Item | Value |
---|---|
geneid | 29969 |
ensemblid | ENSG00000135272.13 |
hgncid | 28870 |
symbol | MDFIC |
name | MyoD family inhibitor domain containing |
refseq_nuc | NM_001166345.3 |
refseq_prot | NP_001159817.1 |
ensembl_nuc | ENST00000393486.6 |
ensembl_prot | ENSP00000377126.1 |
mane_status | MANE Select |
chr | chr7 |
start | 114922094 |
end | 115019917 |
strand | + |
ver | v1.2 |
region | chr7:114922094-115019917 |
region5000 | chr7:114917094-115024917 |
regionname0 | MDFIC_chr7_114922094_115019917 |
regionname5000 | MDFIC_chr7_114917094_115024917 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 246 | 332 | 77 | 68 | 136 | 13 | 36 | 100 | MDFIC_chr7_114917094_115024917 | MDFIC | MSGAG others(241): Show |
chr7 | 114917094 | 115024917 |
a0002 | 0/0 | 246 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | MSGAG others(241): Show |
chr7 | 114917094 | 115024917 |
a0003 | 0/0 | 246 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | MSGAG others(241): Show |
chr7 | 114917094 | 115024917 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 738 | 321 | 70 | 68 | 134 | 13 | 35 | MDFIC_chr7_114917094_115024917 | MDFIC | ATGTC others(733): Show |
chr7 | 114917094 | 115024917 | ||
a0001c0002 | 1/0 | 738 | 5 | 4 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATGTC others(733): Show |
chr7 | 114917094 | 115024917 | ||
a0001c0003 | 0/0 | 738 | 3 | 3 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATGTC others(733): Show |
chr7 | 114917094 | 115024917 | ||
a0001c0006 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATGTC others(733): Show |
chr7 | 114917094 | 115024917 | ||
a0001c0007 | 0/0 | 738 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATGTC others(733): Show |
chr7 | 114917094 | 115024917 | ||
a0001c0008 | 0/0 | 738 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATGTC others(733): Show |
chr7 | 114917094 | 115024917 | ||
a0002c0005 | 0/0 | 738 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATGTC others(733): Show |
chr7 | 114917094 | 115024917 | ||
a0003c0004 | 0/0 | 738 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATGTC others(733): Show |
chr7 | 114917094 | 115024917 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5373 | 50 | 8 | 1 | 36 | 0 | 5 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0002 | 0/0 | 5377 | 35 | 19 | 8 | 0 | 1 | 7 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0003 | 0/0 | 5377 | 22 | 3 | 8 | 7 | 2 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0004 | 0/0 | 5378 | 21 | 0 | 4 | 12 | 3 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5373): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0005 | 0/0 | 5376 | 19 | 2 | 6 | 11 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5371): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0006 | 0/0 | 5382 | 14 | 0 | 0 | 14 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5377): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0007 | 0/0 | 5373 | 13 | 1 | 9 | 0 | 2 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0008 | 0/0 | 5373 | 9 | 4 | 3 | 0 | 2 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0009 | 0/0 | 5377 | 10 | 2 | 8 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0010 | 0/0 | 5377 | 9 | 3 | 0 | 4 | 1 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0011 | 0/0 | 5377 | 9 | 3 | 0 | 2 | 0 | 4 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0012 | 0/0 | 5373 | 6 | 2 | 3 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0013 | 0/0 | 5373 | 8 | 0 | 0 | 8 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0014 | 0/0 | 5369 | 7 | 0 | 0 | 7 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5364): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0015 | 0/0 | 5372 | 7 | 0 | 2 | 5 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5367): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0016 | 0/0 | 5374 | 7 | 0 | 1 | 6 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5369): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0017 | 0/0 | 5373 | 4 | 0 | 2 | 1 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0018 | 0/0 | 5381 | 5 | 0 | 0 | 4 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5376): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0019 | 0/0 | 5365 | 4 | 3 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5360): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0020 | 0/0 | 5378 | 4 | 0 | 4 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5373): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0021 | 0/0 | 5380 | 4 | 0 | 0 | 4 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5375): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0022 | 0/0 | 5365 | 3 | 3 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5360): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0023 | 0/1 | 5381 | 2 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5376): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0024 | 0/0 | 5384 | 3 | 0 | 1 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5379): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0025 | 0/0 | 5373 | 3 | 0 | 2 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0026 | 0/0 | 5373 | 3 | 0 | 0 | 2 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0027 | 0/0 | 5377 | 2 | 2 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0028 | 0/0 | 5378 | 2 | 0 | 0 | 0 | 0 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5373): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0029 | 0/0 | 5382 | 2 | 0 | 0 | 0 | 0 | 2 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5377): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0030 | 0/0 | 5385 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5380): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0032 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0033 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0034 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0035 | 0/0 | 5377 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0037 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0038 | 0/0 | 5376 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5371): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0039 | 0/0 | 5374 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5369): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0040 | 0/0 | 5349 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5344): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0041 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0042 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0044 | 0/0 | 5373 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0045 | 0/0 | 5374 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5369): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0046 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0047 | 0/0 | 5377 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0048 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0049 | 0/0 | 5377 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0050 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0051 | 0/0 | 5384 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5379): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0052 | 0/0 | 5385 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5380): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0053 | 0/0 | 5385 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5380): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0054 | 0/0 | 5386 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5381): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0055 | 0/0 | 5389 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5384): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0056 | 0/0 | 5376 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5371): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0057 | 0/0 | 5377 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0058 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0059 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0060 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0061 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0062 | 0/0 | 5349 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5344): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0063 | 0/0 | 5365 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5360): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0064 | 0/0 | 5377 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0001t0065 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0002t0002 | 0/0 | 5377 | 2 | 2 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0002t0012 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0002t0017 | 1/0 | 5373 | 1 | 0 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0002t0023 | 0/0 | 5381 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5376): Show |
chr7 | 114917094 | 115024917 |
a0001c0003t0031 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0003t0036 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0003t0043 | 0/0 | 5377 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5372): Show |
chr7 | 114917094 | 115024917 |
a0001c0006t0001 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0001c0007t0005 | 0/0 | 5376 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5371): Show |
chr7 | 114917094 | 115024917 |
a0001c0008t0001 | 0/0 | 5373 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0002c0005t0012 | 0/0 | 5373 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
a0003c0004t0008 | 0/0 | 5373 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | ATTCA others(5368): Show |
chr7 | 114917094 | 115024917 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0268 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0197 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0003g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0011 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0004g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0005g0309 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0006g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0007g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0007g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0007g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0007g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0007g0171 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0007g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0007g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0007g0260 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0007g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0007g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0007g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0007g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0008g0009 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0008g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0008g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0008g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0008g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0008g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0008g0300 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0009g0008 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0009g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0009g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0009g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0009g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0009g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0009g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0009g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0010g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0010g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0010g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0010g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0010g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0010g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0010g0232 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0010g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0010g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0011g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0011g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0011g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0011g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0011g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0011g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0011g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0011g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0011g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0012g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0012g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0012g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0012g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0012g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0013g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0013g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0013g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0013g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0013g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0013g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0013g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0013g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0014g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0014g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0014g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0014g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0014g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0014g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0014g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0015g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0015g0012 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0015g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0015g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0015g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0015g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0016g0014 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0016g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0016g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0016g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0016g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0016g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0017g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0017g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0017g0219 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0017g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0018g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0018g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0018g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0018g0254 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0019g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0019g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0019g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0019g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0020g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0020g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0020g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0021g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0021g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0021g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0021g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0022g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0022g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0022g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0023g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0023g0211 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0024g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0024g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0024g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0025g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0025g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0025g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0026g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0026g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0026g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0027g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0027g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0028g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0028g0293 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0029g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0029g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0030g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0030g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0032g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0033g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0034g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0035g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0037g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0038g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0039g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0040g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0041g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0042g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0044g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0045g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0046g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0047g0019 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0048g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0049g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0050g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0051g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0052g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0053g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0054g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0055g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0056g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0057g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0058g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0059g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0060g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0061g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0062g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0063g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0064g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0001t0065g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0002t0002g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0002t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0002t0012g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0002t0017g0020 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0002t0023g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0003t0031g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0003t0036g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0003t0043g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0006t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0007t0005g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0001c0008t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0002c0005t0012g0291 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
a0003c0004t0008g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0007 | g0171 | EUR | GBR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0261 | EUR | GBR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00140 | hp1 | a0001 | c0001 | t0003 | g0237 | EUR | GBR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00140 | hp2 | a0001 | c0001 | t0007 | g0260 | EUR | GBR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00280 | hp1 | a0001 | c0001 | t0018 | g0254 | EUR | FIN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00280 | hp2 | a0001 | c0001 | t0010 | g0232 | EUR | FIN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0161 | EUR | FIN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0255 | EUR | FIN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00408 | hp1 | a0001 | c0001 | t0005 | g0304 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00408 | hp2 | a0001 | c0001 | t0006 | g0246 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00609 | hp2 | a0001 | c0001 | t0004 | g0271 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00621 | hp1 | a0001 | c0001 | t0014 | g0106 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00621 | hp2 | a0001 | c0001 | t0006 | g0178 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00642 | hp1 | a0001 | c0001 | t0055 | g0031 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0210 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00673 | hp2 | a0001 | c0001 | t0016 | g0245 | EAS | CHS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00735 | hp1 | a0001 | c0001 | t0002 | g0236 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00735 | hp2 | a0001 | c0001 | t0005 | g0233 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00738 | hp1 | a0001 | c0001 | t0009 | g0127 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00738 | hp2 | a0001 | c0001 | t0008 | g0038 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00741 | hp1 | a0001 | c0001 | t0025 | g0125 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG00741 | hp2 | a0001 | c0001 | t0007 | g0212 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01069 | hp1 | a0001 | c0001 | t0007 | g0156 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01069 | hp2 | a0001 | c0001 | t0009 | g0121 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01070 | hp1 | a0001 | c0001 | t0020 | g0010 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01070 | hp2 | a0001 | c0001 | t0017 | g0203 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01071 | hp1 | a0001 | c0001 | t0009 | g0122 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01071 | hp2 | a0001 | c0001 | t0020 | g0010 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01081 | hp1 | a0001 | c0001 | t0003 | g0222 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01081 | hp2 | a0001 | c0001 | t0007 | g0276 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0096 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01099 | hp2 | a0001 | c0001 | t0064 | g0120 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01106 | hp1 | a0001 | c0001 | t0004 | g0173 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01106 | hp2 | a0001 | c0001 | t0008 | g0039 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01109 | hp1 | a0001 | c0001 | t0007 | g0230 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01109 | hp2 | a0001 | c0001 | t0012 | g0235 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01167 | hp1 | a0001 | c0001 | t0007 | g0016 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01167 | hp2 | a0001 | c0001 | t0025 | g0126 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01168 | hp1 | a0001 | c0001 | t0009 | g0008 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01168 | hp2 | a0001 | c0001 | t0044 | g0105 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01169 | hp1 | a0001 | c0001 | t0009 | g0008 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01169 | hp2 | a0001 | c0001 | t0007 | g0016 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01175 | hp1 | a0001 | c0001 | t0016 | g0209 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01175 | hp2 | a0001 | c0001 | t0007 | g0277 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01192 | hp1 | a0001 | c0001 | t0002 | g0267 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0193 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01243 | hp1 | a0001 | c0001 | t0057 | g0026 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0187 | AMR | PUR | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0196 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0270 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0225 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01256 | hp2 | a0001 | c0001 | t0015 | g0012 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0207 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01257 | hp2 | a0001 | c0001 | t0007 | g0033 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01346 | hp1 | a0001 | c0001 | t0009 | g0119 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0197 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01358 | hp1 | a0001 | c0001 | t0007 | g0275 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01358 | hp2 | a0001 | c0001 | t0005 | g0012 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01361 | hp1 | a0001 | c0001 | t0012 | g0013 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01361 | hp2 | a0001 | c0001 | t0009 | g0124 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0190 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01433 | hp2 | a0001 | c0001 | t0002 | g0045 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01496 | hp1 | a0001 | c0001 | t0002 | g0231 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01496 | hp2 | a0001 | c0001 | t0008 | g0115 | AMR | CLM | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01515 | hp1 | a0001 | c0001 | t0012 | g0138 | EUR | IBS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01515 | hp2 | a0001 | c0001 | t0008 | g0009 | EUR | IBS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01516 | hp1 | a0002 | c0005 | t0012 | g0291 | EUR | IBS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01516 | hp2 | a0001 | c0001 | t0004 | g0011 | EUR | IBS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01517 | hp1 | a0001 | c0001 | t0004 | g0011 | EUR | IBS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01517 | hp2 | a0001 | c0001 | t0008 | g0009 | EUR | IBS | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01884 | hp1 | a0001 | c0001 | t0045 | g0234 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01884 | hp2 | a0001 | c0001 | t0009 | g0111 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01891 | hp1 | a0001 | c0001 | t0062 | g0118 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0201 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01928 | hp1 | a0001 | c0001 | t0024 | g0148 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01928 | hp2 | a0001 | c0001 | t0003 | g0217 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01943 | hp1 | a0001 | c0001 | t0052 | g0208 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01943 | hp2 | a0001 | c0001 | t0012 | g0195 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01978 | hp1 | a0001 | c0001 | t0009 | g0123 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0282 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01981 | hp1 | a0001 | c0001 | t0020 | g0200 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01981 | hp2 | a0001 | c0001 | t0015 | g0290 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01993 | hp1 | a0001 | c0001 | t0003 | g0198 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG01993 | hp2 | a0001 | c0001 | t0004 | g0259 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0157 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02027 | hp1 | a0001 | c0001 | t0014 | g0273 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02040 | hp2 | a0001 | c0001 | t0010 | g0077 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02055 | hp2 | a0001 | c0001 | t0007 | g0269 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02056 | hp1 | a0001 | c0001 | t0004 | g0172 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02056 | hp2 | a0001 | c0001 | t0017 | g0247 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0181 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02071 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02074 | hp1 | a0001 | c0001 | t0016 | g0014 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02074 | hp2 | a0001 | c0001 | t0049 | g0263 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02080 | hp1 | a0001 | c0001 | t0011 | g0165 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02080 | hp2 | a0001 | c0001 | t0014 | g0289 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02083 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02083 | hp2 | a0001 | c0001 | t0006 | g0223 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02129 | hp1 | a0001 | c0006 | t0001 | g0080 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02129 | hp2 | a0001 | c0001 | t0006 | g0015 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02132 | hp1 | a0001 | c0001 | t0039 | g0151 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02132 | hp2 | a0001 | c0001 | t0026 | g0189 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02135 | hp1 | a0001 | c0001 | t0018 | g0098 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02135 | hp2 | a0001 | c0001 | t0006 | g0097 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02145 | hp1 | a0001 | c0001 | t0012 | g0013 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02148 | hp1 | a0001 | c0001 | t0005 | g0159 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02148 | hp2 | a0001 | c0001 | t0017 | g0219 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02165 | hp1 | a0001 | c0001 | t0024 | g0258 | EAS | CDX | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02165 | hp2 | a0001 | c0001 | t0006 | g0179 | EAS | CDX | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0128 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0101 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02258 | hp1 | a0001 | c0001 | t0061 | g0027 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02258 | hp2 | a0001 | c0001 | t0065 | g0313 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02273 | hp1 | a0001 | c0001 | t0005 | g0309 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02273 | hp2 | a0001 | c0001 | t0038 | g0180 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02280 | hp1 | a0001 | c0001 | t0037 | g0040 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0092 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02293 | hp1 | a0001 | c0001 | t0020 | g0146 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02293 | hp2 | a0001 | c0001 | t0003 | g0199 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02300 | hp1 | a0001 | c0001 | t0003 | g0216 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02300 | hp2 | a0001 | c0001 | t0005 | g0150 | AMR | PEL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0278 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | KHV | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02572 | hp1 | a0001 | c0003 | t0043 | g0023 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0268 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02615 | hp1 | a0001 | c0001 | t0022 | g0054 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0049 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0058 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0093 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02698 | hp1 | a0001 | c0001 | t0047 | g0019 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02717 | hp1 | a0001 | c0001 | t0060 | g0022 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02717 | hp2 | a0001 | c0001 | t0010 | g0056 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0061 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02735 | hp2 | a0001 | c0007 | t0005 | g0182 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02738 | hp1 | a0001 | c0001 | t0028 | g0293 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02738 | hp2 | a0001 | c0001 | t0007 | g0034 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02809 | hp1 | a0001 | c0001 | t0012 | g0021 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02809 | hp2 | a0001 | c0001 | t0027 | g0044 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02818 | hp1 | a0001 | c0001 | t0002 | g0229 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02886 | hp1 | a0001 | c0001 | t0019 | g0279 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02886 | hp2 | a0001 | c0001 | t0023 | g0002 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0042 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02895 | hp2 | a0001 | c0001 | t0011 | g0131 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0050 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02896 | hp2 | a0001 | c0001 | t0011 | g0132 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02922 | hp1 | a0001 | c0002 | t0023 | g0168 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02965 | hp1 | a0001 | c0001 | t0002 | g0252 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02965 | hp2 | a0001 | c0001 | t0002 | g0047 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02970 | hp1 | a0001 | c0001 | t0002 | g0103 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02976 | hp1 | a0001 | c0001 | t0033 | g0104 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02976 | hp2 | a0001 | c0001 | t0042 | g0100 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03041 | hp1 | a0001 | c0001 | t0048 | g0037 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03041 | hp2 | a0001 | c0001 | t0019 | g0133 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03098 | hp1 | a0001 | c0001 | t0041 | g0055 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03098 | hp2 | a0001 | c0001 | t0009 | g0107 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0091 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03130 | hp2 | a0001 | c0001 | t0019 | g0244 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0249 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03139 | hp2 | a0001 | c0001 | t0059 | g0308 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03195 | hp1 | a0001 | c0001 | t0003 | g0280 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0048 | AFR | ESN | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03225 | hp1 | a0001 | c0002 | t0012 | g0028 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03225 | hp2 | a0001 | c0003 | t0031 | g0018 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03453 | hp1 | a0001 | c0002 | t0002 | g0051 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03453 | hp2 | a0001 | c0001 | t0008 | g0017 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03490 | hp1 | a0001 | c0001 | t0017 | g0006 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03490 | hp2 | a0001 | c0001 | t0025 | g0117 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03492 | hp1 | a0001 | c0001 | t0019 | g0006 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03492 | hp2 | a0001 | c0001 | t0028 | g0030 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03540 | hp1 | a0003 | c0004 | t0008 | g0170 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03540 | hp2 | a0001 | c0001 | t0022 | g0052 | AFR | GWD | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0046 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03579 | hp2 | a0001 | c0001 | t0022 | g0053 | AFR | MSL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03654 | hp1 | a0001 | c0001 | t0046 | g0155 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03654 | hp2 | a0001 | c0001 | t0035 | g0204 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03669 | hp2 | a0001 | c0001 | t0063 | g0116 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03704 | hp1 | a0001 | c0001 | t0029 | g0041 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0220 | SAS | PJL | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0166 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03831 | hp2 | a0001 | c0001 | t0011 | g0167 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03834 | hp2 | a0001 | c0001 | t0011 | g0035 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03942 | hp1 | a0001 | c0001 | t0002 | g0087 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG03942 | hp2 | a0001 | c0001 | t0011 | g0192 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG04115 | hp1 | a0001 | c0001 | t0034 | g0221 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG04184 | hp1 | a0001 | c0001 | t0003 | g0214 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG04184 | hp2 | a0001 | c0001 | t0026 | g0163 | SAS | BEB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG04199 | hp1 | a0001 | c0001 | t0011 | g0072 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG04199 | hp2 | a0001 | c0001 | t0004 | g0184 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0032 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG04204 | hp2 | a0001 | c0001 | t0004 | g0256 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG04228 | hp1 | a0001 | c0001 | t0010 | g0083 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG04228 | hp2 | a0001 | c0001 | t0029 | g0312 | SAS | STU | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18522 | hp1 | a0001 | c0001 | t0010 | g0029 | AFR | YRI | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18522 | hp2 | a0001 | c0001 | t0008 | g0139 | AFR | YRI | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18747 | hp1 | a0001 | c0001 | t0006 | g0303 | EAS | CHB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18747 | hp2 | a0001 | c0001 | t0010 | g0242 | EAS | CHB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18906 | hp2 | a0001 | c0003 | t0036 | g0057 | AFR | YRI | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18939 | hp2 | a0001 | c0001 | t0016 | g0014 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18940 | hp1 | a0001 | c0001 | t0005 | g0175 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0062 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18941 | hp1 | a0001 | c0001 | t0013 | g0265 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18941 | hp2 | a0001 | c0001 | t0021 | g0162 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0248 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18946 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18948 | hp1 | a0001 | c0001 | t0010 | g0086 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18948 | hp2 | a0001 | c0001 | t0005 | g0241 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0063 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18951 | hp1 | a0001 | c0001 | t0006 | g0065 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18954 | hp1 | a0001 | c0001 | t0026 | g0164 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18954 | hp2 | a0001 | c0001 | t0006 | g0213 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18963 | hp1 | a0001 | c0001 | t0021 | g0143 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18963 | hp2 | a0001 | c0001 | t0018 | g0005 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18965 | hp1 | a0001 | c0001 | t0013 | g0141 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18965 | hp2 | a0001 | c0001 | t0014 | g0288 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18966 | hp1 | a0001 | c0001 | t0006 | g0227 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18969 | hp1 | a0001 | c0001 | t0013 | g0130 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18969 | hp2 | a0001 | c0001 | t0032 | g0112 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18970 | hp1 | a0001 | c0001 | t0011 | g0306 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18970 | hp2 | a0001 | c0001 | t0005 | g0136 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18971 | hp2 | a0001 | c0001 | t0021 | g0145 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0215 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18973 | hp1 | a0001 | c0001 | t0004 | g0110 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18973 | hp2 | a0001 | c0001 | t0030 | g0068 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18975 | hp1 | a0001 | c0001 | t0005 | g0095 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18977 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18977 | hp2 | a0001 | c0001 | t0004 | g0272 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18979 | hp1 | a0001 | c0001 | t0015 | g0311 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18979 | hp2 | a0001 | c0001 | t0013 | g0283 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18981 | hp1 | a0001 | c0001 | t0004 | g0286 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18981 | hp2 | a0001 | c0001 | t0013 | g0176 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18983 | hp1 | a0001 | c0008 | t0001 | g0287 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18983 | hp2 | a0001 | c0001 | t0014 | g0078 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18984 | hp2 | a0001 | c0001 | t0014 | g0274 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18987 | hp2 | a0001 | c0001 | t0056 | g0224 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18989 | hp2 | a0001 | c0001 | t0051 | g0186 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18990 | hp1 | a0001 | c0001 | t0005 | g0003 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18991 | hp2 | a0001 | c0001 | t0006 | g0066 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18993 | hp1 | a0001 | c0001 | t0013 | g0154 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0251 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18998 | hp1 | a0001 | c0001 | t0004 | g0285 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18998 | hp2 | a0001 | c0001 | t0018 | g0005 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19003 | hp1 | a0001 | c0001 | t0053 | g0075 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0298 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19004 | hp2 | a0001 | c0001 | t0006 | g0158 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19007 | hp1 | a0001 | c0001 | t0006 | g0301 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19007 | hp2 | a0001 | c0001 | t0014 | g0004 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19009 | hp1 | a0001 | c0001 | t0003 | g0218 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19009 | hp2 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19012 | hp1 | a0001 | c0001 | t0021 | g0264 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19012 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19030 | hp1 | a0001 | c0001 | t0002 | g0059 | AFR | LWK | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19030 | hp2 | a0001 | c0001 | t0050 | g0060 | AFR | LWK | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0281 | AFR | LWK | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19043 | hp2 | a0001 | c0001 | t0002 | g0043 | AFR | LWK | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19058 | hp1 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19058 | hp2 | a0001 | c0001 | t0003 | g0099 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19060 | hp1 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19060 | hp2 | a0001 | c0001 | t0030 | g0067 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19064 | hp1 | a0001 | c0001 | t0016 | g0228 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19072 | hp1 | a0001 | c0001 | t0004 | g0297 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19072 | hp2 | a0001 | c0001 | t0018 | g0109 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19076 | hp2 | a0001 | c0001 | t0003 | g0169 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19077 | hp1 | a0001 | c0001 | t0004 | g0250 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19077 | hp2 | a0001 | c0001 | t0013 | g0292 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19078 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19078 | hp2 | a0001 | c0001 | t0024 | g0177 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19081 | hp1 | a0001 | c0001 | t0015 | g0003 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0294 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19083 | hp1 | a0001 | c0001 | t0010 | g0257 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19083 | hp2 | a0001 | c0001 | t0005 | g0094 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19085 | hp1 | a0001 | c0001 | t0016 | g0240 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19086 | hp1 | a0001 | c0001 | t0016 | g0074 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19086 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19087 | hp1 | a0001 | c0001 | t0006 | g0153 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19087 | hp2 | a0001 | c0001 | t0013 | g0284 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19090 | hp1 | a0001 | c0001 | t0015 | g0310 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19090 | hp2 | a0001 | c0001 | t0054 | g0262 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19240 | hp1 | a0001 | c0001 | t0002 | g0102 | AFR | YRI | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA19240 | hp2 | a0001 | c0001 | t0058 | g0253 | AFR | YRI | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA20129 | hp1 | a0001 | c0002 | t0002 | g0024 | AFR | ASW | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA20129 | hp2 | a0001 | c0001 | t0010 | g0089 | AFR | ASW | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0073 | SAS | GIH | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0185 | SAS | GIH | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02109 | hp1 | a0001 | c0001 | t0040 | g0135 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG06807 | hp1 | a0001 | c0001 | t0002 | g0226 | AFR | USA | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
HG06807 | hp2 | a0001 | c0001 | t0027 | g0025 | AFR | USA | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18955 | hp1 | a0001 | c0001 | t0015 | g0174 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA20300 | hp1 | a0001 | c0001 | t0008 | g0300 | AFR | USA | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA20300 | hp2 | a0001 | c0001 | t0005 | g0160 | AFR | USA | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA21309 | hp1 | a0001 | c0001 | t0008 | g0036 | AFR | LWK | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0183 | AFR | LWK | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
homoSapiens | chm13v2 | a0001 | c0001 | t0023 | g0211 | REF | REF | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
homoSapiens | grch38p0 | a0001 | c0002 | t0017 | g0020 | REF | REF | MDFIC_chr7_114917094_115024917 | MDFIC | chr7 | 114917094 | 115024917 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:114942347 | T | A | 1 | a0003 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.167T>A | p.Met56Lys | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/5 | 817/5373 | 167/741 | 56/246 | chr7 | 114942347 | |||
chr7:114979634 | G | A | 1 | a0002 | 1 | HG01516.hp1 | missense_variant | MODERATE | c.346G>A | p.Gly116Arg | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/5 | 996/5373 | 346/741 | 116/246 | chr7 | 114979634 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:114979543 | C | A | 7 | a0001c0001 a0001c0003 a0001c0006 others(4): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
synonymous_variant | LOW | c.255C>A | p.Ala85Ala | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/5 | 905/5373 | 255/741 | 85/246 | chr7 | 114979543 | |||
chr7:114979642 | A | G | 1 | a0001c0008 | 1 | NA18983.hp1 | synonymous_variant | LOW | c.354A>G | p.Ala118Ala | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/5 | 1004/5373 | 354/741 | 118/246 | chr7 | 114979642 | |||
chr7:115015764 | G | A | 1 | a0001c0003 | 3 | HG02572.hp1 HG03225.hp2 NA18906.hp2 |
synonymous_variant | LOW | c.570G>A | p.Ala190Ala | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1220/5373 | 570/741 | 190/246 | chr7 | 115015764 | |||
chr7:115015794 | C | T | 1 | a0001c0007 | 1 | HG02735.hp2 | synonymous_variant | LOW | c.600C>T | p.Cys200Cys | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1250/5373 | 600/741 | 200/246 | chr7 | 115015794 | |||
chr7:115015812 | C | T | 1 | a0001c0006 | 1 | HG02129.hp1 | synonymous_variant | LOW | c.618C>T | p.Asp206Asp | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1268/5373 | 618/741 | 206/246 | chr7 | 115015812 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:114922169 | G | A | 1 | a0001c0003t0031 | 1 | HG03225.hp2 | 5_prime_UTR_variant | MODIFIER | c.-575G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 865 | chr7 | 114922169 | ||||||
chr7:114922213 | G | T | 1 | a0001c0001t0026 | 3 | HG02132.hp2 HG04184.hp2 NA18954.hp1 |
5_prime_UTR_variant | MODIFIER | c.-531G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 821 | chr7 | 114922213 | ||||||
chr7:114922219 | G | A | 1 | a0001c0001t0032 | 1 | NA18969.hp2 | 5_prime_UTR_variant | MODIFIER | c.-525G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 815 | chr7 | 114922219 | ||||||
chr7:114922303 | G | A | 1 | a0001c0001t0033 | 1 | HG02976.hp1 | 5_prime_UTR_variant | MODIFIER | c.-441G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 731 | chr7 | 114922303 | ||||||
chr7:114922368 | C | T | 6 | a0001c0001t0009 a0001c0001t0025 a0001c0001t0062 others(3): Show |
17 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
5_prime_UTR_variant | MODIFIER | c.-376C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 666 | chr7 | 114922368 | ||||||
chr7:114922376 | G | A | 2 | a0001c0001t0034 a0001c0001t0035 |
2 | HG03654.hp2 HG04115.hp1 |
5_prime_UTR_variant | MODIFIER | c.-368G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 658 | chr7 | 114922376 | ||||||
chr7:114922520 | T | C | 1 | a0001c0003t0036 | 1 | NA18906.hp2 | 5_prime_UTR_variant | MODIFIER | c.-224T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/5 | 514 | chr7 | 114922520 | ||||||
chr7:114922982 | C | CGGGCGGC others(5): Show |
1 | a0001c0001t0030 | 2 | NA18973.hp2 NA19060.hp2 |
5_prime_UTR_variant | MODIFIER | c.-51_-40dupGGGCGGCG others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/5 | 39 | INFO_REALIGN_3_PRIME | chr7 | 114922982 | |||||
chr7:114922999 | G | C | 1 | a0001c0001t0030 | 2 | NA18973.hp2 NA19060.hp2 |
5_prime_UTR_variant | MODIFIER | c.-35G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/5 | 35 | chr7 | 114922999 | ||||||
chr7:115016227 | A | G | 4 | a0001c0001t0058 a0001c0001t0059 a0001c0001t0060 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG03139.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*292A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 292 | chr7 | 115016227 | ||||||
chr7:115016240 | T | C | 2 | a0001c0001t0022 a0001c0001t0037 |
4 | HG02280.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*305T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 305 | chr7 | 115016240 | ||||||
chr7:115016323 | C | G | 1 | a0001c0001t0057 | 1 | HG01243.hp1 | 3_prime_UTR_variant | MODIFIER | c.*388C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 388 | chr7 | 115016323 | ||||||
chr7:115016495 | T | C | 1 | a0001c0001t0038 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*560T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 560 | chr7 | 115016495 | ||||||
chr7:115016498 | C | T | 1 | a0001c0001t0056 | 1 | NA18987.hp2 | 3_prime_UTR_variant | MODIFIER | c.*563C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 563 | chr7 | 115016498 | ||||||
chr7:115016558 | G | A | 1 | a0001c0001t0039 | 1 | HG02132.hp1 | 3_prime_UTR_variant | MODIFIER | c.*623G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 623 | chr7 | 115016558 | ||||||
chr7:115016644 | C | CTAAA | 23 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(20): Show |
147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*753dupTAAA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 754 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | |||||
chr7:115016644 | C | CTAAATAA others(1): Show |
6 | a0001c0001t0006 a0001c0001t0018 a0001c0001t0021 others(3): Show |
27 | HG00280.hp1 HG00408.hp2 HG00621.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*746_*753dupTAAATA others(2): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 754 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | |||||
chr7:115016644 | C | CTAAATAA others(5): Show |
4 | a0001c0001t0024 a0001c0001t0052 a0001c0001t0053 others(1): Show |
6 | HG01928.hp1 HG01943.hp1 HG02165.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*742_*753dupTAAATA others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 754 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | |||||
chr7:115016644 | C | CTAAATAA others(9): Show |
1 | a0001c0001t0055 | 1 | HG00642.hp1 | 3_prime_UTR_variant | MODIFIER | c.*738_*753dupTAAATA others(10): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 754 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | |||||
chr7:115016644 | CTAAA | C | 1 | a0001c0001t0014 | 7 | HG00621.hp1 HG02027.hp1 HG02080.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*750_*753delTAAA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 750 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | |||||
chr7:115016644 | CTAAATAA others(1): Show |
C | 3 | a0001c0001t0019 a0001c0001t0022 a0001c0001t0063 |
8 | HG02615.hp1 HG02886.hp1 HG03041.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*746_*753delTAAATA others(2): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 746 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | |||||
chr7:115016644 | CTAAATAA others(17): Show |
C | 2 | a0001c0001t0040 a0001c0001t0062 |
2 | HG01891.hp1 HG02109.hp1 |
3_prime_UTR_variant | MODIFIER | c.*730_*753delTAAATA others(18): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 730 | INFO_REALIGN_3_PRIME | chr7 | 115016644 | |||||
chr7:115016685 | T | C | 7 | a0001c0001t0022 a0001c0001t0037 a0001c0001t0041 others(4): Show |
9 | HG02280.hp1 HG02615.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*750T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 750 | chr7 | 115016685 | ||||||
chr7:115016685 | T | TAAAC | 3 | a0001c0001t0061 a0001c0003t0031 a0001c0003t0043 |
3 | HG02258.hp1 HG02572.hp1 HG03225.hp2 |
3_prime_UTR_variant | MODIFIER | c.*755_*758dupAAAC | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 759 | INFO_REALIGN_3_PRIME | chr7 | 115016685 | |||||
chr7:115016685 | T | TAAATAAA others(5): Show |
1 | a0001c0001t0051 | 1 | NA18989.hp2 | 3_prime_UTR_variant | MODIFIER | c.*753_*754insTAAATA others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 754 | INFO_REALIGN_3_PRIME | chr7 | 115016685 | |||||
chr7:115016835 | G | A | 1 | a0001c0001t0022 | 3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*900G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 900 | chr7 | 115016835 | ||||||
chr7:115016914 | C | T | 1 | a0001c0001t0042 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*979C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 979 | chr7 | 115016914 | ||||||
chr7:115016942 | A | G | 1 | a0001c0001t0042 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1007A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1007 | chr7 | 115016942 | ||||||
chr7:115016990 | A | G | 1 | a0001c0001t0033 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1055A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1055 | chr7 | 115016990 | ||||||
chr7:115017522 | T | C | 1 | a0001c0001t0047 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1587T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1587 | chr7 | 115017522 | ||||||
chr7:115017533 | C | A | 2 | a0001c0001t0022 a0001c0001t0037 |
4 | HG02280.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1598C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1598 | chr7 | 115017533 | ||||||
chr7:115017621 | A | C | 1 | a0001c0001t0060 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1686 | chr7 | 115017621 | ||||||
chr7:115017842 | A | G | 1 | a0001c0001t0020 | 4 | HG01070.hp1 HG01071.hp2 HG01981.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1907A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 1907 | chr7 | 115017842 | ||||||
chr7:115017967 | A | G | 1 | a0001c0001t0046 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2032A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2032 | chr7 | 115017967 | ||||||
chr7:115018140 | G | T | 2 | a0001c0001t0028 a0001c0001t0029 |
4 | HG02738.hp1 HG03492.hp2 HG03704.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2205G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2205 | chr7 | 115018140 | ||||||
chr7:115018166 | A | G | 45 | a0001c0001t0001 a0001c0001t0004 a0001c0001t0006 others(42): Show |
193 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*2231A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2231 | chr7 | 115018166 | ||||||
chr7:115018194 | A | C | 2 | a0001c0001t0042 a0001c0001t0050 |
2 | HG02976.hp2 NA19030.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2259A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2259 | chr7 | 115018194 | ||||||
chr7:115018244 | A | T | 1 | a0001c0001t0045 | 1 | HG01884.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2309A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2309 | chr7 | 115018244 | ||||||
chr7:115018278 | A | C | 1 | a0001c0001t0022 | 3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2343A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2343 | chr7 | 115018278 | ||||||
chr7:115018432 | A | G | 18 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0007 others(15): Show |
89 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(86): Show |
3_prime_UTR_variant | MODIFIER | c.*2497A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2497 | chr7 | 115018432 | ||||||
chr7:115018585 | T | C | 1 | a0001c0001t0044 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2650T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2650 | chr7 | 115018585 | ||||||
chr7:115018751 | C | A | 2 | a0001c0001t0022 a0001c0001t0037 |
4 | HG02280.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2816C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2816 | chr7 | 115018751 | ||||||
chr7:115018892 | A | C | 1 | a0001c0001t0037 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2957A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2957 | chr7 | 115018892 | ||||||
chr7:115018909 | C | T | 2 | a0001c0001t0022 a0001c0001t0037 |
4 | HG02280.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2974C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 2974 | chr7 | 115018909 | ||||||
chr7:115018951 | G | T | 2 | a0001c0001t0022 a0001c0001t0037 |
4 | HG02280.hp1 HG02615.hp1 HG03540.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3016G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3016 | chr7 | 115018951 | ||||||
chr7:115019009 | G | GT | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0016 others(6): Show |
53 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3086dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3087 | INFO_REALIGN_3_PRIME | chr7 | 115019009 | |||||
chr7:115019009 | GT | G | 8 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0021 others(5): Show |
37 | HG00408.hp1 HG00735.hp2 HG01192.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3086delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3086 | INFO_REALIGN_3_PRIME | chr7 | 115019009 | |||||
chr7:115019089 | G | A | 2 | a0001c0001t0048 a0001c0001t0065 |
2 | HG02258.hp2 HG03041.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3154G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3154 | chr7 | 115019089 | ||||||
chr7:115019180 | G | A | 2 | a0001c0001t0013 a0001c0001t0049 |
9 | HG02074.hp2 NA18941.hp1 NA18965.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3245G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3245 | chr7 | 115019180 | ||||||
chr7:115019260 | T | C | 8 | a0001c0001t0001 a0001c0001t0010 a0001c0001t0014 others(5): Show |
74 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*3325T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3325 | chr7 | 115019260 | ||||||
chr7:115019294 | G | C | 9 | a0001c0001t0004 a0001c0001t0006 a0001c0001t0016 others(6): Show |
53 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(50): Show |
3_prime_UTR_variant | MODIFIER | c.*3359G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3359 | chr7 | 115019294 | ||||||
chr7:115019441 | A | T | 9 | a0001c0001t0003 a0001c0001t0012 a0001c0001t0018 others(6): Show |
39 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*3506A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3506 | chr7 | 115019441 | ||||||
chr7:115019483 | A | T | 9 | a0001c0001t0042 a0001c0001t0050 a0001c0001t0058 others(6): Show |
9 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*3548A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3548 | chr7 | 115019483 | ||||||
chr7:115019722 | A | G | 3 | a0001c0001t0059 a0001c0001t0060 a0001c0001t0061 |
3 | HG02258.hp1 HG02717.hp1 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3787A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 5/5 | 3787 | chr7 | 115019722 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:114922762 | G | A | 1 | a0001c0001t0008g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.-108+126G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/4 | chr7 | 114922762 | |||||||
chr7:114922778 | G | GTT | 223 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0113 others(220): Show |
235 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(232): Show |
intron_variant | MODIFIER | c.-108+143_-108+144i others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 1/4 | INFO_REALIGN_3_PRIME | chr7 | 114922778 | ||||||
chr7:114923146 | G | T | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+19G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114923146 | |||||||
chr7:114923225 | G | T | 1 | a0001c0001t0065g0313 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.94+98G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114923225 | |||||||
chr7:114923232 | T | C | 1 | a0001c0001t0014g0106 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.94+105T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114923232 | |||||||
chr7:114923300 | T | C | 2 | a0001c0001t0009g0107 a0001c0001t0065g0313 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.94+173T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114923300 | |||||||
chr7:114924227 | A | G | 1 | a0001c0001t0029g0312 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.94+1100A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114924227 | |||||||
chr7:114924249 | C | A | 1 | a0001c0001t0005g0108 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.94+1122C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114924249 | |||||||
chr7:114924508 | A | C | 3 | a0001c0001t0005g0309 a0001c0001t0015g0310 a0001c0001t0015g0311 |
3 | HG02273.hp1 NA18979.hp1 NA19090.hp1 |
intron_variant | MODIFIER | c.94+1381A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114924508 | |||||||
chr7:114924525 | G | A | 1 | a0001c0001t0018g0109 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.94+1398G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114924525 | |||||||
chr7:114924587 | T | TAGC | 294 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(291): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.94+1461_94+1462ins others(3): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114924587 | ||||||
chr7:114924623 | A | G | 1 | a0001c0001t0059g0308 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.94+1496A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114924623 | |||||||
chr7:114925288 | A | G | 294 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(291): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.94+2161A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114925288 | |||||||
chr7:114925409 | T | C | 1 | a0001c0001t0004g0110 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.94+2282T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114925409 | |||||||
chr7:114925643 | G | A | 1 | a0001c0001t0009g0107 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.94+2516G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114925643 | |||||||
chr7:114926068 | T | C | 1 | a0001c0003t0031g0018 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.94+2941T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926068 | |||||||
chr7:114926214 | A | T | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(271): Show |
288 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(285): Show |
intron_variant | MODIFIER | c.94+3087A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926214 | |||||||
chr7:114926510 | C | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0294 a0001c0001t0001g0295 others(12): Show |
18 | HG00408.hp1 HG02523.hp2 NA18747.hp1 others(15): Show |
intron_variant | MODIFIER | c.94+3383C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926510 | |||||||
chr7:114926535 | G | A | 1 | a0001c0001t0047g0019 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.94+3408G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926535 | |||||||
chr7:114926834 | A | G | 1 | a0001c0001t0028g0293 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.94+3707A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926834 | |||||||
chr7:114926894 | G | T | 1 | a0001c0001t0013g0292 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.94+3767G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926894 | |||||||
chr7:114926937 | C | A | 1 | a0001c0001t0009g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.94+3810C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114926937 | |||||||
chr7:114927325 | C | CT | 305 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(302): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.94+4212dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114927325 | ||||||
chr7:114927325 | C | CTT | 11 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(8): Show |
11 | HG01168.hp2 HG01516.hp1 HG01981.hp2 others(8): Show |
intron_variant | MODIFIER | c.94+4211_94+4212dup others(2): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114927325 | ||||||
chr7:114927455 | C | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(227): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.94+4328C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114927455 | |||||||
chr7:114927517 | A | G | 57 | a0001c0001t0001g0004 a0001c0001t0001g0248 a0001c0001t0001g0251 others(54): Show |
60 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(57): Show |
intron_variant | MODIFIER | c.94+4390A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114927517 | |||||||
chr7:114927741 | C | T | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+4614C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114927741 | |||||||
chr7:114927800 | C | A | 1 | a0001c0001t0010g0089 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.94+4673C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114927800 | |||||||
chr7:114927984 | GC | G | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(227): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.94+4858delC | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114927984 | |||||||
chr7:114928049 | A | G | 48 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0220 others(45): Show |
49 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.94+4922A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114928049 | |||||||
chr7:114928125 | A | T | 1 | a0001c0001t0044g0105 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.94+4998A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114928125 | |||||||
chr7:114928324 | C | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(266): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.94+5197C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114928324 | |||||||
chr7:114928557 | T | C | 38 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0069 others(35): Show |
39 | HG00609.hp1 HG02015.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.94+5430T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114928557 | |||||||
chr7:114928677 | A | C | 1 | a0001c0001t0001g0194 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.94+5550A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114928677 | |||||||
chr7:114929037 | A | G | 6 | a0001c0001t0010g0056 a0001c0001t0022g0052 a0001c0001t0022g0053 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+5910A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929037 | |||||||
chr7:114929055 | A | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0090 others(154): Show |
166 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(163): Show |
intron_variant | MODIFIER | c.94+5928A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929055 | |||||||
chr7:114929084 | G | GATCTATC others(9): Show |
2 | a0001c0001t0005g0128 a0001c0001t0022g0052 |
2 | HG02257.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.94+5961_94+5976dup others(16): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929084 | ||||||
chr7:114929084 | G | GATCTATC others(13): Show |
23 | a0001c0001t0001g0129 a0001c0001t0002g0043 a0001c0001t0002g0202 others(20): Show |
23 | HG01070.hp2 HG01168.hp2 HG01255.hp1 others(20): Show |
intron_variant | MODIFIER | c.94+5976_94+5977ins others(20): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929084 | ||||||
chr7:114929084 | G | GATCTATC others(17): Show |
130 | a0001c0001t0001g0007 a0001c0001t0001g0090 a0001c0001t0001g0091 others(127): Show |
138 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.94+5976_94+5977ins others(24): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929084 | ||||||
chr7:114929084 | G | GATCTATC others(21): Show |
83 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0096 others(80): Show |
88 | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(85): Show |
intron_variant | MODIFIER | c.94+5976_94+5977ins others(28): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929084 | ||||||
chr7:114929084 | G | GATCTATC others(25): Show |
15 | a0001c0001t0001g0191 a0001c0001t0001g0305 a0001c0001t0001g0307 others(12): Show |
15 | HG00621.hp1 HG00738.hp1 HG01167.hp2 others(12): Show |
intron_variant | MODIFIER | c.94+5976_94+5977ins others(32): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929084 | ||||||
chr7:114929084 | G | GATCTATC others(17): Show |
1 | a0001c0001t0005g0193 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.94+5971_94+5972ins others(24): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929084 | ||||||
chr7:114929088 | T | TATCTATC others(10): Show |
39 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0069 others(36): Show |
40 | HG00609.hp1 HG02015.hp2 HG02040.hp2 others(37): Show |
intron_variant | MODIFIER | c.94+5976_94+5977ins others(17): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114929088 | ||||||
chr7:114929273 | A | G | 1 | a0001c0003t0036g0057 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.94+6146A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929273 | |||||||
chr7:114929307 | C | A | 14 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(11): Show |
15 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.94+6180C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929307 | |||||||
chr7:114929327 | C | T | 1 | a0001c0001t0062g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.94+6200C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929327 | |||||||
chr7:114929481 | G | A | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+6354G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929481 | |||||||
chr7:114929547 | A | T | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(227): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.94+6420A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929547 | |||||||
chr7:114929715 | A | C | 1 | a0001c0001t0037g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.94+6588A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929715 | |||||||
chr7:114929722 | A | G | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+6595A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929722 | |||||||
chr7:114929754 | A | C | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(227): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.94+6627A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929754 | |||||||
chr7:114929783 | G | A | 1 | a0001c0001t0020g0010 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.94+6656G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929783 | |||||||
chr7:114929845 | G | A | 4 | a0001c0001t0012g0021 a0001c0001t0037g0040 a0001c0001t0060g0022 others(1): Show |
4 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.94+6718G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114929845 | |||||||
chr7:114930602 | T | G | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+7475T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114930602 | |||||||
chr7:114930797 | T | C | 6 | a0001c0001t0001g0001 a0001c0001t0001g0296 a0001c0001t0001g0302 others(3): Show |
9 | NA18939.hp1 NA18942.hp2 NA18950.hp1 others(6): Show |
intron_variant | MODIFIER | c.94+7670T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114930797 | |||||||
chr7:114931083 | CTCTT | C | 6 | a0001c0001t0010g0056 a0001c0001t0022g0052 a0001c0001t0022g0053 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+7958_94+7961del others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114931083 | ||||||
chr7:114931096 | C | T | 1 | a0001c0003t0036g0057 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.94+7969C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931096 | |||||||
chr7:114931214 | A | G | 1 | a0001c0001t0013g0265 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.94+8087A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931214 | |||||||
chr7:114931290 | G | A | 6 | a0001c0001t0001g0134 a0001c0001t0011g0131 a0001c0001t0011g0132 others(3): Show |
6 | HG02109.hp1 HG02572.hp2 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.94+8163G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931290 | |||||||
chr7:114931308 | C | T | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+8181C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931308 | |||||||
chr7:114931493 | G | A | 1 | a0001c0001t0001g0096 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.94+8366G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931493 | |||||||
chr7:114931795 | G | A | 1 | a0001c0001t0005g0241 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.94+8668G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931795 | |||||||
chr7:114931796 | T | C | 3 | a0001c0001t0003g0169 a0001c0001t0005g0136 a0001c0001t0005g0137 |
3 | NA18970.hp2 NA19058.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.94+8669T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931796 | |||||||
chr7:114931974 | G | A | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18982.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.94+8847G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114931974 | |||||||
chr7:114932000 | C | T | 5 | a0001c0001t0010g0056 a0001c0001t0022g0052 a0001c0001t0022g0053 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+8873C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932000 | |||||||
chr7:114932125 | G | A | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.94+8998G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932125 | |||||||
chr7:114932135 | A | G | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.94+9008A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932135 | |||||||
chr7:114932191 | G | C | 5 | a0001c0001t0010g0056 a0001c0001t0022g0052 a0001c0001t0022g0053 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.94+9064G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932191 | |||||||
chr7:114932526 | G | A | 1 | a0001c0001t0012g0138 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.94+9399G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932526 | |||||||
chr7:114932546 | G | A | 1 | a0001c0001t0006g0097 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.94+9419G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932546 | |||||||
chr7:114932616 | C | T | 1 | a0001c0001t0025g0117 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.94+9489C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932616 | |||||||
chr7:114932670 | G | T | 1 | a0001c0002t0002g0051 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.94+9543G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932670 | |||||||
chr7:114932677 | G | T | 1 | a0001c0001t0011g0167 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.94+9550G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932677 | |||||||
chr7:114932685 | G | A | 1 | a0001c0001t0032g0112 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.94+9558G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932685 | |||||||
chr7:114932739 | G | A | 1 | a0001c0001t0002g0061 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.95-9536G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932739 | |||||||
chr7:114932835 | A | G | 6 | a0001c0001t0010g0056 a0001c0001t0022g0052 a0001c0001t0022g0053 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-9440A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114932835 | |||||||
chr7:114933089 | G | C | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(266): Show |
283 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(280): Show |
intron_variant | MODIFIER | c.95-9186G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933089 | |||||||
chr7:114933253 | C | CA | 3 | a0001c0001t0008g0017 a0001c0001t0008g0139 a0003c0004t0008g0170 |
3 | HG03453.hp2 HG03540.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.95-9022_95-9021ins others(1): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933253 | |||||||
chr7:114933253 | C | CT | 239 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(236): Show |
252 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(249): Show |
intron_variant | MODIFIER | c.95-9005dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114933253 | ||||||
chr7:114933314 | A | G | 2 | a0001c0001t0003g0190 a0001c0001t0011g0167 |
2 | HG01433.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.95-8961A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933314 | |||||||
chr7:114933345 | G | T | 48 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0220 others(45): Show |
49 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(46): Show |
intron_variant | MODIFIER | c.95-8930G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933345 | |||||||
chr7:114933362 | G | A | 1 | a0001c0001t0008g0009 | 2 | HG01515.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.95-8913G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933362 | |||||||
chr7:114933373 | T | C | 275 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(272): Show |
289 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(286): Show |
intron_variant | MODIFIER | c.95-8902T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933373 | |||||||
chr7:114933564 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.95-8711C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933564 | |||||||
chr7:114933777 | A | C | 1 | a0001c0001t0002g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.95-8498A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933777 | |||||||
chr7:114933824 | T | C | 2 | a0001c0001t0002g0225 a0001c0001t0004g0207 |
2 | HG01256.hp1 HG01257.hp1 |
intron_variant | MODIFIER | c.95-8451T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933824 | |||||||
chr7:114933916 | C | T | 1 | a0001c0001t0015g0311 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.95-8359C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933916 | |||||||
chr7:114933917 | G | A | 1 | a0001c0001t0001g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.95-8358G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933917 | |||||||
chr7:114933932 | T | A | 1 | a0001c0001t0004g0063 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.95-8343T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114933932 | |||||||
chr7:114934024 | C | T | 2 | a0001c0001t0008g0038 a0001c0001t0008g0039 |
2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.95-8251C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114934024 | |||||||
chr7:114934025 | G | A | 1 | a0001c0001t0027g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.95-8250G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114934025 | |||||||
chr7:114934184 | A | G | 3 | a0001c0001t0013g0265 a0001c0001t0013g0284 a0001c0001t0021g0264 |
3 | NA18941.hp1 NA19012.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.95-8091A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114934184 | |||||||
chr7:114934552 | A | T | 6 | a0001c0001t0013g0265 a0001c0001t0013g0283 a0001c0001t0013g0284 others(3): Show |
6 | HG02074.hp2 NA18941.hp1 NA18979.hp2 others(3): Show |
intron_variant | MODIFIER | c.95-7723A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114934552 | |||||||
chr7:114934692 | C | T | 16 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(13): Show |
17 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-7583C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114934692 | |||||||
chr7:114935026 | A | G | 1 | a0001c0001t0002g0059 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.95-7249A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935026 | |||||||
chr7:114935037 | G | T | 1 | a0001c0001t0002g0261 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.95-7238G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935037 | |||||||
chr7:114935250 | T | G | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.95-7025T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935250 | |||||||
chr7:114935390 | T | C | 1 | a0001c0001t0001g0251 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.95-6885T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935390 | |||||||
chr7:114935468 | T | A | 1 | a0001c0001t0009g0119 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.95-6807T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935468 | |||||||
chr7:114935532 | G | GT | 229 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(226): Show |
242 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(239): Show |
intron_variant | MODIFIER | c.95-6734dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114935532 | ||||||
chr7:114935800 | T | C | 1 | a0001c0001t0052g0208 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.95-6475T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935800 | |||||||
chr7:114935814 | G | T | 1 | a0001c0001t0012g0138 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.95-6461G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935814 | |||||||
chr7:114935917 | A | G | 1 | a0001c0001t0013g0130 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.95-6358A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114935917 | |||||||
chr7:114936015 | T | C | 1 | a0001c0001t0001g0140 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.95-6260T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114936015 | |||||||
chr7:114936060 | G | T | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.95-6215G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114936060 | |||||||
chr7:114936541 | A | G | 5 | a0001c0001t0010g0056 a0001c0001t0022g0052 a0001c0001t0022g0053 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-5734A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114936541 | |||||||
chr7:114936597 | A | G | 3 | a0001c0001t0013g0265 a0001c0001t0013g0284 a0001c0001t0021g0264 |
3 | NA18941.hp1 NA19012.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.95-5678A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114936597 | |||||||
chr7:114936737 | G | A | 1 | a0001c0001t0001g0064 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.95-5538G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114936737 | |||||||
chr7:114936878 | CATTG | C | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-5393_95-5390del others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114936878 | ||||||
chr7:114936973 | T | A | 230 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(227): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.95-5302T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114936973 | |||||||
chr7:114937054 | A | C | 1 | a0001c0001t0048g0037 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.95-5221A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937054 | |||||||
chr7:114937084 | A | G | 1 | a0001c0001t0002g0282 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.95-5191A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937084 | |||||||
chr7:114937212 | G | A | 1 | a0001c0002t0002g0024 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.95-5063G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937212 | |||||||
chr7:114937330 | T | C | 1 | a0001c0001t0012g0013 | 2 | HG01361.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.95-4945T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937330 | |||||||
chr7:114937458 | T | C | 14 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(11): Show |
15 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(12): Show |
intron_variant | MODIFIER | c.95-4817T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937458 | |||||||
chr7:114937460 | T | A | 8 | a0001c0001t0001g0248 a0001c0001t0004g0015 a0001c0001t0004g0285 others(5): Show |
9 | HG00408.hp2 HG00673.hp2 HG02056.hp2 others(6): Show |
intron_variant | MODIFIER | c.95-4815T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937460 | |||||||
chr7:114937527 | G | C | 7 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0070 others(4): Show |
7 | NA18940.hp2 NA18951.hp1 NA18955.hp2 others(4): Show |
intron_variant | MODIFIER | c.95-4748G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937527 | |||||||
chr7:114937678 | G | A | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.95-4597G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937678 | |||||||
chr7:114937779 | G | A | 1 | a0001c0002t0002g0051 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.95-4496G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937779 | |||||||
chr7:114937798 | C | T | 2 | a0001c0001t0001g0088 a0001c0001t0002g0087 |
2 | HG03834.hp1 HG03942.hp1 |
intron_variant | MODIFIER | c.95-4477C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114937798 | |||||||
chr7:114938474 | C | A | 1 | a0001c0001t0029g0041 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.95-3801C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114938474 | |||||||
chr7:114938741 | G | T | 1 | a0001c0001t0003g0190 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.95-3534G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114938741 | |||||||
chr7:114938799 | AC | A | 315 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(312): Show |
330 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(327): Show |
intron_variant | MODIFIER | c.95-3473delC | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114938799 | ||||||
chr7:114938858 | C | G | 6 | a0001c0001t0010g0056 a0001c0001t0022g0052 a0001c0001t0022g0053 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-3417C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114938858 | |||||||
chr7:114938903 | C | T | 1 | a0001c0001t0011g0165 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.95-3372C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114938903 | |||||||
chr7:114938908 | T | C | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-3367T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114938908 | |||||||
chr7:114939097 | C | CATATG | 11 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(8): Show |
12 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-3178_95-3177ins others(5): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939097 | |||||||
chr7:114939098 | C | G | 11 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(8): Show |
12 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-3177C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939098 | |||||||
chr7:114939099 | A | G | 11 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(8): Show |
12 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-3176A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939099 | |||||||
chr7:114939101 | C | A | 11 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(8): Show |
12 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-3174C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939101 | |||||||
chr7:114939102 | A | G | 11 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(8): Show |
12 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.95-3173A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939102 | |||||||
chr7:114939157 | A | G | 3 | a0001c0001t0026g0163 a0001c0001t0026g0164 a0001c0001t0026g0189 |
3 | HG02132.hp2 HG04184.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.95-3118A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939157 | |||||||
chr7:114939377 | T | C | 4 | a0001c0001t0002g0210 a0001c0001t0002g0226 a0001c0001t0007g0212 others(1): Show |
4 | HG00642.hp2 HG00741.hp2 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2898T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939377 | |||||||
chr7:114939588 | GC | G | 4 | a0001c0001t0012g0021 a0001c0001t0037g0040 a0001c0001t0060g0022 others(1): Show |
4 | HG02280.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.95-2685delC | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114939588 | ||||||
chr7:114939685 | C | G | 2 | a0001c0001t0001g0188 a0001c0001t0006g0301 |
2 | NA18982.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.95-2590C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939685 | |||||||
chr7:114939699 | A | G | 1 | a0001c0001t0004g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.95-2576A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939699 | |||||||
chr7:114939788 | C | T | 1 | a0001c0001t0015g0310 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.95-2487C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939788 | |||||||
chr7:114939924 | A | T | 1 | a0001c0001t0010g0086 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.95-2351A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939924 | |||||||
chr7:114939929 | G | C | 1 | a0001c0001t0010g0086 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.95-2346G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939929 | |||||||
chr7:114939931 | A | C | 1 | a0001c0001t0010g0086 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.95-2344A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939931 | |||||||
chr7:114939980 | T | C | 239 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(236): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.95-2295T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114939980 | |||||||
chr7:114940002 | A | G | 2 | a0001c0001t0001g0004 a0001c0001t0014g0004 |
3 | HG00673.hp1 HG02040.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.95-2273A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940002 | |||||||
chr7:114940016 | T | G | 38 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0069 others(35): Show |
39 | HG00609.hp1 HG02015.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.95-2259T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940016 | |||||||
chr7:114940036 | A | C | 38 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0069 others(35): Show |
39 | HG00609.hp1 HG02015.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.95-2239A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940036 | |||||||
chr7:114940198 | T | C | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-2077T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940198 | |||||||
chr7:114940265 | T | C | 1 | a0001c0001t0027g0025 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.95-2010T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940265 | |||||||
chr7:114940342 | T | G | 6 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(3): Show |
6 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.95-1933T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940342 | |||||||
chr7:114940458 | G | A | 5 | a0001c0001t0010g0056 a0001c0001t0022g0052 a0001c0001t0022g0053 others(2): Show |
5 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.95-1817G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940458 | |||||||
chr7:114940510 | G | A | 1 | a0001c0001t0002g0045 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.95-1765G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940510 | |||||||
chr7:114940553 | A | T | 1 | a0001c0003t0036g0057 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.95-1722A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114940553 | |||||||
chr7:114940977 | GTC | G | 38 | a0001c0001t0001g0062 a0001c0001t0001g0064 a0001c0001t0001g0069 others(35): Show |
39 | HG00609.hp1 HG02015.hp2 HG02040.hp2 others(36): Show |
intron_variant | MODIFIER | c.95-1292_95-1291del others(2): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr7 | 114940977 | ||||||
chr7:114941167 | C | T | 2 | a0001c0001t0022g0052 a0001c0001t0022g0053 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.95-1108C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114941167 | |||||||
chr7:114941346 | G | A | 1 | a0001c0001t0013g0141 | 1 | NA18965.hp1 | intron_variant | MODIFIER | c.95-929G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114941346 | |||||||
chr7:114941453 | C | T | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.95-822C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114941453 | |||||||
chr7:114941674 | A | T | 1 | a0001c0001t0040g0135 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.95-601A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114941674 | |||||||
chr7:114941795 | C | T | 1 | a0001c0002t0002g0051 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.95-480C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114941795 | |||||||
chr7:114941870 | C | T | 1 | a0001c0001t0051g0186 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.95-405C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114941870 | |||||||
chr7:114942034 | G | C | 277 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(274): Show |
291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.95-241G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114942034 | |||||||
chr7:114942107 | A | G | 3 | a0001c0001t0003g0169 a0001c0001t0005g0136 a0001c0001t0005g0137 |
3 | NA18970.hp2 NA19058.hp1 NA19076.hp2 |
intron_variant | MODIFIER | c.95-168A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114942107 | |||||||
chr7:114942136 | G | A | 16 | a0001c0001t0009g0008 a0001c0001t0009g0107 a0001c0001t0009g0111 others(13): Show |
17 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.95-139G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 2/4 | chr7 | 114942136 | |||||||
chr7:114942469 | C | T | 6 | a0001c0001t0010g0056 a0001c0001t0022g0052 a0001c0001t0022g0053 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+72C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114942469 | |||||||
chr7:114942640 | C | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.217+243C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114942640 | |||||||
chr7:114942966 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(229): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.217+569C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114942966 | |||||||
chr7:114942983 | C | T | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+586C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114942983 | |||||||
chr7:114942984 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0090 a0001c0001t0001g0091 others(13): Show |
18 | HG00099.hp1 HG01099.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.217+587G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114942984 | |||||||
chr7:114943033 | C | T | 12 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(9): Show |
13 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.217+636C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943033 | |||||||
chr7:114943043 | T | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(229): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.217+646T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943043 | |||||||
chr7:114943402 | A | G | 1 | a0001c0001t0021g0162 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.217+1005A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943402 | |||||||
chr7:114943432 | A | T | 1 | a0001c0001t0011g0192 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.217+1035A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943432 | |||||||
chr7:114943517 | G | A | 1 | a0001c0001t0004g0297 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.217+1120G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943517 | |||||||
chr7:114943521 | T | C | 1 | a0001c0001t0059g0308 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.217+1124T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943521 | |||||||
chr7:114943622 | A | G | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18982.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.217+1225A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943622 | |||||||
chr7:114943702 | A | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(229): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.217+1305A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114943702 | |||||||
chr7:114943936 | C | CA | 4 | a0001c0001t0010g0029 a0001c0001t0057g0026 a0001c0001t0061g0027 others(1): Show |
4 | HG01243.hp1 HG02258.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+1545dupA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114943936 | ||||||
chr7:114944023 | A | G | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+1626A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944023 | |||||||
chr7:114944256 | G | A | 1 | a0001c0001t0001g0114 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.217+1859G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944256 | |||||||
chr7:114944312 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.217+1915G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944312 | |||||||
chr7:114944398 | T | A | 1 | a0001c0001t0008g0139 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.217+2001T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944398 | |||||||
chr7:114944448 | A | T | 4 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0019g0244 others(1): Show |
4 | HG02886.hp1 HG03130.hp2 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+2051A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944448 | |||||||
chr7:114944477 | T | A | 1 | a0001c0003t0036g0057 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.217+2080T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944477 | |||||||
chr7:114944677 | G | A | 16 | a0001c0001t0001g0007 a0001c0001t0001g0090 a0001c0001t0001g0091 others(13): Show |
18 | HG00099.hp1 HG01099.hp1 HG01516.hp2 others(15): Show |
intron_variant | MODIFIER | c.217+2280G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944677 | |||||||
chr7:114944743 | G | C | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+2346G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944743 | |||||||
chr7:114944992 | T | C | 57 | a0001c0001t0001g0129 a0001c0001t0001g0140 a0001c0001t0001g0144 others(54): Show |
59 | HG00621.hp2 HG01069.hp1 HG01106.hp1 others(56): Show |
intron_variant | MODIFIER | c.217+2595T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114944992 | |||||||
chr7:114945295 | G | T | 2 | a0001c0001t0004g0250 a0001c0001t0004g0278 |
2 | HG02523.hp1 NA19077.hp1 |
intron_variant | MODIFIER | c.217+2898G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114945295 | |||||||
chr7:114945614 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(229): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.217+3217A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114945614 | |||||||
chr7:114945681 | G | C | 6 | a0001c0001t0010g0056 a0001c0001t0022g0052 a0001c0001t0022g0053 others(3): Show |
6 | HG02615.hp1 HG02717.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+3284G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114945681 | |||||||
chr7:114945750 | C | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.217+3353C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114945750 | |||||||
chr7:114945763 | T | C | 1 | a0001c0001t0016g0245 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.217+3366T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114945763 | |||||||
chr7:114946002 | C | T | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+3605C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114946002 | |||||||
chr7:114946225 | A | AGT | 18 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(15): Show |
19 | HG01433.hp2 HG02055.hp1 HG02135.hp2 others(16): Show |
intron_variant | MODIFIER | c.217+3859_217+3860d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114946225 | ||||||
chr7:114946225 | A | AGTGT | 8 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(5): Show |
8 | HG01168.hp2 HG02257.hp2 HG02809.hp2 others(5): Show |
intron_variant | MODIFIER | c.217+3857_217+3860d others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114946225 | ||||||
chr7:114946225 | AGT | A | 167 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(164): Show |
178 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(175): Show |
intron_variant | MODIFIER | c.217+3859_217+3860d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114946225 | ||||||
chr7:114946225 | AGTGT | A | 52 | a0001c0001t0001g0085 a0001c0001t0001g0205 a0001c0001t0001g0206 others(49): Show |
53 | HG00140.hp1 HG00280.hp2 HG00642.hp2 others(50): Show |
intron_variant | MODIFIER | c.217+3857_217+3860d others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114946225 | ||||||
chr7:114946225 | AGTGTGT | A | 14 | a0001c0001t0001g0093 a0001c0001t0002g0282 a0001c0001t0009g0008 others(11): Show |
15 | HG00738.hp1 HG00741.hp1 HG01069.hp2 others(12): Show |
intron_variant | MODIFIER | c.217+3855_217+3860d others(8): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114946225 | ||||||
chr7:114946265 | C | T | 1 | a0001c0001t0003g0190 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.217+3868C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114946265 | |||||||
chr7:114946468 | A | G | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+4071A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114946468 | |||||||
chr7:114946727 | G | A | 1 | a0001c0001t0006g0301 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.217+4330G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114946727 | |||||||
chr7:114946820 | G | C | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(229): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.217+4423G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114946820 | |||||||
chr7:114946848 | C | T | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(229): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.217+4451C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114946848 | |||||||
chr7:114947239 | C | T | 7 | a0001c0001t0002g0261 a0001c0001t0004g0259 a0001c0001t0007g0016 others(4): Show |
8 | HG00099.hp2 HG00140.hp2 HG01081.hp2 others(5): Show |
intron_variant | MODIFIER | c.217+4842C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947239 | |||||||
chr7:114947305 | C | T | 1 | a0001c0001t0005g0157 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.217+4908C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947305 | |||||||
chr7:114947370 | A | G | 232 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(229): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): Show |
intron_variant | MODIFIER | c.217+4973A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947370 | |||||||
chr7:114947377 | A | G | 3 | a0001c0001t0002g0261 a0001c0001t0004g0259 a0001c0001t0007g0260 |
3 | HG00099.hp2 HG00140.hp2 HG01993.hp2 |
intron_variant | MODIFIER | c.217+4980A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947377 | |||||||
chr7:114947534 | T | C | 1 | a0001c0007t0005g0182 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.217+5137T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947534 | |||||||
chr7:114947667 | G | C | 4 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(1): Show |
4 | HG02257.hp2 HG02970.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+5270G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947667 | |||||||
chr7:114947710 | G | A | 34 | a0001c0001t0001g0090 a0001c0001t0001g0140 a0001c0001t0001g0144 others(31): Show |
35 | HG01192.hp2 HG01928.hp1 HG01981.hp2 others(32): Show |
intron_variant | MODIFIER | c.217+5313G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947710 | |||||||
chr7:114947786 | G | A | 1 | a0001c0001t0021g0143 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.217+5389G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947786 | |||||||
chr7:114947938 | G | T | 2 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.217+5541G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114947938 | |||||||
chr7:114948205 | A | G | 1 | a0001c0001t0062g0118 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.217+5808A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948205 | |||||||
chr7:114948222 | C | CT | 294 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(291): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.217+5827dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114948222 | ||||||
chr7:114948254 | G | A | 2 | a0001c0001t0002g0252 a0001c0001t0002g0267 |
2 | HG01192.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.217+5857G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948254 | |||||||
chr7:114948478 | C | T | 1 | a0001c0001t0035g0204 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.217+6081C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948478 | |||||||
chr7:114948485 | A | G | 233 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(230): Show |
246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.217+6088A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948485 | |||||||
chr7:114948505 | C | T | 1 | a0001c0002t0002g0051 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.217+6108C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948505 | |||||||
chr7:114948649 | A | G | 2 | a0001c0001t0002g0185 a0001c0001t0004g0184 |
2 | HG04199.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.217+6252A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948649 | |||||||
chr7:114948820 | C | A | 1 | a0001c0001t0025g0126 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.217+6423C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948820 | |||||||
chr7:114948925 | A | G | 1 | a0001c0001t0024g0177 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.217+6528A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948925 | |||||||
chr7:114948964 | T | C | 4 | a0001c0001t0006g0213 a0001c0001t0006g0227 a0001c0001t0016g0228 others(1): Show |
4 | NA18954.hp2 NA18966.hp1 NA19064.hp1 others(1): Show |
intron_variant | MODIFIER | c.217+6567T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114948964 | |||||||
chr7:114949100 | C | A | 1 | a0001c0001t0002g0282 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.217+6703C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114949100 | |||||||
chr7:114949106 | T | C | 1 | a0001c0001t0006g0097 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.217+6709T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114949106 | |||||||
chr7:114949440 | G | A | 2 | a0001c0001t0002g0058 a0001c0001t0002g0059 |
2 | HG02622.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.217+7043G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114949440 | |||||||
chr7:114949704 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.217+7307T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114949704 | |||||||
chr7:114949790 | TA | T | 295 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(292): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.217+7396delA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114949790 | ||||||
chr7:114949806 | G | A | 1 | a0001c0001t0001g0071 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.217+7409G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114949806 | |||||||
chr7:114949966 | G | A | 1 | a0001c0001t0002g0229 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.217+7569G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114949966 | |||||||
chr7:114950173 | G | A | 238 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(235): Show |
251 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(248): Show |
intron_variant | MODIFIER | c.217+7776G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950173 | |||||||
chr7:114950253 | G | A | 2 | a0001c0001t0009g0107 a0001c0001t0065g0313 |
2 | HG02258.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.217+7856G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950253 | |||||||
chr7:114950282 | T | C | 1 | a0001c0001t0007g0230 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.217+7885T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950282 | |||||||
chr7:114950391 | G | A | 1 | a0001c0001t0007g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.217+7994G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950391 | |||||||
chr7:114950747 | A | T | 2 | a0001c0001t0022g0052 a0001c0001t0022g0053 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.217+8350A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950747 | |||||||
chr7:114950832 | G | A | 1 | a0001c0001t0006g0227 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.217+8435G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950832 | |||||||
chr7:114950874 | A | G | 1 | a0001c0003t0036g0057 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.217+8477A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950874 | |||||||
chr7:114950976 | A | C | 283 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(280): Show |
297 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(294): Show |
intron_variant | MODIFIER | c.217+8579A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114950976 | |||||||
chr7:114951248 | CT | C | 240 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(237): Show |
253 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(250): Show |
intron_variant | MODIFIER | c.217+8852delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951248 | |||||||
chr7:114951345 | GA | G | 58 | a0001c0001t0001g0129 a0001c0001t0001g0140 a0001c0001t0001g0144 others(55): Show |
61 | HG00621.hp2 HG01069.hp1 HG01106.hp1 others(58): Show |
intron_variant | MODIFIER | c.217+8958delA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114951345 | ||||||
chr7:114951407 | C | T | 11 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(8): Show |
12 | HG01433.hp2 HG02055.hp1 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.217+9010C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951407 | |||||||
chr7:114951411 | A | G | 1 | a0001c0001t0001g0084 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.217+9014A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951411 | |||||||
chr7:114951448 | A | G | 7 | a0001c0001t0002g0101 a0001c0001t0002g0102 a0001c0001t0002g0103 others(4): Show |
7 | HG01168.hp2 HG02257.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+9051A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951448 | |||||||
chr7:114951449 | A | G | 1 | a0001c0001t0004g0207 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.217+9052A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951449 | |||||||
chr7:114951610 | C | T | 1 | a0001c0001t0017g0203 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.217+9213C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951610 | |||||||
chr7:114951660 | G | GT | 19 | a0001c0001t0001g0062 a0001c0001t0002g0002 a0001c0001t0002g0042 others(16): Show |
20 | HG01106.hp1 HG01361.hp2 HG01433.hp2 others(17): Show |
intron_variant | MODIFIER | c.217+9272dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114951660 | ||||||
chr7:114951710 | T | G | 1 | a0001c0002t0002g0051 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.217+9313T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951710 | |||||||
chr7:114951869 | C | A | 1 | a0001c0001t0013g0283 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.217+9472C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951869 | |||||||
chr7:114951970 | C | G | 5 | a0001c0001t0003g0280 a0001c0001t0003g0281 a0001c0001t0019g0244 others(2): Show |
5 | HG02572.hp1 HG03130.hp2 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+9573C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951970 | |||||||
chr7:114951979 | G | C | 1 | a0001c0001t0057g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.217+9582G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951979 | |||||||
chr7:114951994 | G | A | 73 | a0001c0001t0001g0085 a0001c0001t0001g0220 a0001c0001t0002g0045 others(70): Show |
75 | HG00099.hp1 HG00280.hp2 HG00642.hp2 others(72): Show |
intron_variant | MODIFIER | c.217+9597G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114951994 | |||||||
chr7:114952121 | T | C | 1 | a0001c0001t0009g0124 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.217+9724T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952121 | |||||||
chr7:114952178 | A | G | 43 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0001g0194 others(40): Show |
44 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(41): Show |
intron_variant | MODIFIER | c.217+9781A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952178 | |||||||
chr7:114952212 | T | C | 44 | a0001c0001t0001g0205 a0001c0001t0001g0206 a0001c0001t0001g0220 others(41): Show |
46 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(43): Show |
intron_variant | MODIFIER | c.217+9815T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952212 | |||||||
chr7:114952328 | C | A | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.217+9931C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952328 | |||||||
chr7:114952349 | G | A | 3 | a0001c0001t0003g0190 a0001c0001t0005g0233 a0001c0001t0012g0235 |
3 | HG00735.hp2 HG01109.hp2 HG01433.hp1 |
intron_variant | MODIFIER | c.217+9952G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952349 | |||||||
chr7:114952382 | C | G | 1 | a0001c0001t0021g0162 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.217+9985C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952382 | |||||||
chr7:114952416 | A | AT | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(107): Show |
117 | HG00099.hp2 HG00609.hp1 HG00621.hp1 others(114): Show |
intron_variant | MODIFIER | c.217+10031dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114952416 | ||||||
chr7:114952461 | A | G | 6 | a0001c0001t0005g0094 a0001c0001t0005g0095 a0001c0001t0005g0150 others(3): Show |
6 | HG00408.hp2 HG01981.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.217+10064A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952461 | |||||||
chr7:114952710 | G | GA | 6 | a0001c0001t0001g0090 a0001c0001t0001g0091 a0001c0001t0001g0092 others(3): Show |
6 | HG01099.hp1 HG02280.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.217+10320dupA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114952710 | ||||||
chr7:114952823 | G | A | 1 | a0001c0001t0002g0268 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.217+10426G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952823 | |||||||
chr7:114952824 | A | T | 5 | a0001c0001t0002g0048 a0001c0001t0002g0101 a0001c0001t0002g0102 others(2): Show |
5 | HG02257.hp2 HG02970.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+10427A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952824 | |||||||
chr7:114952921 | C | T | 1 | a0001c0001t0010g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.217+10524C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952921 | |||||||
chr7:114952931 | A | G | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+10534A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952931 | |||||||
chr7:114952933 | G | A | 73 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0206 others(70): Show |
76 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(73): Show |
intron_variant | MODIFIER | c.217+10536G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114952933 | |||||||
chr7:114953166 | T | C | 4 | a0001c0001t0001g0007 a0001c0001t0022g0052 a0001c0001t0022g0053 others(1): Show |
5 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+10769T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114953166 | |||||||
chr7:114953279 | T | C | 7 | a0001c0001t0002g0045 a0001c0001t0002g0048 a0001c0001t0002g0101 others(4): Show |
7 | HG01433.hp2 HG02257.hp2 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.217+10882T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114953279 | |||||||
chr7:114953604 | T | A | 2 | a0001c0001t0059g0308 a0001c0003t0031g0018 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.217+11207T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114953604 | |||||||
chr7:114953677 | G | A | 2 | a0001c0001t0002g0202 a0001c0001t0008g0300 |
2 | HG02922.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.217+11280G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114953677 | |||||||
chr7:114953810 | A | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(120): Show |
131 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.217+11413A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114953810 | |||||||
chr7:114953834 | A | G | 2 | a0001c0001t0012g0021 a0001c0001t0033g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.217+11437A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114953834 | |||||||
chr7:114954116 | C | T | 2 | a0001c0001t0012g0021 a0001c0001t0033g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.217+11719C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954116 | |||||||
chr7:114954135 | C | A | 1 | a0001c0001t0004g0184 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.217+11738C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954135 | |||||||
chr7:114954257 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0022g0052 a0001c0001t0022g0053 others(1): Show |
5 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+11860G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954257 | |||||||
chr7:114954277 | T | G | 8 | a0001c0001t0001g0114 a0001c0001t0002g0202 a0001c0001t0007g0269 others(5): Show |
8 | HG01496.hp2 HG02055.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.217+11880T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954277 | |||||||
chr7:114954582 | T | G | 1 | a0001c0001t0004g0278 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.217+12185T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954582 | |||||||
chr7:114954750 | C | A | 1 | a0001c0001t0011g0192 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.217+12353C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954750 | |||||||
chr7:114954897 | C | T | 1 | a0001c0001t0007g0171 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.217+12500C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954897 | |||||||
chr7:114954975 | G | C | 2 | a0001c0001t0005g0160 a0001c0001t0005g0304 |
2 | HG00408.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.217+12578G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114954975 | |||||||
chr7:114955190 | A | G | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | NA18944.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.217+12793A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955190 | |||||||
chr7:114955234 | T | C | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(115): Show |
125 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.217+12837T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955234 | |||||||
chr7:114955392 | G | A | 2 | a0001c0001t0001g0294 a0001c0001t0001g0295 |
2 | NA18944.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.217+12995G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955392 | |||||||
chr7:114955392 | G | T | 3 | a0001c0001t0007g0212 a0001c0001t0007g0230 a0001c0001t0007g0260 |
3 | HG00140.hp2 HG00741.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.217+12995G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955392 | |||||||
chr7:114955440 | G | A | 1 | a0001c0001t0018g0098 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.217+13043G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955440 | |||||||
chr7:114955488 | A | G | 1 | a0001c0001t0009g0127 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.217+13091A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955488 | |||||||
chr7:114955779 | C | T | 1 | a0001c0001t0065g0313 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.217+13382C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955779 | |||||||
chr7:114955799 | A | G | 305 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(302): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): Show |
intron_variant | MODIFIER | c.217+13402A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955799 | |||||||
chr7:114955873 | C | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.217+13476C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955873 | |||||||
chr7:114955975 | T | A | 2 | a0001c0001t0019g0244 a0001c0001t0019g0279 |
2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.217+13578T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114955975 | |||||||
chr7:114956162 | G | C | 1 | a0001c0001t0021g0145 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.217+13765G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956162 | |||||||
chr7:114956219 | A | C | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.217+13822A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956219 | |||||||
chr7:114956322 | C | G | 3 | a0001c0001t0004g0015 a0001c0001t0004g0285 a0001c0001t0006g0015 |
3 | HG02071.hp2 HG02129.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.217+13925C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956322 | |||||||
chr7:114956348 | TAC | T | 4 | a0001c0001t0007g0033 a0001c0001t0007g0034 a0001c0001t0007g0156 others(1): Show |
4 | HG01069.hp1 HG01257.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+13961_217+1396 others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114956348 | ||||||
chr7:114956358 | C | CAT | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(109): Show |
120 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(117): Show |
intron_variant | MODIFIER | c.217+13973_217+1397 others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114956358 | ||||||
chr7:114956358 | C | CATAT | 6 | a0001c0001t0001g0248 a0001c0001t0014g0106 a0001c0001t0014g0274 others(3): Show |
6 | HG00621.hp1 HG02080.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.217+13971_217+1397 others(8): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114956358 | ||||||
chr7:114956358 | C | T | 4 | a0001c0001t0007g0033 a0001c0001t0007g0034 a0001c0001t0007g0156 others(1): Show |
4 | HG01069.hp1 HG01257.hp2 HG02738.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+13961C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956358 | |||||||
chr7:114956425 | A | C | 8 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0047 others(5): Show |
9 | HG01361.hp2 HG02055.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.217+14028A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956425 | |||||||
chr7:114956786 | T | G | 25 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(22): Show |
26 | HG01168.hp2 HG01361.hp2 HG01433.hp2 others(23): Show |
intron_variant | MODIFIER | c.217+14389T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956786 | |||||||
chr7:114956951 | G | T | 310 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.217+14554G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114956951 | |||||||
chr7:114957230 | T | A | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(120): Show |
131 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(128): Show |
intron_variant | MODIFIER | c.217+14833T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114957230 | |||||||
chr7:114957258 | G | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(311): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.217+14861G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114957258 | |||||||
chr7:114957402 | G | A | 310 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.217+15005G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114957402 | |||||||
chr7:114957453 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(115): Show |
125 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(122): Show |
intron_variant | MODIFIER | c.217+15056A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114957453 | |||||||
chr7:114958157 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0022g0052 a0001c0001t0022g0053 others(1): Show |
5 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+15760C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958157 | |||||||
chr7:114958202 | C | T | 25 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.217+15805C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958202 | |||||||
chr7:114958208 | T | A | 314 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(311): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.217+15811T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958208 | |||||||
chr7:114958310 | C | A | 4 | a0001c0001t0003g0190 a0001c0001t0005g0233 a0001c0001t0012g0235 others(1): Show |
4 | HG00642.hp1 HG00735.hp2 HG01109.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+15913C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958310 | |||||||
chr7:114958437 | G | A | 2 | a0001c0001t0005g0136 a0001c0001t0005g0137 |
2 | NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.217+16040G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958437 | |||||||
chr7:114958716 | A | T | 1 | a0001c0001t0003g0218 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.217+16319A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958716 | |||||||
chr7:114958852 | C | T | 1 | a0001c0001t0003g0076 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.217+16455C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114958852 | |||||||
chr7:114959506 | A | G | 26 | a0001c0001t0001g0194 a0001c0001t0005g0003 a0001c0001t0005g0012 others(23): Show |
27 | HG00408.hp2 HG01192.hp2 HG01256.hp2 others(24): Show |
intron_variant | MODIFIER | c.217+17109A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114959506 | |||||||
chr7:114959513 | C | T | 1 | a0001c0001t0004g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.217+17116C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114959513 | |||||||
chr7:114959601 | A | G | 1 | a0001c0001t0010g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.217+17204A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114959601 | |||||||
chr7:114959824 | C | CTAA | 100 | a0001c0001t0001g0007 a0001c0001t0001g0188 a0001c0001t0001g0194 others(97): Show |
105 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(102): Show |
intron_variant | MODIFIER | c.217+17456_217+1745 others(7): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114959824 | ||||||
chr7:114959824 | C | CTAATAA | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(152): Show |
163 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(160): Show |
intron_variant | MODIFIER | c.217+17453_217+1745 others(10): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114959824 | ||||||
chr7:114959824 | C | CTAATAAT others(2): Show |
52 | a0001c0001t0001g0079 a0001c0001t0001g0114 a0001c0001t0001g0191 others(49): Show |
54 | HG00099.hp1 HG00140.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.217+17450_217+1745 others(13): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114959824 | ||||||
chr7:114959824 | C | CTAATAAT others(5): Show |
1 | a0001c0001t0010g0242 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.217+17447_217+1745 others(16): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114959824 | ||||||
chr7:114959824 | CTAA | C | 4 | a0001c0001t0010g0056 a0001c0001t0058g0253 a0001c0001t0060g0022 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.217+17456_217+1745 others(7): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114959824 | ||||||
chr7:114959913 | C | T | 1 | a0001c0002t0012g0028 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.217+17516C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114959913 | |||||||
chr7:114960292 | G | A | 1 | a0001c0001t0011g0131 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.217+17895G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960292 | |||||||
chr7:114960395 | C | T | 5 | a0001c0001t0005g0012 a0001c0001t0005g0159 a0001c0001t0005g0309 others(2): Show |
5 | HG01256.hp2 HG01358.hp2 HG01928.hp1 others(2): Show |
intron_variant | MODIFIER | c.217+17998C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960395 | |||||||
chr7:114960484 | A | T | 25 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.217+18087A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960484 | |||||||
chr7:114960494 | G | A | 1 | a0001c0001t0010g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.217+18097G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960494 | |||||||
chr7:114960517 | T | G | 1 | a0001c0001t0027g0025 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.217+18120T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960517 | |||||||
chr7:114960625 | G | A | 4 | a0001c0001t0001g0007 a0001c0001t0022g0052 a0001c0001t0022g0053 others(1): Show |
5 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.217+18228G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960625 | |||||||
chr7:114960628 | T | C | 1 | a0001c0001t0003g0214 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.217+18231T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114960628 | |||||||
chr7:114961039 | G | A | 12 | a0001c0001t0002g0185 a0001c0001t0007g0033 a0001c0001t0007g0034 others(9): Show |
13 | HG00738.hp2 HG01069.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.218-18467G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114961039 | |||||||
chr7:114961280 | T | A | 4 | a0001c0001t0010g0056 a0001c0001t0058g0253 a0001c0001t0060g0022 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-18226T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114961280 | |||||||
chr7:114961413 | G | A | 4 | a0001c0001t0010g0056 a0001c0001t0058g0253 a0001c0001t0060g0022 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-18093G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114961413 | |||||||
chr7:114961421 | G | A | 1 | a0001c0001t0005g0304 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.218-18085G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114961421 | |||||||
chr7:114961472 | G | GTGCTCAA others(38): Show |
1 | a0001c0001t0034g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.218-18031_218-1798 others(49): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114961472 | ||||||
chr7:114961825 | C | T | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218-17681C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114961825 | |||||||
chr7:114962043 | C | T | 1 | a0001c0001t0016g0240 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.218-17463C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962043 | |||||||
chr7:114962318 | T | C | 4 | a0001c0001t0016g0014 a0001c0001t0016g0245 a0001c0001t0017g0247 others(1): Show |
5 | HG00673.hp2 HG02056.hp2 HG02074.hp1 others(2): Show |
intron_variant | MODIFIER | c.218-17188T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962318 | |||||||
chr7:114962446 | C | A | 5 | a0001c0001t0001g0007 a0001c0001t0022g0052 a0001c0001t0022g0053 others(2): Show |
6 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(3): Show |
intron_variant | MODIFIER | c.218-17060C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962446 | |||||||
chr7:114962513 | A | G | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218-16993A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962513 | |||||||
chr7:114962789 | A | G | 1 | a0001c0001t0010g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.218-16717A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962789 | |||||||
chr7:114962817 | A | C | 1 | a0001c0001t0001g0295 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.218-16689A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962817 | |||||||
chr7:114962909 | A | T | 2 | a0001c0001t0012g0021 a0001c0001t0033g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.218-16597A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114962909 | |||||||
chr7:114963003 | G | A | 1 | a0001c0001t0037g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.218-16503G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963003 | |||||||
chr7:114963025 | G | T | 2 | a0001c0001t0059g0308 a0001c0003t0031g0018 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.218-16481G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963025 | |||||||
chr7:114963355 | C | A | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(119): Show |
130 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.218-16151C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963355 | |||||||
chr7:114963372 | T | A | 4 | a0001c0001t0002g0087 a0001c0001t0002g0142 a0001c0001t0002g0231 others(1): Show |
4 | HG01496.hp1 HG02698.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-16134T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963372 | |||||||
chr7:114963498 | A | T | 1 | a0001c0001t0004g0297 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.218-16008A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963498 | |||||||
chr7:114963728 | G | A | 2 | a0001c0001t0022g0052 a0001c0001t0022g0053 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.218-15778G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963728 | |||||||
chr7:114963868 | C | G | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-15638C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963868 | |||||||
chr7:114963931 | T | G | 1 | a0001c0001t0014g0273 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.218-15575T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114963931 | |||||||
chr7:114964043 | T | C | 1 | a0001c0001t0004g0207 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.218-15463T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964043 | |||||||
chr7:114964227 | A | G | 309 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(306): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.218-15279A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964227 | |||||||
chr7:114964492 | TC | T | 150 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0205 others(147): Show |
156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.218-15010delC | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114964492 | ||||||
chr7:114964493 | C | T | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(123): Show |
134 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(131): Show |
intron_variant | MODIFIER | c.218-15013C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964493 | |||||||
chr7:114964494 | C | T | 150 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0205 others(147): Show |
156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.218-15012C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964494 | |||||||
chr7:114964525 | ACTTCCCT others(8): Show |
A | 2 | a0001c0001t0037g0040 a0001c0001t0050g0060 |
2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218-14966_218-1495 others(19): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114964525 | ||||||
chr7:114964622 | C | A | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218-14884C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964622 | |||||||
chr7:114964637 | G | A | 150 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0205 others(147): Show |
156 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.218-14869G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964637 | |||||||
chr7:114964652 | G | A | 1 | a0001c0001t0005g0150 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.218-14854G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964652 | |||||||
chr7:114964693 | G | A | 2 | a0001c0001t0060g0022 a0001c0001t0061g0027 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.218-14813G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964693 | |||||||
chr7:114964709 | C | T | 2 | a0001c0001t0003g0199 a0001c0001t0003g0217 |
2 | HG01928.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.218-14797C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964709 | |||||||
chr7:114964827 | G | C | 1 | a0001c0001t0006g0246 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.218-14679G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964827 | |||||||
chr7:114964828 | C | A | 1 | a0001c0001t0006g0246 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.218-14678C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964828 | |||||||
chr7:114964843 | C | T | 1 | a0001c0001t0024g0258 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.218-14663C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114964843 | |||||||
chr7:114965141 | C | T | 309 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(306): Show |
324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.218-14365C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114965141 | |||||||
chr7:114965444 | G | A | 1 | a0001c0001t0005g0160 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.218-14062G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114965444 | |||||||
chr7:114966054 | A | G | 1 | a0001c0001t0005g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218-13452A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114966054 | |||||||
chr7:114966405 | C | CA | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(120): Show |
130 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(127): Show |
intron_variant | MODIFIER | c.218-13085dupA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114966405 | ||||||
chr7:114966405 | CAAAAAAA | C | 25 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-13091_218-1308 others(11): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114966405 | ||||||
chr7:114966510 | A | T | 1 | a0001c0001t0006g0179 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.218-12996A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114966510 | |||||||
chr7:114966524 | C | T | 105 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(102): Show |
111 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(108): Show |
intron_variant | MODIFIER | c.218-12982C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114966524 | |||||||
chr7:114966979 | T | A | 6 | a0001c0001t0010g0029 a0001c0001t0012g0021 a0001c0001t0012g0138 others(3): Show |
6 | HG01515.hp1 HG02132.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-12527T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114966979 | |||||||
chr7:114967026 | T | A | 2 | a0001c0001t0059g0308 a0001c0003t0031g0018 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.218-12480T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967026 | |||||||
chr7:114967097 | A | G | 2 | a0001c0001t0012g0021 a0001c0001t0033g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.218-12409A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967097 | |||||||
chr7:114967138 | T | G | 4 | a0001c0001t0002g0043 a0001c0001t0002g0046 a0001c0001t0002g0058 others(1): Show |
4 | HG02622.hp1 HG03579.hp1 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-12368T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967138 | |||||||
chr7:114967139 | T | C | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218-12367T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967139 | |||||||
chr7:114967158 | T | G | 3 | a0001c0001t0020g0010 a0001c0001t0020g0146 a0001c0001t0020g0200 |
4 | HG01070.hp1 HG01071.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-12348T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967158 | |||||||
chr7:114967161 | A | G | 25 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-12345A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967161 | |||||||
chr7:114967173 | G | A | 1 | a0001c0001t0001g0188 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.218-12333G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967173 | |||||||
chr7:114967474 | A | G | 307 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(304): Show |
322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.218-12032A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967474 | |||||||
chr7:114967489 | A | C | 1 | a0001c0001t0001g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.218-12017A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967489 | |||||||
chr7:114967546 | C | T | 4 | a0001c0001t0005g0108 a0001c0001t0015g0310 a0001c0001t0015g0311 others(1): Show |
4 | HG02273.hp2 NA18979.hp1 NA19009.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-11960C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967546 | |||||||
chr7:114967568 | A | T | 1 | a0001c0001t0012g0013 | 2 | HG01361.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.218-11938A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967568 | |||||||
chr7:114967597 | G | C | 1 | a0001c0001t0009g0119 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.218-11909G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967597 | |||||||
chr7:114967608 | G | A | 2 | a0001c0001t0030g0067 a0001c0001t0030g0068 |
2 | NA18973.hp2 NA19060.hp2 |
intron_variant | MODIFIER | c.218-11898G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967608 | |||||||
chr7:114967634 | G | T | 12 | a0001c0001t0001g0004 a0001c0001t0001g0248 a0001c0001t0001g0251 others(9): Show |
13 | HG00621.hp1 HG00673.hp1 HG02027.hp1 others(10): Show |
intron_variant | MODIFIER | c.218-11872G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967634 | |||||||
chr7:114967745 | G | C | 3 | a0001c0001t0020g0010 a0001c0001t0020g0146 a0001c0001t0020g0200 |
4 | HG01070.hp1 HG01071.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-11761G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114967745 | |||||||
chr7:114967830 | CT | C | 254 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(251): Show |
267 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.218-11659delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114967830 | ||||||
chr7:114967830 | CTT | C | 48 | a0001c0001t0001g0144 a0001c0001t0001g0181 a0001c0001t0001g0191 others(45): Show |
49 | HG00140.hp2 HG00741.hp2 HG01069.hp2 others(46): Show |
intron_variant | MODIFIER | c.218-11660_218-1165 others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114967830 | ||||||
chr7:114968136 | A | T | 1 | a0001c0001t0006g0178 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.218-11370A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968136 | |||||||
chr7:114968234 | G | T | 2 | a0001c0001t0001g0144 a0001c0001t0001g0149 |
2 | NA18972.hp2 NA19086.hp2 |
intron_variant | MODIFIER | c.218-11272G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968234 | |||||||
chr7:114968336 | A | C | 1 | a0001c0001t0007g0269 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.218-11170A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968336 | |||||||
chr7:114968382 | T | C | 9 | a0001c0001t0001g0007 a0001c0001t0022g0052 a0001c0001t0022g0053 others(6): Show |
10 | HG02280.hp1 HG02615.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.218-11124T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968382 | |||||||
chr7:114968567 | G | A | 1 | a0001c0001t0010g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.218-10939G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968567 | |||||||
chr7:114968814 | A | G | 2 | a0001c0001t0001g0134 a0001c0001t0019g0133 |
2 | HG02572.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.218-10692A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968814 | |||||||
chr7:114968906 | C | T | 2 | a0001c0001t0012g0021 a0001c0001t0033g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.218-10600C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968906 | |||||||
chr7:114968975 | G | A | 144 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0205 others(141): Show |
150 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(147): Show |
intron_variant | MODIFIER | c.218-10531G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114968975 | |||||||
chr7:114969043 | C | T | 4 | a0001c0001t0010g0029 a0001c0001t0012g0021 a0001c0001t0033g0104 others(1): Show |
4 | HG02809.hp1 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-10463C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969043 | |||||||
chr7:114969205 | C | T | 1 | a0001c0001t0051g0186 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.218-10301C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969205 | |||||||
chr7:114969429 | G | A | 1 | a0001c0001t0001g0302 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.218-10077G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969429 | |||||||
chr7:114969439 | C | T | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218-10067C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969439 | |||||||
chr7:114969465 | G | A | 1 | a0001c0001t0003g0076 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.218-10041G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969465 | |||||||
chr7:114969720 | AT | A | 7 | a0001c0001t0001g0007 a0001c0001t0022g0052 a0001c0001t0022g0053 others(4): Show |
8 | HG02280.hp1 HG02615.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.218-9785delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969720 | |||||||
chr7:114969773 | C | A | 1 | a0001c0001t0009g0119 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.218-9733C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114969773 | |||||||
chr7:114970163 | G | A | 2 | a0001c0001t0002g0185 a0001c0001t0047g0019 |
2 | HG02698.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.218-9343G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114970163 | |||||||
chr7:114970197 | G | A | 1 | a0001c0001t0025g0117 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.218-9309G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114970197 | |||||||
chr7:114970445 | C | T | 1 | a0001c0001t0003g0166 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.218-9061C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114970445 | |||||||
chr7:114970609 | C | T | 296 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(293): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.218-8897C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114970609 | |||||||
chr7:114970786 | T | C | 1 | a0001c0001t0001g0096 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.218-8720T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114970786 | |||||||
chr7:114970918 | G | T | 3 | a0001c0001t0003g0201 a0001c0001t0003g0280 a0001c0001t0003g0281 |
3 | HG01891.hp2 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.218-8588G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114970918 | |||||||
chr7:114971248 | A | T | 1 | a0001c0001t0049g0263 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.218-8258A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971248 | |||||||
chr7:114971313 | C | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.218-8193C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971313 | |||||||
chr7:114971362 | G | T | 2 | a0001c0001t0040g0135 a0001c0001t0062g0118 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.218-8144G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971362 | |||||||
chr7:114971447 | C | T | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-8059C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971447 | |||||||
chr7:114971468 | G | A | 1 | a0001c0006t0001g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.218-8038G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971468 | |||||||
chr7:114971479 | A | G | 311 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.218-8027A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971479 | |||||||
chr7:114971515 | T | C | 1 | a0001c0001t0006g0097 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.218-7991T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971515 | |||||||
chr7:114971624 | G | A | 1 | a0001c0001t0010g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.218-7882G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971624 | |||||||
chr7:114971731 | G | C | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.218-7775G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971731 | |||||||
chr7:114971857 | G | T | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218-7649G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971857 | |||||||
chr7:114971872 | G | A | 1 | a0001c0001t0014g0274 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.218-7634G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114971872 | |||||||
chr7:114972054 | C | T | 143 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0205 others(140): Show |
149 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(146): Show |
intron_variant | MODIFIER | c.218-7452C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972054 | |||||||
chr7:114972288 | A | T | 12 | a0001c0001t0002g0185 a0001c0001t0007g0033 a0001c0001t0007g0034 others(9): Show |
13 | HG00738.hp2 HG01069.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.218-7218A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972288 | |||||||
chr7:114972318 | A | C | 2 | a0001c0001t0001g0090 a0001c0001t0002g0229 |
2 | HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.218-7188A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972318 | |||||||
chr7:114972406 | C | T | 4 | a0001c0001t0001g0007 a0001c0001t0022g0052 a0001c0001t0022g0053 others(1): Show |
5 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-7100C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972406 | |||||||
chr7:114972549 | A | G | 2 | a0001c0001t0060g0022 a0001c0001t0061g0027 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.218-6957A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972549 | |||||||
chr7:114972753 | C | T | 25 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-6753C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972753 | |||||||
chr7:114972754 | G | A | 1 | a0001c0001t0004g0173 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.218-6752G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972754 | |||||||
chr7:114972901 | C | T | 1 | a0001c0001t0004g0173 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.218-6605C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972901 | |||||||
chr7:114972928 | C | T | 2 | a0001c0001t0041g0055 a0001c0003t0043g0023 |
2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.218-6578C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972928 | |||||||
chr7:114972953 | C | G | 1 | a0001c0001t0003g0237 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.218-6553C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114972953 | |||||||
chr7:114973090 | C | CAT | 16 | a0001c0001t0002g0059 a0001c0001t0002g0101 a0001c0001t0002g0102 others(13): Show |
16 | HG01516.hp1 HG02257.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.218-6416_218-6415i others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973090 | |||||||
chr7:114973090 | C | CATGT | 155 | a0001c0001t0001g0181 a0001c0001t0001g0188 a0001c0001t0001g0191 others(152): Show |
161 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.218-6416_218-6415i others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973090 | |||||||
chr7:114973090 | C | CATGTGT | 3 | a0001c0001t0002g0231 a0001c0001t0010g0089 a0001c0001t0011g0183 |
3 | HG01496.hp1 NA20129.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.218-6416_218-6415i others(8): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973090 | |||||||
chr7:114973091 | G | A | 131 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(128): Show |
140 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(137): Show |
intron_variant | MODIFIER | c.218-6415G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973091 | |||||||
chr7:114973101 | G | A | 158 | a0001c0001t0001g0181 a0001c0001t0001g0188 a0001c0001t0001g0191 others(155): Show |
164 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(161): Show |
intron_variant | MODIFIER | c.218-6405G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973101 | |||||||
chr7:114973101 | G | GTA | 4 | a0001c0001t0010g0029 a0001c0001t0012g0021 a0001c0001t0033g0104 others(1): Show |
4 | HG02809.hp1 HG02976.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.218-6385_218-6384d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114973101 | ||||||
chr7:114973101 | G | GTGTATA | 5 | a0001c0001t0006g0303 a0001c0001t0007g0212 a0001c0001t0007g0276 others(2): Show |
6 | HG00741.hp2 HG01081.hp2 HG01361.hp1 others(3): Show |
intron_variant | MODIFIER | c.218-6404_218-6403i others(8): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114973101 | ||||||
chr7:114973101 | G | GTGTATAT others(3): Show |
1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.218-6404_218-6403i others(12): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114973101 | ||||||
chr7:114973101 | G | GTGTGTAT others(3): Show |
2 | a0001c0001t0001g0007 a0001c0001t0022g0054 |
3 | HG02615.hp1 HG02970.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.218-6404_218-6403i others(12): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114973101 | ||||||
chr7:114973101 | G | GTGTGTGT others(3): Show |
2 | a0001c0001t0022g0052 a0001c0001t0022g0053 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.218-6404_218-6403i others(12): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114973101 | ||||||
chr7:114973103 | A | G | 117 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(114): Show |
124 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(121): Show |
intron_variant | MODIFIER | c.218-6403A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973103 | |||||||
chr7:114973143 | G | A | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-6363G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973143 | |||||||
chr7:114973220 | A | G | 74 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0206 others(71): Show |
77 | HG00323.hp1 HG00408.hp2 HG00609.hp2 others(74): Show |
intron_variant | MODIFIER | c.218-6286A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973220 | |||||||
chr7:114973281 | C | G | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-6225C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973281 | |||||||
chr7:114973464 | G | T | 1 | a0001c0001t0002g0252 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.218-6042G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973464 | |||||||
chr7:114973783 | T | C | 63 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(60): Show |
67 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(64): Show |
intron_variant | MODIFIER | c.218-5723T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114973783 | |||||||
chr7:114974176 | T | A | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.218-5330T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974176 | |||||||
chr7:114974182 | T | A | 1 | a0001c0001t0004g0207 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.218-5324T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974182 | |||||||
chr7:114974208 | T | C | 2 | a0001c0001t0037g0040 a0001c0001t0050g0060 |
2 | HG02280.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.218-5298T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974208 | |||||||
chr7:114974229 | T | C | 1 | a0001c0001t0005g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.218-5277T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974229 | |||||||
chr7:114974269 | T | C | 1 | a0001c0001t0002g0282 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.218-5237T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974269 | |||||||
chr7:114974297 | TTA | T | 312 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(309): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.218-5195_218-5194d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114974297 | ||||||
chr7:114974359 | G | A | 25 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-5147G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974359 | |||||||
chr7:114974437 | C | G | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-5069C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974437 | |||||||
chr7:114974584 | T | A | 311 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.218-4922T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974584 | |||||||
chr7:114974686 | T | C | 2 | a0001c0001t0001g0090 a0001c0001t0002g0229 |
2 | HG02818.hp1 HG02818.hp2 |
intron_variant | MODIFIER | c.218-4820T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974686 | |||||||
chr7:114974744 | A | G | 1 | a0001c0001t0007g0156 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.218-4762A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974744 | |||||||
chr7:114974762 | A | G | 1 | a0001c0001t0005g0159 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.218-4744A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974762 | |||||||
chr7:114974919 | T | C | 1 | a0001c0001t0002g0282 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.218-4587T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114974919 | |||||||
chr7:114975105 | G | A | 1 | a0001c0001t0004g0063 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.218-4401G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975105 | |||||||
chr7:114975113 | T | C | 311 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.218-4393T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975113 | |||||||
chr7:114975247 | G | A | 1 | a0001c0001t0005g0136 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.218-4259G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975247 | |||||||
chr7:114975261 | G | T | 313 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(310): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.218-4245G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975261 | |||||||
chr7:114975544 | G | A | 2 | a0001c0001t0040g0135 a0001c0001t0062g0118 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.218-3962G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975544 | |||||||
chr7:114975561 | CT | C | 294 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(291): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.218-3932delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114975561 | ||||||
chr7:114975706 | A | G | 1 | a0001c0001t0050g0060 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.218-3800A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975706 | |||||||
chr7:114975890 | A | G | 1 | a0001c0001t0007g0269 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.218-3616A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975890 | |||||||
chr7:114975899 | G | A | 4 | a0001c0001t0002g0048 a0001c0001t0002g0101 a0001c0001t0002g0102 others(1): Show |
4 | HG02257.hp2 HG02970.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-3607G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114975899 | |||||||
chr7:114976152 | C | T | 1 | a0001c0002t0023g0168 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.218-3354C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976152 | |||||||
chr7:114976247 | G | A | 1 | a0001c0001t0001g0205 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.218-3259G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976247 | |||||||
chr7:114976420 | C | T | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-3086C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976420 | |||||||
chr7:114976545 | T | A | 1 | a0001c0001t0015g0174 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.218-2961T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976545 | |||||||
chr7:114976627 | G | C | 9 | a0001c0001t0001g0007 a0001c0001t0022g0052 a0001c0001t0022g0053 others(6): Show |
10 | HG02280.hp1 HG02615.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.218-2879G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976627 | |||||||
chr7:114976633 | A | G | 1 | a0001c0003t0031g0018 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.218-2873A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976633 | |||||||
chr7:114976856 | CT | C | 25 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-2640delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr7 | 114976856 | ||||||
chr7:114976862 | T | C | 1 | a0001c0001t0018g0254 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.218-2644T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114976862 | |||||||
chr7:114977119 | A | T | 25 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-2387A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114977119 | |||||||
chr7:114977495 | C | T | 1 | a0001c0001t0010g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.218-2011C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114977495 | |||||||
chr7:114977547 | C | T | 1 | a0001c0001t0064g0120 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.218-1959C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114977547 | |||||||
chr7:114977591 | C | G | 1 | a0001c0001t0037g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.218-1915C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114977591 | |||||||
chr7:114977792 | T | C | 1 | a0001c0001t0002g0282 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.218-1714T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114977792 | |||||||
chr7:114977875 | A | T | 9 | a0001c0001t0001g0007 a0001c0001t0022g0052 a0001c0001t0022g0053 others(6): Show |
10 | HG02280.hp1 HG02615.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.218-1631A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114977875 | |||||||
chr7:114978004 | A | G | 1 | a0001c0001t0002g0103 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.218-1502A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978004 | |||||||
chr7:114978111 | C | T | 2 | a0001c0001t0040g0135 a0001c0001t0062g0118 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.218-1395C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978111 | |||||||
chr7:114978140 | G | A | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-1366G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978140 | |||||||
chr7:114978141 | C | T | 25 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-1365C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978141 | |||||||
chr7:114978155 | A | G | 1 | a0001c0001t0021g0143 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.218-1351A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978155 | |||||||
chr7:114978393 | C | T | 12 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(9): Show |
13 | HG01361.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.218-1113C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978393 | |||||||
chr7:114978428 | G | T | 1 | a0001c0001t0013g0292 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.218-1078G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978428 | |||||||
chr7:114978450 | A | C | 122 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(119): Show |
129 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.218-1056A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978450 | |||||||
chr7:114978577 | C | T | 311 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(308): Show |
326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.218-929C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978577 | |||||||
chr7:114978635 | T | C | 2 | a0001c0001t0019g0244 a0001c0001t0019g0279 |
2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.218-871T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978635 | |||||||
chr7:114978649 | AC | A | 5 | a0001c0001t0013g0130 a0001c0001t0013g0141 a0001c0001t0013g0154 others(2): Show |
5 | NA18965.hp1 NA18969.hp1 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.218-856delC | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978649 | |||||||
chr7:114978655 | A | G | 2 | a0001c0001t0008g0036 a0001c0001t0044g0105 |
2 | HG01168.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.218-851A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978655 | |||||||
chr7:114978730 | A | G | 4 | a0001c0001t0010g0029 a0001c0001t0012g0021 a0001c0001t0033g0104 others(1): Show |
4 | HG02809.hp1 HG02976.hp1 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.218-776A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978730 | |||||||
chr7:114978857 | A | T | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.218-649A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978857 | |||||||
chr7:114978894 | T | C | 2 | a0001c0001t0059g0308 a0001c0003t0031g0018 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.218-612T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114978894 | |||||||
chr7:114979039 | A | G | 25 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(22): Show |
26 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(23): Show |
intron_variant | MODIFIER | c.218-467A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114979039 | |||||||
chr7:114979152 | A | G | 2 | a0001c0001t0041g0055 a0001c0003t0043g0023 |
2 | HG02572.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.218-354A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114979152 | |||||||
chr7:114979277 | A | G | 1 | a0001c0001t0003g0239 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.218-229A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114979277 | |||||||
chr7:114979460 | A | G | 1 | a0001c0001t0003g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.218-46A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 3/4 | chr7 | 114979460 | |||||||
chr7:114979869 | G | C | 3 | a0001c0001t0002g0049 a0001c0001t0009g0107 a0001c0001t0009g0124 |
3 | HG01361.hp2 HG02615.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.493+88G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114979869 | |||||||
chr7:114979874 | T | C | 1 | a0001c0001t0052g0208 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.493+93T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114979874 | |||||||
chr7:114980027 | G | A | 1 | a0001c0001t0003g0190 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.493+246G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114980027 | |||||||
chr7:114980091 | A | T | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.493+310A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114980091 | |||||||
chr7:114980451 | C | T | 12 | a0001c0001t0002g0185 a0001c0001t0007g0033 a0001c0001t0007g0034 others(9): Show |
13 | HG00738.hp2 HG01069.hp1 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.493+670C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114980451 | |||||||
chr7:114980575 | T | TA | 9 | a0001c0001t0001g0007 a0001c0001t0022g0052 a0001c0001t0022g0053 others(6): Show |
10 | HG02280.hp1 HG02615.hp1 HG02970.hp2 others(7): Show |
intron_variant | MODIFIER | c.493+799dupA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114980575 | ||||||
chr7:114981137 | C | T | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.493+1356C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114981137 | |||||||
chr7:114981396 | C | T | 1 | a0001c0001t0003g0201 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.493+1615C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114981396 | |||||||
chr7:114981405 | G | A | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(104): Show |
113 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(110): Show |
intron_variant | MODIFIER | c.493+1624G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114981405 | |||||||
chr7:114981572 | C | G | 1 | a0001c0001t0010g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+1791C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114981572 | |||||||
chr7:114981588 | A | T | 2 | a0001c0001t0012g0021 a0001c0001t0033g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.493+1807A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114981588 | |||||||
chr7:114981732 | G | A | 1 | a0001c0001t0004g0256 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.493+1951G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114981732 | |||||||
chr7:114982037 | G | T | 2 | a0001c0001t0048g0037 a0001c0001t0065g0313 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.493+2256G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982037 | |||||||
chr7:114982467 | A | T | 1 | a0001c0001t0009g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.493+2686A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982467 | |||||||
chr7:114982470 | G | A | 13 | a0001c0001t0001g0114 a0001c0001t0002g0185 a0001c0001t0002g0202 others(10): Show |
14 | HG00738.hp2 HG01106.hp2 HG01496.hp2 others(11): Show |
intron_variant | MODIFIER | c.493+2689G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982470 | |||||||
chr7:114982504 | A | G | 175 | a0001c0001t0001g0181 a0001c0001t0001g0188 a0001c0001t0001g0191 others(172): Show |
182 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(179): Show |
intron_variant | MODIFIER | c.493+2723A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982504 | |||||||
chr7:114982658 | A | G | 2 | a0001c0001t0001g0113 a0001c0001t0032g0112 |
2 | NA18969.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.493+2877A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982658 | |||||||
chr7:114982725 | A | G | 1 | a0001c0001t0001g0188 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.493+2944A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982725 | |||||||
chr7:114982809 | G | A | 35 | a0001c0001t0002g0032 a0001c0001t0002g0061 a0001c0001t0002g0210 others(32): Show |
37 | HG00099.hp2 HG00642.hp2 HG00735.hp1 others(34): Show |
intron_variant | MODIFIER | c.493+3028G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982809 | |||||||
chr7:114982910 | C | T | 2 | a0001c0001t0006g0097 a0001c0001t0007g0275 |
2 | HG01358.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.493+3129C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982910 | |||||||
chr7:114982920 | C | G | 4 | a0001c0001t0001g0007 a0001c0001t0022g0052 a0001c0001t0022g0053 others(1): Show |
5 | HG02615.hp1 HG02970.hp2 HG03540.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+3139C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982920 | |||||||
chr7:114982951 | C | T | 2 | a0001c0001t0012g0021 a0001c0001t0033g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.493+3170C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114982951 | |||||||
chr7:114983308 | T | C | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(112): Show |
122 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.493+3527T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983308 | |||||||
chr7:114983387 | G | A | 2 | a0001c0001t0017g0006 a0001c0001t0019g0006 |
2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.493+3606G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983387 | |||||||
chr7:114983452 | G | A | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.493+3671G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983452 | |||||||
chr7:114983503 | T | G | 2 | a0001c0001t0022g0052 a0001c0001t0022g0053 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.493+3722T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983503 | |||||||
chr7:114983511 | A | G | 104 | a0001c0001t0001g0181 a0001c0001t0001g0188 a0001c0001t0001g0191 others(101): Show |
108 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(105): Show |
intron_variant | MODIFIER | c.493+3730A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983511 | |||||||
chr7:114983514 | G | A | 3 | a0001c0001t0003g0166 a0001c0001t0003g0222 a0001c0001t0003g0255 |
3 | HG00323.hp2 HG01081.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.493+3733G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983514 | |||||||
chr7:114983563 | C | CT | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(118): Show |
129 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(126): Show |
intron_variant | MODIFIER | c.493+3804dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114983563 | ||||||
chr7:114983563 | C | CTT | 93 | a0001c0001t0001g0062 a0001c0001t0001g0129 a0001c0001t0001g0149 others(90): Show |
97 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(94): Show |
intron_variant | MODIFIER | c.493+3803_493+3804d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114983563 | ||||||
chr7:114983563 | C | CTTT | 11 | a0001c0001t0001g0181 a0001c0001t0002g0046 a0001c0001t0002g0059 others(8): Show |
11 | HG00280.hp1 HG01175.hp2 HG01928.hp2 others(8): Show |
intron_variant | MODIFIER | c.493+3802_493+3804d others(5): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114983563 | ||||||
chr7:114983636 | C | T | 1 | a0001c0001t0006g0246 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.493+3855C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983636 | |||||||
chr7:114983687 | C | T | 4 | a0001c0001t0003g0198 a0001c0001t0003g0199 a0001c0001t0003g0217 others(1): Show |
4 | HG01928.hp2 HG01943.hp2 HG01993.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+3906C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983687 | |||||||
chr7:114983713 | G | A | 1 | a0001c0002t0023g0168 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.493+3932G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983713 | |||||||
chr7:114983725 | G | A | 1 | a0001c0001t0005g0147 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.493+3944G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983725 | |||||||
chr7:114983764 | T | A | 2 | a0001c0001t0059g0308 a0001c0003t0031g0018 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.493+3983T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983764 | |||||||
chr7:114983861 | A | G | 2 | a0001c0001t0059g0308 a0001c0003t0031g0018 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.493+4080A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983861 | |||||||
chr7:114983929 | C | T | 2 | a0001c0001t0012g0021 a0001c0001t0033g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.493+4148C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983929 | |||||||
chr7:114983973 | A | T | 1 | a0001c0001t0005g0193 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.493+4192A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114983973 | |||||||
chr7:114984074 | T | C | 6 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(3): Show |
6 | HG01099.hp1 HG02280.hp2 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.493+4293T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984074 | |||||||
chr7:114984089 | C | T | 8 | a0001c0001t0005g0012 a0001c0001t0005g0147 a0001c0001t0005g0159 others(5): Show |
8 | HG01256.hp2 HG01358.hp2 HG01928.hp1 others(5): Show |
intron_variant | MODIFIER | c.493+4308C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984089 | |||||||
chr7:114984115 | A | G | 4 | a0001c0001t0007g0016 a0001c0001t0007g0275 a0001c0001t0007g0276 others(1): Show |
5 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+4334A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984115 | |||||||
chr7:114984475 | A | C | 2 | a0001c0001t0012g0021 a0001c0001t0033g0104 |
2 | HG02809.hp1 HG02976.hp1 |
intron_variant | MODIFIER | c.493+4694A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984475 | |||||||
chr7:114984547 | T | A | 1 | a0001c0001t0018g0109 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.493+4766T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984547 | |||||||
chr7:114984625 | C | A | 3 | a0001c0001t0007g0212 a0001c0001t0007g0230 a0001c0001t0007g0260 |
3 | HG00140.hp2 HG00741.hp2 HG01109.hp1 |
intron_variant | MODIFIER | c.493+4844C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984625 | |||||||
chr7:114984674 | C | T | 2 | a0001c0001t0005g0136 a0001c0001t0005g0137 |
2 | NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.493+4893C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984674 | |||||||
chr7:114984713 | A | G | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+4932A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984713 | |||||||
chr7:114984718 | G | A | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(122): Show |
132 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(129): Show |
intron_variant | MODIFIER | c.493+4937G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984718 | |||||||
chr7:114984839 | C | A | 1 | a0001c0001t0024g0258 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.493+5058C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114984839 | |||||||
chr7:114985111 | C | T | 2 | a0001c0001t0060g0022 a0001c0001t0061g0027 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.493+5330C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985111 | |||||||
chr7:114985145 | G | C | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.493+5364G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985145 | |||||||
chr7:114985171 | G | A | 1 | a0001c0001t0002g0252 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.493+5390G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985171 | |||||||
chr7:114985291 | T | A | 59 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(56): Show |
62 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(59): Show |
intron_variant | MODIFIER | c.493+5510T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985291 | |||||||
chr7:114985367 | A | G | 1 | a0001c0003t0036g0057 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.493+5586A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985367 | |||||||
chr7:114985482 | C | G | 79 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0206 others(76): Show |
83 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(80): Show |
intron_variant | MODIFIER | c.493+5701C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985482 | |||||||
chr7:114985484 | G | C | 2 | a0001c0001t0002g0045 a0001c0001t0002g0249 |
2 | HG01433.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.493+5703G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985484 | |||||||
chr7:114985554 | G | T | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+5773G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985554 | |||||||
chr7:114985599 | T | G | 1 | a0001c0001t0011g0072 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.493+5818T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985599 | |||||||
chr7:114985659 | T | C | 15 | a0001c0001t0001g0114 a0001c0001t0002g0185 a0001c0001t0002g0202 others(12): Show |
16 | HG00738.hp2 HG01106.hp2 HG01496.hp2 others(13): Show |
intron_variant | MODIFIER | c.493+5878T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985659 | |||||||
chr7:114985719 | A | G | 1 | a0001c0001t0003g0215 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.493+5938A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985719 | |||||||
chr7:114985734 | G | T | 16 | a0001c0001t0001g0188 a0001c0001t0004g0161 a0001c0001t0004g0184 others(13): Show |
16 | HG00323.hp1 HG00408.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.493+5953G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114985734 | |||||||
chr7:114986032 | G | GT | 76 | a0001c0001t0001g0149 a0001c0001t0001g0152 a0001c0001t0001g0194 others(73): Show |
81 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(78): Show |
intron_variant | MODIFIER | c.493+6266dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114986032 | ||||||
chr7:114986032 | GT | G | 90 | a0001c0001t0001g0069 a0001c0001t0001g0188 a0001c0001t0002g0002 others(87): Show |
93 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(90): Show |
intron_variant | MODIFIER | c.493+6266delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114986032 | ||||||
chr7:114986032 | GTT | G | 29 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+6265_493+6266d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114986032 | ||||||
chr7:114986202 | T | C | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+6421T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986202 | |||||||
chr7:114986262 | C | T | 75 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0206 others(72): Show |
79 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+6481C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986262 | |||||||
chr7:114986274 | T | G | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.493+6493T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986274 | |||||||
chr7:114986294 | C | A | 126 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(123): Show |
133 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(130): Show |
intron_variant | MODIFIER | c.493+6513C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986294 | |||||||
chr7:114986385 | A | G | 296 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(293): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.493+6604A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986385 | |||||||
chr7:114986648 | GTT | G | 28 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(25): Show |
29 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.493+6869_493+6870d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114986648 | ||||||
chr7:114986825 | T | C | 29 | a0001c0001t0001g0181 a0001c0001t0001g0191 a0001c0001t0002g0073 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+7044T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986825 | |||||||
chr7:114986848 | G | A | 1 | a0001c0001t0004g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.493+7067G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114986848 | |||||||
chr7:114987043 | A | G | 3 | a0001c0001t0003g0201 a0001c0001t0003g0280 a0001c0001t0003g0281 |
3 | HG01891.hp2 HG03195.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.493+7262A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987043 | |||||||
chr7:114987139 | A | G | 75 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0206 others(72): Show |
79 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(76): Show |
intron_variant | MODIFIER | c.493+7358A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987139 | |||||||
chr7:114987209 | G | A | 1 | a0001c0001t0006g0097 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.493+7428G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987209 | |||||||
chr7:114987529 | G | A | 1 | a0001c0001t0002g0282 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.493+7748G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987529 | |||||||
chr7:114987592 | A | G | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+7811A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987592 | |||||||
chr7:114987804 | T | A | 5 | a0001c0001t0037g0040 a0001c0001t0050g0060 a0001c0001t0059g0308 others(2): Show |
5 | HG01099.hp2 HG02280.hp1 HG03139.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+8023T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987804 | |||||||
chr7:114987845 | G | C | 2 | a0001c0001t0014g0106 a0001c0001t0014g0274 |
2 | HG00621.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.493+8064G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987845 | |||||||
chr7:114987929 | A | G | 2 | a0001c0001t0060g0022 a0001c0001t0061g0027 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.493+8148A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114987929 | |||||||
chr7:114988064 | T | G | 2 | a0001c0001t0019g0244 a0001c0001t0019g0279 |
2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.493+8283T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114988064 | |||||||
chr7:114988210 | A | G | 313 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(310): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.493+8429A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114988210 | |||||||
chr7:114988437 | C | A | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.493+8656C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114988437 | |||||||
chr7:114988464 | C | T | 1 | a0001c0001t0029g0312 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.493+8683C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114988464 | |||||||
chr7:114988667 | TAGG | T | 3 | a0001c0001t0022g0052 a0001c0001t0022g0053 a0001c0001t0022g0054 |
3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.493+8891_493+8893d others(5): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114988667 | ||||||
chr7:114989057 | G | A | 1 | a0001c0001t0063g0116 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.493+9276G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989057 | |||||||
chr7:114989064 | G | A | 1 | a0001c0001t0004g0207 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.493+9283G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989064 | |||||||
chr7:114989080 | A | G | 1 | a0001c0001t0002g0042 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.493+9299A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989080 | |||||||
chr7:114989155 | G | T | 3 | a0001c0001t0022g0052 a0001c0001t0022g0053 a0001c0001t0022g0054 |
3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.493+9374G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989155 | |||||||
chr7:114989231 | G | A | 58 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(55): Show |
61 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.493+9450G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989231 | |||||||
chr7:114989290 | G | A | 1 | a0001c0001t0033g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.493+9509G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989290 | |||||||
chr7:114989642 | T | C | 1 | a0001c0001t0027g0044 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.493+9861T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989642 | |||||||
chr7:114989665 | C | A | 1 | a0001c0001t0037g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.493+9884C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989665 | |||||||
chr7:114989769 | G | A | 1 | a0001c0001t0004g0187 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.493+9988G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114989769 | |||||||
chr7:114990103 | A | G | 1 | a0001c0001t0010g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+10322A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990103 | |||||||
chr7:114990193 | T | A | 2 | a0001c0001t0011g0131 a0001c0001t0011g0132 |
2 | HG02895.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.493+10412T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990193 | |||||||
chr7:114990357 | T | C | 2 | a0001c0001t0060g0022 a0001c0001t0061g0027 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.493+10576T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990357 | |||||||
chr7:114990483 | A | C | 1 | a0001c0001t0003g0238 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.493+10702A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990483 | |||||||
chr7:114990498 | C | T | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+10717C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990498 | |||||||
chr7:114990552 | A | G | 3 | a0001c0001t0033g0104 a0001c0001t0048g0037 a0001c0001t0065g0313 |
3 | HG02258.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.493+10771A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990552 | |||||||
chr7:114990583 | G | T | 1 | a0001c0001t0003g0197 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.493+10802G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990583 | |||||||
chr7:114990603 | G | T | 29 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0007g0016 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+10822G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990603 | |||||||
chr7:114990669 | G | A | 10 | a0001c0001t0001g0114 a0001c0001t0002g0202 a0001c0001t0008g0009 others(7): Show |
11 | HG00738.hp2 HG01106.hp2 HG01496.hp2 others(8): Show |
intron_variant | MODIFIER | c.493+10888G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990669 | |||||||
chr7:114990683 | C | A | 1 | a0001c0001t0010g0242 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.493+10902C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990683 | |||||||
chr7:114990695 | T | G | 1 | a0001c0001t0010g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.493+10914T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990695 | |||||||
chr7:114990755 | G | A | 1 | a0001c0003t0036g0057 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.493+10974G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990755 | |||||||
chr7:114990816 | C | T | 5 | a0001c0001t0001g0062 a0001c0001t0001g0069 a0001c0001t0001g0070 others(2): Show |
5 | HG02523.hp2 NA18940.hp2 NA18955.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+11035C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990816 | |||||||
chr7:114990842 | A | G | 1 | a0001c0001t0004g0286 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.493+11061A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990842 | |||||||
chr7:114990929 | T | C | 313 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(310): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.493+11148T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114990929 | |||||||
chr7:114991002 | T | C | 153 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0205 others(150): Show |
160 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.493+11221T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991002 | |||||||
chr7:114991007 | C | A | 1 | a0001c0001t0018g0109 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.493+11226C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991007 | |||||||
chr7:114991007 | C | T | 152 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0205 others(149): Show |
159 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.493+11226C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991007 | |||||||
chr7:114991046 | T | C | 1 | a0001c0001t0004g0011 | 2 | HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.493+11265T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991046 | |||||||
chr7:114991095 | G | A | 1 | a0001c0001t0033g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.493+11314G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991095 | |||||||
chr7:114991142 | G | A | 1 | a0001c0001t0057g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.493+11361G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991142 | |||||||
chr7:114991176 | G | A | 1 | a0001c0001t0028g0293 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.493+11395G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991176 | |||||||
chr7:114991250 | T | C | 58 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(55): Show |
61 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.493+11469T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991250 | |||||||
chr7:114991357 | G | C | 1 | a0001c0001t0016g0074 | 1 | NA19086.hp1 | intron_variant | MODIFIER | c.493+11576G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991357 | |||||||
chr7:114991455 | T | G | 1 | a0001c0001t0003g0190 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.493+11674T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991455 | |||||||
chr7:114991705 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(112): Show |
122 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.493+11924C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991705 | |||||||
chr7:114991708 | T | C | 153 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0205 others(150): Show |
160 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.493+11927T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991708 | |||||||
chr7:114991738 | T | G | 29 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0007g0016 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+11957T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991738 | |||||||
chr7:114991979 | T | G | 1 | a0001c0001t0016g0240 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.493+12198T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114991979 | |||||||
chr7:114992010 | T | C | 1 | a0001c0001t0024g0177 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.493+12229T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992010 | |||||||
chr7:114992034 | G | C | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+12253G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992034 | |||||||
chr7:114992077 | G | A | 1 | a0001c0001t0011g0192 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.493+12296G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992077 | |||||||
chr7:114992123 | G | A | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(96): Show |
105 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.493+12342G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992123 | |||||||
chr7:114992287 | A | T | 1 | a0001c0001t0018g0109 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.493+12506A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992287 | |||||||
chr7:114992329 | A | T | 1 | a0001c0001t0001g0152 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.493+12548A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992329 | |||||||
chr7:114992382 | CTA | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(309): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.493+12603_493+1260 others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114992382 | ||||||
chr7:114992431 | T | A | 1 | a0001c0001t0044g0105 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.493+12650T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992431 | |||||||
chr7:114992445 | C | T | 28 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0007g0016 others(25): Show |
29 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.493+12664C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992445 | |||||||
chr7:114992637 | A | C | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.493+12856A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992637 | |||||||
chr7:114992652 | T | C | 2 | a0001c0001t0002g0045 a0001c0001t0002g0249 |
2 | HG01433.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.493+12871T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992652 | |||||||
chr7:114992752 | A | G | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.493+12971A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992752 | |||||||
chr7:114992832 | A | C | 2 | a0001c0001t0003g0238 a0001c0001t0003g0239 |
2 | NA18977.hp1 NA19012.hp2 |
intron_variant | MODIFIER | c.493+13051A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992832 | |||||||
chr7:114992839 | G | C | 4 | a0001c0001t0007g0016 a0001c0001t0007g0275 a0001c0001t0007g0276 others(1): Show |
5 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.493+13058G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992839 | |||||||
chr7:114992865 | A | G | 56 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(53): Show |
60 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.493+13084A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992865 | |||||||
chr7:114992987 | T | G | 74 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0206 others(71): Show |
78 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.493+13206T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992987 | |||||||
chr7:114992999 | T | C | 28 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0007g0016 others(25): Show |
29 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.493+13218T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114992999 | |||||||
chr7:114993202 | C | G | 3 | a0001c0001t0002g0032 a0001c0001t0009g0008 a0001c0001t0017g0219 |
4 | HG01168.hp1 HG01169.hp1 HG02148.hp2 others(1): Show |
intron_variant | MODIFIER | c.493+13421C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993202 | |||||||
chr7:114993266 | C | T | 78 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0206 others(75): Show |
82 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(79): Show |
intron_variant | MODIFIER | c.493+13485C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993266 | |||||||
chr7:114993508 | A | G | 16 | a0001c0001t0001g0188 a0001c0001t0004g0161 a0001c0001t0004g0184 others(13): Show |
16 | HG00323.hp1 HG00408.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.493+13727A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993508 | |||||||
chr7:114993517 | T | G | 1 | a0001c0001t0053g0075 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.493+13736T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993517 | |||||||
chr7:114993728 | T | C | 1 | a0001c0001t0010g0232 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.493+13947T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993728 | |||||||
chr7:114993795 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(112): Show |
122 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.493+14014C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993795 | |||||||
chr7:114993801 | G | C | 23 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(20): Show |
24 | HG01243.hp1 HG01361.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.493+14020G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993801 | |||||||
chr7:114993815 | T | G | 1 | a0001c0001t0008g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.493+14034T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114993815 | |||||||
chr7:114994004 | A | T | 2 | a0001c0001t0001g0004 a0001c0001t0014g0004 |
3 | HG00673.hp1 HG02040.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.493+14223A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994004 | |||||||
chr7:114994050 | A | G | 1 | a0001c0001t0013g0283 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.493+14269A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994050 | |||||||
chr7:114994103 | A | G | 1 | a0001c0001t0001g0220 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.493+14322A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994103 | |||||||
chr7:114994112 | T | G | 1 | a0001c0001t0024g0148 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.493+14331T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994112 | |||||||
chr7:114994266 | T | G | 29 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0007g0016 others(26): Show |
30 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.493+14485T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994266 | |||||||
chr7:114994275 | C | CAATACAA others(11): Show |
3 | a0001c0001t0009g0123 a0001c0001t0025g0117 a0001c0001t0063g0116 |
3 | HG01978.hp1 HG03490.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.493+14495_493+1449 others(22): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114994275 | ||||||
chr7:114994277 | C | G | 3 | a0001c0001t0009g0123 a0001c0001t0025g0117 a0001c0001t0063g0116 |
3 | HG01978.hp1 HG03490.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.493+14496C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994277 | |||||||
chr7:114994405 | G | A | 4 | a0001c0001t0010g0029 a0001c0001t0012g0021 a0001c0001t0041g0055 others(1): Show |
4 | HG02572.hp1 HG02809.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.493+14624G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994405 | |||||||
chr7:114994668 | A | G | 1 | a0001c0001t0004g0278 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.493+14887A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994668 | |||||||
chr7:114994686 | C | A | 6 | a0001c0001t0010g0029 a0001c0001t0010g0056 a0001c0001t0012g0021 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.493+14905C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994686 | |||||||
chr7:114994709 | G | A | 2 | a0001c0001t0048g0037 a0001c0001t0065g0313 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.493+14928G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994709 | |||||||
chr7:114994775 | C | T | 1 | a0001c0001t0001g0152 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.493+14994C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994775 | |||||||
chr7:114994967 | T | C | 1 | a0001c0001t0005g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.493+15186T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994967 | |||||||
chr7:114994968 | G | A | 1 | a0001c0001t0005g0128 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.493+15187G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114994968 | |||||||
chr7:114995057 | A | G | 22 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(19): Show |
23 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(20): Show |
intron_variant | MODIFIER | c.493+15276A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995057 | |||||||
chr7:114995104 | C | T | 1 | a0001c0003t0036g0057 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.493+15323C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995104 | |||||||
chr7:114995111 | T | G | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.493+15330T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995111 | |||||||
chr7:114995270 | A | G | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+15489A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995270 | |||||||
chr7:114995323 | G | A | 3 | a0001c0001t0033g0104 a0001c0001t0048g0037 a0001c0001t0065g0313 |
3 | HG02258.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.493+15542G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995323 | |||||||
chr7:114995329 | A | T | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+15548A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995329 | |||||||
chr7:114995348 | G | A | 1 | a0001c0001t0034g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.493+15567G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995348 | |||||||
chr7:114995388 | G | A | 35 | a0001c0001t0003g0076 a0001c0001t0003g0099 a0001c0001t0003g0166 others(32): Show |
37 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.493+15607G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995388 | |||||||
chr7:114995406 | G | C | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+15625G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995406 | |||||||
chr7:114995425 | G | T | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.493+15644G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995425 | |||||||
chr7:114995483 | C | A | 152 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0205 others(149): Show |
159 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.493+15702C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995483 | |||||||
chr7:114995564 | G | T | 1 | a0001c0001t0001g0149 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.493+15783G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995564 | |||||||
chr7:114995755 | A | C | 2 | a0001c0001t0019g0244 a0001c0001t0019g0279 |
2 | HG02886.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.493+15974A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995755 | |||||||
chr7:114995755 | A | T | 23 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(20): Show |
24 | HG01243.hp1 HG01361.hp2 HG01433.hp2 others(21): Show |
intron_variant | MODIFIER | c.493+15974A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995755 | |||||||
chr7:114995874 | G | A | 2 | a0001c0001t0059g0308 a0001c0003t0031g0018 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.493+16093G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995874 | |||||||
chr7:114995905 | A | C | 1 | a0001c0001t0011g0035 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.493+16124A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995905 | |||||||
chr7:114995943 | T | C | 313 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(310): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.493+16162T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114995943 | |||||||
chr7:114996421 | T | C | 35 | a0001c0001t0003g0076 a0001c0001t0003g0099 a0001c0001t0003g0166 others(32): Show |
37 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.493+16640T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996421 | |||||||
chr7:114996427 | G | T | 2 | a0001c0001t0008g0036 a0001c0001t0044g0105 |
2 | HG01168.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.493+16646G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996427 | |||||||
chr7:114996555 | G | A | 1 | a0001c0001t0037g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.493+16774G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996555 | |||||||
chr7:114996602 | G | A | 1 | a0001c0001t0012g0138 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.493+16821G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996602 | |||||||
chr7:114996652 | G | A | 2 | a0001c0001t0060g0022 a0001c0001t0061g0027 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.493+16871G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996652 | |||||||
chr7:114996695 | A | C | 28 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0007g0016 others(25): Show |
29 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.493+16914A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996695 | |||||||
chr7:114996771 | G | A | 1 | a0001c0001t0033g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.493+16990G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996771 | |||||||
chr7:114996813 | G | A | 1 | a0001c0001t0009g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.493+17032G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996813 | |||||||
chr7:114996897 | A | T | 16 | a0001c0001t0001g0114 a0001c0001t0002g0202 a0001c0001t0007g0269 others(13): Show |
17 | HG00738.hp2 HG01106.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.493+17116A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996897 | |||||||
chr7:114996962 | C | A | 1 | a0001c0001t0033g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.493+17181C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114996962 | |||||||
chr7:114997009 | T | C | 1 | a0001c0001t0003g0215 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.493+17228T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997009 | |||||||
chr7:114997015 | G | A | 1 | a0001c0001t0002g0049 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.493+17234G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997015 | |||||||
chr7:114997400 | A | G | 1 | a0001c0001t0003g0169 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.493+17619A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997400 | |||||||
chr7:114997408 | A | ATG | 6 | a0001c0001t0001g0090 a0001c0001t0001g0113 a0001c0001t0002g0229 others(3): Show |
6 | HG00280.hp2 HG02818.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.493+17644_493+1764 others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114997408 | ||||||
chr7:114997425 | T | C | 1 | a0001c0001t0033g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.493+17644T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997425 | |||||||
chr7:114997521 | G | A | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.493+17740G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997521 | |||||||
chr7:114997576 | GA | G | 184 | a0001c0001t0001g0181 a0001c0001t0001g0194 a0001c0001t0001g0205 others(181): Show |
192 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.493+17812delA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114997576 | ||||||
chr7:114997576 | GAA | G | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(96): Show |
105 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.493+17811_493+1781 others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 114997576 | ||||||
chr7:114997734 | T | C | 2 | a0001c0001t0048g0037 a0001c0001t0065g0313 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.493+17953T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997734 | |||||||
chr7:114997773 | G | T | 74 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0206 others(71): Show |
78 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.494-17915G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997773 | |||||||
chr7:114997838 | G | T | 2 | a0001c0001t0022g0052 a0001c0001t0022g0053 |
2 | HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.494-17850G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997838 | |||||||
chr7:114997849 | G | A | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494-17839G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114997849 | |||||||
chr7:114998025 | A | T | 1 | a0001c0003t0036g0057 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.494-17663A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998025 | |||||||
chr7:114998026 | C | T | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494-17662C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998026 | |||||||
chr7:114998105 | A | C | 1 | a0001c0001t0002g0231 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.494-17583A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998105 | |||||||
chr7:114998135 | G | A | 1 | a0001c0001t0010g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.494-17553G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998135 | |||||||
chr7:114998276 | G | A | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494-17412G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998276 | |||||||
chr7:114998328 | G | A | 2 | a0001c0001t0001g0071 a0001c0001t0001g0081 |
2 | HG02602.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.494-17360G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998328 | |||||||
chr7:114998469 | A | G | 2 | a0001c0001t0060g0022 a0001c0001t0061g0027 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.494-17219A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998469 | |||||||
chr7:114998483 | T | A | 4 | a0001c0001t0018g0005 a0001c0001t0018g0098 a0001c0001t0018g0109 others(1): Show |
5 | HG02135.hp1 NA18963.hp2 NA18998.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-17205T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998483 | |||||||
chr7:114998681 | T | C | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.494-17007T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998681 | |||||||
chr7:114998832 | G | A | 6 | a0001c0001t0010g0029 a0001c0001t0010g0056 a0001c0001t0012g0021 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.494-16856G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998832 | |||||||
chr7:114998923 | T | C | 35 | a0001c0001t0003g0076 a0001c0001t0003g0099 a0001c0001t0003g0166 others(32): Show |
37 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.494-16765T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114998923 | |||||||
chr7:114999338 | C | T | 313 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(310): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.494-16350C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999338 | |||||||
chr7:114999391 | C | T | 313 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(310): Show |
328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.494-16297C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999391 | |||||||
chr7:114999538 | T | C | 16 | a0001c0001t0001g0188 a0001c0001t0004g0161 a0001c0001t0004g0184 others(13): Show |
16 | HG00323.hp1 HG00408.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.494-16150T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999538 | |||||||
chr7:114999583 | A | G | 1 | a0001c0001t0009g0119 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.494-16105A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999583 | |||||||
chr7:114999619 | T | C | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.494-16069T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999619 | |||||||
chr7:114999650 | A | G | 1 | a0001c0001t0034g0221 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.494-16038A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999650 | |||||||
chr7:114999692 | G | A | 300 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(297): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): Show |
intron_variant | MODIFIER | c.494-15996G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999692 | |||||||
chr7:114999779 | C | CA | 268 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(265): Show |
282 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(279): Show |
intron_variant | MODIFIER | c.494-15909_494-1590 others(5): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999779 | |||||||
chr7:114999828 | A | T | 3 | a0001c0001t0033g0104 a0001c0001t0048g0037 a0001c0001t0065g0313 |
3 | HG02258.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.494-15860A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999828 | |||||||
chr7:114999840 | A | C | 1 | a0001c0001t0010g0077 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.494-15848A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999840 | |||||||
chr7:114999896 | G | A | 3 | a0001c0001t0003g0099 a0001c0001t0003g0215 a0001c0001t0003g0218 |
3 | NA18972.hp1 NA19009.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.494-15792G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 114999896 | |||||||
chr7:115000023 | T | C | 1 | a0001c0001t0003g0237 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.494-15665T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000023 | |||||||
chr7:115000184 | A | C | 1 | a0001c0001t0033g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.494-15504A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000184 | |||||||
chr7:115000263 | G | C | 1 | a0001c0001t0015g0290 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.494-15425G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000263 | |||||||
chr7:115000305 | A | G | 153 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0205 others(150): Show |
160 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.494-15383A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000305 | |||||||
chr7:115000425 | G | T | 1 | a0001c0001t0010g0029 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.494-15263G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000425 | |||||||
chr7:115000505 | G | A | 1 | a0001c0001t0033g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.494-15183G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000505 | |||||||
chr7:115000524 | A | G | 1 | a0001c0001t0002g0046 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.494-15164A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000524 | |||||||
chr7:115000553 | C | T | 1 | a0001c0001t0004g0286 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.494-15135C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000553 | |||||||
chr7:115000645 | T | G | 2 | a0001c0001t0005g0136 a0001c0001t0005g0137 |
2 | NA18970.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.494-15043T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000645 | |||||||
chr7:115000660 | G | T | 1 | a0001c0001t0021g0264 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.494-15028G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000660 | |||||||
chr7:115000772 | C | T | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(112): Show |
122 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.494-14916C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115000772 | |||||||
chr7:115001017 | C | T | 1 | a0001c0001t0033g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.494-14671C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115001017 | |||||||
chr7:115001287 | T | A | 1 | a0001c0001t0008g0115 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.494-14401T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115001287 | |||||||
chr7:115001323 | C | T | 1 | a0001c0001t0001g0129 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.494-14365C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115001323 | |||||||
chr7:115001445 | T | C | 2 | a0001c0001t0040g0135 a0001c0001t0062g0118 |
2 | HG01891.hp1 HG02109.hp1 |
intron_variant | MODIFIER | c.494-14243T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115001445 | |||||||
chr7:115001720 | A | AT | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(112): Show |
122 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(119): Show |
intron_variant | MODIFIER | c.494-13962dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115001720 | ||||||
chr7:115001939 | C | T | 16 | a0001c0001t0001g0188 a0001c0001t0004g0161 a0001c0001t0004g0184 others(13): Show |
16 | HG00323.hp1 HG00408.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.494-13749C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115001939 | |||||||
chr7:115002078 | C | T | 1 | a0001c0001t0001g0206 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.494-13610C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002078 | |||||||
chr7:115002146 | AAAACAAA others(1): Show |
A | 74 | a0001c0001t0001g0194 a0001c0001t0001g0205 a0001c0001t0001g0206 others(71): Show |
78 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(75): Show |
intron_variant | MODIFIER | c.494-13526_494-1351 others(12): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115002146 | ||||||
chr7:115002204 | T | C | 6 | a0001c0001t0010g0029 a0001c0001t0010g0056 a0001c0001t0012g0021 others(3): Show |
6 | HG02572.hp1 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.494-13484T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002204 | |||||||
chr7:115002265 | C | T | 1 | a0001c0001t0016g0245 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.494-13423C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002265 | |||||||
chr7:115002466 | T | A | 3 | a0001c0001t0033g0104 a0001c0001t0048g0037 a0001c0001t0065g0313 |
3 | HG02258.hp2 HG02976.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.494-13222T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002466 | |||||||
chr7:115002577 | G | C | 2 | a0001c0001t0002g0073 a0001c0001t0011g0072 |
2 | HG04199.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.494-13111G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002577 | |||||||
chr7:115002797 | T | C | 3 | a0001c0001t0009g0123 a0001c0001t0025g0117 a0001c0001t0063g0116 |
3 | HG01978.hp1 HG03490.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.494-12891T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002797 | |||||||
chr7:115002852 | T | C | 2 | a0001c0001t0001g0205 a0001c0001t0001g0206 |
2 | NA18982.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.494-12836T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002852 | |||||||
chr7:115002863 | T | C | 312 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(309): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.494-12825T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002863 | |||||||
chr7:115002874 | A | G | 152 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0205 others(149): Show |
159 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.494-12814A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002874 | |||||||
chr7:115002876 | A | G | 2 | a0001c0001t0059g0308 a0001c0003t0031g0018 |
2 | HG03139.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.494-12812A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115002876 | |||||||
chr7:115003055 | C | T | 299 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(296): Show |
314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.494-12633C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003055 | |||||||
chr7:115003252 | T | A | 58 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(55): Show |
61 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.494-12436T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003252 | |||||||
chr7:115003319 | G | A | 1 | a0001c0001t0002g0087 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.494-12369G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003319 | |||||||
chr7:115003474 | G | A | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.494-12214G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003474 | |||||||
chr7:115003476 | T | C | 1 | a0001c0006t0001g0080 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.494-12212T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003476 | |||||||
chr7:115003584 | A | G | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.494-12104A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003584 | |||||||
chr7:115003649 | T | C | 4 | a0001c0001t0007g0016 a0001c0001t0007g0275 a0001c0001t0007g0276 others(1): Show |
5 | HG01081.hp2 HG01167.hp1 HG01169.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-12039T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003649 | |||||||
chr7:115003810 | T | G | 1 | a0001c0001t0033g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.494-11878T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003810 | |||||||
chr7:115003874 | G | A | 152 | a0001c0001t0001g0188 a0001c0001t0001g0194 a0001c0001t0001g0205 others(149): Show |
159 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.494-11814G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003874 | |||||||
chr7:115003904 | C | T | 58 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(55): Show |
61 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(58): Show |
intron_variant | MODIFIER | c.494-11784C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115003904 | |||||||
chr7:115004139 | C | T | 1 | a0001c0001t0011g0192 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.494-11549C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115004139 | |||||||
chr7:115004233 | G | C | 1 | a0001c0001t0004g0243 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.494-11455G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115004233 | |||||||
chr7:115004403 | A | C | 99 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(96): Show |
105 | HG00099.hp2 HG00280.hp2 HG00609.hp1 others(102): Show |
intron_variant | MODIFIER | c.494-11285A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115004403 | |||||||
chr7:115004432 | A | C | 1 | a0001c0001t0004g0173 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.494-11256A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115004432 | |||||||
chr7:115004637 | C | T | 1 | a0001c0001t0017g0203 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.494-11051C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115004637 | |||||||
chr7:115004987 | C | T | 1 | a0001c0001t0004g0259 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.494-10701C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115004987 | |||||||
chr7:115005189 | A | G | 1 | a0001c0001t0046g0155 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.494-10499A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115005189 | |||||||
chr7:115005252 | G | C | 2 | a0001c0001t0048g0037 a0001c0001t0065g0313 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.494-10436G>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115005252 | |||||||
chr7:115005328 | ATTAATTG others(57): Show |
A | 1 | a0001c0003t0043g0023 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.494-10355_494-1029 others(68): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115005328 | ||||||
chr7:115005593 | A | G | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.494-10095A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115005593 | |||||||
chr7:115005718 | A | T | 1 | a0001c0001t0006g0097 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.494-9970A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115005718 | |||||||
chr7:115005990 | C | T | 1 | a0001c0001t0037g0040 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.494-9698C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115005990 | |||||||
chr7:115006060 | G | A | 28 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0007g0016 others(25): Show |
29 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.494-9628G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006060 | |||||||
chr7:115006114 | T | C | 12 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(9): Show |
13 | HG01361.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.494-9574T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006114 | |||||||
chr7:115006164 | C | T | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.494-9524C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006164 | |||||||
chr7:115006295 | A | T | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494-9393A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006295 | |||||||
chr7:115006669 | G | A | 312 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(309): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): Show |
intron_variant | MODIFIER | c.494-9019G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006669 | |||||||
chr7:115006683 | A | G | 10 | a0001c0001t0010g0029 a0001c0001t0010g0056 a0001c0001t0012g0021 others(7): Show |
10 | HG02258.hp1 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.494-9005A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006683 | |||||||
chr7:115006935 | G | GTTTTACT others(8): Show |
310 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(307): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.494-8750_494-8749i others(17): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115006935 | ||||||
chr7:115006977 | A | T | 28 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0007g0016 others(25): Show |
29 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(26): Show |
intron_variant | MODIFIER | c.494-8711A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115006977 | |||||||
chr7:115007175 | A | C | 1 | a0001c0001t0004g0272 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.494-8513A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007175 | |||||||
chr7:115007362 | G | T | 5 | a0001c0001t0001g0082 a0001c0001t0001g0191 a0001c0001t0026g0163 others(2): Show |
5 | HG02015.hp2 HG02132.hp2 HG04184.hp2 others(2): Show |
intron_variant | MODIFIER | c.494-8326G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007362 | |||||||
chr7:115007430 | T | C | 1 | a0001c0001t0003g0255 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.494-8258T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007430 | |||||||
chr7:115007506 | T | C | 1 | a0001c0001t0042g0100 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.494-8182T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007506 | |||||||
chr7:115007630 | G | A | 2 | a0001c0001t0010g0056 a0001c0001t0058g0253 |
2 | HG02717.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.494-8058G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007630 | |||||||
chr7:115007630 | G | GTA | 23 | a0001c0001t0001g0181 a0001c0001t0002g0073 a0001c0001t0002g0101 others(20): Show |
24 | HG00140.hp2 HG00741.hp2 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.494-8032_494-8031d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | ||||||
chr7:115007630 | G | GTATA | 9 | a0001c0001t0007g0156 a0001c0001t0011g0035 a0001c0001t0011g0072 others(6): Show |
9 | HG01069.hp1 HG02258.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.494-8034_494-8031d others(6): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | ||||||
chr7:115007630 | G | GTATATA | 3 | a0001c0001t0011g0167 a0001c0001t0041g0055 a0001c0001t0046g0155 |
3 | HG03098.hp1 HG03654.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.494-8036_494-8031d others(8): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | ||||||
chr7:115007630 | G | GTATATAT others(1): Show |
3 | a0001c0001t0002g0043 a0001c0001t0007g0034 a0001c0001t0007g0171 |
3 | HG00099.hp1 HG02738.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.494-8038_494-8031d others(10): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | ||||||
chr7:115007630 | G | GTATATAT others(5): Show |
1 | a0001c0001t0007g0033 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.494-8042_494-8031d others(14): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | ||||||
chr7:115007630 | G | GTGTATAT others(3): Show |
1 | a0001c0001t0061g0027 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.494-8057_494-8056i others(12): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | ||||||
chr7:115007630 | G | GTGTGTAT others(21): Show |
1 | a0001c0001t0022g0052 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.494-8057_494-8056i others(30): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | ||||||
chr7:115007630 | G | GTGTGTAT others(27): Show |
1 | a0001c0001t0022g0053 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.494-8057_494-8056i others(36): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | ||||||
chr7:115007630 | G | GTGTGTAT others(29): Show |
1 | a0001c0001t0022g0054 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.494-8057_494-8056i others(38): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | ||||||
chr7:115007630 | GTATATAT others(5): Show |
G | 2 | a0001c0001t0004g0011 a0001c0001t0004g0207 |
3 | HG01257.hp1 HG01516.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.494-8042_494-8031d others(14): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | ||||||
chr7:115007630 | GTATATAT others(7): Show |
G | 243 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(240): Show |
255 | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(252): Show |
intron_variant | MODIFIER | c.494-8044_494-8031d others(16): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007630 | ||||||
chr7:115007806 | C | T | 16 | a0001c0001t0001g0188 a0001c0001t0004g0161 a0001c0001t0004g0184 others(13): Show |
16 | HG00323.hp1 HG00408.hp1 HG02165.hp1 others(13): Show |
intron_variant | MODIFIER | c.494-7882C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007806 | |||||||
chr7:115007862 | A | AT | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(131): Show |
141 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(138): Show |
intron_variant | MODIFIER | c.494-7810dupT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007862 | ||||||
chr7:115007862 | A | ATT | 12 | a0001c0001t0001g0114 a0001c0001t0002g0202 a0001c0001t0007g0277 others(9): Show |
13 | HG01106.hp2 HG01175.hp2 HG01496.hp2 others(10): Show |
intron_variant | MODIFIER | c.494-7811_494-7810d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115007862 | ||||||
chr7:115007940 | G | T | 1 | a0001c0001t0011g0183 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.494-7748G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007940 | |||||||
chr7:115007987 | C | T | 1 | a0001c0001t0001g0082 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.494-7701C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115007987 | |||||||
chr7:115008011 | C | T | 2 | a0001c0001t0060g0022 a0001c0001t0061g0027 |
2 | HG02258.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.494-7677C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008011 | |||||||
chr7:115008065 | G | T | 314 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(311): Show |
329 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(326): Show |
intron_variant | MODIFIER | c.494-7623G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008065 | |||||||
chr7:115008169 | C | A | 207 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(204): Show |
217 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(214): Show |
intron_variant | MODIFIER | c.494-7519C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008169 | |||||||
chr7:115008199 | G | A | 279 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(276): Show |
293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.494-7489G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008199 | |||||||
chr7:115008212 | A | C | 3 | a0001c0001t0020g0010 a0001c0001t0020g0146 a0001c0001t0020g0200 |
4 | HG01070.hp1 HG01071.hp2 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-7476A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008212 | |||||||
chr7:115008523 | C | T | 2 | a0001c0001t0048g0037 a0001c0001t0065g0313 |
2 | HG02258.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.494-7165C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008523 | |||||||
chr7:115008608 | C | T | 2 | a0001c0001t0002g0045 a0001c0001t0002g0249 |
2 | HG01433.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.494-7080C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008608 | |||||||
chr7:115008779 | G | T | 1 | a0001c0001t0057g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.494-6909G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008779 | |||||||
chr7:115008874 | G | A | 1 | a0001c0001t0008g0017 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.494-6814G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008874 | |||||||
chr7:115008895 | C | G | 1 | a0001c0001t0002g0058 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.494-6793C>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115008895 | |||||||
chr7:115009088 | A | G | 1 | a0001c0001t0002g0267 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.494-6600A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115009088 | |||||||
chr7:115009097 | G | A | 2 | a0001c0001t0004g0243 a0001c0001t0016g0074 |
2 | NA19085.hp2 NA19086.hp1 |
intron_variant | MODIFIER | c.494-6591G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115009097 | |||||||
chr7:115009777 | G | A | 7 | a0001c0001t0010g0029 a0001c0001t0010g0056 a0001c0001t0012g0021 others(4): Show |
7 | HG02258.hp1 HG02717.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.494-5911G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115009777 | |||||||
chr7:115010064 | CTTA | C | 23 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(20): Show |
24 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.494-5623_494-5621d others(5): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010064 | |||||||
chr7:115010069 | GA | G | 23 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(20): Show |
24 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.494-5617delA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115010069 | ||||||
chr7:115010071 | A | T | 23 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(20): Show |
24 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.494-5617A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010071 | |||||||
chr7:115010073 | AGG | A | 23 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(20): Show |
24 | HG01361.hp2 HG01433.hp2 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.494-5612_494-5611d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115010073 | ||||||
chr7:115010130 | T | A | 25 | a0001c0001t0001g0001 a0001c0001t0001g0062 a0001c0001t0001g0064 others(22): Show |
28 | HG00609.hp1 HG02015.hp2 HG02132.hp2 others(25): Show |
intron_variant | MODIFIER | c.494-5558T>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010130 | |||||||
chr7:115010131 | A | T | 1 | a0001c0001t0016g0240 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.494-5557A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010131 | |||||||
chr7:115010547 | T | G | 3 | a0001c0001t0022g0052 a0001c0001t0022g0053 a0001c0001t0022g0054 |
3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.494-5141T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010547 | |||||||
chr7:115010763 | C | T | 2 | a0001c0001t0002g0142 a0001c0001t0002g0185 |
2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.494-4925C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010763 | |||||||
chr7:115010915 | A | T | 3 | a0001c0001t0002g0229 a0001c0001t0002g0252 a0001c0001t0002g0267 |
3 | HG01192.hp1 HG02818.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.494-4773A>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010915 | |||||||
chr7:115010977 | A | G | 35 | a0001c0001t0003g0076 a0001c0001t0003g0099 a0001c0001t0003g0166 others(32): Show |
37 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(34): Show |
intron_variant | MODIFIER | c.494-4711A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115010977 | |||||||
chr7:115011178 | A | G | 4 | a0001c0001t0011g0131 a0001c0001t0011g0132 a0001c0001t0040g0135 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-4510A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011178 | |||||||
chr7:115011260 | G | A | 1 | a0001c0001t0033g0104 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.494-4428G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011260 | |||||||
chr7:115011261 | G | A | 2 | a0001c0001t0002g0142 a0001c0001t0002g0185 |
2 | HG02698.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.494-4427G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011261 | |||||||
chr7:115011602 | A | G | 1 | a0001c0001t0004g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.494-4086A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011602 | |||||||
chr7:115011640 | A | G | 49 | a0001c0001t0004g0011 a0001c0001t0004g0015 a0001c0001t0004g0063 others(46): Show |
52 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.494-4048A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011640 | |||||||
chr7:115011697 | CAT | C | 4 | a0001c0001t0058g0253 a0001c0001t0059g0308 a0001c0001t0060g0022 others(1): Show |
4 | HG02258.hp1 HG02717.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-3990_494-3989d others(4): Show |
MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011697 | |||||||
chr7:115011876 | C | T | 37 | a0001c0001t0004g0161 a0001c0001t0005g0003 a0001c0001t0005g0012 others(34): Show |
38 | HG00323.hp1 HG00408.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.494-3812C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011876 | |||||||
chr7:115011877 | G | A | 12 | a0001c0001t0002g0002 a0001c0001t0002g0042 a0001c0001t0002g0043 others(9): Show |
13 | HG01361.hp2 HG02055.hp1 HG02145.hp2 others(10): Show |
intron_variant | MODIFIER | c.494-3811G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011877 | |||||||
chr7:115011916 | A | C | 1 | a0001c0001t0002g0073 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.494-3772A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115011916 | |||||||
chr7:115012021 | C | T | 58 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0062 others(55): Show |
62 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(59): Show |
intron_variant | MODIFIER | c.494-3667C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115012021 | |||||||
chr7:115012266 | A | G | 1 | a0001c0001t0004g0161 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.494-3422A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115012266 | |||||||
chr7:115012379 | G | A | 1 | a0001c0001t0041g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.494-3309G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115012379 | |||||||
chr7:115012382 | G | A | 4 | a0001c0001t0011g0131 a0001c0001t0011g0132 a0001c0001t0040g0135 others(1): Show |
4 | HG01891.hp1 HG02109.hp1 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-3306G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115012382 | |||||||
chr7:115012786 | T | C | 1 | a0001c0001t0041g0055 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.494-2902T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115012786 | |||||||
chr7:115012935 | C | T | 2 | a0001c0001t0007g0276 a0001c0001t0050g0060 |
2 | HG01081.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.494-2753C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115012935 | |||||||
chr7:115013321 | G | T | 1 | a0001c0001t0001g0062 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.494-2367G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115013321 | |||||||
chr7:115013344 | GA | G | 179 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(176): Show |
189 | HG00099.hp1 HG00140.hp2 HG00280.hp2 others(186): Show |
intron_variant | MODIFIER | c.494-2342delA | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | INFO_REALIGN_3_PRIME | chr7 | 115013344 | ||||||
chr7:115013369 | A | G | 1 | a0001c0001t0001g0092 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.494-2319A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115013369 | |||||||
chr7:115013389 | A | G | 2 | a0001c0001t0006g0153 a0001c0001t0054g0262 |
2 | NA19087.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.494-2299A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115013389 | |||||||
chr7:115013415 | G | A | 3 | a0001c0001t0022g0052 a0001c0001t0022g0053 a0001c0001t0022g0054 |
3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.494-2273G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115013415 | |||||||
chr7:115013564 | A | G | 69 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(66): Show |
74 | HG00280.hp2 HG00609.hp1 HG00621.hp1 others(71): Show |
intron_variant | MODIFIER | c.494-2124A>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115013564 | |||||||
chr7:115013985 | C | T | 33 | a0001c0001t0007g0016 a0001c0001t0007g0033 a0001c0001t0007g0034 others(30): Show |
34 | HG00099.hp1 HG00140.hp2 HG00741.hp2 others(31): Show |
intron_variant | MODIFIER | c.494-1703C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115013985 | |||||||
chr7:115014045 | C | A | 49 | a0001c0001t0004g0011 a0001c0001t0004g0015 a0001c0001t0004g0063 others(46): Show |
52 | HG00408.hp2 HG00609.hp2 HG00621.hp2 others(49): Show |
intron_variant | MODIFIER | c.494-1643C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014045 | |||||||
chr7:115014085 | T | G | 2 | a0001c0001t0004g0285 a0001c0001t0006g0301 |
2 | NA18998.hp1 NA19007.hp1 |
intron_variant | MODIFIER | c.494-1603T>G | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014085 | |||||||
chr7:115014119 | G | A | 1 | a0001c0001t0057g0026 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.494-1569G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014119 | |||||||
chr7:115014127 | T | C | 1 | a0001c0001t0010g0242 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.494-1561T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014127 | |||||||
chr7:115014184 | G | A | 2 | a0001c0001t0003g0214 a0001c0001t0035g0204 |
2 | HG03654.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.494-1504G>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014184 | |||||||
chr7:115014274 | G | T | 1 | a0001c0001t0058g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.494-1414G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014274 | |||||||
chr7:115014475 | C | T | 1 | a0001c0001t0030g0068 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.494-1213C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014475 | |||||||
chr7:115014484 | G | T | 1 | a0001c0001t0001g0079 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.494-1204G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014484 | |||||||
chr7:115014488 | T | C | 4 | a0001c0001t0008g0017 a0001c0001t0008g0115 a0001c0001t0008g0139 others(1): Show |
4 | HG01496.hp2 HG03453.hp2 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.494-1200T>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014488 | |||||||
chr7:115014541 | G | T | 4 | a0001c0001t0028g0030 a0001c0001t0028g0293 a0001c0001t0029g0041 others(1): Show |
4 | HG02738.hp1 HG03492.hp2 HG03704.hp1 others(1): Show |
intron_variant | MODIFIER | c.494-1147G>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014541 | |||||||
chr7:115014562 | C | T | 1 | a0001c0001t0010g0083 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.494-1126C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014562 | |||||||
chr7:115014628 | C | A | 1 | a0001c0001t0011g0072 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.494-1060C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014628 | |||||||
chr7:115014779 | CT | C | 3 | a0001c0001t0022g0052 a0001c0001t0022g0053 a0001c0001t0022g0054 |
3 | HG02615.hp1 HG03540.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.494-908delT | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014779 | |||||||
chr7:115014963 | C | A | 1 | a0001c0001t0039g0151 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.494-725C>A | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115014963 | |||||||
chr7:115015058 | C | T | 1 | a0001c0001t0058g0253 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.494-630C>T | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115015058 | |||||||
chr7:115015314 | A | C | 1 | a0001c0001t0014g0289 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.494-374A>C | MDFIC | ENSG00000135272.13 | transcript | ENST00000393486.6 | protein_coding | 4/4 | chr7 | 115015314 |