a0001c0001t0002g0252 a0001c0001t0002g0253 others(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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0004g0243 | 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 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0002g0016 |
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 | a0001c0001t0002g0090 | 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 | a0001c0001t0001g0120 a0001c0001t0001g0121 a0001c0001t0001g0123 others(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 | a0001c0001t0003g0245 | 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 | 114 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): 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 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | 51 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0024 others(48): Show |
52 | HG00323.hp2 HG00597.hp1 HG00609.hp2 others(49): 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 | a0001c0001t0001g0211 | 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 | 62 | a0001c0001t0001g0156 a0001c0001t0001g0270 a0001c0001t0002g0238 others(59): 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 | a0001c0001t0033g0209 | 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 | 141 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(138): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): Show |
intron_variant | MODIFIER | c.799+2798T>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77818029 | |||||||
chr1:77818036 | G | A | 141 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(138): Show |
143 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(140): 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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0002t0003g0267 |
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 | 114 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): 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 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0002g0226 others(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 | a0001c0001t0001g0092 a0001c0001t0002g0229 a0001c0001t0003g0039 others(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 | 114 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): Show |
intron_variant | MODIFIER | c.799+3113A>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77818344 | |||||||
chr1:77818526 | A | G | 140 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(137): Show |
142 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(139): 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 | a0001c0001t0035g0272 | 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 | a0001c0002t0003g0267 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0093 others(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 | 4 | a0001c0001t0003g0012 a0001c0001t0007g0001 a0001c0001t0007g0013 others(1): 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 | a0001c0001t0009g0265 | 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 | a0001c0002t0003g0267 | 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 | a0001c0001t0002g0049 | 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 | a0001c0001t0011g0164 | 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 | a0001c0001t0002g0259 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.799+4560A>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77819791 | |||||||
chr1:77820106 | CT | C | 18 | a0001c0001t0001g0025 a0001c0001t0001g0052 a0001c0001t0001g0086 others(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 | a0001c0001t0011g0163 | 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 | a0001c0001t0001g0064 | 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 | a0001c0001t0009g0006 a0001c0001t0009g0265 a0001c0001t0009g0273 |
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 | a0001c0001t0003g0245 | 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 | a0001c0001t0015g0010 | 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 | 114 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): 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 | a0001c0001t0001g0134 a0001c0001t0010g0135 a0001c0001t0010g0232 |
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 | 115 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(112): Show |
116 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(113): 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 | a0001c0001t0001g0025 a0001c0001t0001g0175 a0001c0001t0001g0225 others(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 | a0001c0001t0015g0010 | 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 | a0001c0001t0002g0224 | 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 | a0001c0001t0002g0108 | 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 | a0001c0001t0023g0188 | 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 | a0001c0001t0002g0202 | 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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | 140 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(137): Show |
142 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(139): 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 | a0001c0001t0001g0174 a0001c0001t0001g0175 a0001c0001t0001g0186 others(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 | 114 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(111): Show |
115 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(112): 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 | a0001c0001t0001g0019 a0001c0001t0001g0022 a0001c0001t0001g0023 others(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 | 19 | a0001c0001t0001g0031 a0001c0001t0001g0034 a0001c0001t0001g0045 others(16): Show |
19 | HG01358.hp1 HG01358.hp2 HG01891.hp1 others(16): 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 | a0001c0001t0001g0174 a0001c0001t0001g0186 a0001c0001t0001g0195 others(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 | a0001c0001t0002g0274 | 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 | a0001c0001t0001g0241 a0001c0001t0005g0178 |
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 | a0001c0001t0002g0018 | 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 | a0001c0001t0001g0051 a0001c0001t0002g0102 |
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 | a0001c0001t0007g0183 | 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 | a0001c0001t0003g0251 | 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 | a0001c0001t0002g0016 | 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 | a0001c0001t0002g0057 a0001c0001t0002g0082 |
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 | a0001c0001t0003g0251 | 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 | a0001c0001t0003g0260 | 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 | 4 | a0001c0001t0003g0012 a0001c0001t0007g0001 a0001c0001t0007g0013 others(1): 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 | a0001c0001t0003g0251 | 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 | a0001c0001t0001g0270 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0002g0238 a0001c0001t0017g0239 a0001c0001t0017g0248 |
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 | a0001c0001t0001g0270 a0001c0001t0002g0252 a0001c0001t0002g0253 others(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 | a0001c0001t0004g0157 | 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 | a0001c0001t0003g0245 | 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 | a0001c0001t0031g0017 | 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 | a0001c0001t0004g0136 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0003g0251 a0001c0001t0026g0250 a0001c0001t0035g0272 |
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 | 98 | a0001c0001t0001g0011 a0001c0001t0001g0015 a0001c0001t0001g0019 others(95): Show |
98 | HG00099.hp2 HG00597.hp1 HG00609.hp2 others(95): 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 | a0001c0001t0001g0002 a0001c0001t0001g0047 a0001c0001t0002g0044 others(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 | a0001c0001t0001g0241 a0001c0001t0001g0246 a0001c0001t0004g0037 others(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 | a0001c0001t0001g0052 a0001c0001t0002g0053 |
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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0003g0072 | 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 | a0001c0001t0002g0016 | 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 | a0001c0001t0036g0207 | 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 | a0001c0001t0001g0067 | 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 | 7 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0103 others(4): 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 | a0001c0001t0001g0103 a0001c0001t0001g0111 |
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 | a0001c0001t0001g0045 a0001c0001t0001g0047 a0001c0001t0001g0050 others(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 | 36 | a0001c0001t0001g0156 a0001c0001t0002g0143 a0001c0001t0004g0004 others(33): 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 | a0001c0001t0003g0177 | 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 | a0001c0001t0001g0204 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0204 | 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 | a0001c0001t0002g0238 a0001c0001t0017g0239 a0001c0001t0017g0248 |
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 | a0001c0001t0002g0118 | 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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0002g0060 | 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 | a0001c0001t0001g0270 a0001c0001t0002g0252 a0001c0001t0002g0253 others(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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0001g0120 | 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 | 2 | a0001c0001t0007g0001 a0001c0001t0007g0014 |
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 | a0001c0001t0009g0273 | 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 | a0001c0001t0003g0260 | 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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0001g0246 | 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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0025g0187 | 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 | a0001c0001t0002g0090 | 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 | a0001c0001t0001g0204 a0001c0001t0007g0244 a0001c0001t0035g0272 |
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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | 36 | a0001c0001t0001g0156 a0001c0001t0002g0143 a0001c0001t0004g0004 others(33): 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 | |||||||
chr1:77828502 | A | G | 2 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0007g0014 | 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 | a0001c0001t0003g0206 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0026g0250 | 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 | a0001c0001t0001g0156 a0001c0001t0002g0143 a0001c0001t0004g0137 others(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 | a0001c0001t0003g0251 a0001c0001t0026g0250 |
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 | a0001c0001t0025g0187 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0050 a0001c0001t0001g0093 others(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 | a0001c0001t0001g0222 a0001c0001t0002g0223 |
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 | a0001c0001t0002g0032 | 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 | 28 | a0001c0001t0001g0061 a0001c0001t0001g0204 a0001c0001t0001g0205 others(25): 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 | a0001c0001t0003g0260 | 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 | a0001c0001t0001g0094 | 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 | a0001c0001t0001g0015 a0001c0001t0001g0050 a0001c0001t0002g0046 others(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 | a0001c0001t0002g0070 | 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 | a0001c0001t0024g0219 | 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 | a0001c0001t0003g0245 | 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 | 265 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(262): Show |
270 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(267): 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 | a0001c0001t0006g0257 | 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 | a0001c0001t0002g0082 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | a0001c0001t0005g0234 | 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 | a0001c0001t0001g0051 | 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 | a0001c0001t0004g0142 | 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 | a0001c0001t0001g0092 | 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 | a0001c0001t0001g0094 a0001c0001t0001g0095 a0001c0001t0001g0240 |
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 | a0001c0001t0002g0238 | 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 | a0001c0001t0001g0019 | 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 | 33 | a0001c0001t0004g0004 a0001c0001t0004g0037 a0001c0001t0004g0136 others(30): 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 | a0001c0001t0003g0245 | 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 | a0001c0001t0011g0160 a0001c0001t0011g0162 a0001c0001t0011g0163 others(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 | a0001c0001t0010g0020 | 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 | a0001c0001t0001g0204 | 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 | 18 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(15): 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 | a0001c0001t0005g0234 | 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0001g0218 | 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | 17 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(14): 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 | a0001c0001t0014g0036 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0005g0191 | 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 | a0001c0001t0004g0140 | 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 | a0001c0001t0002g0126 | 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 | a0001c0001t0003g0206 | 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0004g0138 a0001c0001t0004g0148 |
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 | a0001c0001t0001g0236 | 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 | a0001c0001t0001g0133 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0008g0113 | 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 | a0001c0001t0015g0009 | 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 | a0001c0001t0001g0050 a0001c0001t0002g0252 a0001c0001t0002g0253 others(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 | a0001c0001t0009g0006 a0001c0001t0009g0264 a0001c0001t0009g0265 others(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 | a0001c0001t0002g0057 a0001c0001t0002g0082 |
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 | a0001c0001t0001g0133 | 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 | a0001c0001t0003g0245 | 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 | 150 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): 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 | a0001c0001t0003g0196 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0004g0037 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0005g0212 | 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 | a0001c0001t0005g0212 | 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 | a0001c0001t0008g0200 a0001c0001t0008g0208 |
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 | 8 | a0001c0001t0003g0117 a0001c0001t0007g0001 a0001c0001t0007g0014 others(5): 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 | a0001c0001t0014g0036 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0001g0221 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0173 |
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 | a0001c0001t0026g0250 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | a0001c0001t0002g0090 | 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 | a0001c0001t0002g0238 | 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 | a0001c0001t0003g0262 a0001c0001t0006g0263 a0001c0001t0007g0244 others(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 | 228 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(225): Show |
233 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(230): 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 | a0001c0001t0017g0125 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0064 others(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 | a0001c0001t0003g0245 | 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 | a0001c0001t0002g0032 | 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 | 150 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): Show |
intron_variant | MODIFIER | c.800-3209T>G | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 7/15 | chr1 | 77840098 | |||||||
chr1:77840174 | G | T | 66 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0038 others(63): 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 | a0001c0001t0002g0090 | 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 | a0001c0001t0001g0241 | 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 | a0001c0001t0001g0270 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0019g0182 | 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 | a0001c0001t0019g0182 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | a0001c0001t0017g0248 | 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 | a0001c0001t0002g0143 a0001c0003t0001g0115 |
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 | a0001c0001t0001g0174 | 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 | 229 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(226): Show |
234 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(231): 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 | 151 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): 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 | a0001c0001t0001g0089 a0001c0001t0001g0186 a0001c0001t0001g0270 others(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 | a0001c0001t0001g0121 | 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 | a0001c0001t0017g0125 a0001c0001t0017g0239 a0001c0001t0017g0248 others(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 | 150 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(147): Show |
150 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(147): 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 | a0001c0001t0015g0009 | 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 | a0001c0001t0008g0033 | 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 | a0001c0001t0005g0212 | 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 | a0001c0001t0001g0067 | 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 | a0001c0001t0003g0012 a0001c0001t0007g0013 |
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 | a0001c0001t0001g0024 a0001c0001t0001g0195 |
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 | a0001c0001t0001g0233 | 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 | a0001c0001t0004g0140 a0001c0001t0004g0146 a0001c0001t0004g0152 others(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 | a0001c0001t0001g0061 a0001c0001t0001g0091 a0001c0001t0001g0240 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0195 a0001c0001t0003g0072 others(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 | a0001c0001t0003g0039 a0001c0001t0003g0168 |
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 | a0001c0001t0035g0272 | 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 | a0001c0001t0003g0177 a0001c0001t0003g0193 a0001c0001t0003g0206 others(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 | a0001c0001t0001g0022 a0001c0001t0001g0051 a0001c0001t0001g0062 others(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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0265 others(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 | a0001c0001t0004g0149 a0001c0001t0004g0150 a0001c0001t0004g0165 |
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 | a0001c0001t0001g0211 a0001c0001t0002g0053 a0001c0001t0003g0012 others(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 | 5 | a0001c0001t0001g0227 a0001c0001t0001g0246 a0001c0001t0003g0117 others(2): 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 |
1 | a0001c0001t0003g0003 | 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 | a0001c0001t0003g0170 a0001c0001t0007g0261 |
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 | a0001c0001t0001g0007 a0001c0001t0001g0103 a0001c0001t0001g0111 others(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 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | 25 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0027 others(22): Show |
25 | HG01106.hp2 HG02080.hp2 HG02083.hp1 others(22): 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 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0015 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0047 a0001c0001t0001g0121 a0001c0001t0001g0222 others(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 | a0001c0001t0001g0019 a0001c0001t0001g0025 a0001c0001t0001g0027 others(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 | a0001c0001t0001g0027 a0001c0001t0001g0050 a0001c0001t0001g0064 others(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 | a0001c0001t0003g0251 | 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 | a0001c0001t0035g0272 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0245 a0001c0001t0003g0260 others(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 | a0001c0001t0009g0264 | 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 | a0001c0001t0017g0125 a0001c0001t0017g0239 a0001c0001t0017g0248 others(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 | a0001c0001t0017g0125 a0001c0001t0017g0239 a0001c0001t0017g0248 others(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 | a0001c0001t0001g0174 a0001c0001t0003g0085 a0001c0001t0003g0196 others(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 | a0001c0001t0005g0191 | 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 | a0001c0001t0007g0244 a0001c0001t0017g0125 a0001c0001t0017g0239 others(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 | a0001c0001t0001g0023 a0001c0001t0001g0034 a0001c0001t0005g0181 |
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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0047 a0001c0001t0001g0121 others(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 | a0001c0001t0001g0225 a0001c0001t0002g0046 a0001c0001t0003g0039 others(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 | 191 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(188): Show |
192 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(189): Show |
intron_variant | MODIFIER | c.900+732G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844139 | |||||||
chr1:77844143 | G | T | 153 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(150): Show |
154 | HG00099.hp2 HG00438.hp2 HG00597.hp1 others(151): Show |
intron_variant | MODIFIER | c.900+736G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77844143 | |||||||
chr1:77844147 | G | T | 35 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0103 others(32): 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 | 151 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0052 a0001c0001t0002g0053 |
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 | a0001c0001t0004g0154 | 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 | a0001c0001t0004g0149 | 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 | a0001c0001t0004g0145 | 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0003g0251 | 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 | 12 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(9): 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 | a0001c0001t0002g0259 | 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 | a0001c0001t0017g0248 | 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 | 17 | a0001c0001t0001g0233 a0001c0001t0003g0003 a0001c0001t0003g0012 others(14): 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 | a0001c0001t0003g0260 | 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 | a0001c0001t0011g0160 a0001c0001t0011g0162 a0001c0001t0011g0163 others(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 | a0001c0001t0002g0032 a0001c0001t0005g0234 |
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 | a0001c0001t0001g0029 | 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 | a0001c0001t0003g0058 | 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 | 231 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(228): Show |
236 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(233): 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 | a0001c0001t0007g0244 | 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 | a0001c0001t0014g0036 a0001c0001t0035g0272 |
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 | a0001c0001t0003g0081 | 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 | 237 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(234): Show |
242 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(239): 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 | a0001c0001t0005g0234 | 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 | a0001c0002t0003g0267 | 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 | a0001c0001t0014g0036 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0009g0264 | 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 | 230 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(227): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): 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 | a0001c0004t0001g0030 | 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0013g0213 | 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 | a0001c0001t0001g0029 | 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 | a0001c0001t0014g0036 | 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 | 151 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): 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 | a0001c0001t0002g0060 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.900+5003G>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77848410 | |||||||
chr1:77848613 | A | G | 1 | a0001c0001t0035g0272 | 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 | 26 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0064 others(23): Show |
26 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(23): 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 | a0001c0001t0013g0005 | 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 | a0001c0001t0001g0222 a0001c0001t0002g0223 a0001c0001t0002g0274 |
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 | a0001c0001t0003g0083 | 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 | 230 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(227): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): Show |
intron_variant | MODIFIER | c.900+5813C>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77849220 | |||||||
chr1:77849480 | G | A | 25 | a0001c0001t0004g0004 a0001c0001t0004g0037 a0001c0001t0004g0136 others(22): 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 | 1 | a0001c0001t0004g0004 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0052 a0001c0001t0001g0111 others(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 | a0001c0002t0003g0267 a0001c0002t0005g0192 |
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 | a0001c0002t0003g0267 a0001c0002t0005g0192 |
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 | a0001c0001t0033g0209 | 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 | a0001c0001t0003g0260 | 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 | 153 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(150): Show |
153 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(150): 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 | a0001c0001t0005g0176 a0001c0001t0014g0266 |
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 | a0001c0001t0010g0020 | 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 | a0001c0001t0007g0013 | 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 | a0001c0001t0001g0007 a0001c0001t0001g0008 |
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 | 33 | a0001c0001t0004g0004 a0001c0001t0004g0037 a0001c0001t0004g0136 others(30): 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 | 116 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0015 others(113): 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 | 59 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0022 others(56): Show |
59 | HG00099.hp2 HG00323.hp2 HG00597.hp1 others(56): 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 | a0001c0001t0001g0221 | 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 | 151 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): 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 | a0001c0001t0029g0043 | 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 | 237 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(234): Show |
242 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(239): Show |
intron_variant | MODIFIER | c.901-6443G>A | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 8/15 | chr1 | 77852495 | |||||||
chr1:77852934 | G | A | 14 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(11): 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | 151 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): 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 | a0001c0001t0009g0055 | 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 | a0001c0001t0016g0199 | 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 | a0001c0001t0026g0250 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | a0001c0002t0005g0192 | 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 | a0001c0001t0035g0272 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | a0001c0001t0017g0239 | 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 | a0001c0001t0007g0183 | 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 | a0001c0001t0001g0211 | 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 | a0001c0001t0003g0077 | 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 | 25 | a0001c0001t0004g0004 a0001c0001t0004g0037 a0001c0001t0004g0136 others(22): 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 | a0001c0001t0028g0151 | 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 | a0001c0001t0029g0043 | 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 | a0001c0001t0002g0074 a0001c0001t0002g0078 a0001c0001t0002g0079 others(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 | a0001c0001t0007g0244 a0001c0001t0033g0209 |
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 | 18 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(15): 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 | a0001c0001t0003g0196 a0001c0001t0005g0181 |
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 | a0001c0001t0002g0102 | 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 | 33 | a0001c0001t0004g0004 a0001c0001t0004g0037 a0001c0001t0004g0136 others(30): 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 | a0001c0001t0035g0272 | 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 | a0001c0001t0003g0260 | 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 | 33 | a0001c0001t0004g0004 a0001c0001t0004g0037 a0001c0001t0004g0136 others(30): 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 | a0001c0001t0001g0242 | 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 | a0001c0001t0015g0010 | 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 | a0001c0001t0017g0125 a0001c0001t0017g0239 a0001c0001t0017g0248 others(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 | a0001c0001t0002g0126 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0035g0272 | 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 | 18 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(15): 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 | a0001c0001t0014g0036 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | a0001c0001t0028g0151 | 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 | a0001c0001t0004g0136 | 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 | a0001c0001t0001g0174 | 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 | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(159): 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 | a0001c0001t0024g0219 | 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 | a0001c0001t0005g0215 | 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 | a0001c0001t0002g0197 | 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 | a0001c0001t0007g0183 a0001c0001t0014g0036 a0001c0001t0014g0266 others(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 | 162 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(159): Show |
162 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(159): 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 | a0001c0001t0003g0245 | 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 | a0001c0001t0028g0151 | 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 | a0001c0001t0028g0151 | 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 | a0001c0001t0003g0262 a0001c0001t0006g0263 a0001c0001t0007g0261 |
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 | 14 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(11): 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 | a0001c0001t0017g0125 a0001c0001t0017g0239 a0001c0001t0017g0248 others(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 | a0001c0001t0003g0169 | 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 | 41 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0064 others(38): Show |
41 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(38): 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 | a0001c0001t0002g0084 a0001c0001t0002g0107 a0001c0001t0002g0252 others(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 | 2 | a0001c0001t0003g0003 a0001c0001t0003g0117 |
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 | a0001c0001t0028g0151 | 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 | a0001c0001t0028g0151 | 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 | 14 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(11): 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 | 18 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(15): 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 | a0001c0001t0002g0223 | 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 | a0001c0001t0017g0125 a0001c0001t0017g0239 a0001c0001t0017g0248 others(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 | 15 | a0001c0001t0001g0174 a0001c0001t0003g0003 a0001c0001t0003g0012 others(12): 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0002g0087 others(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 | a0001c0001t0005g0191 | 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 | a0001c0001t0035g0272 | 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0017g0125 a0001c0001t0017g0239 a0001c0001t0017g0248 others(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 | a0001c0001t0005g0191 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0002g0032 | 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 | a0001c0001t0002g0118 | 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 | a0001c0001t0020g0269 | 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 | 271 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(268): Show |
276 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(273): 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | 28 | a0001c0001t0004g0004 a0001c0001t0004g0037 a0001c0001t0004g0136 others(25): 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 | a0001c0001t0004g0037 a0001c0001t0011g0160 a0001c0001t0011g0162 others(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 | a0001c0001t0026g0250 | 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0265 others(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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | a0001c0001t0004g0136 | 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 | a0001c0001t0009g0264 | 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 | 236 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(238): 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 | a0001c0001t0002g0118 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | a0001c0001t0001g0088 a0001c0001t0001g0089 a0001c0001t0002g0087 others(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 | a0001c0001t0001g0225 a0001c0001t0001g0242 a0001c0001t0002g0048 others(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 | a0001c0001t0014g0266 a0001c0001t0014g0268 a0001c0001t0019g0182 others(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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | a0001c0001t0001g0129 | 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 | a0001c0001t0001g0019 a0001c0001t0001g0023 a0001c0001t0001g0025 others(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 | a0001c0001t0007g0244 | 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 | a0001c0001t0002g0224 a0001c0001t0002g0228 a0001c0001t0005g0214 others(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 | a0001c0001t0003g0081 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0002g0228 a0001c0001t0003g0054 |
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 | a0001c0001t0014g0036 a0001c0001t0014g0266 a0001c0001t0014g0268 others(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 | 230 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(227): Show |
235 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(232): 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 | a0001c0001t0014g0036 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(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 | a0001c0001t0011g0160 a0001c0001t0011g0162 a0001c0001t0011g0163 others(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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0020g0269 | 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 | a0001c0001t0003g0251 | 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 | a0001c0001t0011g0160 a0001c0001t0011g0162 a0001c0001t0012g0161 |
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 | 94 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0064 others(91): Show |
99 | HG00099.hp1 HG00438.hp2 HG00639.hp1 others(96): 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 | a0001c0001t0002g0259 a0001c0001t0004g0037 a0001c0001t0004g0147 others(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 | a0001c0001t0001g0002 a0001c0001t0006g0002 |
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 | a0001c0001t0010g0114 | 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0026g0250 | 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 | a0001c0001t0003g0262 a0001c0001t0006g0263 a0001c0001t0007g0261 |
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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0001g0091 | 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 | a0001c0001t0007g0261 | 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 | 151 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): 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 | a0001c0001t0017g0125 a0001c0001t0017g0239 a0001c0001t0017g0248 others(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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0246 | 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 | a0001c0001t0003g0172 a0001c0001t0003g0173 |
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 | 237 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(234): Show |
242 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(239): 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | a0001c0001t0001g0249 a0001c0001t0013g0213 a0001c0001t0014g0268 others(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 | a0001c0001t0003g0262 a0001c0001t0005g0212 a0001c0001t0006g0263 others(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 | a0001c0001t0027g0080 | 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 | 14 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(11): 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 | a0001c0001t0003g0260 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0024 a0001c0001t0001g0026 others(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 | a0001c0001t0005g0180 | 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 | a0001c0001t0002g0046 a0001c0001t0002g0228 a0001c0001t0003g0054 others(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 | a0001c0001t0014g0036 | 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 | a0001c0001t0003g0206 | 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 | a0001c0001t0001g0240 | 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0002g0127 | 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 | a0001c0001t0002g0127 | 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0002g0049 | 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 | a0001c0001t0003g0169 a0001c0001t0003g0170 a0001c0001t0007g0171 |
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 | a0001c0001t0015g0194 a0001c0001t0023g0188 a0001c0001t0025g0187 |
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 | a0001c0001t0017g0125 a0001c0001t0017g0239 a0001c0001t0017g0248 others(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 | a0001c0001t0027g0080 | 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 | 25 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0064 others(22): Show |
25 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(22): 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 | a0001c0001t0005g0215 | 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 | a0001c0001t0026g0250 | 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 | 4 | a0001c0001t0003g0012 a0001c0001t0007g0001 a0001c0001t0007g0013 others(1): 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 | a0001c0001t0004g0139 | 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 | 236 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(233): Show |
241 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(238): 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 | a0001c0001t0013g0005 a0001c0001t0013g0190 a0001c0001t0013g0213 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0011 others(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 | 47 | a0001c0001t0001g0123 a0001c0001t0001g0134 a0001c0001t0002g0048 others(44): 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 | 25 | a0001c0001t0001g0249 a0001c0001t0004g0004 a0001c0001t0004g0037 others(22): 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 | a0001c0001t0003g0038 a0001c0001t0003g0245 a0001c0001t0003g0251 others(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 | a0001c0001t0015g0010 | 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0015g0194 | 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 | a0001c0001t0005g0180 | 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 | a0001c0001t0001g0205 a0001c0001t0009g0055 a0001c0001t0009g0265 |
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 | a0001c0001t0001g0093 a0001c0001t0001g0096 a0001c0001t0002g0098 |
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 | a0001c0001t0001g0091 | 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 | a0001c0001t0003g0072 a0001c0001t0003g0077 a0001c0001t0003g0081 others(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 | a0001c0001t0001g0052 a0001c0001t0002g0048 a0001c0001t0002g0053 |
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 | a0001c0001t0035g0272 | 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 | a0001c0001t0003g0245 | 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 | a0001c0001t0035g0272 | 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0026g0250 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0039 a0001c0001t0003g0168 others(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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0003g0003 others(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 | 160 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(157): Show |
162 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(159): 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 | a0001c0001t0001g0026 a0001c0001t0001g0110 |
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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(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 | 33 | a0001c0001t0004g0004 a0001c0001t0004g0037 a0001c0001t0004g0136 others(30): 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0003g0168 | 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 | a0001c0001t0001g0227 | 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 | a0001c0001t0035g0272 | 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 | 14 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(11): 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 | a0001c0001t0033g0209 | 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 | a0001c0001t0007g0261 | 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 | 18 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(15): 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 | a0001c0001t0001g0011 a0001c0001t0001g0029 a0001c0001t0001g0134 others(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 | a0001c0001t0017g0125 a0001c0001t0017g0239 a0001c0001t0017g0248 others(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 | a0001c0001t0003g0168 | 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 | a0001c0001t0026g0250 | 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 | 203 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(200): Show |
208 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(205): 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0006g0263 | 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 | a0001c0001t0001g0123 a0001c0001t0001g0128 a0001c0001t0001g0129 others(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 | a0001c0001t0001g0088 | 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 | a0001c0001t0001g0088 | 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 | a0001c0001t0017g0125 a0001c0001t0017g0239 a0001c0001t0017g0248 others(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 | a0001c0001t0012g0167 | 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 | a0001c0001t0017g0125 a0001c0001t0017g0239 a0001c0001t0017g0248 others(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 | a0001c0001t0002g0021 | 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 | a0001c0001t0002g0021 | 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 | a0001c0001t0001g0086 | 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 | a0001c0001t0009g0006 a0001c0001t0009g0055 a0001c0001t0009g0264 others(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 | a0001c0001t0001g0067 a0001c0001t0001g0203 a0001c0001t0002g0238 others(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 | a0001c0001t0017g0125 a0001c0001t0017g0248 a0001c0001t0034g0132 |
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 | a0001c0001t0001g0050 a0001c0001t0001g0061 a0001c0001t0001g0089 others(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 | a0001c0001t0003g0012 a0001c0001t0003g0072 a0001c0001t0003g0077 others(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 | a0001c0001t0001g0007 a0001c0001t0001g0008 a0001c0001t0001g0015 others(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 | a0001c0001t0003g0262 | 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 | a0001c0001t0007g0261 | 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 | a0001c0001t0004g0140 | 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 |
26 | a0001c0001t0003g0003 a0001c0001t0003g0038 a0001c0001t0003g0039 others(23): 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 | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0022 others(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 |
31 | a0001c0001t0004g0004 a0001c0001t0004g0037 a0001c0001t0004g0136 others(28): 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 | a0001c0001t0003g0168 a0001c0001t0003g0245 a0001c0001t0003g0260 others(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 |
21 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0028 others(18): Show |
21 | HG00099.hp1 HG01106.hp2 HG01496.hp1 others(18): 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 | a0001c0001t0001g0110 a0001c0001t0001g0225 a0001c0001t0001g0242 others(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 | a0001c0001t0001g0026 a0001c0001t0002g0070 a0001c0001t0002g0074 others(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 | a0001c0001t0002g0254 | 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 | a0001c0001t0006g0263 | 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 | a0001c0001t0002g0259 a0001c0001t0006g0255 |
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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0018g0258 |
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 | a0001c0001t0001g0011 | 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 | a0001c0001t0002g0256 | 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 | a0001c0001t0017g0248 | 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 | a0001c0001t0017g0125 | 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 | a0001c0001t0034g0132 | 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 | a0001c0001t0017g0239 | 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 | a0001c0001t0017g0239 | 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 | a0001c0001t0003g0012 | 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 | a0001c0001t0003g0196 a0001c0001t0005g0181 |
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 | a0001c0001t0003g0262 a0001c0001t0007g0261 |
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 | 34 | a0001c0001t0001g0045 a0001c0001t0004g0004 a0001c0001t0004g0037 others(31): 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 | a0001c0001t0001g0022 a0001c0001t0001g0051 a0001c0001t0001g0086 others(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 | a0001c0001t0001g0235 a0001c0001t0001g0237 a0001c0001t0010g0114 |
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 | a0001c0001t0001g0174 a0001c0001t0001g0203 a0001c0001t0001g0221 |
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 | a0001c0001t0004g0157 | 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 | a0001c0001t0035g0272 | 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 | a0001c0001t0006g0217 | 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 | a0001c0001t0002g0119 | 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 | 25 | a0001c0001t0001g0002 a0001c0001t0001g0011 a0001c0001t0001g0064 others(22): Show |
25 | HG00099.hp1 HG00639.hp1 HG00741.hp2 others(22): Show |
intron_variant | MODIFIER | c.1584+676A>T | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77873796 | |||||||
chr1:77873969 | G | T | 14 | a0001c0001t0003g0003 a0001c0001t0003g0012 a0001c0001t0003g0117 others(11): 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 | a0001c0001t0002g0226 | 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 | a0001c0001t0009g0273 | 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 | a0001c0001t0004g0142 a0001c0001t0004g0157 |
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 | 151 | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0008 others(148): Show |
151 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(148): 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 | a0001c0001t0002g0252 a0001c0001t0002g0253 a0001c0001t0002g0254 others(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 | a0001c0001t0035g0272 | 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 | a0001c0001t0035g0272 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1585-86G>C | MIGA1 | ENSG00000180488.17 | transcript | ENST00000370791.9 | protein_coding | 15/15 | chr1 | 77874760 |