Item | Value |
---|---|
geneid | 54468 |
ensemblid | ENSG00000164654.16 |
hgncid | 21905 |
symbol | MIOS |
name | meiosis regulator for oocyte development |
refseq_nuc | NM_019005.4 |
refseq_prot | NP_061878.3 |
ensembl_nuc | ENST00000340080.9 |
ensembl_prot | ENSP00000339881.4 |
mane_status | MANE Select |
chr | chr7 |
start | 7566884 |
end | 7608932 |
strand | + |
ver | v1.2 |
region | chr7:7566884-7608932 |
region5000 | chr7:7561884-7613932 |
regionname0 | MIOS_chr7_7566884_7608932 |
regionname5000 | MIOS_chr7_7561884_7613932 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 875 | 324 | 82 | 56 | 138 | 12 | 34 | 112 | MIOS_chr7_7561884_7613932 | MIOS | MSGTK others(870): Show |
chr7 | 7561884 | 7613932 |
a0002 | 0/0 | 875 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | MSGTK others(870): Show |
chr7 | 7561884 | 7613932 |
a0003 | 0/0 | 875 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | MSGTK others(870): Show |
chr7 | 7561884 | 7613932 |
a0004 | 0/0 | 875 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | MSGTK others(870): Show |
chr7 | 7561884 | 7613932 |
a0005 | 0/0 | 875 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | MSGTK others(870): Show |
chr7 | 7561884 | 7613932 |
a0006 | 0/0 | 875 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | MSGTK others(870): Show |
chr7 | 7561884 | 7613932 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 2625 | 192 | 39 | 40 | 87 | 11 | 14 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0001c0002 | 0/0 | 2625 | 64 | 15 | 6 | 34 | 1 | 8 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0001c0003 | 0/0 | 2625 | 30 | 10 | 4 | 12 | 0 | 4 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0001c0004 | 0/0 | 2625 | 11 | 11 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0001c0005 | 0/0 | 2625 | 7 | 1 | 2 | 1 | 0 | 3 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0001c0006 | 0/0 | 2625 | 6 | 0 | 0 | 3 | 0 | 3 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0001c0007 | 1/0 | 2625 | 4 | 0 | 2 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0001c0008 | 0/0 | 2625 | 3 | 3 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0001c0009 | 0/0 | 2625 | 3 | 0 | 2 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0001c0011 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0001c0013 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0001c0017 | 0/0 | 2625 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0002c0010 | 0/0 | 2625 | 2 | 2 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0003c0015 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0004c0014 | 0/0 | 2625 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0005c0012 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 | ||
a0006c0016 | 0/0 | 2625 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | ATGAG others(2620): Show |
chr7 | 7561884 | 7613932 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 4878 | 155 | 12 | 35 | 83 | 11 | 13 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0001t0003 | 0/0 | 4878 | 10 | 9 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0001t0006 | 0/0 | 4875 | 7 | 7 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4870): Show |
chr7 | 7561884 | 7613932 |
a0001c0001t0008 | 0/0 | 4878 | 5 | 4 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0001t0009 | 0/0 | 4878 | 5 | 4 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0001t0012 | 0/0 | 4878 | 3 | 2 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0001t0014 | 0/0 | 4878 | 2 | 0 | 0 | 2 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0001t0016 | 0/0 | 4878 | 2 | 0 | 1 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0001t0020 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0001t0021 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0001t0026 | 0/0 | 4879 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4874): Show |
chr7 | 7561884 | 7613932 |
a0001c0002t0001 | 0/0 | 4878 | 42 | 5 | 6 | 25 | 1 | 5 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0002t0004 | 0/0 | 4878 | 8 | 0 | 0 | 8 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0002t0006 | 0/0 | 4875 | 2 | 2 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4870): Show |
chr7 | 7561884 | 7613932 |
a0001c0002t0010 | 0/0 | 4878 | 3 | 3 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0002t0015 | 0/0 | 4878 | 2 | 1 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0002t0019 | 0/0 | 4878 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0002t0022 | 0/0 | 4878 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0002t0023 | 0/0 | 4875 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4870): Show |
chr7 | 7561884 | 7613932 |
a0001c0002t0025 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0002t0028 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0002t0029 | 0/0 | 4877 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4872): Show |
chr7 | 7561884 | 7613932 |
a0001c0002t0031 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0003t0002 | 0/0 | 4878 | 21 | 2 | 3 | 12 | 0 | 4 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0003t0007 | 0/0 | 4878 | 9 | 8 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0004t0001 | 0/0 | 4878 | 5 | 5 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0004t0003 | 0/0 | 4878 | 4 | 4 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0004t0010 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0004t0027 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0005t0002 | 0/0 | 4878 | 6 | 1 | 2 | 1 | 0 | 2 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0005t0024 | 0/0 | 4878 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0006t0005 | 0/0 | 4878 | 6 | 0 | 0 | 3 | 0 | 3 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0007t0013 | 1/0 | 4877 | 3 | 0 | 1 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4872): Show |
chr7 | 7561884 | 7613932 |
a0001c0007t0030 | 0/0 | 4877 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4872): Show |
chr7 | 7561884 | 7613932 |
a0001c0008t0005 | 0/0 | 4878 | 3 | 3 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0009t0011 | 0/0 | 4879 | 3 | 0 | 2 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4874): Show |
chr7 | 7561884 | 7613932 |
a0001c0011t0017 | 0/0 | 4878 | 2 | 2 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0013t0003 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0001c0017t0001 | 0/0 | 4878 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0002c0010t0018 | 0/0 | 4878 | 2 | 2 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCTTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0003c0015t0003 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0004c0014t0003 | 0/0 | 4878 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0005c0012t0004 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
a0006c0016t0001 | 0/0 | 4878 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | CCCTT others(4873): Show |
chr7 | 7561884 | 7613932 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 10 | 1 | 1 | 6 | 0 | 2 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0004 | 0/0 | 5 | 0 | 3 | 1 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0005 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0007 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0011 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0012 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0013 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0023 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0024 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0025 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0026 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0028 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0033 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0125 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0003g0030 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0003g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0003g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0003g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0003g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0003g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0006g0003 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0006g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0008g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0008g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0008g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0008g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0008g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0009g0014 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0009g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0009g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0012g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0012g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0014g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0014g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0016g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0016g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0020g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0021g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0001t0026g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0006 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0004g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0004g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0004g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0004g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0004g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0006g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0006g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0010g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0010g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0010g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0015g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0015g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0019g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0022g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0023g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0025g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0028g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0029g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0002t0031g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0002g0002 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0002g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0002g0009 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0002g0018 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0002g0019 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0002g0052 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0002g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0002g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0007g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0007g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0007g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0007g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0007g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0007g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0007g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0003t0007g0260 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0004t0001g0015 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0004t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0004t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0004t0003g0016 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0004t0003g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0004t0010g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0004t0027g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0005t0002g0008 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0005t0002g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0005t0002g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0005t0002g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0005t0002g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0005t0024g0051 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0006t0005g0029 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0006t0005g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0006t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0006t0005g0215 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0006t0005g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0007t0013g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0007t0013g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0007t0013g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0007t0030g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0008t0005g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0008t0005g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0008t0005g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0009t0011g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0009t0011g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0011t0017g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0011t0017g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0013t0003g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0001c0017t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0002c0010t0018g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0002c0010t0018g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0003c0015t0003g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0004c0014t0003g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0005c0012t0004g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
a0006c0016t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0026 | EUR | GBR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0032 | EUR | GBR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00280 | hp2 | a0001 | c0002 | t0001 | g0079 | EUR | FIN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0027 | EUR | FIN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0026 | EUR | FIN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | CHS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | CHS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00544 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | CHS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | CHS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00621 | hp2 | a0001 | c0002 | t0001 | g0077 | EAS | CHS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00639 | hp1 | a0001 | c0001 | t0016 | g0121 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0203 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0139 | EAS | CHS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00733 | hp2 | a0001 | c0005 | t0002 | g0055 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00741 | hp1 | a0001 | c0003 | t0002 | g0056 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0112 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0035 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01081 | hp2 | a0001 | c0001 | t0008 | g0222 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01106 | hp1 | a0001 | c0002 | t0001 | g0115 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01106 | hp2 | a0001 | c0007 | t0013 | g0251 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01109 | hp1 | a0001 | c0003 | t0002 | g0050 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01109 | hp2 | a0001 | c0001 | t0009 | g0185 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0129 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01243 | hp2 | a0001 | c0001 | t0012 | g0045 | AMR | PUR | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0148 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01256 | hp2 | a0001 | c0002 | t0001 | g0081 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0127 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01257 | hp2 | a0001 | c0005 | t0002 | g0054 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01261 | hp1 | a0001 | c0003 | t0002 | g0009 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0141 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01346 | hp2 | a0001 | c0003 | t0007 | g0254 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0088 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0235 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0178 | EUR | IBS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0225 | EUR | IBS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0023 | EUR | IBS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0033 | EUR | IBS | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0157 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0216 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01891 | hp2 | a0001 | c0001 | t0003 | g0031 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01934 | hp1 | a0001 | c0007 | t0030 | g0248 | AMR | PEL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01952 | hp2 | a0001 | c0009 | t0011 | g0017 | AMR | PEL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01978 | hp1 | a0001 | c0002 | t0001 | g0082 | AMR | PEL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0143 | AMR | PEL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01981 | hp1 | a0001 | c0002 | t0001 | g0078 | AMR | PEL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0024 | AMR | PEL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PEL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PEL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02015 | hp1 | a0001 | c0009 | t0011 | g0048 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0111 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0147 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02055 | hp1 | a0001 | c0003 | t0007 | g0256 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02055 | hp2 | a0001 | c0001 | t0003 | g0218 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02056 | hp2 | a0001 | c0002 | t0025 | g0060 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02080 | hp1 | a0001 | c0002 | t0001 | g0063 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02083 | hp1 | a0001 | c0001 | t0021 | g0234 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02129 | hp2 | a0001 | c0002 | t0004 | g0106 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02132 | hp2 | a0001 | c0006 | t0005 | g0210 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | KHV | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02145 | hp1 | a0001 | c0001 | t0008 | g0221 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02145 | hp2 | a0001 | c0003 | t0007 | g0260 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02257 | hp1 | a0001 | c0004 | t0010 | g0253 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02257 | hp2 | a0001 | c0002 | t0001 | g0085 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02293 | hp1 | a0001 | c0009 | t0011 | g0017 | AMR | PEL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02451 | hp1 | a0001 | c0001 | t0026 | g0197 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02451 | hp2 | a0001 | c0002 | t0001 | g0087 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02572 | hp1 | a0001 | c0004 | t0003 | g0043 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02572 | hp2 | a0001 | c0001 | t0009 | g0014 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02615 | hp1 | a0001 | c0003 | t0002 | g0009 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02615 | hp2 | a0001 | c0002 | t0023 | g0200 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02622 | hp1 | a0001 | c0001 | t0006 | g0046 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02622 | hp2 | a0001 | c0003 | t0002 | g0009 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02630 | hp1 | a0001 | c0002 | t0031 | g0252 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0176 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0162 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02647 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02698 | hp1 | a0001 | c0001 | t0016 | g0150 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02698 | hp2 | a0001 | c0002 | t0019 | g0092 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02717 | hp1 | a0001 | c0004 | t0003 | g0016 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02717 | hp2 | a0001 | c0001 | t0009 | g0014 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02723 | hp1 | a0001 | c0001 | t0009 | g0014 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02723 | hp2 | a0001 | c0003 | t0007 | g0258 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02735 | hp2 | a0001 | c0006 | t0005 | g0215 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02809 | hp1 | a0001 | c0004 | t0001 | g0186 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0175 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02818 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02818 | hp2 | a0001 | c0004 | t0001 | g0187 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0204 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02886 | hp2 | a0001 | c0002 | t0006 | g0198 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02895 | hp1 | a0002 | c0010 | t0018 | g0041 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02895 | hp2 | a0001 | c0011 | t0017 | g0123 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02897 | hp1 | a0001 | c0003 | t0007 | g0259 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02897 | hp2 | a0001 | c0011 | t0017 | g0122 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02922 | hp1 | a0001 | c0003 | t0007 | g0034 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02922 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02965 | hp1 | a0001 | c0002 | t0001 | g0086 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02965 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02970 | hp1 | a0001 | c0001 | t0008 | g0224 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02970 | hp2 | a0001 | c0004 | t0003 | g0016 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02976 | hp1 | a0003 | c0015 | t0003 | g0220 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02976 | hp2 | a0001 | c0003 | t0007 | g0255 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03041 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03041 | hp2 | a0001 | c0004 | t0027 | g0183 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0205 | AFR | MSL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03098 | hp2 | a0001 | c0002 | t0029 | g0247 | AFR | MSL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03130 | hp1 | a0001 | c0003 | t0007 | g0034 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03139 | hp1 | a0001 | c0001 | t0003 | g0030 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03139 | hp2 | a0001 | c0001 | t0006 | g0003 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0223 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03195 | hp2 | a0001 | c0001 | t0012 | g0044 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03209 | hp1 | a0001 | c0001 | t0012 | g0047 | AFR | MSL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03209 | hp2 | a0001 | c0002 | t0010 | g0244 | AFR | MSL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03225 | hp1 | a0001 | c0008 | t0005 | g0214 | AFR | MSL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03225 | hp2 | a0001 | c0003 | t0007 | g0257 | AFR | MSL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0120 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0126 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | MSL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03453 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | MSL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | MSL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03486 | hp2 | a0002 | c0010 | t0018 | g0042 | AFR | MSL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03491 | hp1 | a0001 | c0006 | t0005 | g0029 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03491 | hp2 | a0001 | c0002 | t0022 | g0119 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03492 | hp1 | a0001 | c0006 | t0005 | g0029 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0151 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03516 | hp1 | a0001 | c0008 | t0005 | g0213 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ESN | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03540 | hp1 | a0004 | c0014 | t0003 | g0031 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03540 | hp2 | a0001 | c0002 | t0001 | g0083 | AFR | GWD | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | MSL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03579 | hp2 | a0001 | c0001 | t0003 | g0236 | AFR | MSL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03654 | hp1 | a0001 | c0003 | t0002 | g0008 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03654 | hp2 | a0001 | c0002 | t0001 | g0102 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03669 | hp2 | a0001 | c0002 | t0015 | g0233 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03688 | hp1 | a0001 | c0002 | t0001 | g0100 | SAS | STU | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0166 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0152 | SAS | PJL | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03834 | hp1 | a0001 | c0002 | t0001 | g0006 | SAS | BEB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03834 | hp2 | a0001 | c0003 | t0002 | g0018 | SAS | BEB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03927 | hp1 | a0001 | c0003 | t0002 | g0018 | SAS | BEB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03927 | hp2 | a0001 | c0001 | t0001 | g0142 | SAS | BEB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03942 | hp1 | a0001 | c0017 | t0001 | g0049 | SAS | BEB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG03942 | hp2 | a0001 | c0007 | t0013 | g0250 | SAS | BEB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG04184 | hp1 | a0001 | c0002 | t0001 | g0080 | SAS | BEB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | BEB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG04199 | hp1 | a0001 | c0002 | t0001 | g0005 | SAS | STU | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG04199 | hp2 | a0001 | c0005 | t0002 | g0061 | SAS | STU | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG04204 | hp1 | a0001 | c0005 | t0002 | g0053 | SAS | STU | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG04204 | hp2 | a0001 | c0003 | t0002 | g0052 | SAS | STU | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18522 | hp1 | a0001 | c0013 | t0003 | g0238 | AFR | YRI | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18522 | hp2 | a0001 | c0002 | t0006 | g0199 | AFR | YRI | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18612 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | CHB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | CHB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | YRI | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18906 | hp2 | a0001 | c0002 | t0001 | g0084 | AFR | YRI | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18939 | hp2 | a0005 | c0012 | t0004 | g0232 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18948 | hp1 | a0001 | c0001 | t0020 | g0072 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0037 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18952 | hp1 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18952 | hp2 | a0001 | c0006 | t0005 | g0240 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18957 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18960 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18961 | hp1 | a0001 | c0002 | t0001 | g0068 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18963 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18963 | hp2 | a0001 | c0002 | t0001 | g0067 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0036 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18964 | hp2 | a0001 | c0002 | t0001 | g0116 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18968 | hp2 | a0001 | c0006 | t0005 | g0211 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0096 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18971 | hp2 | a0001 | c0001 | t0014 | g0022 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18974 | hp2 | a0001 | c0002 | t0001 | g0076 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18977 | hp2 | a0001 | c0002 | t0001 | g0021 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18980 | hp1 | a0001 | c0002 | t0001 | g0108 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18982 | hp1 | a0001 | c0003 | t0002 | g0057 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18982 | hp2 | a0001 | c0002 | t0001 | g0159 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18983 | hp1 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18987 | hp1 | a0001 | c0002 | t0004 | g0069 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18987 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18992 | hp2 | a0006 | c0016 | t0001 | g0105 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18993 | hp1 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18993 | hp2 | a0001 | c0002 | t0001 | g0138 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18994 | hp1 | a0001 | c0002 | t0001 | g0158 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18995 | hp1 | a0001 | c0002 | t0001 | g0094 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18997 | hp1 | a0001 | c0002 | t0001 | g0073 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18997 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18998 | hp2 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19000 | hp2 | a0001 | c0002 | t0001 | g0066 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19001 | hp1 | a0001 | c0002 | t0001 | g0074 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19004 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19005 | hp1 | a0001 | c0005 | t0002 | g0008 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19006 | hp1 | a0001 | c0002 | t0004 | g0070 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0022 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19010 | hp2 | a0001 | c0003 | t0002 | g0058 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19043 | hp1 | a0001 | c0002 | t0010 | g0245 | AFR | LWK | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19043 | hp2 | a0001 | c0001 | t0003 | g0219 | AFR | LWK | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19054 | hp1 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19064 | hp2 | a0001 | c0003 | t0002 | g0019 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19067 | hp2 | a0001 | c0001 | t0014 | g0107 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19070 | hp2 | a0001 | c0002 | t0004 | g0020 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19072 | hp2 | a0001 | c0002 | t0004 | g0071 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19082 | hp1 | a0001 | c0002 | t0004 | g0020 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19082 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19084 | hp2 | a0001 | c0003 | t0002 | g0002 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19085 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19085 | hp2 | a0001 | c0002 | t0001 | g0065 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19087 | hp1 | a0001 | c0003 | t0002 | g0059 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19089 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0243 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0177 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19240 | hp1 | a0001 | c0001 | t0003 | g0237 | AFR | YRI | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA19240 | hp2 | a0001 | c0001 | t0003 | g0217 | AFR | YRI | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA20129 | hp1 | a0001 | c0001 | t0006 | g0003 | AFR | ASW | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA20129 | hp2 | a0001 | c0001 | t0009 | g0184 | AFR | ASW | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | GIH | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA20905 | hp2 | a0001 | c0005 | t0024 | g0051 | SAS | GIH | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG01123 | hp2 | a0001 | c0002 | t0001 | g0110 | AMR | CLM | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02109 | hp1 | a0001 | c0005 | t0002 | g0008 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02109 | hp2 | a0001 | c0002 | t0028 | g0261 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02486 | hp1 | a0001 | c0008 | t0005 | g0212 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02486 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02559 | hp1 | a0001 | c0002 | t0015 | g0130 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
HG02559 | hp2 | a0001 | c0004 | t0003 | g0016 | AFR | ACB | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18955 | hp1 | a0001 | c0002 | t0001 | g0006 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA20300 | hp1 | a0001 | c0002 | t0010 | g0246 | AFR | USA | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | USA | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0125 | REF | REF | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
homoSapiens | grch38p0 | a0001 | c0007 | t0013 | g0249 | REF | REF | MIOS_chr7_7561884_7613932 | MIOS | chr7 | 7561884 | 7613932 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:7573487 | A | G | 1 | a0003 | 1 | HG02976.hp1 | missense_variant | MODERATE | c.1012A>G | p.Met338Val | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 4/13 | 1421/4877 | 1012/2628 | 338/875 | chr7 | 7573487 | |||
chr7:7573661 | C | G | 1 | a0004 | 1 | HG03540.hp1 | missense_variant | MODERATE | c.1186C>G | p.Leu396Val | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 4/13 | 1595/4877 | 1186/2628 | 396/875 | chr7 | 7573661 | |||
chr7:7583209 | G | C | 1 | a0006 | 1 | NA18992.hp2 | missense_variant | MODERATE | c.1485G>C | p.Gln495His | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/13 | 1894/4877 | 1485/2628 | 495/875 | chr7 | 7583209 | |||
chr7:7589448 | C | A | 1 | a0002 | 2 | HG02895.hp1 HG03486.hp2 |
missense_variant | MODERATE | c.1928C>A | p.Ala643Asp | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/13 | 2337/4877 | 1928/2628 | 643/875 | chr7 | 7589448 | |||
chr7:7589528 | G | C | 1 | a0005 | 1 | NA18939.hp2 | missense_variant | MODERATE | c.2008G>C | p.Gly670Arg | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/13 | 2417/4877 | 2008/2628 | 670/875 | chr7 | 7589528 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:7573222 | A | G | 1 | a0001c0017 | 1 | HG03942.hp1 | synonymous_variant | LOW | c.747A>G | p.Ala249Ala | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 4/13 | 1156/4877 | 747/2628 | 249/875 | chr7 | 7573222 | |||
chr7:7573252 | A | G | 1 | a0001c0011 | 2 | HG02895.hp2 HG02897.hp2 |
synonymous_variant | LOW | c.777A>G | p.Pro259Pro | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 4/13 | 1186/4877 | 777/2628 | 259/875 | chr7 | 7573252 | |||
chr7:7573408 | C | T | 2 | a0001c0003 a0001c0005 |
37 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(34): Show |
synonymous_variant | LOW | c.933C>T | p.Pro311Pro | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 4/13 | 1342/4877 | 933/2628 | 311/875 | chr7 | 7573408 | |||
chr7:7573480 | A | G | 1 | a0006c0016 | 1 | NA18992.hp2 | synonymous_variant | LOW | c.1005A>G | p.Gln335Gln | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 4/13 | 1414/4877 | 1005/2628 | 335/875 | chr7 | 7573480 | |||
chr7:7585736 | A | G | 1 | a0001c0009 | 3 | HG01952.hp2 HG02015.hp1 HG02293.hp1 |
synonymous_variant | LOW | c.1749A>G | p.Leu583Leu | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/13 | 2158/4877 | 1749/2628 | 583/875 | chr7 | 7585736 | |||
chr7:7588500 | T | C | 1 | a0001c0008 | 3 | HG02486.hp1 HG03225.hp1 HG03516.hp1 |
splice_region_variant&synonymous_variant | LOW | c.1821T>C | p.Tyr607Tyr | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 8/13 | 2230/4877 | 1821/2628 | 607/875 | chr7 | 7588500 | |||
chr7:7596364 | G | A | 1 | a0001c0013 | 1 | NA18522.hp1 | synonymous_variant | LOW | c.2304G>A | p.Thr768Thr | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/13 | 2713/4877 | 2304/2628 | 768/875 | chr7 | 7596364 | |||
chr7:7606036 | C | T | 2 | a0001c0006 a0001c0008 |
9 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(6): Show |
synonymous_variant | LOW | c.2496C>T | p.His832His | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 12/13 | 2905/4877 | 2496/2628 | 832/875 | chr7 | 7606036 | |||
chr7:7607020 | G | T | 16 | a0001c0001 a0001c0002 a0001c0003 others(13): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
synonymous_variant | LOW | c.2556G>T | p.Ser852Ser | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 2965/4877 | 2556/2628 | 852/875 | chr7 | 7607020 | |||
chr7:7607056 | A | G | 7 | a0001c0001 a0001c0005 a0001c0008 others(4): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(203): Show |
synonymous_variant | LOW | c.2592A>G | p.Thr864Thr | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 3001/4877 | 2592/2628 | 864/875 | chr7 | 7607056 | |||
chr7:7607089 | A | G | 2 | a0001c0004 a0001c0011 |
13 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(10): Show |
synonymous_variant | LOW | c.2625A>G | p.Pro875Pro | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 3034/4877 | 2625/2628 | 875/875 | chr7 | 7607089 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:7566886 | C | T | 1 | a0002c0010t0018 | 2 | HG02895.hp1 HG03486.hp2 |
5_prime_UTR_variant | MODIFIER | c.-407C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/13 | 5590 | chr7 | 7566886 | ||||||
chr7:7566902 | G | A | 1 | a0001c0002t0019 | 1 | HG02698.hp2 | 5_prime_UTR_variant | MODIFIER | c.-391G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/13 | 5574 | chr7 | 7566902 | ||||||
chr7:7566908 | G | C | 20 | a0001c0001t0001 a0001c0001t0014 a0001c0001t0016 others(17): Show |
254 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(251): Show |
5_prime_UTR_variant | MODIFIER | c.-385G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/13 | 5568 | chr7 | 7566908 | ||||||
chr7:7566922 | C | G | 1 | a0001c0001t0016 | 2 | HG00639.hp1 HG02698.hp1 |
5_prime_UTR_variant | MODIFIER | c.-371C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/13 | 5554 | chr7 | 7566922 | ||||||
chr7:7566930 | T | G | 1 | a0001c0011t0017 | 2 | HG02895.hp2 HG02897.hp2 |
5_prime_UTR_variant | MODIFIER | c.-363T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/13 | 5546 | chr7 | 7566930 | ||||||
chr7:7566975 | G | C | 38 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(35): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
5_prime_UTR_variant | MODIFIER | c.-318G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/13 | 5501 | chr7 | 7566975 | ||||||
chr7:7567630 | A | G | 6 | a0001c0002t0025 a0001c0002t0028 a0001c0003t0002 others(3): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
5_prime_UTR_variant | MODIFIER | c.-197A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 2/13 | 4846 | chr7 | 7567630 | ||||||
chr7:7568036 | A | C | 5 | a0001c0002t0025 a0001c0003t0002 a0001c0003t0007 others(2): Show |
38 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
5_prime_UTR_variant | MODIFIER | c.-128A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/13 | 4440 | chr7 | 7568036 | ||||||
chr7:7568036 | A | G | 1 | a0001c0004t0027 | 1 | HG03041.hp2 | 5_prime_UTR_variant | MODIFIER | c.-128A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/13 | 4440 | chr7 | 7568036 | ||||||
chr7:7607485 | C | T | 1 | a0001c0002t0025 | 1 | HG02056.hp2 | 3_prime_UTR_variant | MODIFIER | c.*393C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 393 | chr7 | 7607485 | ||||||
chr7:7607530 | G | A | 1 | a0001c0002t0029 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*438G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 438 | chr7 | 7607530 | ||||||
chr7:7607535 | C | T | 1 | a0001c0001t0012 | 3 | HG01243.hp2 HG03195.hp2 HG03209.hp1 |
3_prime_UTR_variant | MODIFIER | c.*443C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 443 | chr7 | 7607535 | ||||||
chr7:7607557 | C | T | 40 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(37): Show |
319 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(316): Show |
3_prime_UTR_variant | MODIFIER | c.*465C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 465 | chr7 | 7607557 | ||||||
chr7:7607560 | A | AT | 5 | a0001c0001t0006 a0001c0001t0026 a0001c0002t0006 others(2): Show |
14 | HG01952.hp2 HG02015.hp1 HG02293.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*473dupT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 474 | INFO_REALIGN_3_PRIME | chr7 | 7607560 | |||||
chr7:7607628 | A | T | 1 | a0001c0007t0030 | 1 | HG01934.hp1 | 3_prime_UTR_variant | MODIFIER | c.*536A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 536 | chr7 | 7607628 | ||||||
chr7:7607645 | T | C | 1 | a0001c0005t0024 | 1 | NA20905.hp2 | 3_prime_UTR_variant | MODIFIER | c.*553T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 553 | chr7 | 7607645 | ||||||
chr7:7607679 | T | C | 23 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0014 others(20): Show |
246 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(243): Show |
3_prime_UTR_variant | MODIFIER | c.*587T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 587 | chr7 | 7607679 | ||||||
chr7:7607930 | A | G | 2 | a0001c0002t0004 a0005c0012t0004 |
9 | HG00544.hp2 HG02129.hp2 NA18939.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*838A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 838 | chr7 | 7607930 | ||||||
chr7:7608083 | G | A | 41 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(38): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*991G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 991 | chr7 | 7608083 | ||||||
chr7:7608150 | T | G | 41 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(38): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*1058T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 1058 | chr7 | 7608150 | ||||||
chr7:7608165 | A | AT | 41 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(38): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*1082dupT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 1083 | INFO_REALIGN_3_PRIME | chr7 | 7608165 | |||||
chr7:7608183 | ATAGC | A | 3 | a0001c0001t0006 a0001c0002t0006 a0001c0002t0023 |
10 | HG02615.hp2 HG02622.hp1 HG02818.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*1095_*1098delCTAG | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 1095 | INFO_REALIGN_3_PRIME | chr7 | 7608183 | |||||
chr7:7608198 | T | G | 1 | a0001c0001t0020 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1106T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 1106 | chr7 | 7608198 | ||||||
chr7:7608244 | A | G | 41 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0006 others(38): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*1152A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 1152 | chr7 | 7608244 | ||||||
chr7:7608404 | G | T | 1 | a0001c0001t0021 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1312G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 1312 | chr7 | 7608404 | ||||||
chr7:7608451 | G | A | 4 | a0001c0001t0006 a0001c0001t0026 a0001c0002t0006 others(1): Show |
11 | HG02451.hp1 HG02615.hp2 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1359G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 1359 | chr7 | 7608451 | ||||||
chr7:7608693 | C | A | 1 | a0001c0001t0009 | 5 | HG01109.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1601C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 1601 | chr7 | 7608693 | ||||||
chr7:7608736 | T | C | 6 | a0001c0002t0022 a0001c0002t0025 a0001c0003t0002 others(3): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*1644T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 1644 | chr7 | 7608736 | ||||||
chr7:7608838 | G | A | 1 | a0001c0001t0014 | 2 | NA18971.hp2 NA19067.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1746G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 13/13 | 1746 | chr7 | 7608838 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:7567093 | T | C | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(244): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-221+21T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/12 | chr7 | 7567093 | |||||||
chr7:7567137 | G | C | 1 | a0001c0001t0001g0035 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.-221+65G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/12 | chr7 | 7567137 | |||||||
chr7:7567221 | C | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.-221+149C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/12 | chr7 | 7567221 | |||||||
chr7:7567256 | C | T | 1 | a0001c0004t0003g0016 | 3 | HG02559.hp2 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-221+184C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/12 | chr7 | 7567256 | |||||||
chr7:7567436 | C | A | 5 | a0001c0001t0001g0036 a0001c0001t0001g0037 a0001c0001t0001g0038 others(2): Show |
5 | NA18941.hp1 NA18951.hp2 NA18964.hp1 others(2): Show |
intron_variant | MODIFIER | c.-220-171C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/12 | chr7 | 7567436 | |||||||
chr7:7567438 | C | G | 2 | a0001c0001t0001g0242 a0001c0001t0001g0243 |
2 | NA18980.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.-220-169C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/12 | chr7 | 7567438 | |||||||
chr7:7567475 | CT | C | 12 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(9): Show |
20 | HG01243.hp2 HG01952.hp2 HG02015.hp1 others(17): Show |
intron_variant | MODIFIER | c.-220-131delT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/12 | chr7 | 7567475 | |||||||
chr7:7567533 | A | G | 1 | a0001c0001t0003g0241 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-220-74A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 1/12 | chr7 | 7567533 | |||||||
chr7:7567732 | C | A | 215 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(212): Show |
274 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(271): Show |
intron_variant | MODIFIER | c.-139+44C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 2/12 | chr7 | 7567732 | |||||||
chr7:7567791 | G | A | 4 | a0001c0001t0001g0206 a0001c0001t0001g0207 a0001c0001t0001g0208 others(1): Show |
4 | HG00544.hp1 HG02135.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.-139+103G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 2/12 | chr7 | 7567791 | |||||||
chr7:7567818 | A | G | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG00639.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-139+130A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 2/12 | chr7 | 7567818 | |||||||
chr7:7567924 | T | G | 1 | a0001c0017t0001g0049 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-138-102T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 2/12 | chr7 | 7567924 | |||||||
chr7:7567953 | T | C | 10 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(7): Show |
17 | HG01243.hp2 HG02257.hp1 HG02559.hp2 others(14): Show |
intron_variant | MODIFIER | c.-138-73T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 2/12 | chr7 | 7567953 | |||||||
chr7:7567955 | A | T | 189 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(186): Show |
236 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(233): Show |
intron_variant | MODIFIER | c.-138-71A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 2/12 | chr7 | 7567955 | |||||||
chr7:7567980 | A | G | 1 | a0001c0005t0002g0061 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.-138-46A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 2/12 | chr7 | 7567980 | |||||||
chr7:7568007 | CTG | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(67): Show |
77 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.-138-17_-138-16del others(2): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr7 | 7568007 | ||||||
chr7:7568187 | A | G | 4 | a0001c0003t0007g0034 a0001c0003t0007g0258 a0001c0003t0007g0259 others(1): Show |
5 | HG02145.hp2 HG02723.hp2 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.-41+64A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7568187 | |||||||
chr7:7568220 | C | G | 1 | a0001c0001t0001g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.-41+97C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7568220 | |||||||
chr7:7568410 | T | A | 1 | a0001c0001t0016g0121 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.-41+287T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7568410 | |||||||
chr7:7568633 | A | ACATTGTA others(312): Show |
1 | a0001c0001t0001g0202 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-41+527_-41+528ins others(319): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr7 | 7568633 | ||||||
chr7:7568635 | A | C | 26 | a0001c0002t0025g0060 a0001c0003t0002g0002 a0001c0003t0002g0008 others(23): Show |
38 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.-41+512A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7568635 | |||||||
chr7:7568660 | G | A | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-41+537G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7568660 | |||||||
chr7:7568684 | C | T | 1 | a0001c0004t0003g0016 | 3 | HG02559.hp2 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.-41+561C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7568684 | |||||||
chr7:7568701 | A | G | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-41+578A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7568701 | |||||||
chr7:7568732 | C | G | 4 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-41+609C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7568732 | |||||||
chr7:7568732 | C | T | 2 | a0001c0001t0001g0201 a0001c0006t0005g0240 |
2 | NA18952.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.-41+609C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7568732 | |||||||
chr7:7568957 | T | C | 260 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(257): Show |
323 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(320): Show |
intron_variant | MODIFIER | c.-41+834T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7568957 | |||||||
chr7:7568967 | C | T | 26 | a0001c0002t0025g0060 a0001c0003t0002g0002 a0001c0003t0002g0008 others(23): Show |
38 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.-41+844C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7568967 | |||||||
chr7:7569000 | T | C | 1 | a0001c0001t0026g0197 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-41+877T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569000 | |||||||
chr7:7569069 | A | T | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-41+946A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569069 | |||||||
chr7:7569086 | A | C | 1 | a0001c0001t0001g0239 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.-41+963A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569086 | |||||||
chr7:7569230 | G | A | 2 | a0001c0011t0017g0122 a0001c0011t0017g0123 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-41+1107G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569230 | |||||||
chr7:7569252 | C | T | 1 | a0001c0013t0003g0238 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.-41+1129C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569252 | |||||||
chr7:7569339 | C | A | 8 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(5): Show |
9 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41+1216C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569339 | |||||||
chr7:7569472 | G | A | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.-41+1349G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569472 | |||||||
chr7:7569475 | C | G | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(244): Show |
309 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(306): Show |
intron_variant | MODIFIER | c.-41+1352C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569475 | |||||||
chr7:7569494 | G | A | 1 | a0001c0001t0001g0062 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.-41+1371G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569494 | |||||||
chr7:7569531 | G | C | 104 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(101): Show |
137 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(134): Show |
intron_variant | MODIFIER | c.-41+1408G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569531 | |||||||
chr7:7569634 | C | A | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-41+1511C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569634 | |||||||
chr7:7569637 | A | G | 8 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(5): Show |
9 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.-41+1514A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569637 | |||||||
chr7:7569763 | G | A | 3 | a0001c0002t0010g0244 a0001c0002t0010g0245 a0001c0002t0010g0246 |
3 | HG03209.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.-41+1640G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569763 | |||||||
chr7:7569804 | T | G | 1 | a0001c0003t0002g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-41+1681T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569804 | |||||||
chr7:7569870 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(5): Show |
15 | HG01243.hp2 HG02257.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-41+1747G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7569870 | |||||||
chr7:7570032 | A | AGG | 148 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(145): Show |
172 | HG00140.hp2 HG00280.hp2 HG00438.hp2 others(169): Show |
intron_variant | MODIFIER | c.-41+1910_-41+1911d others(4): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | INFO_REALIGN_3_PRIME | chr7 | 7570032 | ||||||
chr7:7570109 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(5): Show |
15 | HG01243.hp2 HG02257.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-41+1986G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7570109 | |||||||
chr7:7570445 | C | G | 26 | a0001c0002t0025g0060 a0001c0003t0002g0002 a0001c0003t0002g0008 others(23): Show |
38 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.-40-1991C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7570445 | |||||||
chr7:7570474 | G | C | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | HG00735.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.-40-1962G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7570474 | |||||||
chr7:7570486 | G | A | 1 | a0001c0002t0029g0247 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.-40-1950G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7570486 | |||||||
chr7:7570575 | C | A | 92 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(89): Show |
123 | HG00140.hp1 HG00280.hp1 HG00323.hp1 others(120): Show |
intron_variant | MODIFIER | c.-40-1861C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7570575 | |||||||
chr7:7570738 | C | T | 2 | a0001c0009t0011g0017 a0001c0009t0011g0048 |
3 | HG01952.hp2 HG02015.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.-40-1698C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7570738 | |||||||
chr7:7570908 | C | T | 1 | a0001c0002t0022g0119 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.-40-1528C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7570908 | |||||||
chr7:7570926 | C | T | 3 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 |
5 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-1510C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7570926 | |||||||
chr7:7571007 | A | C | 26 | a0001c0002t0025g0060 a0001c0003t0002g0002 a0001c0003t0002g0008 others(23): Show |
38 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.-40-1429A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571007 | |||||||
chr7:7571081 | T | C | 2 | a0002c0010t0018g0041 a0002c0010t0018g0042 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-40-1355T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571081 | |||||||
chr7:7571176 | T | C | 2 | a0001c0001t0001g0023 a0001c0001t0001g0127 |
3 | HG01257.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.-40-1260T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571176 | |||||||
chr7:7571235 | G | C | 1 | a0001c0001t0008g0216 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-40-1201G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571235 | |||||||
chr7:7571286 | G | A | 8 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(5): Show |
15 | HG01243.hp2 HG02257.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.-40-1150G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571286 | |||||||
chr7:7571291 | C | T | 1 | a0001c0001t0026g0197 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-40-1145C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571291 | |||||||
chr7:7571359 | C | T | 3 | a0001c0001t0003g0235 a0001c0001t0003g0236 a0001c0001t0003g0237 |
3 | HG01496.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.-40-1077C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571359 | |||||||
chr7:7571496 | G | A | 1 | a0001c0002t0001g0063 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-40-940G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571496 | |||||||
chr7:7571559 | A | G | 4 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-40-877A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571559 | |||||||
chr7:7571699 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(121): Show |
159 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.-40-737A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571699 | |||||||
chr7:7571717 | A | G | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-40-719A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571717 | |||||||
chr7:7571825 | G | A | 3 | a0001c0002t0006g0198 a0001c0002t0006g0199 a0001c0002t0023g0200 |
3 | HG02615.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-40-611G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571825 | |||||||
chr7:7571888 | A | G | 1 | a0001c0004t0001g0187 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-40-548A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571888 | |||||||
chr7:7571909 | A | C | 7 | a0001c0003t0007g0034 a0001c0003t0007g0255 a0001c0003t0007g0256 others(4): Show |
8 | HG02055.hp1 HG02145.hp2 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.-40-527A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571909 | |||||||
chr7:7571965 | GC | G | 3 | a0001c0001t0009g0014 a0001c0001t0009g0184 a0001c0001t0009g0185 |
5 | HG01109.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.-40-470delC | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571965 | |||||||
chr7:7571991 | T | C | 3 | a0001c0006t0005g0210 a0001c0006t0005g0211 a0001c0006t0005g0240 |
3 | HG02132.hp2 NA18952.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.-40-445T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7571991 | |||||||
chr7:7572050 | A | G | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.-40-386A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7572050 | |||||||
chr7:7572133 | T | C | 1 | a0001c0001t0001g0190 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.-40-303T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7572133 | |||||||
chr7:7572218 | G | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(143): Show |
189 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(186): Show |
intron_variant | MODIFIER | c.-40-218G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7572218 | |||||||
chr7:7572334 | G | C | 10 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(7): Show |
11 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.-40-102G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7572334 | |||||||
chr7:7572352 | T | G | 2 | a0001c0001t0001g0128 a0001c0001t0001g0129 |
2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.-40-84T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 3/12 | chr7 | 7572352 | |||||||
chr7:7573866 | A | G | 1 | a0001c0001t0021g0234 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1294+97A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 4/12 | chr7 | 7573866 | |||||||
chr7:7573922 | C | T | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1294+153C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 4/12 | chr7 | 7573922 | |||||||
chr7:7573961 | G | C | 3 | a0001c0004t0003g0016 a0001c0004t0003g0043 a0001c0004t0010g0253 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1295-137G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 4/12 | chr7 | 7573961 | |||||||
chr7:7574288 | T | A | 10 | a0001c0001t0003g0030 a0001c0001t0003g0217 a0001c0001t0003g0218 others(7): Show |
11 | HG01496.hp1 HG01891.hp1 HG02055.hp2 others(8): Show |
intron_variant | MODIFIER | c.1393+92T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7574288 | |||||||
chr7:7574450 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1393+254A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7574450 | |||||||
chr7:7574620 | A | G | 1 | a0001c0002t0001g0116 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1393+424A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7574620 | |||||||
chr7:7574626 | C | T | 14 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(11): Show |
16 | HG01496.hp1 HG01891.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.1393+430C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7574626 | |||||||
chr7:7574714 | C | T | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(138): Show |
184 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.1393+518C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7574714 | |||||||
chr7:7574715 | G | A | 1 | a0001c0002t0015g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1393+519G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7574715 | |||||||
chr7:7574784 | C | CT | 65 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(62): Show |
72 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.1393+600dupT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr7 | 7574784 | ||||||
chr7:7574823 | T | C | 1 | a0001c0001t0001g0131 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1393+627T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7574823 | |||||||
chr7:7574853 | A | G | 116 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(113): Show |
148 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.1393+657A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7574853 | |||||||
chr7:7574955 | T | C | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(116): Show |
153 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.1393+759T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7574955 | |||||||
chr7:7575373 | A | G | 3 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 |
5 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1393+1177A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7575373 | |||||||
chr7:7575439 | A | G | 11 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0009g0014 others(8): Show |
20 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1393+1243A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7575439 | |||||||
chr7:7575442 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1393+1246A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7575442 | |||||||
chr7:7575594 | G | A | 4 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1393+1398G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7575594 | |||||||
chr7:7575678 | T | C | 5 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(2): Show |
10 | HG01243.hp2 HG02622.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1393+1482T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7575678 | |||||||
chr7:7575745 | G | A | 3 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 |
5 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1393+1549G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7575745 | |||||||
chr7:7575908 | T | TTTGTTTC others(303): Show |
1 | a0001c0009t0011g0017 | 2 | HG01952.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1393+1720_1393+172 others(314): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr7 | 7575908 | ||||||
chr7:7575908 | T | TTTGTTTC others(323): Show |
1 | a0001c0009t0011g0048 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.1393+1720_1393+172 others(334): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr7 | 7575908 | ||||||
chr7:7576333 | A | G | 5 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 others(2): Show |
7 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1393+2137A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7576333 | |||||||
chr7:7576431 | G | C | 22 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0206 others(19): Show |
24 | HG00140.hp2 HG00544.hp1 HG00642.hp1 others(21): Show |
intron_variant | MODIFIER | c.1393+2235G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7576431 | |||||||
chr7:7576519 | A | G | 1 | a0001c0003t0007g0257 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1393+2323A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7576519 | |||||||
chr7:7576680 | C | T | 1 | a0001c0002t0001g0115 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1393+2484C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7576680 | |||||||
chr7:7576695 | A | G | 2 | a0001c0013t0003g0238 a0003c0015t0003g0220 |
2 | HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1393+2499A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7576695 | |||||||
chr7:7576729 | A | G | 1 | a0001c0001t0001g0131 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.1393+2533A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7576729 | |||||||
chr7:7576889 | A | G | 1 | a0001c0002t0031g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1393+2693A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7576889 | |||||||
chr7:7577034 | T | C | 7 | a0001c0006t0005g0210 a0001c0006t0005g0211 a0001c0006t0005g0215 others(4): Show |
7 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1393+2838T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7577034 | |||||||
chr7:7577048 | A | G | 5 | a0001c0001t0008g0216 a0001c0001t0008g0221 a0001c0001t0008g0222 others(2): Show |
5 | HG01081.hp2 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1393+2852A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7577048 | |||||||
chr7:7577199 | A | C | 2 | a0001c0001t0001g0179 a0001c0001t0001g0180 |
2 | NA18975.hp1 NA19080.hp2 |
intron_variant | MODIFIER | c.1393+3003A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7577199 | |||||||
chr7:7577209 | G | C | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1393+3013G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7577209 | |||||||
chr7:7577265 | C | T | 1 | a0001c0002t0025g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1393+3069C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7577265 | |||||||
chr7:7577417 | T | C | 1 | a0001c0004t0003g0016 | 3 | HG02559.hp2 HG02717.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1393+3221T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7577417 | |||||||
chr7:7577476 | C | A | 7 | a0001c0006t0005g0210 a0001c0006t0005g0211 a0001c0006t0005g0215 others(4): Show |
7 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(4): Show |
intron_variant | MODIFIER | c.1393+3280C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7577476 | |||||||
chr7:7577588 | G | C | 1 | a0001c0002t0029g0247 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1393+3392G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7577588 | |||||||
chr7:7577591 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1393+3395A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7577591 | |||||||
chr7:7577687 | A | G | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
243 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(240): Show |
intron_variant | MODIFIER | c.1393+3491A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7577687 | |||||||
chr7:7577815 | G | A | 3 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 |
3 | HG02451.hp1 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1393+3619G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7577815 | |||||||
chr7:7577987 | T | G | 1 | a0001c0001t0026g0197 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1393+3791T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7577987 | |||||||
chr7:7578048 | G | T | 1 | a0001c0003t0002g0009 | 3 | HG01261.hp1 HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1393+3852G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578048 | |||||||
chr7:7578099 | G | C | 3 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 |
5 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1393+3903G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578099 | |||||||
chr7:7578319 | A | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0009g0014 others(5): Show |
15 | HG01109.hp2 HG01243.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.1393+4123A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578319 | |||||||
chr7:7578357 | A | T | 26 | a0001c0002t0025g0060 a0001c0003t0002g0002 a0001c0003t0002g0008 others(23): Show |
38 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1393+4161A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578357 | |||||||
chr7:7578462 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(5): Show |
15 | HG01243.hp2 HG02257.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1393+4266C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578462 | |||||||
chr7:7578521 | G | C | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(105): Show |
136 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(133): Show |
intron_variant | MODIFIER | c.1393+4325G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578521 | |||||||
chr7:7578711 | A | G | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | HG01070.hp2 HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1394-4407A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578711 | |||||||
chr7:7578743 | C | T | 1 | a0001c0002t0001g0118 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.1394-4375C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578743 | |||||||
chr7:7578792 | C | T | 1 | a0001c0002t0001g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1394-4326C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578792 | |||||||
chr7:7578885 | A | T | 1 | a0001c0001t0001g0040 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1394-4233A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578885 | |||||||
chr7:7578886 | T | C | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1394-4232T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578886 | |||||||
chr7:7578926 | G | T | 3 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 |
3 | HG01070.hp2 HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1394-4192G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578926 | |||||||
chr7:7578935 | T | G | 1 | a0001c0001t0001g0062 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1394-4183T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578935 | |||||||
chr7:7578991 | A | G | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(106): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1394-4127A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7578991 | |||||||
chr7:7579051 | C | T | 8 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(5): Show |
15 | HG01243.hp2 HG02257.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1394-4067C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579051 | |||||||
chr7:7579089 | A | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(125): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1394-4029A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579089 | |||||||
chr7:7579099 | C | G | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(125): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1394-4019C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579099 | |||||||
chr7:7579142 | A | G | 1 | a0001c0001t0001g0196 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1394-3976A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579142 | |||||||
chr7:7579235 | T | C | 1 | a0001c0004t0001g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1394-3883T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579235 | |||||||
chr7:7579313 | T | C | 6 | a0001c0001t0001g0010 a0001c0002t0004g0010 a0001c0002t0004g0020 others(3): Show |
8 | HG00544.hp2 HG02129.hp1 NA18987.hp1 others(5): Show |
intron_variant | MODIFIER | c.1394-3805T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579313 | |||||||
chr7:7579379 | C | A | 26 | a0001c0002t0025g0060 a0001c0003t0002g0002 a0001c0003t0002g0008 others(23): Show |
38 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1394-3739C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579379 | |||||||
chr7:7579519 | A | T | 18 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(15): Show |
21 | HG01496.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.1394-3599A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579519 | |||||||
chr7:7579582 | C | G | 2 | a0002c0010t0018g0041 a0002c0010t0018g0042 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1394-3536C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579582 | |||||||
chr7:7579636 | G | T | 3 | a0001c0002t0006g0198 a0001c0002t0006g0199 a0001c0002t0023g0200 |
3 | HG02615.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1394-3482G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579636 | |||||||
chr7:7579781 | C | T | 2 | a0002c0010t0018g0041 a0002c0010t0018g0042 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1394-3337C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579781 | |||||||
chr7:7579823 | C | A | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1394-3295C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579823 | |||||||
chr7:7579892 | T | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1394-3226T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579892 | |||||||
chr7:7579901 | A | G | 1 | a0001c0001t0001g0027 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.1394-3217A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579901 | |||||||
chr7:7579922 | G | A | 3 | a0001c0001t0001g0132 a0001c0001t0001g0133 a0001c0001t0001g0134 |
3 | NA18974.hp1 NA18978.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1394-3196G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579922 | |||||||
chr7:7579971 | T | C | 8 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(5): Show |
9 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1394-3147T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7579971 | |||||||
chr7:7580064 | T | A | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(125): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1394-3054T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580064 | |||||||
chr7:7580129 | C | T | 2 | a0001c0003t0007g0259 a0001c0003t0007g0260 |
2 | HG02145.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1394-2989C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580129 | |||||||
chr7:7580220 | A | G | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1394-2898A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580220 | |||||||
chr7:7580226 | T | C | 128 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(125): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.1394-2892T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580226 | |||||||
chr7:7580466 | C | T | 1 | a0001c0004t0001g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1394-2652C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580466 | |||||||
chr7:7580494 | A | T | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.1394-2624A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580494 | |||||||
chr7:7580547 | A | G | 1 | a0001c0007t0013g0251 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1394-2571A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580547 | |||||||
chr7:7580618 | A | G | 1 | a0001c0006t0005g0211 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1394-2500A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580618 | |||||||
chr7:7580638 | A | G | 1 | a0001c0003t0002g0009 | 3 | HG01261.hp1 HG02615.hp1 HG02622.hp2 |
intron_variant | MODIFIER | c.1394-2480A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580638 | |||||||
chr7:7580678 | C | G | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1394-2440C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580678 | |||||||
chr7:7580680 | A | G | 104 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(101): Show |
124 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1394-2438A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580680 | |||||||
chr7:7580694 | C | CT | 200 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(197): Show |
248 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(245): Show |
intron_variant | MODIFIER | c.1394-2407dupT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr7 | 7580694 | ||||||
chr7:7580694 | C | CTT | 50 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0174 others(47): Show |
65 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(62): Show |
intron_variant | MODIFIER | c.1394-2408_1394-240 others(6): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr7 | 7580694 | ||||||
chr7:7580709 | T | G | 1 | a0001c0001t0020g0072 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.1394-2409T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580709 | |||||||
chr7:7580712 | A | T | 1 | a0001c0001t0003g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1394-2406A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580712 | |||||||
chr7:7580720 | A | G | 1 | a0001c0002t0006g0199 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1394-2398A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580720 | |||||||
chr7:7580768 | C | T | 1 | a0001c0001t0001g0039 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1394-2350C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580768 | |||||||
chr7:7580789 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(106): Show |
137 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(134): Show |
intron_variant | MODIFIER | c.1394-2329C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580789 | |||||||
chr7:7580844 | A | C | 1 | a0001c0001t0001g0173 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1394-2274A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580844 | |||||||
chr7:7580861 | A | G | 1 | a0001c0003t0002g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1394-2257A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580861 | |||||||
chr7:7580883 | T | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1394-2235T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580883 | |||||||
chr7:7580914 | C | T | 71 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(68): Show |
78 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(75): Show |
intron_variant | MODIFIER | c.1394-2204C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580914 | |||||||
chr7:7580976 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(106): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1394-2142G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580976 | |||||||
chr7:7580982 | T | C | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(173): Show |
231 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(228): Show |
intron_variant | MODIFIER | c.1394-2136T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7580982 | |||||||
chr7:7581050 | G | T | 1 | a0001c0001t0001g0126 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1394-2068G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581050 | |||||||
chr7:7581119 | C | G | 2 | a0001c0002t0001g0110 a0001c0002t0001g0115 |
2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1394-1999C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581119 | |||||||
chr7:7581124 | A | C | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1394-1994A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581124 | |||||||
chr7:7581131 | G | A | 1 | a0001c0001t0001g0135 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.1394-1987G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581131 | |||||||
chr7:7581131 | G | C | 1 | a0003c0015t0003g0220 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1394-1987G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581131 | |||||||
chr7:7581191 | G | A | 19 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(16): Show |
22 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(19): Show |
intron_variant | MODIFIER | c.1394-1927G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581191 | |||||||
chr7:7581211 | G | C | 2 | a0001c0001t0012g0044 a0001c0001t0012g0045 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1394-1907G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581211 | |||||||
chr7:7581248 | C | CTGA | 105 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(102): Show |
125 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(122): Show |
intron_variant | MODIFIER | c.1394-1869_1394-186 others(7): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr7 | 7581248 | ||||||
chr7:7581420 | G | A | 255 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(252): Show |
318 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(315): Show |
intron_variant | MODIFIER | c.1394-1698G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581420 | |||||||
chr7:7581436 | T | A | 8 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(5): Show |
9 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1394-1682T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581436 | |||||||
chr7:7581511 | C | T | 3 | a0001c0004t0003g0016 a0001c0004t0003g0043 a0001c0004t0010g0253 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.1394-1607C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581511 | |||||||
chr7:7581530 | A | C | 1 | a0001c0002t0015g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1394-1588A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581530 | |||||||
chr7:7581532 | G | A | 1 | a0001c0002t0015g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1394-1586G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581532 | |||||||
chr7:7581557 | T | C | 2 | a0001c0001t0012g0044 a0001c0001t0012g0045 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1394-1561T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581557 | |||||||
chr7:7581718 | G | A | 1 | a0001c0002t0010g0244 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1394-1400G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581718 | |||||||
chr7:7581745 | C | A | 2 | a0001c0011t0017g0122 a0001c0011t0017g0123 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1394-1373C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581745 | |||||||
chr7:7581763 | T | C | 2 | a0001c0001t0012g0044 a0001c0001t0012g0045 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1394-1355T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581763 | |||||||
chr7:7581812 | C | T | 1 | a0001c0004t0001g0186 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1394-1306C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581812 | |||||||
chr7:7581813 | G | C | 1 | a0001c0002t0001g0064 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1394-1305G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581813 | |||||||
chr7:7581831 | A | G | 145 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(142): Show |
185 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.1394-1287A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581831 | |||||||
chr7:7581882 | C | A | 4 | a0001c0001t0003g0031 a0001c0013t0003g0238 a0003c0015t0003g0220 others(1): Show |
4 | HG01891.hp2 HG02976.hp1 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1394-1236C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581882 | |||||||
chr7:7581882 | C | T | 3 | a0001c0001t0003g0237 a0001c0004t0001g0015 a0001c0004t0001g0187 |
5 | HG02647.hp2 HG02818.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1394-1236C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7581882 | |||||||
chr7:7582048 | G | A | 2 | a0001c0002t0001g0073 a0001c0002t0001g0074 |
2 | NA18997.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.1394-1070G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7582048 | |||||||
chr7:7582213 | G | C | 1 | a0001c0009t0011g0017 | 2 | HG01952.hp2 HG02293.hp1 |
intron_variant | MODIFIER | c.1394-905G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7582213 | |||||||
chr7:7582305 | T | C | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1394-813T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7582305 | |||||||
chr7:7582433 | C | A | 5 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(2): Show |
10 | HG01243.hp2 HG02622.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1394-685C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7582433 | |||||||
chr7:7582556 | A | G | 2 | a0001c0006t0005g0029 a0001c0006t0005g0215 |
3 | HG02735.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1394-562A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7582556 | |||||||
chr7:7582731 | G | A | 2 | a0001c0011t0017g0122 a0001c0011t0017g0123 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1394-387G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7582731 | |||||||
chr7:7582842 | T | C | 1 | a0001c0002t0001g0075 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1394-276T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7582842 | |||||||
chr7:7583011 | C | T | 2 | a0001c0001t0003g0219 a0001c0001t0003g0241 |
2 | HG02486.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.1394-107C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7583011 | |||||||
chr7:7583049 | C | T | 2 | a0002c0010t0018g0041 a0002c0010t0018g0042 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1394-69C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7583049 | |||||||
chr7:7583065 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1394-53C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 5/12 | chr7 | 7583065 | |||||||
chr7:7583692 | T | TA | 26 | a0001c0002t0025g0060 a0001c0003t0002g0002 a0001c0003t0002g0008 others(23): Show |
38 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1648+323dupA | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr7 | 7583692 | ||||||
chr7:7583710 | T | G | 1 | a0001c0006t0005g0211 | 1 | NA18968.hp2 | intron_variant | MODIFIER | c.1648+338T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7583710 | |||||||
chr7:7583729 | C | T | 16 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(13): Show |
24 | HG01243.hp2 HG01952.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.1648+357C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7583729 | |||||||
chr7:7583890 | G | A | 3 | a0001c0001t0001g0203 a0001c0001t0001g0204 a0001c0001t0001g0205 |
3 | HG00639.hp2 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.1648+518G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7583890 | |||||||
chr7:7583898 | T | G | 11 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0009g0014 others(8): Show |
20 | HG01109.hp2 HG01243.hp2 HG02257.hp1 others(17): Show |
intron_variant | MODIFIER | c.1648+526T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7583898 | |||||||
chr7:7583903 | A | G | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(121): Show |
164 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(161): Show |
intron_variant | MODIFIER | c.1648+531A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7583903 | |||||||
chr7:7584000 | T | G | 8 | a0001c0001t0003g0030 a0001c0001t0003g0217 a0001c0001t0003g0218 others(5): Show |
9 | HG01496.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.1648+628T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584000 | |||||||
chr7:7584112 | G | T | 17 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(14): Show |
20 | HG01496.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1648+740G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584112 | |||||||
chr7:7584207 | A | G | 1 | a0001c0001t0001g0171 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1648+835A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584207 | |||||||
chr7:7584236 | TCA | T | 17 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(14): Show |
20 | HG01496.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.1648+866_1648+867d others(4): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr7 | 7584236 | ||||||
chr7:7584344 | A | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(69): Show |
81 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1648+972A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584344 | |||||||
chr7:7584409 | C | T | 2 | a0001c0006t0005g0029 a0001c0006t0005g0215 |
3 | HG02735.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1648+1037C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584409 | |||||||
chr7:7584491 | T | C | 26 | a0001c0002t0025g0060 a0001c0003t0002g0002 a0001c0003t0002g0008 others(23): Show |
38 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1648+1119T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584491 | |||||||
chr7:7584728 | T | G | 1 | a0001c0002t0031g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1649-908T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584728 | |||||||
chr7:7584809 | A | G | 3 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 |
5 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649-827A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584809 | |||||||
chr7:7584850 | C | T | 3 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 |
5 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1649-786C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584850 | |||||||
chr7:7584884 | T | C | 2 | a0001c0011t0017g0122 a0001c0011t0017g0123 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1649-752T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584884 | |||||||
chr7:7584911 | C | G | 1 | a0001c0002t0031g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.1649-725C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584911 | |||||||
chr7:7584919 | C | G | 10 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(7): Show |
11 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(8): Show |
intron_variant | MODIFIER | c.1649-717C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584919 | |||||||
chr7:7584954 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.1649-682G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7584954 | |||||||
chr7:7585095 | T | G | 2 | a0001c0009t0011g0017 a0001c0009t0011g0048 |
3 | HG01952.hp2 HG02015.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1649-541T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7585095 | |||||||
chr7:7585208 | T | C | 2 | a0001c0001t0001g0136 a0001c0001t0001g0202 |
2 | NA18995.hp2 NA19005.hp2 |
intron_variant | MODIFIER | c.1649-428T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7585208 | |||||||
chr7:7585230 | C | T | 1 | a0001c0001t0001g0170 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1649-406C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7585230 | |||||||
chr7:7585261 | T | C | 1 | a0001c0002t0015g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1649-375T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7585261 | |||||||
chr7:7585281 | G | C | 2 | a0001c0011t0017g0122 a0001c0011t0017g0123 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1649-355G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7585281 | |||||||
chr7:7585408 | AC | A | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(115): Show |
156 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(153): Show |
intron_variant | MODIFIER | c.1649-220delC | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr7 | 7585408 | ||||||
chr7:7585416 | C | CT | 8 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(5): Show |
9 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1649-206dupT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr7 | 7585416 | ||||||
chr7:7585416 | C | T | 1 | a0001c0001t0001g0173 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1649-220C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7585416 | |||||||
chr7:7585416 | CT | C | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(75): Show |
89 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(86): Show |
intron_variant | MODIFIER | c.1649-206delT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr7 | 7585416 | ||||||
chr7:7585417 | T | C | 42 | a0001c0001t0003g0030 a0001c0001t0003g0217 a0001c0001t0003g0218 others(39): Show |
55 | HG00733.hp2 HG00741.hp1 HG01081.hp2 others(52): Show |
intron_variant | MODIFIER | c.1649-219T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7585417 | |||||||
chr7:7585418 | T | C | 28 | a0001c0002t0001g0076 a0001c0002t0001g0077 a0001c0002t0025g0060 others(25): Show |
40 | HG00621.hp2 HG00733.hp2 HG00741.hp1 others(37): Show |
intron_variant | MODIFIER | c.1649-218T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7585418 | |||||||
chr7:7585419 | T | C | 26 | a0001c0002t0025g0060 a0001c0003t0002g0002 a0001c0003t0002g0008 others(23): Show |
38 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(35): Show |
intron_variant | MODIFIER | c.1649-217T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7585419 | |||||||
chr7:7585463 | A | G | 2 | a0001c0003t0002g0008 a0001c0005t0002g0008 |
3 | HG02109.hp1 HG03654.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.1649-173A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7585463 | |||||||
chr7:7585468 | A | G | 1 | a0001c0001t0001g0114 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1649-168A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7585468 | |||||||
chr7:7585608 | T | C | 2 | a0001c0009t0011g0017 a0001c0009t0011g0048 |
3 | HG01952.hp2 HG02015.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1649-28T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 6/12 | chr7 | 7585608 | |||||||
chr7:7585928 | A | G | 5 | a0001c0001t0008g0216 a0001c0001t0008g0221 a0001c0001t0008g0222 others(2): Show |
5 | HG01081.hp2 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.1818+123A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7585928 | |||||||
chr7:7586094 | A | G | 1 | a0001c0002t0015g0233 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1818+289A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7586094 | |||||||
chr7:7586150 | ATGCACGT others(13): Show |
A | 2 | a0002c0010t0018g0041 a0002c0010t0018g0042 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.1818+348_1818+367d others(22): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586150 | ||||||
chr7:7586155 | C | CGT | 3 | a0001c0007t0013g0250 a0001c0007t0013g0251 a0001c0007t0030g0248 |
3 | HG01106.hp2 HG01934.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1818+389_1818+390d others(4): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586155 | ||||||
chr7:7586155 | CGT | C | 22 | a0001c0001t0003g0031 a0001c0002t0025g0060 a0001c0003t0002g0002 others(19): Show |
33 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(30): Show |
intron_variant | MODIFIER | c.1818+389_1818+390d others(4): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586155 | ||||||
chr7:7586155 | CGTGTGT | C | 4 | a0001c0002t0006g0198 a0001c0002t0006g0199 a0001c0002t0023g0200 others(1): Show |
4 | HG02615.hp2 HG02886.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1818+385_1818+390d others(8): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586155 | ||||||
chr7:7586155 | CGTGTGTG others(1): Show |
C | 14 | a0001c0001t0026g0197 a0001c0004t0003g0016 a0001c0004t0003g0043 others(11): Show |
17 | HG02132.hp2 HG02257.hp1 HG02451.hp1 others(14): Show |
intron_variant | MODIFIER | c.1818+383_1818+390d others(10): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586155 | ||||||
chr7:7586155 | CGTGTGTG others(3): Show |
C | 5 | a0001c0001t0006g0003 a0001c0001t0009g0014 a0001c0001t0009g0184 others(2): Show |
7 | HG01109.hp2 HG02109.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1818+381_1818+390d others(12): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586155 | ||||||
chr7:7586155 | CGTGTGTG others(5): Show |
C | 12 | a0001c0001t0003g0030 a0001c0001t0003g0217 a0001c0001t0003g0218 others(9): Show |
16 | HG01243.hp2 HG01891.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1818+379_1818+390d others(14): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586155 | ||||||
chr7:7586155 | CGTGTGTG others(7): Show |
C | 21 | a0001c0001t0001g0025 a0001c0001t0001g0027 a0001c0001t0001g0152 others(18): Show |
24 | HG00280.hp1 HG00323.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.1818+377_1818+390d others(16): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586155 | ||||||
chr7:7586155 | CGTGTGTG others(9): Show |
C | 172 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(169): Show |
206 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.1818+375_1818+390d others(18): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586155 | ||||||
chr7:7586155 | CGTGTGTG others(11): Show |
C | 1 | a0001c0001t0001g0229 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1818+373_1818+390d others(20): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586155 | ||||||
chr7:7586155 | CGTGTGTG others(13): Show |
C | 2 | a0001c0011t0017g0122 a0001c0011t0017g0123 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1818+371_1818+390d others(22): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586155 | ||||||
chr7:7586196 | A | G | 2 | a0001c0009t0011g0017 a0001c0009t0011g0048 |
3 | HG01952.hp2 HG02015.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1818+391A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7586196 | |||||||
chr7:7586213 | C | CA | 3 | a0001c0002t0006g0198 a0001c0002t0006g0199 a0001c0002t0023g0200 |
3 | HG02615.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.1818+409dupA | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586213 | ||||||
chr7:7586264 | A | G | 2 | a0001c0001t0001g0168 a0001c0001t0001g0169 |
2 | HG02135.hp2 NA18966.hp1 |
intron_variant | MODIFIER | c.1818+459A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7586264 | |||||||
chr7:7586464 | A | C | 8 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(5): Show |
9 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.1818+659A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7586464 | |||||||
chr7:7586482 | A | G | 3 | a0001c0006t0005g0210 a0001c0006t0005g0211 a0001c0006t0005g0240 |
3 | HG02132.hp2 NA18952.hp2 NA18968.hp2 |
intron_variant | MODIFIER | c.1818+677A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7586482 | |||||||
chr7:7586702 | T | C | 71 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(68): Show |
80 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1818+897T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7586702 | |||||||
chr7:7586988 | C | CT | 11 | a0001c0001t0008g0216 a0001c0001t0008g0221 a0001c0001t0008g0222 others(8): Show |
11 | HG01081.hp2 HG01884.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1818+1203dupT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586988 | ||||||
chr7:7586988 | CT | C | 22 | a0001c0001t0001g0134 a0001c0001t0001g0195 a0001c0001t0006g0003 others(19): Show |
32 | HG01109.hp2 HG01243.hp2 HG01952.hp2 others(29): Show |
intron_variant | MODIFIER | c.1818+1203delT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586988 | ||||||
chr7:7586988 | CTT | C | 202 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(199): Show |
251 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(248): Show |
intron_variant | MODIFIER | c.1818+1202_1818+120 others(6): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7586988 | ||||||
chr7:7587000 | T | G | 9 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0009g0014 others(6): Show |
18 | HG01109.hp2 HG02257.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.1818+1195T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587000 | |||||||
chr7:7587003 | T | G | 15 | a0001c0001t0003g0235 a0001c0001t0006g0003 a0001c0001t0006g0046 others(12): Show |
25 | HG01109.hp2 HG01243.hp2 HG01496.hp1 others(22): Show |
intron_variant | MODIFIER | c.1818+1198T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587003 | |||||||
chr7:7587003 | T | TG | 17 | a0001c0001t0003g0030 a0001c0001t0003g0217 a0001c0001t0003g0218 others(14): Show |
21 | HG01891.hp1 HG02055.hp2 HG02132.hp2 others(18): Show |
intron_variant | MODIFIER | c.1818+1198_1818+119 others(5): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587003 | |||||||
chr7:7587006 | T | G | 250 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(247): Show |
313 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(310): Show |
intron_variant | MODIFIER | c.1818+1201T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587006 | |||||||
chr7:7587030 | G | C | 2 | a0001c0001t0012g0044 a0001c0001t0012g0045 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1818+1225G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587030 | |||||||
chr7:7587049 | T | C | 71 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(68): Show |
80 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1818+1244T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587049 | |||||||
chr7:7587097 | A | G | 5 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0003t0002g0057 others(2): Show |
12 | NA18612.hp1 NA18957.hp2 NA18960.hp1 others(9): Show |
intron_variant | MODIFIER | c.1818+1292A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587097 | |||||||
chr7:7587268 | A | C | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.1819-1230A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587268 | |||||||
chr7:7587276 | T | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(5): Show |
15 | HG01243.hp2 HG02257.hp1 HG02559.hp2 others(12): Show |
intron_variant | MODIFIER | c.1819-1222T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587276 | |||||||
chr7:7587284 | T | A | 1 | a0001c0002t0001g0138 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1819-1214T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587284 | |||||||
chr7:7587307 | G | A | 104 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(101): Show |
124 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1819-1191G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587307 | |||||||
chr7:7587314 | C | A | 13 | a0001c0001t0001g0120 a0001c0002t0001g0078 a0001c0002t0001g0079 others(10): Show |
13 | HG00280.hp2 HG01106.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1819-1184C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587314 | |||||||
chr7:7587371 | T | C | 2 | a0001c0001t0006g0003 a0001c0001t0006g0046 |
7 | HG02622.hp1 HG02818.hp1 HG02922.hp2 others(4): Show |
intron_variant | MODIFIER | c.1819-1127T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587371 | |||||||
chr7:7587478 | A | G | 77 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(74): Show |
85 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(82): Show |
intron_variant | MODIFIER | c.1819-1020A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587478 | |||||||
chr7:7587722 | GA | G | 4 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1819-770delA | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr7 | 7587722 | ||||||
chr7:7587801 | G | A | 104 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(101): Show |
124 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(121): Show |
intron_variant | MODIFIER | c.1819-697G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587801 | |||||||
chr7:7587839 | T | C | 2 | a0001c0009t0011g0017 a0001c0009t0011g0048 |
3 | HG01952.hp2 HG02015.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.1819-659T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587839 | |||||||
chr7:7587912 | C | T | 3 | a0001c0002t0010g0244 a0001c0002t0010g0245 a0001c0002t0010g0246 |
3 | HG03209.hp2 NA19043.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1819-586C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7587912 | |||||||
chr7:7588040 | G | A | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.1819-458G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7588040 | |||||||
chr7:7588040 | G | T | 1 | a0001c0001t0009g0185 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1819-458G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7588040 | |||||||
chr7:7588160 | A | G | 5 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 others(2): Show |
5 | HG02257.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.1819-338A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7588160 | |||||||
chr7:7588344 | C | G | 13 | a0001c0001t0001g0120 a0001c0002t0001g0078 a0001c0002t0001g0079 others(10): Show |
13 | HG00280.hp2 HG01106.hp1 HG01123.hp2 others(10): Show |
intron_variant | MODIFIER | c.1819-154C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7588344 | |||||||
chr7:7588363 | T | C | 227 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(224): Show |
286 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.1819-135T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7588363 | |||||||
chr7:7588425 | A | G | 1 | a0001c0006t0005g0240 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.1819-73A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 7/12 | chr7 | 7588425 | |||||||
chr7:7588644 | C | T | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.1884+81C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 8/12 | chr7 | 7588644 | |||||||
chr7:7588744 | T | G | 2 | a0001c0001t0003g0031 a0004c0014t0003g0031 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1884+181T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 8/12 | chr7 | 7588744 | |||||||
chr7:7588785 | G | A | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(106): Show |
139 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.1884+222G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 8/12 | chr7 | 7588785 | |||||||
chr7:7588906 | G | A | 2 | a0001c0011t0017g0122 a0001c0011t0017g0123 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1884+343G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 8/12 | chr7 | 7588906 | |||||||
chr7:7588906 | G | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(67): Show |
77 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1884+343G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 8/12 | chr7 | 7588906 | |||||||
chr7:7588924 | C | T | 86 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(83): Show |
101 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(98): Show |
intron_variant | MODIFIER | c.1884+361C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 8/12 | chr7 | 7588924 | |||||||
chr7:7588948 | A | G | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(160): Show |
210 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(207): Show |
intron_variant | MODIFIER | c.1884+385A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 8/12 | chr7 | 7588948 | |||||||
chr7:7588992 | G | C | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(67): Show |
77 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.1885-413G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 8/12 | chr7 | 7588992 | |||||||
chr7:7589164 | G | C | 2 | a0001c0002t0001g0110 a0001c0002t0001g0115 |
2 | HG01106.hp1 HG01123.hp2 |
intron_variant | MODIFIER | c.1885-241G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 8/12 | chr7 | 7589164 | |||||||
chr7:7589291 | T | C | 16 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(13): Show |
24 | HG01243.hp2 HG01952.hp2 HG02015.hp1 others(21): Show |
intron_variant | MODIFIER | c.1885-114T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 8/12 | chr7 | 7589291 | |||||||
chr7:7589356 | A | T | 1 | a0001c0001t0001g0166 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1885-49A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 8/12 | chr7 | 7589356 | |||||||
chr7:7589597 | T | G | 8 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(5): Show |
9 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2043+34T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7589597 | |||||||
chr7:7589622 | TC | T | 4 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2043+60delC | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7589622 | |||||||
chr7:7589698 | C | G | 1 | a0001c0001t0003g0237 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.2043+135C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7589698 | |||||||
chr7:7589712 | T | C | 28 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0002t0028g0261 others(25): Show |
40 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(37): Show |
intron_variant | MODIFIER | c.2043+149T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7589712 | |||||||
chr7:7589762 | C | A | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(67): Show |
77 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.2043+199C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7589762 | |||||||
chr7:7589780 | C | A | 14 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(11): Show |
15 | HG01952.hp2 HG02015.hp1 HG02132.hp2 others(12): Show |
intron_variant | MODIFIER | c.2043+217C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7589780 | |||||||
chr7:7589991 | G | A | 1 | a0001c0001t0001g0206 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.2043+428G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7589991 | |||||||
chr7:7590044 | A | G | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00642.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.2043+481A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7590044 | |||||||
chr7:7590142 | C | G | 1 | a0001c0003t0007g0254 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2043+579C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7590142 | |||||||
chr7:7590210 | T | C | 3 | a0001c0004t0003g0016 a0001c0004t0003g0043 a0001c0004t0010g0253 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2043+647T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7590210 | |||||||
chr7:7590282 | T | C | 2 | a0001c0009t0011g0017 a0001c0009t0011g0048 |
3 | HG01952.hp2 HG02015.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2043+719T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7590282 | |||||||
chr7:7590534 | T | C | 1 | a0001c0001t0001g0139 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2043+971T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7590534 | |||||||
chr7:7590607 | G | A | 8 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(5): Show |
9 | HG01952.hp2 HG02015.hp1 HG02293.hp1 others(6): Show |
intron_variant | MODIFIER | c.2043+1044G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7590607 | |||||||
chr7:7590937 | C | G | 2 | a0001c0001t0003g0031 a0004c0014t0003g0031 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2043+1374C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7590937 | |||||||
chr7:7591174 | C | G | 1 | a0001c0003t0007g0256 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2043+1611C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7591174 | |||||||
chr7:7591297 | G | GT | 115 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(112): Show |
144 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.2043+1750dupT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7591297 | ||||||
chr7:7591297 | G | GTT | 19 | a0001c0001t0001g0012 a0001c0001t0001g0124 a0001c0001t0001g0129 others(16): Show |
21 | HG00438.hp1 HG00544.hp1 HG00621.hp1 others(18): Show |
intron_variant | MODIFIER | c.2043+1749_2043+175 others(6): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7591297 | ||||||
chr7:7591384 | A | G | 1 | a0001c0001t0001g0182 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.2043+1821A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7591384 | |||||||
chr7:7591427 | C | T | 9 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(6): Show |
16 | HG01106.hp1 HG01243.hp2 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.2043+1864C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7591427 | |||||||
chr7:7591526 | C | T | 5 | a0001c0001t0001g0160 a0001c0001t0026g0197 a0001c0002t0006g0198 others(2): Show |
5 | HG01934.hp2 HG02451.hp1 HG02615.hp2 others(2): Show |
intron_variant | MODIFIER | c.2043+1963C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7591526 | |||||||
chr7:7591539 | G | A | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2043+1976G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7591539 | |||||||
chr7:7591571 | C | T | 11 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(8): Show |
12 | HG01496.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.2043+2008C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7591571 | |||||||
chr7:7591704 | A | G | 2 | a0002c0010t0018g0041 a0002c0010t0018g0042 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2043+2141A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7591704 | |||||||
chr7:7591908 | A | G | 2 | a0001c0009t0011g0017 a0001c0009t0011g0048 |
3 | HG01952.hp2 HG02015.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2043+2345A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7591908 | |||||||
chr7:7591908 | A | T | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2043+2345A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7591908 | |||||||
chr7:7591984 | AT | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(241): Show |
306 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(303): Show |
intron_variant | MODIFIER | c.2043+2435delT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7591984 | ||||||
chr7:7592005 | G | C | 87 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(84): Show |
97 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(94): Show |
intron_variant | MODIFIER | c.2043+2442G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592005 | |||||||
chr7:7592042 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2043+2479A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592042 | |||||||
chr7:7592087 | C | T | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(105): Show |
138 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(135): Show |
intron_variant | MODIFIER | c.2043+2524C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592087 | |||||||
chr7:7592088 | G | A | 11 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(8): Show |
12 | HG01496.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.2043+2525G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592088 | |||||||
chr7:7592236 | G | A | 1 | a0001c0002t0001g0088 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2043+2673G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592236 | |||||||
chr7:7592276 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2044-2704G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592276 | |||||||
chr7:7592284 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2044-2696T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592284 | |||||||
chr7:7592310 | C | G | 8 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(5): Show |
9 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2044-2670C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592310 | |||||||
chr7:7592316 | C | G | 1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.2044-2664C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592316 | |||||||
chr7:7592481 | G | C | 8 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(5): Show |
9 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2044-2499G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592481 | |||||||
chr7:7592490 | A | G | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2044-2490A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592490 | |||||||
chr7:7592562 | A | G | 1 | a0001c0002t0001g0088 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2044-2418A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592562 | |||||||
chr7:7592644 | C | T | 1 | a0001c0002t0031g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2044-2336C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592644 | |||||||
chr7:7592650 | G | A | 1 | a0001c0002t0029g0247 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2044-2330G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592650 | |||||||
chr7:7592687 | C | T | 3 | a0001c0004t0003g0016 a0001c0004t0003g0043 a0001c0004t0010g0253 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044-2293C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592687 | |||||||
chr7:7592782 | G | A | 1 | a0001c0001t0021g0234 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.2044-2198G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592782 | |||||||
chr7:7592796 | C | T | 53 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(50): Show |
69 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(66): Show |
intron_variant | MODIFIER | c.2044-2184C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592796 | |||||||
chr7:7592870 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2044-2110G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592870 | |||||||
chr7:7592981 | G | A | 3 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0225 |
5 | HG00140.hp2 HG01496.hp2 HG01515.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044-1999G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7592981 | |||||||
chr7:7593052 | G | C | 1 | a0001c0001t0012g0044 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.2044-1928G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593052 | |||||||
chr7:7593299 | G | T | 1 | a0001c0001t0006g0046 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2044-1681G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593299 | |||||||
chr7:7593315 | G | A | 1 | a0001c0001t0001g0242 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2044-1665G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593315 | |||||||
chr7:7593334 | A | G | 1 | a0001c0001t0001g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2044-1646A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593334 | |||||||
chr7:7593433 | G | A | 1 | a0001c0002t0010g0246 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2044-1547G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593433 | |||||||
chr7:7593466 | G | A | 6 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(3): Show |
7 | HG01952.hp2 HG02015.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.2044-1514G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593466 | |||||||
chr7:7593611 | C | T | 3 | a0001c0002t0001g0138 a0001c0002t0001g0158 a0001c0002t0001g0159 |
3 | NA18982.hp2 NA18993.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.2044-1369C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593611 | |||||||
chr7:7593622 | G | A | 92 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(89): Show |
102 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.2044-1358G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593622 | |||||||
chr7:7593634 | G | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.2044-1346G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593634 | |||||||
chr7:7593699 | G | A | 22 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(19): Show |
25 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.2044-1281G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593699 | |||||||
chr7:7593718 | A | AC | 92 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(89): Show |
102 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(99): Show |
intron_variant | MODIFIER | c.2044-1258dupC | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7593718 | ||||||
chr7:7593879 | C | CA | 10 | a0001c0001t0001g0140 a0001c0001t0001g0141 a0001c0001t0001g0142 others(7): Show |
10 | HG00544.hp1 HG01261.hp2 HG01978.hp2 others(7): Show |
intron_variant | MODIFIER | c.2044-1085dupA | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7593879 | ||||||
chr7:7593879 | C | CAA | 14 | a0001c0001t0003g0031 a0001c0001t0008g0216 a0001c0001t0008g0222 others(11): Show |
16 | HG01081.hp2 HG01346.hp2 HG01884.hp2 others(13): Show |
intron_variant | MODIFIER | c.2044-1086_2044-108 others(6): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7593879 | ||||||
chr7:7593879 | C | CAAA | 15 | a0001c0001t0008g0221 a0001c0002t0022g0119 a0001c0002t0025g0060 others(12): Show |
20 | HG00741.hp1 HG01109.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.2044-1087_2044-108 others(7): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7593879 | ||||||
chr7:7593879 | C | CAAAA | 7 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0003t0002g0052 others(4): Show |
14 | HG02055.hp1 HG04204.hp2 NA18612.hp1 others(11): Show |
intron_variant | MODIFIER | c.2044-1088_2044-108 others(8): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7593879 | ||||||
chr7:7593885 | AAAAAAAA others(4): Show |
A | 78 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(75): Show |
86 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(83): Show |
intron_variant | MODIFIER | c.2044-1089_2044-107 others(15): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7593885 | ||||||
chr7:7593891 | AAAAAG | A | 17 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(14): Show |
19 | HG01952.hp2 HG02015.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.2044-1084_2044-108 others(9): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7593891 | ||||||
chr7:7593896 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(157): Show |
213 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(210): Show |
intron_variant | MODIFIER | c.2044-1084G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593896 | |||||||
chr7:7593902 | G | A | 1 | a0001c0013t0003g0238 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2044-1078G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593902 | |||||||
chr7:7593907 | G | A | 16 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(13): Show |
17 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2044-1073G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593907 | |||||||
chr7:7593993 | T | C | 14 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0009g0014 others(11): Show |
23 | HG01109.hp2 HG01243.hp2 HG02572.hp2 others(20): Show |
intron_variant | MODIFIER | c.2044-987T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7593993 | |||||||
chr7:7594074 | C | T | 2 | a0001c0011t0017g0122 a0001c0011t0017g0123 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2044-906C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594074 | |||||||
chr7:7594094 | G | A | 2 | a0001c0001t0008g0216 a0001c0001t0008g0222 |
2 | HG01081.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.2044-886G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594094 | |||||||
chr7:7594126 | G | A | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.2044-854G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594126 | |||||||
chr7:7594182 | G | T | 69 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(66): Show |
76 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(73): Show |
intron_variant | MODIFIER | c.2044-798G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594182 | |||||||
chr7:7594227 | C | T | 1 | a0001c0003t0002g0050 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2044-753C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594227 | |||||||
chr7:7594235 | C | T | 1 | a0001c0001t0001g0124 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2044-745C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594235 | |||||||
chr7:7594241 | T | C | 5 | a0001c0001t0008g0216 a0001c0001t0008g0221 a0001c0001t0008g0222 others(2): Show |
5 | HG01081.hp2 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044-739T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594241 | |||||||
chr7:7594267 | C | A | 3 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 |
5 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-713C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594267 | |||||||
chr7:7594269 | G | C | 1 | a0001c0001t0001g0036 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.2044-711G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594269 | |||||||
chr7:7594311 | C | CT | 68 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(65): Show |
75 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.2044-655dupT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7594311 | ||||||
chr7:7594311 | CT | C | 111 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(108): Show |
143 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(140): Show |
intron_variant | MODIFIER | c.2044-655delT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7594311 | ||||||
chr7:7594351 | G | C | 1 | a0001c0006t0005g0240 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2044-629G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594351 | |||||||
chr7:7594374 | T | C | 3 | a0001c0004t0003g0016 a0001c0004t0003g0043 a0001c0004t0010g0253 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2044-606T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594374 | |||||||
chr7:7594383 | TGCAACTT others(2): Show |
T | 3 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 |
5 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2044-594_2044-586d others(11): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7594383 | ||||||
chr7:7594447 | A | G | 2 | a0001c0009t0011g0017 a0001c0009t0011g0048 |
3 | HG01952.hp2 HG02015.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2044-533A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594447 | |||||||
chr7:7594531 | G | C | 11 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(8): Show |
12 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.2044-449G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594531 | |||||||
chr7:7594534 | A | G | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(67): Show |
77 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.2044-446A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594534 | |||||||
chr7:7594537 | C | T | 17 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(14): Show |
20 | HG01496.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2044-443C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594537 | |||||||
chr7:7594580 | C | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG02135.hp2 NA18966.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2044-400C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594580 | |||||||
chr7:7594587 | G | A | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2044-393G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594587 | |||||||
chr7:7594636 | C | G | 1 | a0001c0006t0005g0240 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.2044-344C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594636 | |||||||
chr7:7594706 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.2044-274A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594706 | |||||||
chr7:7594862 | C | CA | 116 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(113): Show |
139 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(136): Show |
intron_variant | MODIFIER | c.2044-103dupA | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7594862 | ||||||
chr7:7594862 | C | CAA | 33 | a0001c0001t0001g0226 a0001c0001t0003g0030 a0001c0001t0003g0031 others(30): Show |
41 | HG01081.hp2 HG01109.hp2 HG01243.hp2 others(38): Show |
intron_variant | MODIFIER | c.2044-104_2044-103d others(4): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7594862 | ||||||
chr7:7594862 | C | CAAA | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(105): Show |
140 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(137): Show |
intron_variant | MODIFIER | c.2044-105_2044-103d others(5): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | INFO_REALIGN_3_PRIME | chr7 | 7594862 | ||||||
chr7:7594900 | C | T | 1 | a0001c0002t0001g0111 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.2044-80C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594900 | |||||||
chr7:7594950 | C | G | 5 | a0001c0001t0003g0030 a0001c0001t0003g0217 a0001c0001t0003g0218 others(2): Show |
6 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2044-30C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 9/12 | chr7 | 7594950 | |||||||
chr7:7595141 | A | G | 3 | a0001c0001t0003g0031 a0001c0013t0003g0238 a0004c0014t0003g0031 |
3 | HG01891.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2196+9A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595141 | |||||||
chr7:7595230 | A | C | 1 | a0001c0001t0001g0239 | 1 | NA19054.hp2 | intron_variant | MODIFIER | c.2196+98A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595230 | |||||||
chr7:7595248 | T | C | 1 | a0001c0001t0001g0091 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.2196+116T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595248 | |||||||
chr7:7595305 | A | G | 17 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(14): Show |
19 | HG01952.hp2 HG02015.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.2196+173A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595305 | |||||||
chr7:7595317 | G | C | 8 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0009g0014 others(5): Show |
15 | HG01109.hp2 HG01243.hp2 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2196+185G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595317 | |||||||
chr7:7595331 | C | A | 2 | a0001c0001t0001g0131 a0001c0001t0001g0144 |
2 | NA18961.hp2 NA19072.hp1 |
intron_variant | MODIFIER | c.2196+199C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595331 | |||||||
chr7:7595390 | G | T | 3 | a0001c0001t0001g0028 a0001c0001t0001g0179 a0001c0001t0001g0180 |
4 | NA18975.hp1 NA19080.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.2196+258G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595390 | |||||||
chr7:7595465 | G | A | 5 | a0001c0001t0008g0216 a0001c0001t0008g0221 a0001c0001t0008g0222 others(2): Show |
5 | HG01081.hp2 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2196+333G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595465 | |||||||
chr7:7595533 | T | C | 5 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 others(2): Show |
7 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2196+401T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595533 | |||||||
chr7:7595586 | C | T | 16 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(13): Show |
17 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2196+454C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595586 | |||||||
chr7:7595699 | C | G | 22 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(19): Show |
25 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(22): Show |
intron_variant | MODIFIER | c.2197-558C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595699 | |||||||
chr7:7595845 | A | T | 1 | a0001c0001t0001g0133 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2197-412A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595845 | |||||||
chr7:7595846 | G | T | 70 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(67): Show |
77 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(74): Show |
intron_variant | MODIFIER | c.2197-411G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595846 | |||||||
chr7:7595946 | A | G | 3 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 |
5 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2197-311A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595946 | |||||||
chr7:7595969 | A | G | 5 | a0001c0001t0003g0030 a0001c0001t0003g0217 a0001c0001t0003g0218 others(2): Show |
6 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2197-288A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7595969 | |||||||
chr7:7596069 | A | G | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(115): Show |
155 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.2197-188A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7596069 | |||||||
chr7:7596124 | G | A | 16 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(13): Show |
17 | HG01081.hp2 HG01496.hp1 HG01884.hp2 others(14): Show |
intron_variant | MODIFIER | c.2197-133G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 10/12 | chr7 | 7596124 | |||||||
chr7:7596545 | T | G | 2 | a0001c0004t0003g0043 a0001c0004t0010g0253 |
2 | HG02257.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.2401+84T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7596545 | |||||||
chr7:7596631 | A | G | 1 | a0001c0001t0001g0178 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2401+170A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7596631 | |||||||
chr7:7596747 | C | A | 1 | a0001c0001t0001g0145 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2401+286C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7596747 | |||||||
chr7:7596756 | C | G | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(69): Show |
81 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.2401+295C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7596756 | |||||||
chr7:7596803 | G | C | 11 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(8): Show |
12 | HG01496.hp1 HG01891.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.2401+342G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7596803 | |||||||
chr7:7596845 | C | T | 3 | a0001c0001t0001g0164 a0001c0001t0001g0168 a0001c0001t0001g0169 |
3 | HG02135.hp2 NA18966.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.2401+384C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7596845 | |||||||
chr7:7596861 | T | C | 3 | a0001c0001t0009g0014 a0001c0001t0009g0184 a0001c0001t0009g0185 |
5 | HG01109.hp2 HG02572.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.2401+400T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7596861 | |||||||
chr7:7596900 | T | C | 1 | a0001c0002t0015g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2401+439T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7596900 | |||||||
chr7:7596935 | C | T | 2 | a0001c0001t0001g0191 a0001c0001t0001g0194 |
2 | NA18969.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.2401+474C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7596935 | |||||||
chr7:7597039 | T | A | 2 | a0001c0001t0012g0044 a0001c0001t0012g0045 |
2 | HG01243.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.2401+578T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597039 | |||||||
chr7:7597109 | A | G | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.2401+648A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597109 | |||||||
chr7:7597153 | C | T | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2401+692C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597153 | |||||||
chr7:7597207 | T | C | 5 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 others(2): Show |
7 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2401+746T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597207 | |||||||
chr7:7597251 | G | A | 1 | a0001c0001t0001g0146 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.2401+790G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597251 | |||||||
chr7:7597265 | G | T | 1 | a0001c0001t0001g0145 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.2401+804G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597265 | |||||||
chr7:7597270 | G | A | 6 | a0001c0001t0001g0007 a0001c0001t0001g0147 a0001c0001t0001g0164 others(3): Show |
9 | HG02027.hp2 HG02135.hp2 NA18948.hp2 others(6): Show |
intron_variant | MODIFIER | c.2401+809G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597270 | |||||||
chr7:7597281 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.2401+820A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597281 | |||||||
chr7:7597289 | G | A | 1 | a0001c0001t0001g0162 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.2401+828G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597289 | |||||||
chr7:7597331 | TA | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(69): Show |
81 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.2401+882delA | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597331 | ||||||
chr7:7597331 | TAA | T | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(151): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.2401+881_2401+882d others(4): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597331 | ||||||
chr7:7597345 | G | T | 2 | a0001c0001t0003g0031 a0004c0014t0003g0031 |
2 | HG01891.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2401+884G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597345 | |||||||
chr7:7597444 | C | A | 1 | a0001c0003t0002g0019 | 2 | NA18983.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.2401+983C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597444 | |||||||
chr7:7597449 | T | A | 8 | a0001c0001t0003g0030 a0001c0001t0003g0217 a0001c0001t0003g0218 others(5): Show |
9 | HG01496.hp1 HG01891.hp1 HG02055.hp2 others(6): Show |
intron_variant | MODIFIER | c.2401+988T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597449 | |||||||
chr7:7597467 | TTTATATA others(4): Show |
T | 1 | a0001c0005t0002g0053 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2401+1008_2401+101 others(15): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597467 | ||||||
chr7:7597468 | TTA | T | 15 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0012 others(12): Show |
21 | HG00621.hp1 HG01106.hp2 HG01109.hp2 others(18): Show |
intron_variant | MODIFIER | c.2401+1055_2401+105 others(6): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597468 | TTATA | T | 12 | a0001c0001t0001g0001 a0001c0001t0001g0007 a0001c0001t0001g0040 others(9): Show |
12 | HG01069.hp2 HG01255.hp1 HG02109.hp2 others(9): Show |
intron_variant | MODIFIER | c.2401+1053_2401+105 others(8): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597468 | TTATATA | T | 11 | a0001c0001t0001g0128 a0001c0001t0001g0129 a0001c0001t0001g0139 others(8): Show |
13 | HG00544.hp1 HG00673.hp2 HG01243.hp1 others(10): Show |
intron_variant | MODIFIER | c.2401+1051_2401+105 others(10): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597468 | TTATATAT others(1): Show |
T | 12 | a0001c0001t0001g0001 a0001c0001t0006g0003 a0001c0001t0012g0047 others(9): Show |
12 | HG00673.hp1 HG00741.hp1 HG01346.hp2 others(9): Show |
intron_variant | MODIFIER | c.2401+1049_2401+105 others(12): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597468 | TTATATAT others(3): Show |
T | 8 | a0001c0001t0003g0031 a0001c0001t0006g0003 a0001c0003t0007g0034 others(5): Show |
8 | HG01891.hp2 HG02055.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.2401+1047_2401+105 others(14): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597468 | TTATATAT others(5): Show |
T | 24 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0012g0044 others(21): Show |
36 | HG00639.hp1 HG00733.hp2 HG01109.hp1 others(33): Show |
intron_variant | MODIFIER | c.2401+1045_2401+105 others(16): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597468 | TTATATAT others(7): Show |
T | 2 | a0001c0001t0001g0165 a0001c0002t0015g0233 |
2 | HG03669.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.2401+1043_2401+105 others(18): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597468 | TTATATAT others(11): Show |
T | 1 | a0001c0001t0001g0203 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2401+1039_2401+105 others(22): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597468 | TTATATAT others(17): Show |
T | 3 | a0001c0001t0003g0235 a0001c0001t0003g0236 a0001c0001t0003g0237 |
3 | HG01496.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2401+1033_2401+105 others(28): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597468 | TTATATAT others(21): Show |
T | 3 | a0001c0004t0003g0016 a0001c0004t0003g0043 a0001c0004t0010g0253 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2401+1029_2401+105 others(32): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597468 | TTATATAT others(23): Show |
T | 2 | a0001c0001t0001g0132 a0001c0001t0001g0134 |
2 | NA18974.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.2401+1027_2401+105 others(34): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597468 | TTATATAT others(25): Show |
T | 3 | a0001c0001t0001g0001 a0001c0009t0011g0017 a0001c0009t0011g0048 |
4 | HG01192.hp1 HG01952.hp2 HG02015.hp1 others(1): Show |
intron_variant | MODIFIER | c.2401+1025_2401+105 others(36): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597468 | TTATATAT others(29): Show |
T | 4 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2401+1021_2401+105 others(40): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597468 | ||||||
chr7:7597479 | T | A | 71 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(68): Show |
80 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.2401+1018T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597479 | |||||||
chr7:7597497 | T | A | 1 | a0001c0002t0004g0070 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2401+1036T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597497 | |||||||
chr7:7597511 | T | A | 1 | a0001c0003t0002g0052 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.2401+1050T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597511 | |||||||
chr7:7597513 | T | A | 4 | a0001c0001t0001g0005 a0001c0002t0001g0005 a0001c0002t0019g0092 others(1): Show |
6 | HG02698.hp2 HG03942.hp1 HG04199.hp1 others(3): Show |
intron_variant | MODIFIER | c.2401+1052T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597513 | |||||||
chr7:7597515 | T | A | 96 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(93): Show |
129 | HG00544.hp1 HG00621.hp1 HG00639.hp1 others(126): Show |
intron_variant | MODIFIER | c.2401+1054T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597515 | |||||||
chr7:7597515 | T | TAA | 14 | a0001c0001t0001g0032 a0001c0001t0001g0137 a0001c0001t0001g0151 others(11): Show |
15 | HG00140.hp2 HG00733.hp1 HG01496.hp2 others(12): Show |
intron_variant | MODIFIER | c.2401+1055_2401+105 others(6): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7597515 | ||||||
chr7:7597517 | T | A | 115 | a0001c0001t0001g0001 a0001c0001t0001g0005 a0001c0001t0001g0007 others(112): Show |
154 | HG00140.hp2 HG00544.hp1 HG00621.hp1 others(151): Show |
intron_variant | MODIFIER | c.2401+1056T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TAAAA | 11 | a0001c0001t0001g0024 a0001c0001t0001g0027 a0001c0001t0001g0033 others(8): Show |
14 | HG00280.hp1 HG00323.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(8): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATAAAA | 12 | a0001c0001t0001g0025 a0001c0001t0001g0136 a0001c0001t0001g0147 others(9): Show |
15 | HG01070.hp1 HG02004.hp2 HG02027.hp2 others(12): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(10): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATAAA others(1): Show |
11 | a0001c0001t0001g0004 a0001c0001t0001g0023 a0001c0001t0001g0028 others(8): Show |
17 | HG00642.hp2 HG01167.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(12): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATAAA others(3): Show |
4 | a0001c0001t0001g0013 a0001c0001t0001g0093 a0001c0001t0001g0177 others(1): Show |
6 | HG02080.hp1 NA19002.hp2 NA19007.hp1 others(3): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(14): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(3): Show |
6 | a0001c0001t0001g0026 a0001c0001t0001g0133 a0001c0001t0003g0218 others(3): Show |
8 | HG00140.hp1 HG00323.hp2 HG02055.hp2 others(5): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(14): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(5): Show |
10 | a0001c0001t0001g0062 a0001c0001t0001g0089 a0001c0001t0001g0095 others(7): Show |
11 | HG01070.hp2 HG01981.hp1 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(16): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(5): Show |
12 | a0001c0001t0001g0039 a0001c0001t0001g0154 a0001c0001t0001g0155 others(9): Show |
13 | HG00438.hp1 HG00741.hp2 HG01884.hp1 others(10): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(16): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(7): Show |
9 | a0001c0001t0001g0006 a0001c0001t0001g0091 a0001c0001t0001g0097 others(6): Show |
11 | HG00280.hp2 HG00438.hp2 HG01255.hp2 others(8): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(18): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(7): Show |
10 | a0001c0001t0001g0011 a0001c0001t0001g0156 a0001c0001t0001g0189 others(7): Show |
12 | HG00735.hp1 HG00735.hp2 HG01069.hp1 others(9): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(18): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(9): Show |
9 | a0001c0001t0001g0010 a0001c0001t0001g0098 a0001c0002t0001g0073 others(6): Show |
10 | HG00544.hp2 HG02129.hp1 HG04184.hp1 others(7): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(20): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(9): Show |
4 | a0001c0001t0001g0163 a0001c0001t0008g0222 a0001c0001t0008g0224 others(1): Show |
4 | HG01081.hp2 HG02970.hp1 NA18968.hp2 others(1): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(20): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(11): Show |
9 | a0001c0001t0001g0090 a0001c0001t0001g0099 a0001c0001t0014g0022 others(6): Show |
9 | HG02027.hp1 HG02129.hp2 NA18906.hp2 others(6): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(22): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(11): Show |
4 | a0001c0001t0001g0124 a0001c0001t0001g0179 a0001c0002t0001g0066 others(1): Show |
4 | HG01123.hp2 NA18906.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(22): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(12): Show |
1 | a0001c0002t0001g0065 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2401+1056_2401+105 others(23): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(13): Show |
8 | a0001c0001t0001g0101 a0001c0002t0001g0082 a0001c0002t0001g0085 others(5): Show |
9 | HG01978.hp1 HG02257.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(24): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(13): Show |
4 | a0001c0001t0001g0127 a0001c0001t0001g0166 a0001c0001t0001g0180 others(1): Show |
4 | HG01257.hp1 HG03704.hp1 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(24): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(15): Show |
5 | a0001c0001t0001g0113 a0001c0002t0001g0067 a0001c0002t0001g0081 others(2): Show |
5 | HG01256.hp2 HG02004.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(26): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(17): Show |
1 | a0001c0002t0001g0088 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2401+1056_2401+105 others(28): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(17): Show |
5 | a0001c0001t0001g0103 a0001c0001t0001g0109 a0001c0001t0001g0120 others(2): Show |
5 | HG01106.hp1 HG03239.hp1 NA18975.hp2 others(2): Show |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(28): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(19): Show |
2 | a0001c0001t0001g0104 a0001c0001t0020g0072 |
2 | NA18948.hp1 NA18951.hp1 |
intron_variant | MODIFIER | c.2401+1056_2401+105 others(30): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(19): Show |
1 | a0001c0001t0001g0193 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2401+1056_2401+105 others(30): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597517 | T | TATATATA others(21): Show |
1 | a0001c0001t0001g0143 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.2401+1056_2401+105 others(32): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597517 | |||||||
chr7:7597573 | C | G | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2401+1112C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597573 | |||||||
chr7:7597622 | T | A | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.2401+1161T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597622 | |||||||
chr7:7597666 | A | T | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2401+1205A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597666 | |||||||
chr7:7597679 | C | G | 1 | a0001c0002t0001g0096 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2401+1218C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597679 | |||||||
chr7:7597693 | G | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2401+1232G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597693 | |||||||
chr7:7597804 | C | T | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2401+1343C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597804 | |||||||
chr7:7597827 | C | T | 1 | a0003c0015t0003g0220 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2401+1366C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597827 | |||||||
chr7:7597839 | A | G | 3 | a0001c0001t0003g0031 a0001c0013t0003g0238 a0004c0014t0003g0031 |
3 | HG01891.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2401+1378A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597839 | |||||||
chr7:7597873 | C | A | 1 | a0001c0002t0029g0247 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2401+1412C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597873 | |||||||
chr7:7597903 | G | T | 10 | a0001c0001t0001g0028 a0001c0001t0001g0156 a0001c0001t0001g0189 others(7): Show |
11 | HG00735.hp1 HG00741.hp2 HG01069.hp1 others(8): Show |
intron_variant | MODIFIER | c.2401+1442G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7597903 | |||||||
chr7:7598010 | T | C | 2 | a0001c0009t0011g0017 a0001c0009t0011g0048 |
3 | HG01952.hp2 HG02015.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2401+1549T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598010 | |||||||
chr7:7598099 | A | G | 1 | a0001c0001t0001g0152 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.2401+1638A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598099 | |||||||
chr7:7598164 | G | A | 1 | a0001c0002t0001g0076 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.2401+1703G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598164 | |||||||
chr7:7598259 | C | T | 1 | a0001c0001t0001g0139 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.2401+1798C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598259 | |||||||
chr7:7598304 | A | T | 1 | a0001c0001t0012g0047 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2401+1843A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598304 | |||||||
chr7:7598351 | C | T | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2401+1890C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598351 | |||||||
chr7:7598386 | C | T | 5 | a0001c0003t0002g0002 a0001c0003t0002g0019 a0001c0003t0002g0057 others(2): Show |
12 | NA18612.hp1 NA18957.hp2 NA18960.hp1 others(9): Show |
intron_variant | MODIFIER | c.2401+1925C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598386 | |||||||
chr7:7598574 | A | ACAGACAT others(31): Show |
3 | a0001c0004t0003g0016 a0001c0004t0003g0043 a0001c0004t0010g0253 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2401+2113_2401+211 others(42): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598574 | |||||||
chr7:7598584 | C | T | 3 | a0001c0001t0003g0235 a0001c0001t0003g0236 a0001c0001t0003g0237 |
3 | HG01496.hp1 HG03579.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.2401+2123C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598584 | |||||||
chr7:7598608 | G | A | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2401+2147G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598608 | |||||||
chr7:7598662 | T | G | 3 | a0002c0010t0018g0041 a0002c0010t0018g0042 a0003c0015t0003g0220 |
3 | HG02895.hp1 HG02976.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2401+2201T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598662 | |||||||
chr7:7598752 | C | G | 3 | a0001c0004t0003g0016 a0001c0004t0003g0043 a0001c0004t0010g0253 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2401+2291C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598752 | |||||||
chr7:7598785 | A | C | 1 | a0001c0001t0001g0160 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.2401+2324A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598785 | |||||||
chr7:7598838 | T | C | 1 | a0001c0001t0001g0172 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2401+2377T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598838 | |||||||
chr7:7598936 | T | C | 1 | a0001c0002t0001g0094 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.2401+2475T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598936 | |||||||
chr7:7598944 | A | G | 1 | a0001c0001t0001g0194 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.2401+2483A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7598944 | |||||||
chr7:7599086 | C | A | 3 | a0001c0001t0003g0031 a0001c0013t0003g0238 a0004c0014t0003g0031 |
3 | HG01891.hp2 HG03540.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.2401+2625C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599086 | |||||||
chr7:7599144 | A | G | 1 | a0001c0002t0001g0088 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.2401+2683A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599144 | |||||||
chr7:7599177 | T | G | 1 | a0001c0001t0026g0197 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2401+2716T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599177 | |||||||
chr7:7599194 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2401+2733A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599194 | |||||||
chr7:7599231 | A | G | 3 | a0001c0001t0001g0028 a0001c0001t0001g0179 a0001c0001t0001g0180 |
4 | NA18975.hp1 NA19080.hp2 NA19084.hp1 others(1): Show |
intron_variant | MODIFIER | c.2401+2770A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599231 | |||||||
chr7:7599268 | C | T | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2401+2807C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599268 | |||||||
chr7:7599290 | G | A | 1 | a0001c0002t0025g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2401+2829G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599290 | |||||||
chr7:7599347 | T | C | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2401+2886T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599347 | |||||||
chr7:7599378 | A | C | 1 | a0001c0001t0001g0101 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2401+2917A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599378 | |||||||
chr7:7599379 | C | T | 1 | a0001c0001t0001g0101 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.2401+2918C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599379 | |||||||
chr7:7599450 | T | C | 39 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0009g0014 others(36): Show |
60 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(57): Show |
intron_variant | MODIFIER | c.2401+2989T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599450 | |||||||
chr7:7599467 | G | C | 1 | a0001c0001t0001g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2401+3006G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599467 | |||||||
chr7:7599489 | G | A | 1 | a0001c0001t0001g0172 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.2401+3028G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599489 | |||||||
chr7:7599576 | T | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2401+3115T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599576 | |||||||
chr7:7599699 | G | A | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2401+3238G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599699 | |||||||
chr7:7599840 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2401+3379A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599840 | |||||||
chr7:7599846 | C | G | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2401+3385C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7599846 | |||||||
chr7:7600043 | C | G | 1 | a0001c0003t0007g0254 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2401+3582C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600043 | |||||||
chr7:7600077 | C | G | 1 | a0003c0015t0003g0220 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2401+3616C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600077 | |||||||
chr7:7600080 | G | C | 5 | a0001c0001t0008g0216 a0001c0001t0008g0221 a0001c0001t0008g0222 others(2): Show |
5 | HG01081.hp2 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2401+3619G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600080 | |||||||
chr7:7600095 | C | T | 1 | a0001c0001t0016g0121 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2401+3634C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600095 | |||||||
chr7:7600155 | C | T | 1 | a0001c0001t0001g0153 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2401+3694C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600155 | |||||||
chr7:7600200 | A | AT | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(258): Show |
324 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(321): Show |
intron_variant | MODIFIER | c.2401+3748dupT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7600200 | ||||||
chr7:7600326 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2401+3865G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600326 | |||||||
chr7:7600361 | A | C | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2401+3900A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600361 | |||||||
chr7:7600411 | C | G | 1 | a0001c0001t0001g0133 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2401+3950C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600411 | |||||||
chr7:7600479 | C | T | 11 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(8): Show |
12 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.2401+4018C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600479 | |||||||
chr7:7600522 | C | G | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2401+4061C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600522 | |||||||
chr7:7600586 | A | G | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2401+4125A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600586 | |||||||
chr7:7600595 | T | C | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(69): Show |
81 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.2401+4134T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600595 | |||||||
chr7:7600721 | T | C | 5 | a0001c0001t0003g0030 a0001c0001t0003g0217 a0001c0001t0003g0218 others(2): Show |
6 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2401+4260T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600721 | |||||||
chr7:7600881 | T | A | 2 | a0001c0001t0001g0230 a0001c0001t0001g0231 |
2 | HG00642.hp1 HG01167.hp1 |
intron_variant | MODIFIER | c.2401+4420T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600881 | |||||||
chr7:7600914 | C | A | 1 | a0001c0001t0001g0097 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.2401+4453C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600914 | |||||||
chr7:7600919 | C | A | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2401+4458C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600919 | |||||||
chr7:7600951 | G | C | 1 | a0001c0001t0003g0235 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2401+4490G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600951 | |||||||
chr7:7600974 | A | T | 1 | a0001c0001t0001g0149 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.2401+4513A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7600974 | |||||||
chr7:7601070 | G | GT | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(160): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2401+4612dupT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7601070 | ||||||
chr7:7601106 | G | A | 2 | a0001c0001t0026g0197 a0001c0002t0006g0199 |
2 | HG02451.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.2401+4645G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601106 | |||||||
chr7:7601150 | T | G | 11 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(8): Show |
12 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.2401+4689T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601150 | |||||||
chr7:7601163 | G | A | 2 | a0001c0001t0001g0182 a0001c0001t0001g0201 |
2 | NA19000.hp1 NA19006.hp2 |
intron_variant | MODIFIER | c.2401+4702G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601163 | |||||||
chr7:7601245 | C | G | 2 | a0002c0010t0018g0041 a0002c0010t0018g0042 |
2 | HG02895.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.2402-4697C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601245 | |||||||
chr7:7601293 | T | C | 3 | a0001c0001t0001g0036 a0001c0001t0001g0039 a0001c0001t0001g0040 |
3 | NA18964.hp1 NA19007.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.2402-4649T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601293 | |||||||
chr7:7601294 | G | C | 107 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(104): Show |
135 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(132): Show |
intron_variant | MODIFIER | c.2402-4648G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601294 | |||||||
chr7:7601366 | G | A | 1 | a0001c0013t0003g0238 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2402-4576G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601366 | |||||||
chr7:7601399 | G | A | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2402-4543G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601399 | |||||||
chr7:7601427 | G | A | 1 | a0001c0002t0004g0070 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.2402-4515G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601427 | |||||||
chr7:7601443 | C | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2402-4499C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601443 | |||||||
chr7:7601468 | C | G | 2 | a0001c0006t0005g0029 a0001c0006t0005g0215 |
3 | HG02735.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2402-4474C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601468 | |||||||
chr7:7601472 | A | G | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2402-4470A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601472 | |||||||
chr7:7601557 | A | C | 5 | a0001c0001t0003g0030 a0001c0001t0003g0217 a0001c0001t0003g0218 others(2): Show |
6 | HG01891.hp1 HG02055.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.2402-4385A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601557 | |||||||
chr7:7601607 | G | C | 146 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(143): Show |
195 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.2402-4335G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601607 | |||||||
chr7:7601717 | T | C | 1 | a0001c0002t0029g0247 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2402-4225T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601717 | |||||||
chr7:7601752 | TG | T | 2 | a0001c0006t0005g0029 a0001c0006t0005g0215 |
3 | HG02735.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2402-4188delG | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7601752 | ||||||
chr7:7601814 | A | G | 1 | a0001c0002t0001g0086 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2402-4128A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601814 | |||||||
chr7:7601857 | C | T | 1 | a0001c0001t0001g0135 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2402-4085C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601857 | |||||||
chr7:7601895 | C | T | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(69): Show |
81 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.2402-4047C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601895 | |||||||
chr7:7601910 | G | A | 17 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(14): Show |
20 | HG01496.hp1 HG01891.hp1 HG01891.hp2 others(17): Show |
intron_variant | MODIFIER | c.2402-4032G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601910 | |||||||
chr7:7601917 | C | T | 163 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(160): Show |
214 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.2402-4025C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601917 | |||||||
chr7:7601964 | A | C | 196 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(193): Show |
236 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(233): Show |
intron_variant | MODIFIER | c.2402-3978A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7601964 | |||||||
chr7:7602087 | C | G | 1 | a0003c0015t0003g0220 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2402-3855C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602087 | |||||||
chr7:7602111 | A | G | 1 | a0003c0015t0003g0220 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2402-3831A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602111 | |||||||
chr7:7602130 | A | G | 1 | a0001c0001t0001g0193 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2402-3812A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602130 | |||||||
chr7:7602158 | T | G | 17 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(14): Show |
19 | HG01952.hp2 HG02015.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.2402-3784T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602158 | |||||||
chr7:7602171 | G | C | 1 | a0005c0012t0004g0232 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.2402-3771G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602171 | |||||||
chr7:7602233 | A | G | 8 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(5): Show |
9 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2402-3709A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602233 | |||||||
chr7:7602253 | G | A | 3 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 |
5 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.2402-3689G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602253 | |||||||
chr7:7602328 | T | C | 2 | a0001c0009t0011g0017 a0001c0009t0011g0048 |
3 | HG01952.hp2 HG02015.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2402-3614T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602328 | |||||||
chr7:7602330 | G | T | 5 | a0001c0001t0008g0216 a0001c0001t0008g0221 a0001c0001t0008g0222 others(2): Show |
5 | HG01081.hp2 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2402-3612G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602330 | |||||||
chr7:7602435 | C | A | 4 | a0001c0005t0002g0053 a0001c0005t0002g0054 a0001c0005t0002g0055 others(1): Show |
4 | HG00733.hp2 HG01257.hp2 HG04199.hp2 others(1): Show |
intron_variant | MODIFIER | c.2402-3507C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602435 | |||||||
chr7:7602567 | A | G | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2402-3375A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602567 | |||||||
chr7:7602576 | G | C | 2 | a0001c0001t0001g0154 a0001c0001t0001g0162 |
2 | HG02647.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.2402-3366G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602576 | |||||||
chr7:7602581 | A | C | 1 | a0001c0001t0001g0027 | 2 | HG00280.hp1 HG00323.hp1 |
intron_variant | MODIFIER | c.2402-3361A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602581 | |||||||
chr7:7602597 | A | C | 72 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0010 others(69): Show |
81 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.2402-3345A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602597 | |||||||
chr7:7602600 | C | G | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2402-3342C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602600 | |||||||
chr7:7602612 | G | T | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2402-3330G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602612 | |||||||
chr7:7602670 | G | A | 17 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(14): Show |
19 | HG01952.hp2 HG02015.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.2402-3272G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602670 | |||||||
chr7:7602789 | C | T | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2402-3153C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602789 | |||||||
chr7:7602822 | C | T | 4 | a0001c0002t0001g0084 a0001c0002t0001g0085 a0001c0002t0001g0086 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2402-3120C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602822 | |||||||
chr7:7602837 | A | G | 4 | a0001c0002t0001g0084 a0001c0002t0001g0085 a0001c0002t0001g0086 others(1): Show |
4 | HG02257.hp2 HG02451.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2402-3105A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602837 | |||||||
chr7:7602889 | G | A | 29 | a0001c0001t0006g0003 a0001c0001t0006g0046 a0001c0001t0009g0014 others(26): Show |
40 | HG01109.hp2 HG01243.hp2 HG01952.hp2 others(37): Show |
intron_variant | MODIFIER | c.2402-3053G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602889 | |||||||
chr7:7602923 | A | G | 2 | a0001c0011t0017g0122 a0001c0011t0017g0123 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2402-3019A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602923 | |||||||
chr7:7602959 | A | C | 11 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(8): Show |
12 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.2402-2983A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602959 | |||||||
chr7:7602963 | A | G | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2402-2979A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7602963 | |||||||
chr7:7603074 | A | G | 1 | a0001c0001t0001g0147 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.2402-2868A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603074 | |||||||
chr7:7603093 | G | A | 1 | a0001c0004t0027g0183 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.2402-2849G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603093 | |||||||
chr7:7603107 | C | T | 1 | a0001c0001t0001g0242 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.2402-2835C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603107 | |||||||
chr7:7603131 | A | G | 1 | a0001c0005t0002g0055 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.2402-2811A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603131 | |||||||
chr7:7603131 | A | T | 1 | a0001c0002t0031g0252 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.2402-2811A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603131 | |||||||
chr7:7603200 | C | A | 4 | a0001c0002t0001g0065 a0001c0002t0001g0066 a0001c0002t0001g0067 others(1): Show |
4 | NA18961.hp1 NA18963.hp2 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.2402-2742C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603200 | |||||||
chr7:7603203 | A | G | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2402-2739A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603203 | |||||||
chr7:7603247 | G | T | 1 | a0001c0002t0025g0060 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.2402-2695G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603247 | |||||||
chr7:7603303 | T | C | 1 | a0001c0003t0002g0058 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2402-2639T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603303 | |||||||
chr7:7603304 | G | A | 1 | a0001c0003t0002g0058 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2402-2638G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603304 | |||||||
chr7:7603341 | G | T | 1 | a0001c0013t0003g0238 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2402-2601G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603341 | |||||||
chr7:7603354 | G | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.2402-2588G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603354 | |||||||
chr7:7603410 | C | G | 135 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(132): Show |
168 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.2402-2532C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603410 | |||||||
chr7:7603486 | GA | G | 44 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(41): Show |
58 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(55): Show |
intron_variant | MODIFIER | c.2402-2453delA | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7603486 | ||||||
chr7:7603525 | C | G | 3 | a0001c0002t0006g0198 a0001c0002t0006g0199 a0001c0002t0023g0200 |
3 | HG02615.hp2 HG02886.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.2402-2417C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603525 | |||||||
chr7:7603531 | A | G | 3 | a0001c0004t0003g0016 a0001c0004t0003g0043 a0001c0004t0010g0253 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2402-2411A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603531 | |||||||
chr7:7603539 | G | A | 6 | a0001c0001t0001g0037 a0001c0002t0006g0198 a0001c0002t0006g0199 others(3): Show |
7 | HG01952.hp2 HG02015.hp1 HG02293.hp1 others(4): Show |
intron_variant | MODIFIER | c.2402-2403G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603539 | |||||||
chr7:7603567 | T | G | 1 | a0001c0001t0001g0133 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.2402-2375T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603567 | |||||||
chr7:7603574 | G | C | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2402-2368G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603574 | |||||||
chr7:7603579 | T | C | 4 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2402-2363T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603579 | |||||||
chr7:7603635 | A | G | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2402-2307A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603635 | |||||||
chr7:7603655 | G | A | 1 | a0001c0002t0028g0261 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2402-2287G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603655 | |||||||
chr7:7603701 | T | G | 2 | a0001c0011t0017g0122 a0001c0011t0017g0123 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2402-2241T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603701 | |||||||
chr7:7603817 | A | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.2402-2125A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603817 | |||||||
chr7:7603887 | AAAT | A | 17 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(14): Show |
19 | HG01952.hp2 HG02015.hp1 HG02132.hp2 others(16): Show |
intron_variant | MODIFIER | c.2402-2054_2402-205 others(7): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603887 | |||||||
chr7:7603950 | A | G | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(109): Show |
142 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(139): Show |
intron_variant | MODIFIER | c.2402-1992A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603950 | |||||||
chr7:7603953 | A | G | 4 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2402-1989A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603953 | |||||||
chr7:7603978 | C | T | 3 | a0001c0004t0003g0016 a0001c0004t0003g0043 a0001c0004t0010g0253 |
5 | HG02257.hp1 HG02559.hp2 HG02572.hp1 others(2): Show |
intron_variant | MODIFIER | c.2402-1964C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7603978 | |||||||
chr7:7604052 | C | T | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2402-1890C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604052 | |||||||
chr7:7604071 | C | G | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.2402-1871C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604071 | |||||||
chr7:7604075 | G | GA | 3 | a0001c0001t0001g0174 a0001c0001t0008g0224 a0001c0002t0001g0073 |
3 | HG02970.hp1 HG03516.hp2 NA18997.hp1 |
intron_variant | MODIFIER | c.2402-1865dupA | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7604075 | ||||||
chr7:7604102 | A | T | 1 | a0001c0002t0029g0247 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2402-1840A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604102 | |||||||
chr7:7604180 | G | A | 2 | a0001c0001t0001g0013 a0001c0001t0001g0177 |
4 | NA19007.hp1 NA19011.hp2 NA19068.hp1 others(1): Show |
intron_variant | MODIFIER | c.2402-1762G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604180 | |||||||
chr7:7604200 | A | C | 1 | a0001c0001t0001g0148 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.2402-1742A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604200 | |||||||
chr7:7604221 | T | A | 17 | a0001c0001t0001g0032 a0001c0001t0001g0033 a0001c0001t0001g0137 others(14): Show |
19 | HG00140.hp2 HG00544.hp1 HG00642.hp1 others(16): Show |
intron_variant | MODIFIER | c.2402-1721T>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604221 | |||||||
chr7:7604224 | A | G | 8 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(5): Show |
9 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(6): Show |
intron_variant | MODIFIER | c.2402-1718A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604224 | |||||||
chr7:7604359 | G | C | 257 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(254): Show |
320 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(317): Show |
intron_variant | MODIFIER | c.2402-1583G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604359 | |||||||
chr7:7604498 | A | G | 1 | a0001c0001t0001g0120 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2402-1444A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604498 | |||||||
chr7:7604504 | AAGAAG | A | 5 | a0001c0001t0008g0216 a0001c0001t0008g0221 a0001c0001t0008g0222 others(2): Show |
5 | HG01081.hp2 HG01884.hp2 HG02145.hp1 others(2): Show |
intron_variant | MODIFIER | c.2402-1436_2402-143 others(9): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7604504 | ||||||
chr7:7604509 | G | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(249): Show |
315 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(312): Show |
intron_variant | MODIFIER | c.2402-1433G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604509 | |||||||
chr7:7604523 | C | T | 1 | a0001c0002t0006g0199 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2402-1419C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604523 | |||||||
chr7:7604651 | T | C | 4 | a0001c0001t0026g0197 a0001c0002t0006g0198 a0001c0002t0006g0199 others(1): Show |
4 | HG02451.hp1 HG02615.hp2 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.2402-1291T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604651 | |||||||
chr7:7604735 | G | C | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2402-1207G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604735 | |||||||
chr7:7604773 | A | G | 1 | a0001c0008t0005g0213 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2402-1169A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604773 | |||||||
chr7:7604859 | A | T | 1 | a0001c0001t0001g0141 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.2402-1083A>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604859 | |||||||
chr7:7604882 | C | T | 1 | a0001c0003t0002g0057 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2402-1060C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604882 | |||||||
chr7:7604894 | ATATTT | A | 5 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 others(2): Show |
7 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2402-1042_2402-103 others(9): Show |
MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7604894 | ||||||
chr7:7604947 | T | G | 1 | a0001c0002t0015g0130 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2402-995T>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7604947 | |||||||
chr7:7605026 | C | G | 1 | a0001c0009t0011g0048 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2402-916C>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605026 | |||||||
chr7:7605077 | C | A | 2 | a0001c0011t0017g0122 a0001c0011t0017g0123 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2402-865C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605077 | |||||||
chr7:7605094 | G | A | 1 | a0001c0001t0006g0046 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.2402-848G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605094 | |||||||
chr7:7605139 | G | A | 1 | a0001c0007t0030g0248 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.2402-803G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605139 | |||||||
chr7:7605215 | C | T | 2 | a0001c0004t0003g0016 a0001c0004t0010g0253 |
4 | HG02257.hp1 HG02559.hp2 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.2402-727C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605215 | |||||||
chr7:7605260 | G | A | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2402-682G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605260 | |||||||
chr7:7605297 | A | AT | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(121): Show |
163 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(160): Show |
intron_variant | MODIFIER | c.2402-630dupT | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr7 | 7605297 | ||||||
chr7:7605372 | G | T | 2 | a0001c0009t0011g0017 a0001c0009t0011g0048 |
3 | HG01952.hp2 HG02015.hp1 HG02293.hp1 |
intron_variant | MODIFIER | c.2402-570G>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605372 | |||||||
chr7:7605417 | C | T | 11 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(8): Show |
12 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.2402-525C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605417 | |||||||
chr7:7605456 | G | C | 1 | a0001c0001t0001g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2402-486G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605456 | |||||||
chr7:7605457 | G | C | 1 | a0001c0001t0001g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2402-485G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605457 | |||||||
chr7:7605553 | C | T | 27 | a0001c0002t0022g0119 a0001c0002t0025g0060 a0001c0003t0002g0002 others(24): Show |
39 | HG00733.hp2 HG00741.hp1 HG01109.hp1 others(36): Show |
intron_variant | MODIFIER | c.2402-389C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605553 | |||||||
chr7:7605585 | A | C | 1 | a0001c0001t0001g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2402-357A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605585 | |||||||
chr7:7605586 | C | A | 1 | a0001c0001t0001g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2402-356C>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605586 | |||||||
chr7:7605587 | A | C | 1 | a0001c0001t0001g0165 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.2402-355A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605587 | |||||||
chr7:7605661 | A | G | 1 | a0001c0003t0007g0034 | 2 | HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2402-281A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605661 | |||||||
chr7:7605689 | C | T | 5 | a0001c0004t0001g0015 a0001c0004t0001g0186 a0001c0004t0001g0187 others(2): Show |
7 | HG02647.hp2 HG02809.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.2402-253C>T | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605689 | |||||||
chr7:7605788 | T | C | 2 | a0001c0011t0017g0122 a0001c0011t0017g0123 |
2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.2402-154T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605788 | |||||||
chr7:7605836 | G | C | 1 | a0003c0015t0003g0220 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2402-106G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605836 | |||||||
chr7:7605904 | A | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(259): Show |
325 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(322): Show |
intron_variant | MODIFIER | c.2402-38A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605904 | |||||||
chr7:7605910 | T | C | 11 | a0001c0006t0005g0029 a0001c0006t0005g0210 a0001c0006t0005g0211 others(8): Show |
12 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(9): Show |
intron_variant | MODIFIER | c.2402-32T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 11/12 | chr7 | 7605910 | |||||||
chr7:7606112 | G | A | 1 | a0001c0001t0001g0207 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.2531+41G>A | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 12/12 | chr7 | 7606112 | |||||||
chr7:7606153 | A | G | 1 | a0001c0001t0001g0181 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2531+82A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 12/12 | chr7 | 7606153 | |||||||
chr7:7606175 | A | G | 136 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0007 others(133): Show |
176 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.2531+104A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 12/12 | chr7 | 7606175 | |||||||
chr7:7606278 | A | G | 5 | a0001c0002t0001g0083 a0001c0002t0001g0084 a0001c0002t0001g0085 others(2): Show |
5 | HG02257.hp2 HG02451.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2531+207A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 12/12 | chr7 | 7606278 | |||||||
chr7:7606396 | A | C | 15 | a0001c0001t0003g0030 a0001c0001t0003g0031 a0001c0001t0003g0217 others(12): Show |
16 | HG01109.hp2 HG01496.hp1 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.2531+325A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 12/12 | chr7 | 7606396 | |||||||
chr7:7606468 | A | G | 2 | a0001c0006t0005g0029 a0001c0006t0005g0215 |
3 | HG02735.hp2 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.2531+397A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 12/12 | chr7 | 7606468 | |||||||
chr7:7606483 | A | C | 1 | a0001c0002t0022g0119 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.2531+412A>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 12/12 | chr7 | 7606483 | |||||||
chr7:7606535 | T | C | 1 | a0001c0001t0001g0144 | 1 | NA18961.hp2 | intron_variant | MODIFIER | c.2532-461T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 12/12 | chr7 | 7606535 | |||||||
chr7:7606553 | T | C | 9 | a0001c0002t0015g0233 a0001c0006t0005g0029 a0001c0006t0005g0210 others(6): Show |
10 | HG02132.hp2 HG02486.hp1 HG02735.hp2 others(7): Show |
intron_variant | MODIFIER | c.2532-443T>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 12/12 | chr7 | 7606553 | |||||||
chr7:7606710 | G | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(255): Show |
321 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(318): Show |
intron_variant | MODIFIER | c.2532-286G>C | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 12/12 | chr7 | 7606710 | |||||||
chr7:7606742 | A | G | 259 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0005 others(256): Show |
322 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(319): Show |
intron_variant | MODIFIER | c.2532-254A>G | MIOS | ENSG00000164654.16 | transcript | ENST00000340080.9 | protein_coding | 12/12 | chr7 | 7606742 |